Lisbon Other11 Job Listings - OK

Browse

Antiques & Collectibles

Baby & Kids Items

Books · Movies & Music

Garden & Outdoor

Health & Beauty

Musical Instruments

Office Supplies

Agriculture & Industry

Building Materials

Property For Sale

Property For Rent

Domestic services

Information technology

Transport/Moves

Professionals Liberals

Activities & Groups

Artists & Musicians

Classes & Lessons

Friendship & Networking

Skills & Language Swap

Travel & Travel Partners

Administration Office Support

Advertising Arts Media

Banking Financial Services

Call Center Customer Service

Ceo General Management

Community Services Dev

Consulting Strategy

Design Architecture

Education Training

Farming Animals Conservation

Government Defense

Healthcare Medical

Hospitality Tourism

Human Resources Recruitment

Info Comm Technology

Mfg Transport Logistics

Marketing Communications1

Mining Resources Energy

Real Estate Property

Retail Consumer Products

Science Technology

Self Employment1

Sport Recreation

Trades Services

···

Log in / Register

Other11 in Lisbon

Best Match

Filter·1

Other11

Lisbon

Salary

Job Type

Workplace type

Unit

Location:Lisbon

Category:Other11

Sr Project Manager, RWLP ** open to several EMEA locations **64705443042561120

Sr Project Manager, RWLP ** open to several EMEA locations **

**Description** Sr Project Manager, RWLP \*\* open to several EMEA locations \*\* Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** Project Leadership and Delivery: * Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP’s, and regulatory requirements. * Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer’s and the Company’s contractual agreement. * Lead project team to ensure quality, timelines and budget management. * Accountable for the financial performance of each project. * Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues. * Ensure studies are conducted in compliance with GCP, relevant SOP’s and regulatory requirements. * Accountable for all project deliverables for each project assigned. Documentation and Reporting: * Responsible for quality and completeness of TMF for assigned projects. * Accountable for maintenance of study information on a variety of databases and systems. * Responsible for study management components of inspection readiness for all aspects of the study conduct. * Oversight for development and implementation of project plans. * Plan, coordinate and present at internal and external meetings. * Prepare project management reports for clients and management. * Developing contingency planning and risk mitigation strategies to ensure successful delivery of study goals. Business Development: * Develops strong relationships with current clients to generate new and/or add\-on business for the future. * May participate in bid defense meetings where presented as potential project manager. Management: * May be required to line manage other project management team members and clinical monitoring staff. **QUALIFICATION REQUIREMENTS;** * Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience. * Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements * **Prior experience as Project Manager in a CRO environment is required.** * **Prior experience in Phase IV is a plus.** * Strong organizational skills. * Strong ability to manage time and work independently. * Direct therapeutic area expertise. * Ability to embrace new technologies. * Excellent communication, presentation, interpersonal skills, both written and spoken. * Ability to travel as necessary (approximately 25%). **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Av. João Crisóstomo 57, 1050-126 Lisboa, Portugal

Medical Editor - II (Formatting Regulatory Documents) - Home Based64694284691713121

Medical Editor - II (Formatting Regulatory Documents) - Home Based

**Description** Medical Editor \- II (Formatting Regulatory Documents) \- Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** **Roles and Responsibilities:** * Defines scope of formatting of clinical and regulatory documents with the document author. Coordinates and track activities and perform detailed quality reviews. Import and route documents in the regulatory information management systems (RIMS). * Ensure document format and styles are consistent with the defined in RIMS and are consistent with the clinical and regulatory templates. Ensure document properties and naming conventions are used. Maintain strong knowledge of RIMS styes and formatting standards. * Effectively communicates deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills. * Effectively attends to multiple tasks within overlapping timeframes; builds positive and productive relationships that enable high quality documents to be completed on time. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for ensuring the quality of clinical and regulatory documents are formatted to the requirements in the AbbVie style guide and document templates.

Av. João Crisóstomo 57, 1050-126 Lisboa, Portugal

Manager, Medical Writing - Regulatory64616285094018122

Manager, Medical Writing - Regulatory

**Description** Manager, Medical Writing \- Regulatory Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Project\-specific management responsibilities for medical writing staff members. Recommends courses of action on salary administration, interviewing and selection, terminations, professional development, performance appraisals, job description preparation, and employee counseling. Works with and advises staff on administrative policies and procedures, technical problems, priorities, and methods. * Reviews and edits departmental work products for completeness, accuracy, and overall quality; assumes responsibility for quality of departmental work products. * Ensures adherence to Sponsor objectives and that quality standards are maintained. * Supports the company’s MW leadership team in the planning, development and implementation of document development strategies and development and presentation of quarterly business updates. * Assists with the preparation of budgets and timelines for medical writing activities (full\-service clinical development projects and stand\-alone medical writing projects) as needed. * Assists with budgeting, revenue, invoicing, and forecasting as requested. * Assists with budgeting, revenue, invoicing, and forecasting as requested. * Contributes to departmental metrics by assisting in the tracking, maintaining and reviewing project metrics. * Supports business development by assisting with proposal and costing development as well as bid defenses and customer meetings. * Builds and maintain relationships with internal and external customers. * Forms, maintains and leads productive cross\-functional working teams, including addressing issues that arise. * Reviews performance of medical writing personnel (direct reports). * Develops and maintains departmental SOPs and templates and acts as resource for implementation. * Participates in the planning, writing, and assembly of medical writing deliverables, as needed. * Performs senior reviews of medical writing deliverables, as well as reviews of statistical analysis plans and table/figure/listing. * Performs other work\-related duties as assigned. Minimal travel may be required (up to 25%). **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Responsible for the task\-specific supervision of the medical writing staff members. Coordinates resources and medical writing activities to ensure that medical writing deliverables are high\-quality, clear and accurate, and meet regulatory standards, customer needs, and internal requirements.

Av. João Crisóstomo 57, 1050-126 Lisboa, Portugal

Meeting and Contracting Capability Manager64411760722947123

Meeting and Contracting Capability Manager

Join our team at **AMGEN Capability Center Portugal**, number 1 company in Best Workplaces \- https://www.greatplacetowork.pt/ \- ranking in Portugal in 2024 (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 500 talented people and more than 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **Meeting and Contracting Capability Manager** **LIVE** **WHAT YOU WILL DO** The Meeting and Contracting Capability Manager is accountable for efficiently managing daily meetings and providing contracting support across various functions at Amgen. Their responsibilities include coordinating logistics for both internal and external events organized by Amgen, engaging with agencies, managing contracts, overseeing the lifecycle of purchase orders (POs), facilitating contracts for Healthcare Professionals, and supporting processes related to sponsorships, fees for services, donations, and education. They also align with the continuous improvement agenda of the ACCP. They will lead a team responsible for executing day\-to\-day support across various functions at Amgen. Additional responsibilities will include: * Coordinating system workflows for Amgen\-organized internal and external meetings, sponsorships, donations, fees for service, educational support requests, and disclosure reporting. * Adhering to Amgen policies, SOPs, and ensuring compliant usage of business systems and tools. * Providing audit support to the responsible Amgen employee. * Supporting the continuous improvement agenda. * Monitoring ACCP meeting and contracting capability service levels and satisfaction to ensure that outputs meet the agreed expectation. * Managing the performance and development the team. Lead performance management processes, including setting goals and conducting performance evaluations, and providing feedback for continuous improvement. **WIN** **WHAT WE EXPECT OF YOU** Our ideal candidate is strategic in decision\-making and planning. They are customer\-focused, result\-oriented, and set on problem solving. They have excellent presentation skills and can manage multiple tasks, prioritizing logically. They should possess strong leadership skills, with a proven ability to motivate and develop diverse teams. Minimum requirements: * Master’s degree, preferably in Business Management. * Minimum 6\-8 years of directly related experience with a successful track record in administration and meeting \& contracting support. * Project Management and/or compliance experience is an asset. * Fluency in English, in written and verbal communication. * Proven people management experience. The ideal candidate will have experience in a people management role, overseeing teams of up to 10 employees. Experience in conflict resolution, recruitment, and training is essential, along with a commitment to fostering a diverse and inclusive work environment. Preferred Requirements: * Knowledge of the Pharmaceutical industry. * Experience in using contracting/compliance soft. * German fluency will be considered a plus **THRIVE** **WHAT CAN YOU EXPECT OF US** As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well\-being. * Vast opportunities to learn, develop, and move up and across our global organization. * A diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits. * Flexible work arrangements. **APPLY NOW** **FOR A CAREER THAT DEFIES IMAGINATION** In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us. **CAREERS.AMGEN.COM** **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Director – Digital GBS & GCA Tech Strategist64361985059842124

Director – Digital GBS & GCA Tech Strategist

Are you ready to lead the charge in revolutionizing Global Business Services (GBS) and Global Corporate Affairs (GCA) through digital innovation? As the Director, Digital GBS \& GCA Tech Strategist, you will be at the forefront of transforming how we work, communicate, and engage with stakeholders. Your mission is to unlock enterprise value by strategically adopting AI, leveraging advanced technologies, and implementing digital operating models. You'll spearhead innovation, ensure responsible technology governance, and drive significant improvements in business performance and stakeholder trust. Are you prepared to make a difference? **Accountabilities:** * Lead enterprise\-wide digital transformation for GBS \& GCA, integrating AI, GenAI, advanced analytics, and next\-generation technology into all aspects of service delivery, communication, and stakeholder engagement. * Design and implement AI\-first strategies to create efficient, predictive, and personalized employee and stakeholder experiences. * Overhaul traditional operating models by embedding intelligent automation, digital agents, and cognitive platforms into core processes. * Activate real\-time, connected digital ecosystems for seamless cross\-functional, cross\-geographical collaboration. * Establish and scale innovative solutions using disruptive technologies such as quantum AI, immersive platforms, and Web3 infrastructure. * Implement robust governance and ethical frameworks to guide responsible, transparent, and compliant AI use. * Leverage advanced analytics for real\-time operational insights, reputational risk, and sustainability impact measurement. * Drive enterprise\-wide cultural adoption of AI and digital innovation through targeted change leadership and reskilling. * Advise and influence executive leadership and board\-level conversations on digital risk, innovation, and long\-term value creation. * Serve as an external thought leader and ambassador for digital transformation in GBS, GCA, and corporate resilience. **Essential Skills/Experience:** * Bachelor’s degree in Computer Science, Engineering, Business Information Systems, or a related field; Master’s (MBA/MSc or equivalent) strongly preferred. * 12\+ years’ progressive leadership experience in digital transformation, enterprise IT strategy, or innovation roles within global, matrixed organisations. * Proven success leading large\-scale, AI\-enabled transformations in GBS, shared services, corporate affairs, or enterprise functions. * Deep expertise in translating emerging technologies (AI/ML, GenAI, automation, analytics, cloud, Web3\) into scalable business solutions. * Demonstrated experience driving enterprise\-wide operating model transformation with intelligent automation and digital platforms. * Hands\-on exposure working with external innovation ecosystems—startups, accelerators, venture labs, or academia. * Knowledge of corporate affairs domains such as ESG, public affairs, reputation management, and strategic communications. * Strong understanding of AI ethics, regulatory frameworks (GDPR, DS, NIS2, AI Act), and data governance. * Ability to define and execute digital strategy with a clear vision and scalable implementation plan. * Excellent executive presence, communication, storytelling, and influencing skills at the highest enterprise levels. **Desirable Skills/Experience:** * Visionary and future\-focused, able to anticipate digital disruption and proactively shape business strategies. * Digital innovation leader with a strong values\-based approach focused on responsible technology, sustainability, and inclusivity. * Skilled in agile transformation, design thinking, stakeholder engagement, and change leadership across global and diverse teams. * Highly collaborative, adaptive, resilient, and committed to fostering continuous learning and digital fluency. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life\-changing medicines. In\-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, our work directly impacts patients by transforming our ability to develop life\-changing medicines. We empower the business to perform at its peak by combining cutting\-edge science with leading digital technology platforms. Our dynamic environment offers countless opportunities to learn and grow. Here you can innovate freely while contributing to something far bigger. With investment behind us and a commitment to disrupt the industry through technology and data\-led strategies, there's no better place to make a meaningful impact. Ready to take the next step in your career? Apply now to join us on this exciting journey!

R. do Salitre 195, 1269-063 Lisboa, Portugal

PV Officer, Team Lead - Russian language required64221617738881125

PV Officer, Team Lead - Russian language required

**Company Description** We are PrimeVigilance (part of Ergomed Group), a specialised mid\-size pharmacovigilance service provider established in 2008\. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives. **Job Description*** Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader * Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process * Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management Role and Responsibilities * Providing support to other activities undertaken by the project team on behalf of the client and the company * Line Manages assigned ICSR staff * Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency) * Proposes process changes to ICSR Operational Lead * Manages ICSR deviations with ICSR Operational Lead support * Reviews trackers and timesheet data and ensures accuracy * Is involved in ICSR processing and 2nd QC of cases * Operates as the assigned team SME and supports other SMEs **Qualifications** * Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance * Extensive experience in pharmacovigilance within which demonstrated work experience in line manager role. * Excellent communication (written and verbal) skills, Russian and English * Organization skills, including attention to details and multitasking * Delegation skills * Planning and time management * Technical skills * Team working **Additional Information** Why PrimeVigilance? We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer: * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join! * Quality * Integrity \& Trust * Drive \& Passion * Agility \& Responsiveness * Belonging * Collaborative Partnerships We look forward to welcoming your application.

PV49+C7 Lisbon, Portugal

Medical Reviewer I64212408346113126

Medical Reviewer I

**Company Description** We are PrimeVigilance (part of Ergomed PLC), a specialised mid\-size pharmacovigilance service provider established in 2008\. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. **Job Description** Responsibilities include: * To review and approve post\-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, listedness / expectedness and Company causality, as well as writing of Company comment, follow\-up questions and Analysis of Similar Events, when required. Including completion of all required supporting documentation such as trackers. * To review literature screening search strategy * To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings * Reviewing database outputs * To review and provide input in Periodic Safety Update Reports * To review and provide input in Development Safety Update Reports * Participating in signal detection activities including meetings and writing signal detection reports * Proposing a course of action whenever a possible signal is identified **Qualifications** * Medically qualified as a physician with demonstrated experience in Pharmacovigilance * Any experience in aggregate reports and signal detection is desirable * Excellent interpersonal skills * Ability to plan, organise, prioritise and execute multiple tasks * Ability to work effectively cross culturally and cross functionally and value the importance of teamwork * Communication skills * Presentation skills **Additional Information** We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us. **We offer:** * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join! * Quality * Integrity \& Trust * Drive \& Passion * Agility \& Responsiveness * Belonging * Collaborative Partnerships Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application!

PV49+C7 Lisbon, Portugal

Sr Mgr Information Systems64178905977473127

Sr Mgr Information Systems

Join our team at Amgen Capability Center Portugal, ranked the \#1 Best Workplace in Portugal in 2024 (201–500 employees’ category) by the Great Place to Work Institute. With over 300 talented professionals representing more than 35 nationalities, we are shaping the future of healthcare across diverse areas such as Cybersecurity, Data \& Analytics, Digital Innovation, Finance, HR, Regulatory Affairs, and more. Located in the heart of Lisbon, our office fosters innovation, excellence, and inspiration. Come thrive with us at Amgen, supporting our mission To Serve Patients. What we do at Amgen matters in people’s lives. **SENIOR MANAGER INFORMATION SYSTEMS** At Amgen, Technology isn’t just a support function—it’s a catalyst for discovery, transformation, and real\-world impact. Here, your ideas fuel innovation that improves and saves lives of patients in dire need of our medicines. Are you ready to do meaningful work that matters? **LIVE** **What will you do** In this role you will be accountable for leading, developing, and supporting a hard\-working technology team within a matrixed, global organization. This position focuses on people leadership, talent management, organizational development, and fostering a culture of collaboration, inclusion, and continuous improvement. You will be responsible for coaching and developing employees, managing performance, and ensuring alignment of team capabilities with organizational objectives. Success in this role requires strong interpersonal and leadership skills, the ability to influence across diverse teams, and a passion for building an engaged and empowered workforce. Your leadership and strategic approach will enable you to drive innovation and enhance the overall IT capabilities to support the company's goals. Responsibilities will include: * Lead, inspire, and run a diverse technology team, creating an engaged and hard\-working environment. * Provide coaching, mentoring, and career development support to help employees achieve their goals. * Oversee performance management, including feedback, evaluations, and recognition. * Manage workforce planning, recruitment, and onboarding to ensure the right skills and capabilities. * Champion diversity, equity, and inclusion across all team practices. * Drive succession planning and leadership pipeline development. * Work with Product Owners, Service Owners and/or delivery teams to ensure delivery of commitments. * Foster a culture of collaboration and continuous improvement. * Align team goals with organizational strategy and represent employee perspectives in leadership forums. * Partner with HR and business leaders to implement people\-focused initiatives. * Ensure compliance with organizational policies and standards. * Monitor retention, engagement, and development metrics to drive improvement. **WIN** **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The tech professional we seek is a creative problem\-solver and a team player with these qualifications: * Bachelor’s or Master’s degree in Computer Science, Engineering, Data Science, or a related field. * Master’s degree with 8–10 years of dynamic experience in people leadership, HR\-focused management, or organizational development roles; OR * Bachelor’s degree with 10–14 years of equivalent leadership and management experience. * Strong experience in leading, coaching, and developing teams with varied strengths. * Knowledge of HR standards, including performance management, employee engagement, and workforce planning. * Shown success in leading organizational change and driving cultural transformation. * Strong ability to partner with senior leaders, HR, and business partners. * Strong verbal and written interpersonal and communication skills. * Ability to work effectively with global, virtual teams. * High degree of initiative and self\-motivation. * Strong organizational skills to manage multiple priorities successfully. * Strong presentation and public speaking skills. * A passion for applying technology to make a real\-world impact. * Fluency in English. **THRIVE** ---------- **What you can expect of us** As we work to develop treatments that take care of others, we also care deeply for our teammates’ well\-being and growth. * **Work That Matters** – Build tech that accelerates scientific breakthroughs and helps patients worldwide. * **Modern Tech Stack** – Cloud\-first, automation\-focused, AI\-powered. * **Global Scale, Agile Mindset** – Collaborate across continents while working in nimble, high\-impact teams. * **Continuous Learning** – Access to certifications, trainings, mentorship, and career mobility. * **Amgen Total Rewards Plan** – Comprehensive benefits in healthcare, finance, and well\-being. * **Flexibility** – Hybrid work model with time split between our Lisbon office and remote work. **Apply now** ------------- Join us in our mission to serve patients. **careers.amgen.com** --------------------- **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Medical Writer - Promotional Review - German64170784296578128

Medical Writer - Promotional Review - German

**Senior Scientific Communications Specialist \- German** **(Medical Writer / Promo Review)** Location: Fully Remote Europe Essentials **Degree:** Advanced degree in Pharmacy (PharmD preferred), advanced healthcare degree, or equivalent clinical experience. **Experience:** 24 years in scientific content creation within the pharmaceutical industry, medical education, or academia. Languages: Fluent in English and German (C1/C2\). **Position Summary** The Senior Scientific Communications Specialist provides scientific and medical writing support across multiple therapeutic areas. This role ensures the delivery of accurate, balanced, and compliant content for internal stakeholders, healthcare professionals, and consumers. The position supports client needs, aligns with Medical Affairs and brand strategies, and may lead team members or client projects. **Key Responsibilities** * Develop, review, and edit scientific and medical materials (e.g., standard/custom responses, slide decks, manuscripts, dossiers, and promotional materials). * Ensure content accuracy, scientific integrity, and compliance with regulatory standards. * Apply and maintain approved content and style guidelines in content management systems. * Respond to medical information requests via email, web, or calls; conduct scientific exchanges as needed. * Participate in scientific and brand training to maintain expertise. * Meet quality and turnaround targets while adhering to legal, regulatory, and compliance policies. * Mentor or train new staff; may lead teams supporting specific clients or brands. * Serve as primary contact between Med Communications and clients for project coordination and updates. * Support quality assurance activities and participate in special projects, pilots, or client initiatives. * Provide medical information support through virtual sessions or medical meeting coverage. **Qualifications \& Competencies** * Strong attention to detail, communication, and organizational skills. * Proficiency in Microsoft Office; familiarity with Embase, Ovid, and content management systems preferred. * Solid understanding of pharmaceutical, regulatory, and compliance environments (FDA, EMA). * Demonstrated expertise in drug information communication and scientific content management. * Team\-oriented, adaptable, and able to manage multiple priorities in a fast\-paced, client\-driven setting. * Displays professionalism, initiative, and leadership in cross\-functional collaborations. **Core Competencies:** Accuracy Time Management Communication Leadership Collaboration Innovation Customer Focus Work Ethic Self\-Motivation Technical Aptitude Applied Learning **Work Environment** **Remote position** within Europe for Med Communications International. Candidates must submit an **English CV**. **Equal Opportunity:** Med Communications, Inc. is an equal opportunity employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, national origin, age, disability, or veteran status. **Note to Recruitment Agencies:** Please be aware that any unsolicited CVs or candidate profiles received without prior engagement or agreement with our recruitment team will be considered free and carry no obligation on the part of Med Communications. We thank you for your compliance with our policy. **Privacy Notice:** By submitting your CV, you consent to the processing and international transfer of your personal data in accordance with the Med Communications Inc \- Privacy Policy.

PV49+C7 Lisbon, Portugal

Senior Associate Finance64101828272513129

Senior Associate Finance

Join our team at AMGEN Capability Center Portugal, number 1 company in Best Workplaces \- https://www.greatplacetowork.pt/ \- ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 400 talented people and 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **SENIOR ASSOCIATE FINANCE** **LIVE** **WHAT YOU WILL DO** Let’s do this. Let’s change the world! We are looking for a highly motivated Senior Associate Finance to serve as a member of the Operations Financial Planning and Analysis team (FP\&A) that supports Amgen Manufacturing Limited LLC in Puerto Rico (Juncos site). In this role, you will be responsible for handling budgeting, forecasting, and reporting and closing activities of critical functions within the site. This role is expected to partner with some site clients to ensure accurate and timely forecast submissions and monthly reporting. The role requires close collaboration with functional stakeholders to understand business drivers and support decision\-making through data\-driven insights. **Key Responsibilities:** * Support business planning and decision making through financial analysis. * Manage the standard cost development for raw material during the standard cost process. * Raw Materials, Purchase price variance, consumables and freight analysis. * Perform month\-end, quarter\-end, year\-end closing activities including accruals and journal entries, perform variance analysis. * Monthly actuals financial reporting. * Perform, compile and analyze ad hoc requests. * Support transformational initiatives through automation and financial process improvements. * Collaborate with cross\-functional teams and support site objectives as required. **WIN** **WHAT WE EXPECT OF YOU** We are all different, yet we all use our unique contributions to serve patients! The Finance Manager professional we seek is an individual contributor leader with these qualifications: **Minimum requirements:** * Master’s degree and 2 years of Finance or Accounting experience or * Bachelor’s degree and 4 years of experience in finance, accounting, or related fields * Relevant experience in financial planning and analysis, accounting, and manufacturing industry * Strong analytical skills with the ability to analyze data and present results in a clear and concise manner * Experience with SAP and Hyperion planning system and/or other ERP and consolidation tools * Proficient with MS Office systems, particularly Excel and Power Point and visualization tools * Detail oriented and able to handle fast paced environment while delivering timely results * Fluency in English and Spanish, both in written and oral communication **Preferred requirements:** * Prior experience supporting operations, supply chain, or manufacturing environments preferred * Experience with raw material standard costing * Data analytics or data visualization and dashboard experience (e.g., Tableau, Power BI, Smartsheet, Alteryx, SQL) * Understand Continuous Improvement concepts * Strong problem\-solving and analytical skills. * Excellent verbal and written communication and presentation skills (English) * Ability to work cross\-functionally and influence stakeholders. * Energetic, detail oriented, highly motivated with a “can do” outlook * Flexibility to work with different time zones. **THRIVE** **WHAT YOU CAN EXPECT OF US** * Vast opportunities to learn, develop, and move up and across our global organization. * A diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits. * Flexible work arrangements. **APPLY NOW** **Objects in your future are closer than they appear. Join us.** **CAREERS.AMGEN.COM** **EQUAL OPPORTUNITY** **STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Senior Auditor (Financial Services)640888806749461210

Senior Auditor (Financial Services)

At Forvis Mazars, we are looking for dynamic, creative individuals committed to their technical and professional growth. We highly value teamwork and the willingness to learn, and we seek those who share our commitment to excellence and innovation. As an Organization, we are committed to contributing to the development of your career, making Forvis Mazars learning a unique experience that will accompany and drive you throughout your professional life, wherever it may lead. The Senior Auditor will be involved in diverse client projects within the financial sector – Banking, Insurance, and Asset Management (financial statement audit/financial audit, internal control and risk management, specific audits, analysis of prospective financial information) and other regulatory work required by law (BdP, ASF, and CMVM). **Who we are looking for:** Professional experience between 3 to 5 years in auditing, preferably in an international environment; Interest in the financial sector; Higher academic degree in Management, Economics, Finance, Taxation, Accounting, or similar; Knowledge of International Financial Reporting Standards (IFRS) and applicable financial sector regulations issued by Banco de Portugal, ASF, and CMVM; Fluency in English (preferred); Advanced knowledge of Office tools; High level of commitment, positive attitude, dynamic and proactive; Enjoy client interaction; Strong communication skills; What we offer Integration into a global and dynamic company; Opportunity to join a young and significantly growing team specialized in the financial sector, with excellent career progression prospects; Continuous training. **How you can apply:** You should send your updated CV by email with the subject "AuditSeniorFS".

PV49+C7 Lisbon, Portugal

Pharmaceutical Trainee - Regulatory Affairs640888806951691211

Pharmaceutical Trainee - Regulatory Affairs

**Trainee** Hybrid, Full time Pharegistrum is a pharmaceutical and technical consulting company based in Lisbon, providing services in the areas of Regulatory Affairs, Quality Assurance, Pharmacovigilance, among others, to a diverse range of national and international clients. We are currently seeking a Pharmacist or a Master's graduate in Pharmaceutical Sciences with interest in these fields to undertake an internship within our company. **Responsibilities** Support a qualified team through active participation in pharmaceutical consulting projects and daily activities, gaining practical knowledge and experience in the pharmaceutical sector, aiming to contribute to the company’s mission while developing professionally. **Qualifications** \- Pharmacist or Master's degree in Pharmaceutical Sciences; \- Strong command of English. Additional languages are an asset; \- Ability to interpret and communicate effectively; \- Strong sense of commitment; \- Ability to adapt to multiple tasks and functional areas; \- Motivation to learn and grow along with the company’s development. Interested candidates should send their full CV in English, quoting reference 2025/T, to the email address info@pharegistrum.com. Job type: Temporary or Fixed-term employment contract Contract duration: 9\-12 months Salary: 10,800.00€ \- 16,800.00€ per year Education: * Master's degree (Mandatory) Language: * Portuguese (Mandatory)

PV49+C7 Lisbon, Portugal

€ 10,800-16,800/year

Software Development Engineer - Test I640888806355231212

Software Development Engineer - Test I

Join our team at AMGEN Capability Center Portugal, number 1 company in Best Workplaces \- https://www.greatplacetowork.pt/ \- ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 400 talented people and 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **Software Development Engineer \- Test I** **LIVE** **WHAT YOU WILL DO** **Role Description:** The Software Development Engineer \- Test position offers a unique opportunity to join a fun, innovative engineering team within the AI \& Data Science (AI\&D) \- Enterprise Automation organization. You’ll work on next\-generation capabilities and services in Applied AI \& Automation using innovative COTS products, open\-source software, frameworks, tools, and cloud computing services. The role also emphasizes demonstrating these capabilities to support critical business operations and initiatives, in ensuring quality, compliance, and performance across Amgen’s Applied AI \& Automation Footprint. In this role, you will be responsible for ensuring the quality and compliance of enterprise automation solutions \& platforms, with a strong focus on computer systems validation including test automation, test planning, execution, and defect management. You will work closely with product owners, developers, and QA teams to validate systems against business and regulatory requirements. This role is critical in ensuring that automation solutions meet performance, security, and compliance expectations across the development lifecycle, especially in GxP\-regulated environments. **Roles \& Responsibilities:** * Build out test engineering practices, standards, community and lead by execution in creating a new culture around the test automation demeanor. * Design, develop and maintain automated and manual test cases based on functional and non\-functional requirements. * Perform responsibilities in compliance with GxP and Computer System Validation (CSV) regulations, ensuring proper documentation, execution, and adherence to regulatory standards. * Create and maintain the Requirement Traceability Matrix (RTM) to ensure full test coverage. * Log, track and manage defects using tools such as HP ALM or JIRA, ensuring clear documentation and traceability. * Assist in User Acceptance Testing (UAT), working closely with business stakeholders. * Execute tests including Systems Integration Testing (SIT), Operational Qualification (OQ), and regression testing. * Execute test scripts provided by analysts, focusing on accuracy and completeness of testing. * Collaborate with developers to ensure all identified bugs and issues are addressed and resolved effectively. * Support automation testing efforts by building and maintaining scripts in tools like UiPath Test Suite, Selenium, or similar tools. * Maintain detailed documentation of test cycles, supporting audit readiness and compliance. **WIN** **WHAT WE EXPECT OF YOU** **Basic Qualifications:** * Bachelor’s degree and 0 to 3 years of Computer Science, IT or related field experience * OR * Diploma and 4 to 7 years of Computer Science, IT or related field experience **Preferred Qualifications:** * BS/MS in Computer Science, Information Systems, or related field * 3\+ years of experience in application testing and automation frameworks **Must\-Have Skills:** * Strong experience in designing and executing both manual and automated test cases based on functional and non\-functional requirements. * Strong knowledge of test lifecycle documentation including test plans, RTMs, OQ protocols, and summary reports * Hands\-on experience with UiPath Test Suite, Selenium, Postman, or similar tools. * Experience in validated (GxP) environments and with CSV practices **Good\-to\-Have Skills:** * Develop, enhance, and maintain test automation scripts using data\-driven, keyword\-driven, or hybrid frameworks, enabling reusable, scalable, and maintainable test coverage across systems. * Proficient in creating test lifecycle documentation (RTMs, OQ protocols, test plans, reports) and supporting end\-to\-end testing within regulated GxP and CSV\-compliant computer systems, ensuring adherence to validation, audit, and documentation standards * Familiarity with Agile/Scrum methodologies and continuous testing practices * Strong test design and problem\-solving skills. * Familiarity with Jenkins, GitHub Actions, or similar tools for integrating testing into DevOps pipelines. * Experience collaborating with Cross\-Functional teams, particularly within healthcare or pharmaceutical environments. * Experience in handling product features for PI planning and developing product roadmaps and user journeys * Able to communicate complex subject matters in business terms * Familiarity with GxP, CFR 21 Part 11 and systems validation **Professional Certifications:** * ISTQB Foundation or Advanced Level Certification (Optional but valuable) * Certified CSV/Validation Professional (Optional but valuable) * SAFe Agile Tester Certification (Optional but valuable) **Soft Skills:** * Excellent critical\-thinking and problem\-solving skills * Strong communication and collaboration skills * Demonstrated awareness of how to function in a team setting * Demonstrated awareness of presentation skills **THRIVE** **WHAT YOU CAN EXPECT OF US** * Vast opportunities to learn, develop, and move up and across our global organization. * A diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits. * Flexible work arrangements. **APPLY NOW** Objects in your future are closer than they appear. Join us. **CAREERS.AMGEN.COM** **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Artwork Specialist638229112555531213

Artwork Specialist

share mail share share Artwork Specialist **Country:** Portugal **City:** Lisbon **Department:** Global Operations \& Production **Job ID:** 44747 **Job Grade:** PT10F **Hiring Manager:** Alexandra Lopes **Internal Posting Date:** \- Professional \| Permanent \| Full\-time \| Hybrid Our people in **Manufacturing \& Global Operations** share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain – from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future. **What the job looks like** Each day you’ll enjoy a variety of challenges, such as: * Management of artworks for regulatory and technical changes affecting printed packaging materials e.g., labels, leaflets, folding boxes, foils etc.) for Grünenthal and Clients products’ portfolio; * Diligent check of the correctness/compliance of the created artworks in multilingual files; * Proper archive and diligent share of final approved master artworks with the respective business functions; * Maintenance of packaging material master data and bill of materials in the relevant systems; * Cross functional collaboration to ensure the timely delivery of quality artwork in an international environment (across regions); * Monitor implementation of label changes for GRT products, according to regulatory timelines; * Support new business integrations with strategy and planning concerning artworks; * Creation, maintenance and archiving of standard operating procedures (SOP), packaging documentation and GMP\-relevant documents. **What you'll bring to the table** To make the most of this role and truly thrive, you should have: * High school degree or graduation in life sciences; * Minimum 2 years experience in pharmaceutical industry areas such as Regulatory Affairs, Supply, Quality, Production; * Previous experience in artwork development for pharmaceutical industry (preferred) or equivalent industry (e.g., Medical Devices, Cosmetics); * Good verbal and written English. German and Spanish language skills are an advantage; * Good knowledge of MS Office and SAP (preferred); * Good knowledge of regulatory terminology and labeling guidelines; * Basic knowledge of GMP regulations and guidelines. **\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_** Alexandra Lopes, the Hiring Manager About Grünenthal Grünenthal is a global leader in pain management and related diseases. As a science\-based, privately\-owned pharmaceutical company, we have a long track record of bringing innovative treatments and state\-of\-the\-art technologies to patients worldwide. Our purpose is to change lives for the better – and innovation is our passion. We are focussing all of our activities and efforts on working towards our vision of a world free of pain. Grünenthal is headquartered in Aachen, Germany, and has affiliates in 28 countries across Europe, Latin America and the US. Our products are available in more than 100 countries. In 2024, Grünenthal employed around 4,300 people and achieved sales of € 1\.8 billion. Your HR contact: Sara Marques

PV49+C7 Lisbon, Portugal

Senior Pharmacovigilance Physician I638229112724491214

Senior Pharmacovigilance Physician I

**Company Description** We are PrimeVigilance (part of Ergomed PLC), a specialised mid\-size pharmacovigilance service provider established in 2008\. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. **Job Description** * To review and approve post\-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding, assessment of seriousness, expectedness, and Company causality, as well as writing of Company comment, follow\-up questions and Analysis of Similar Events. This includes completion of all required supporting documentation such as trackers. * To support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues * To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings * Reviewing database outputs **Qualifications** * Medical qualification as a Physician * Ability to work effectively cross culturally and value the importance of teamwork * Presentation skills * Advanced knowledge of English and MS Office **Additional Information** We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us. **We offer:** * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join! * Quality * Integrity \& Trust * Drive \& Passion * Agility \& Responsiveness * Belonging * Collaborative Partnerships Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application!

PV49+C7 Lisbon, Portugal

Principal Data Engineer638229113040671215

Principal Data Engineer

Join our team at **AMGEN Capability Center Portugal**, number 1 company in Best WorkplacesTM https://www.greatplacetowork.pt/ ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 300 talented people and more than 35 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **PRINCIPAL DATA ENGINEER** At Amgen, Technology isn’t just a support function—it’s a catalyst for discovery, transformation, and real\-world impact. Here, your ideas fuel innovation that improves and saves lives of patients in dire need of our medicines. Are you ready to do meaningful work that matters? **LIVE** **WHAT YOU WILL DO** -------------------- As a Principal Data Engineer at Amgen, you’ll work at the intersection of science, data, and innovation. You’ll collaborate with world\-class experts across domains to build high\-impact digital solutions that accelerate research, streamline operations, and empower better patient outcomes. You will lead the design and implementation of scalable data infrastructure. You’ll collaborate across teams to build robust data platforms, develop pipelines, and drive integration efforts. This role combines deep technical expertise with leadership, as you guide a team of engineers and help shape the Amgen's data strategy. **Responsibilities will include:** ---------------------------------- * Provide expert guidance and mentorship to the data engineering team, fostering a culture of innovation and standard processes. * Design, develop, and implement robust data architectures and platforms to support business objectives. * Oversee the development and optimization of data pipelines, and data integration solutions. * Establish and maintain data governance policies and standards to ensure data quality, security, and compliance. * Architect and manage cloud\-based data solutions, using AWS or other preferred platforms. * Lead and motivate a hard\-working data engineering team to deliver exceptional results. * Identify, analyze, and resolve complex data\-related challenges. * Work closely with business partners to understand data requirements and translate them into technical solutions. * Stay abreast of emerging data technologies and explore opportunities for innovation. **WIN** **WHAT WE EXPECT OF YOU** We are all different, yet we all use our unique contributions to serve patients. The tech professional we seek is a creative problem\-solver and a team player with these qualifications: **Minimum Requirements** ------------------------ * Bachelor’s degree in computer science and engineering preferred, other Engineering field is considered; Master’s degree and 6\+ years' experience OR Bachelor’s degree and 8\+ years' experience. * Strong rapid prototyping skills and can quickly translate concepts into working code. * Showed talent in using cloud platforms (AWS, Azure, GCP) for data engineering solutions. Strong understanding of cloud architecture principles and cost optimization strategies. * Proficient on experience in Python, PySpark, SQL. Hands\-on experience with bid data ETL performance tuning. * Ability to lead and develop hard\-working data engineering teams. * Strong problem\-solving, analytical, and critical thinking skills to address complex data challenges. * Strong verbal and written communication skills. * Ability to work effectively with global, remote teams. * Ability to manage multiple priorities successfully. * Team\-oriented, with a focus on achieving team goals. Strong presentation and public speaking skills. **Preferred Requirements** * Experienced with data modeling and performance tuning for both OLAP and OLTP databases. * Experienced with Apache Spark, Apache Airflow. * Experienced with software engineering best\-practices, including but not limited to version control (Git, Subversion, etc.), CI/CD (Jenkins, Maven etc.), automated unit testing, and Dev Ops. * Experienced with AWS, GCP or Azure cloud services. * AWS Certified Data Engineer preferred. * Databricks Certificate preferred. **THRIVE** ---------- **WHAT YOU CAN EXPECT OF US** As we work to develop treatments that take care of others, we also care deeply for our teammates’ well\-being and growth. * **Work That Matters** – Build tech that accelerates scientific breakthroughs and helps patients worldwide. * **Modern Tech Stack** – Cloud\-first, automation\-focused, AI\-powered. * **Global Scale, Agile Mindset** – Collaborate across continents while working in nimble, high\-impact teams. * **Continuous Learning** – Access to certifications, trainings, mentorship, and career mobility. * **Amgen Total Rewards Plan** – Comprehensive benefits in healthcare, finance, and well\-being. * **Flexibility** – Hybrid work model with time split between our Lisbon office and remote work. **Apply now** ------------- Join us in our mission to serve patients. **careers.amgen.com** --------------------- **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Pharmacovigilance Medical Writer II (Aggregate report writing experience required)638229113199391216

Pharmacovigilance Medical Writer II (Aggregate report writing experience required)

**Company Description** We are PrimeVigilance (part of Ergomed Group), a specialised mid\-size pharmacovigilance service provider initially established in 2008\. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. **Job Description** We are looking for a pharmacovigilance medical writer to join our team. The Medical Writer will be responsible for medical writing including: * PSURs/PBRERs * PADERs * ACOs * DSURs * RMPs * QC and review of all written output from the operations team as required * Supporting the project managers to determine scheduling of the aggregate reports for which they are responsible * In conjunction with the Quality, Compliance and Training Manager identify areas for improvement and address via training, clarifying changes to SOPs/OGs/templates * Complete quality documentation of aggregate reports * Attending kick off meetings with new clients as required * Attending audits and inspections as required * Providing aggregate report training **Qualifications** * MD, pharmacy or Life Science degree (Masters or PhD is desirable) * Strong previous experience in Pharmacovigilance (Aggregate report writing, case processing, signal detection or risk management) within ideally a CRO environment * Ability to manage multiple and varied tasks and prioritize workload with attention to detail * Ability to effectively train and mentor Associate Medical Writers * Must be a strong team player * Fluency in English, an additional language is a benefit **Additional Information** **Why PrimeVigilance** We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. **We offer:** * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join! * Quality * Integrity \& Trust * Drive \& Passion * Agility \& Responsiveness * Belonging * Collaborative Partnerships Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.

PV49+C7 Lisbon, Portugal

German-speaking Document Control Coordinator638229113360671217

German-speaking Document Control Coordinator

Join our team at **AMGEN Capability Center Portugal**, number 1 company in Best Workplaces \- https://www.greatplacetowork.pt/ \- ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 400 dedicated people and 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **German Speaking Document Coordinator** **LIVE** **What you will do** You will be responsible for supporting contract management, Purchase Order (PO) lifecycle management, Healthcare Professionals (HCP) Contracting and sponsorships/fees for service/donations/educational processes support. Also, you will adhere to the continuous improvement agenda of the ACCP, provide specific legal support for the function including corporate administration and intercompany agreement management. Additional responsibilities will include: * Handling contract templates and contract repositories creation (non legal). * Support the audit team with any requirements/information. * Recognizing and escalating problems or risks, as and when they arise in line with the business requirements. * Adapt, support and contribute to the growth and continuous improvement of the department and ACCP. **WIN** **What we expect of you** Our ideal candidate has presentations and data compilation skills. He/she has developed skills in following the processes and procedures necessary to succeed; understand how to collaborate, work in a team and is set on Project Delivery. Proven experience and skills needed: * University Degree, preferably in the business area, or high school completion and 2 years in a similar role * Familiarity working with compliance processes and procedures * Detail oriented and organized * Personal credibility and flexibility * Service\-minded, proactive and committed attitude * Fluency in German and English, both in written and verbal communication. Preferred Requirements * Experience in an administrative role supporting teams at different levels * Knowledge of Pharmaceutical industry * Familiar with MS Office, SAP tools * Fluency in another European language **THRIVE** **WHAT YOU CAN EXPECT OF US** * Vast opportunities to learn, develop, and move up and across our global organization. * Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits. * Flexible work arrangements. **APPLY NOW FOR A CAREER THAT DEFIES IMAGINATION** In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us. **CAREERS.AMGEN.COM** **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

PV Officer, Team Lead/Case Processing Manager (Pharmacovigilance), Team Lead (Europe remote/hybrid position)638229113520651218

PV Officer, Team Lead/Case Processing Manager (Pharmacovigilance), Team Lead (Europe remote/hybrid position)

**Company Description** We are PrimeVigilance (part of Ergomed Group), a specialised mid\-size pharmacovigilance service provider established in 2008\. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. We love investing in our staff by providing an excellent training and development platform. We value employee experience, well\-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high\-quality client service can be achieved. Come and join us in this exciting journey to make a positive impact in patient’s lives. **Job Description** * Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader * Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process * Assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management * Contributes to achieving company´s goals and objectives * Works under supervision of ICSR Operational Lead * Providing support to other activities undertaken by the project team on behalf of the client and the company * Line Manages assigned ICSR staff * Creates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures, trainings and any other actions to increase ICSR team efficiency) * Proposes process changes to ICSR Operational Lead * Manages ICSR deviations with ICSR Operational Lead support * Reviews trackers and timesheet data and ensures accuracy * Is involved in ICSR processing and 2nd QC of cases * Support other departments, as approved and instructed by ICSR Operational Lead **Qualifications** * Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance * Strong previous experience of PV in ideally a CRO environment * Previous experience in a Line Management position * Excellent communication (written and verbal) skills * Organization skills, including attention to details and multitasking * Delegation skills * Planning and time management * Technical skills * Team working * English – fluent (spoken, written) **Additional Information** We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human\-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow. To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. We offer: * Training and career development opportunities internally * Strong emphasis on personal and professional growth * Friendly, supportive working environment * Opportunity to work with colleagues based all over the world, with English as the company language Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join! * Quality * Integrity \& Trust * Drive \& Passion * Agility \& Responsiveness * Belonging * Collaborative Partnerships

PV49+C7 Lisbon, Portugal

Business, Data Analytics and Insights Senior Associate638229112056331219

Business, Data Analytics and Insights Senior Associate

Join our team at **AMGEN Capability Center Portugal**, number 1 company in Best WorkplacesTM https://www.greatplacetowork.pt/ ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 300 talented people and more than 35 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives Business, Data Analytics and Insights Senior Associate **LIVE** **WHAT YOU WILL DO** You, as our Business, Data Analytics and Insights Senior Associate, will play a pivotal role as a strategic partner to Commercial leadership, offering data\-backed insights crucial for driving commercial success. You will be responsible for forecasting, producing budgeting and planning reports, data analysis, and supporting wider Business Units within the ACCP. Other responsibilities will include: * Understand business drivers to create, prepare, and maintain patient and demand\-based forecasts and scenarios * Contribute to regular forecast cycles including multiple cycles of annual long\-range forecast, and short\-term forecast * Perform in\-depth data analysis to build robust assumptions, scenarios, and forecast inputs * Present and defend forecast approach, methodology, assumptions, and outputs in team discussions * Collecting feedback and preparing communication plans to share outputs. * Taking ownership of complex calculations through understanding inputs and their relationships to the problem. * Supporting ACCP continuous improvement activities. * Supporting wider business units on an ad hoc basis (Finance/FP\&A/Business Enablement). **WIN** **WHAT WE EXPECT OF YOU** Our ideal candidate is a team player with customer focus. The ideal candidate is is problem solving and result oriented and has time and process management skills and can compile data. Proven experience and skills needed: * University Degree in commerce, finance, economics, mathematics, healthcare or related field. * 3\+ years working in a finance/data related field ideally Data and Analytics. * Forecasting and Modelling experience * Fluency in English, both in written and oral communication. * Strong Excel knowledge Preferred Requirements: * Working knowledge of IS systems (including demonstrated capability of other MS Office applications, SQL, Hyperion Pillar, Tableau, Anaplan). * Demonstrates a service\-minded attitude. * Experience in the Pharmaceutical industry. * Clearly explains processes and procedures. * Fluency in multiple European languages. **THRIVE** **WHAT YOU CAN EXPECT OF US** * Vast opportunities to learn, develop, and move up and across our global organization. * Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits. * Flexible work arrangements. **APPLY NOW** Objects in your future are closer than they appear. Join us. **CAREERS.AMGEN.COM** **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Senior Associate Data Acquisition and Governance638229112392991220

Senior Associate Data Acquisition and Governance

Join our team at **AMGEN Capability Center Portugal**, number 1 company in Best WorkplacesTM https://www.greatplacetowork.pt/ ranking in Portugal (category 201\-500 employees) by the Great Place to Work Institute. We have a team of over 300 talented people and more than 35 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. This is your chance to explore a world of opportunities in different areas such as Cybersecurity, Data \& Analytics, Digital, Technology and Innovation, Finance, General \& Admin, Human Resources, Regulatory Affairs and many more. In Lisbon's city center, our AMGEN office fosters innovation, excellence, and inspiration. Come thrive with us at AMGEN, supporting our mission To Serve Patients. What we do at AMGEN matters in people’s lives. **SENIOR ASSOCIATE DATA ACQUISITION AND GOVERNANCE** **LIVE** **WHAT YOU WILL DO** In this vital role you will support Amgen’s Customer Data \& Analytics (CD\&A) strategy by managing key operational processes and documentation workflows to ensure compliance and audit readiness. You’ll collaborate with cross\-functional teams and external vendors to oversee and lead the full lifecycle of Third Party Agreements (TPAs), Fair Market Value (FMV) documentation, product intake forms, and data catalog metadata—contributing to effective data acquisition and governance. The responsibilities of the role will include: * Coordinate with Legal, Compliance, Procurement, and business stakeholders to support timely contract execution and documentation workflows. * Manage and track data vendor investigations with third\-party vendors, acting as a central point of coordination between vendors, internal data stewards, and business stakeholders to track, document, and resolve issues in alignment with service level agreements. * Maintain the Commercial Global Data Catalog, including metadata standardization and asset tracking. * Support documentation intake processes and develop stakeholder\-facing materials such as SOPs, training guides, and visual tools to improve data literacy. * Ensure accurate documentation control, versioning, and consistency across compliance records and internal trackers. **WIN** **WHAT WE EXPECT OF YOU** Our ideal candidate is a collaborative, adaptable and autonomous individual, with customer focus, organization and attention to detail skills. **Proven experience and skills needed:** * Minimum 3 years of experience in data management, data governance, contracting, or related business field. * University Degree in business administration, commerce, finance, economics, healthcare or related field. * Excellent communication skills and previous stakeholder and project management experience * Proficiency in English, both in written and verbal communication. **Preferred Requirements:** * Experience with commonly used biopharmaceutical industry secondary datasets and databases. * Experience with FMV documentation or audit preparation in biotech/pharma/healthcare. * Familiarity with Third Party Agreement management or vendor contracting workflows. * Experience with data catalog tools or metadata governance. **THRIVE** **WHAT YOU CAN EXPECT OF US** * Vast opportunities to learn, develop, and move up and across our global organization. * Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act. * Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth, and career benefits. * Flexible work arrangements. L**OCATION:**Ability to work flexibly from home with regular office work in our Lisbon workspace. **APPLY NOW** Objects in your future are closer than they appear. Join us. **careers.amgen.com** **EQUAL OPPORTUNITY STATEMENT** Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

PV49+C7 Lisbon, Portugal

Popular Jobs

Popular Cities

Retail Assistants Recruitment Acct Relationship Mgmt Recruitment Advertising Arts Media Recruitment Accounting Recruitment Other14 Recruitment Other9 Recruitment Other4 Recruitment Mfg Transport Logistics Recruitment Info Comm Technology Recruitment Sales Recruitment

Mira Other11 Recruitment Guimaraes Other11 Recruitment Porto Other11 Recruitment Braga Other11 Recruitment Coimbra Other11 Recruitment Vila Nova de Gaia Other11 Recruitment Aveiro Other11 Recruitment Lisbon Other11 Recruitment Ovar Other11 Recruitment

Help

Support and feedback

Cookie

Cookie Settings

Our Apps

Download on the

APP Store

Download

Get it on

Google Play

© 2025 Servanan International Pte. Ltd.