Loures Pharma Medical Devices Job Listings

Technical Director – Sintra Warehouse64731744626689120

Indeed

Technical Director – Sintra Warehouse

### **Join DHL Supply Chain and become part of the world’s leading contract logistics company.** **In Portugal, we are a benchmark in integrated supply chain management, with over 10 sites, 200,000 m², and more than 1,000 employees. We are certified as a** **Great Place to Work®****, because we believe people are our greatest strength.** Globally, DHL Supply Chain is recognized for its high level of expertise in supporting clients in the **Life Sciences & Healthcare** sector, delivering secure, efficient solutions compliant with the most stringent regulatory standards. We work to connect people and improve lives, ensuring critical products reach where they are needed—safely and reliably. #### **What will you do in this role?** As **Technical Director**, you will be a key player in ensuring our processes meet the highest standards of quality and safety. Your mission will include: * Ensuring compliance with **Good Distribution Practices (GDP)** for human medicinal products and medical devices. * Supporting the **Quality Management System**, certified to ISO 9001:2015. * Close collaboration with operations, logistics, and quality teams to integrate excellence practices. * Managing complaints, deviations, non-conformities, product recalls, and returns. * Participating in audits and occasional visits to other warehouses. #### **What are we looking for?** * **Education**: Bachelor’s or Integrated Master’s degree in Pharmaceutical Sciences (mandatory). * **Registration with the Portuguese Pharmaceutical Society** (mandatory). * Fluency in English. * Up to 5 years’ experience in Technical Director roles. #### **Why choose DHL Supply Chain?** At DHL, we believe **your development is as important as our success**. We offer: * An environment that fosters continuous learning and professional growth. * Challenging projects and real impact across the supply chain. * An inclusive culture and global programs such as **GoGreen, GoHelp, GoTrade, and GoTeach**, reflecting our commitment to sustainability and social responsibility. **Join a team that connects people and improves lives.** Apply now and discover what it’s like to work for a company recognized as a **Great Employer for All** and **Highly Reliable**.

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Pharmaceutical Technician - Sacavém64088894045954121

Indeed

Pharmaceutical Technician - Sacavém

We are recruiting a Pharmaceutical Technician to join the team of a pharmacy located in Sacavém. **Main responsibilities:** * Customer service and advisory on health and wellness products; * Dispensing of prescription and non-prescription medications; * Collaboration in pharmaceutical services provided by the pharmacy; * Support in receiving, storing, and inventory management; * Contribution to the smooth daily operation and organization of the space. **Requirements:** * Bachelor's degree in Pharmacy; * Enjoyment in customer service and commitment to service quality; * Organizational skills, responsibility, and teamwork spirit. **Offer:** * Integration into a solid and well-structured pharmacy; * Attractive remuneration, adjusted to profile and experience; * Opportunity to access continuous training programs; * Collaborative work environment focused on team development. Type of offer: Full-time/Full\-time

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Indeed

QA Trainee

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are **In it for life.** You will be responsible to:: * Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured; * Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports; * Prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following\-up action plans as necessary; * Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits; * Periodic follow\-up of ongoing deviations and Change Controls (PdAs) to assure timely closure of deviations and approval of PdAs, as appropriate; * Prepares SOPs, department IOPs, quality related reports and change control documents (PdAs) as required and appropriate; * Review process master documentation, revision of executed batch documentation and product specifications as required and appropriate; * Review regulatory documentation and co\-ordination of site documentation to support regulatory requirements; * Authorize the usage of production equipment/utilities when qualification required. We are looking to recruit a Candidate:: * University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory); * Requires educational / training experience in Chemical environment (desirable); * Fluency in English is a requirement; * Computer literate with good working knowledge of the MS Office package; * Good documentation skills and attention to detail. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity. ***Notice to Agencies and Search Firms Representatives*** *Hovione does not accept unsolicited résumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third\-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral. Thank you for your understanding.*

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Quality Control Manager64088839110530123

Indeed

Quality Control Manager

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * Coordinate and supervise activities within the area and prioritize activities in case of conflict between simultaneous production lines / projects to ensure that the deliverables of each project are dealt in the team within the timeframes defined, with the appropriate quality and according to cGMP and that an outstanding service is provided to all customers (internal and external) * Ensure that all TMs of the team have suitable training and qualifications to the work they perform * Participate in client meetings, external and internal audits and Product/Project teams representing own area specialization * Review and approve analytical test methods to be executed in own laboratory * Review and approve reports prepared in own laboratory * Check and approve raw material, intermediate and final product batches, stability samples, In Process and COL samples and/or all samples sent for QC from own laboratory * Manage all defined stability programs in terms of protocl preparation, inventory management, analytical testing execution and data release * Ensure all safety and quality events are investigated and root cause determined with CAPA’s identified and executed * Coordinate the timely execution of the preventive maintenance program and execution of corrective maintenance. * Keep up to date on new analysis techniques relevant to the laboratory, by means of literature, training, seminars or conferences * Coordinate the TMs assigned to his/her area of responsibility, namely in terms of recruitment, integration, training needs and performance management in accordance with the company's HR policies, in order to ensure all TMs are aligned and motivated towards achieving Hovione's goals, values and culture by promoting their personal and professional development whilst maximizing productivity * Develop and propose for superior approval the activity plan and related budget for the Area under responsibility in line with the unit's strategy, in order to align activities with area strategic objectives * Monitor Communication´s budget, by controlling budget evolution, identifying any deviations between the real and the foreseen and taking corrective measures * Ensure compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others) within his/ her TMs * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. We are looking to recruit a Candidate:: * Masters’ degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or in similar Chemistry/ Biochemistry/ Health Sciences fields * Technical background preferred * Typically requires 5 years of relevant experience in an Analytical Chemistry / Quality Control laboratory, preferably in a GMP environment * Experience in leading others in project context * Effective time management skills and the ability to multitask. * Track record of overachieving targets * Possess solid knowledge of Analytical Chemistry / Quality Control principles and practices * Knowledge and experience of GMP and ICH guidelines * Good communication skills (verbal and written) \- Skilled at managing processes and tools \- Fluency in English is a requirement * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

QC Specialist - Temporary64088839130113124

Indeed

QC Specialist - Temporary

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * Manage and support quality control projects while ensuring compliance with GMP, operational standards, and legal regulations; * Use analytical techniques and instrumentation, such as gas and high\-performance liquid chromatography (HPLC) amongst others; * Perform method development, validation, transfer, and reporting in a timely and cost\-effective manner; * Address analytical challenges proactively, provide support across departments, and escalate unresolved issues; * Ensure a seamless flow of information within teams and external stakeholders to maintain project efficiency; * Investigate CAPAs, deviations, and incidents while assisting with audits and compliance reporting; * Maintain hygiene, perform equipment calibrations, and accurately utilize laboratory information systems; * Support the onboarding of new team members and contribute to the advancement of analytical chemistry expertise; * Analyze and interpret laboratory data, ensuring accuracy in documentation and adherence to GLP standards; * Make informed quality control decisions while supporting KPI generation and reporting processes; * Uphold all GMP, HSE, and company\-specific procedures, ensuring a safe and high\-quality operational environment (COPs, HBR, SOPs and others); * Assist with audits / investigations as required, following the instruction of QC Management. We are looking to recruit a Candidate:: * Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field; * Typically requires 3\-5 years of relevant experience in a pharmaceutical QC laboratory environment (mandatory); * Hands\-on experience in Analytical Chemistry and QC procedures (mandatory); * Training and experience of GMP and ICH guidelines standards (mandatory); * Knowledge on HPLC and GC, and familiarity with Empower Software (desirable); * Strong understanding and knowledge of GMP practices, analytical theory and techniques; * Fluency in English is a requirement; * Computer literate with good working knowledge of the MS Office package; * Good documentation skills and attention to detail. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity. ***Notice to Agencies and Search Firms Representatives*** *Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third\-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.*

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Qualification & Validation Specialist63822737365507125

Indeed

Qualification & Validation Specialist

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: As a **Qualification \& Validation Specialist**, you will play a key role in ensuring that our facilities, equipment, and systems are fit for purpose and compliant with applicable quality standards. You will work cross\-functionally to define and implement best practices in qualification and validation, supporting both local and global initiatives. **Key Responsibilities*** Ensure cGMP compliance before, during, and after qualification/validation activities. * Validate systems, equipment, and processes according to intended use and product requirements. * Support continuous improvement and promote a quality\-driven culture. * Align qualification and validation procedures across Hovione sites. * Collaborate with Engineering, Maintenance, Production, and Quality Control to ensure system compliance. * Participate in project design reviews to ensure GMP compliance. * Develop and approve validation protocols, VMPs, and related documentation. * Support audits and inspections, and manage deviations, CAPAs, and change controls. * Provide training and contribute to the development of quality system methodologies. * Ensure safe work practices and compliance with HSE and GMP guidelines. We are looking to recruit a Candidate:: **Education \& Experience:*** University degree in Chemistry, Chemical Engineering, Mechanical Engineering, or a related scientific field (mandatory). * 3–5 years of experience in Qualification \& Validation, preferably in a GMP\-regulated environment. **Technical Skills:*** Strong knowledge of cGMP, ICH, ISO guidelines, and risk assessment methodologies. * Experience with process and HVAC systems is a plus. * Fluent in English; proficient in MS Office. **Soft Skills:*** Strong problem\-solving and decision\-making abilities. * Ability to work independently and collaboratively. * Excellent communication and documentation skills. **Why Join Us?*** Be part of a mission\-driven organization that values quality, innovation, and collaboration. * Work in a dynamic, high\-impact environment with opportunities for growth. * Contribute to global projects and continuous improvement initiatives. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Indeed

Analyst

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * To organize and define daily priorities within their assigned tasks in order to accurately and promptly perform the allocated sample analysis to meet the requirements of the periodic laboratory plan and area KPIs. * To adhere to the laboratory testing schedule in order to achieve an efficient Quality Control (QC) system. * Take responsibility for all data individually generated and ensure it is in accordance with all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities. * To maintain all checklists, laboratory records and notebooks in which he/she is involved to an acceptable GMP standard and in accordance with Hovione internal procedures. * To maintain good hygiene and housekeeping within the laboratory. * To perform routine calibration and both corrective and preventative maintenance of designated laboratory instruments, requesting any instrument parts and consumables required by the area. * Comply with the high standards in the QC Laboratories. * To bring any discrepancies, deviations or non\-conformance in testing or work practice to the attention of QC management in accordance with Hovione internal procedures. * To issue events and support the investigation of OOS/OOT/atypical results, deviations and QC incidents generated in the QC Laboratories. * Ensure appropriate communication with other internal department in relation to QC work by using the appropriate Hovione processes and their IT platforms. * Assist with audits as required, following the instruction of QC Management. * Undertake any additional tasks to support the laboratory activities as and when required. * Seek out additional information when one feels that the available information is not enough. * Follow all annual performance review requirements, including completion of the self\-assessment. * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. * Ensure facility activities are carried out in compliance with all GMP, legal and HSE regulations and applicable standards in the country of operation, complying with and enforcing all Hovione processes and good practice. We are looking to recruit a Candidate:: * High School diploma (mandatory) * Qualification in a relevant chemistry, analytical chemistry, chemical engineering, pharmaceutical\-related or other science\-related field (mandatory) * Relevant work experience * Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (mandatory) * Experience of GMP practices and HSE standards (preferable) \- Technical understanding of GMP practices, analytical theory and techniques \- Clear and open communication skills (written and verbal) * Competent (written and verbal) English (preferable for sites where English is not the first language) * Ability and availability to work in shift patterns, as required by business needs * Computer literate with knowledge of the MS Office package AK382 * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

QC Technical Specialist63822737250819127

Indeed

QC Technical Specialist

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Defines and implements quality control techniques in order to verify the quality of raw materials, intermediate and end products as well as any other analytical services relevant to our client base and according to regulatory requirements. Manage and control all Quality Control activities in accordance with identified quality assurance standards, company procedures, client specifications, contract requirements, and regulatory guidelines. * Ensure the effective and proactive flow of information and requests between the QC team and the internal and external (if applicable) stakeholders * Participate in meetings with internal and external customers as representative of analytical area, providing information on the status of activities * Provide collaborative and timely support in the resolution of analytical problems relating to assigned projects / initiatives * Propose and prepare changes to QC procedures or analytical methods for onwards approval and implementation * Assure product specifications are maintained in accordance with appropriate standards and propose revisions as required * Issue and follow\-up change controls * Assure good functioning equipment, planning and managing the maintenance, internal calibration plans, reference standards and internal qualifications of designated laboratory instruments * Accurately use and maintain all laboratory information systems, participating in the implementation of lab systems improvements as required * Prepare protocols, reports, QC documentation and review records to ensure compliance with cGMP and HSEE standards * Request quotations and propose the acquisition of instruments, materials and reagents to guarantee the stock control and operation of the laboratories * Manage reserve/retention samples * Initiate events and deviations in the CAPA system in accordance with the required timeframes and in partnership with appropriate colleagues, complete relevant section/s of the event or deviation * Lead and participate in root\-cause investigations, guiding colleagues (as required) in the necessary investigative testing, and ensuring appropriate corrective and preventative actions are determined * Determine the root cause of events and deviations based upon the data and information obtained through the investigation, ensuring appropriate corrective and preventative actions are determined * Complete or support the completion/close out of OOS/OOT laboratory deviation investigations and QC incidents * Monitor progress and follow\-up corrective and preventative actions * Monitor the status of open events and deviations and provide periodic status reports to QC management * Assess the impact of changes to facilities/systems/equipment/stability and processing of change control documents * Perform periodic checks of laboratory documentation to ensure compliance with applicable operating procedures and identify and implement updates/improvements to current procedures * Be an advocate for safe operating and high\-quality performance within the area, alerting the management of the area to any potential risks, discrepancies, deviations or non\-conformance in accordance with Hovione internal procedures, suggesting optimizations or improvements * Prepare and participate in internal/external audits as requiredSupport the compilation of audit responses for QC * Ensure all assigned tasks are planned and delivered on time, safely, efficiently, reliably and in a cost\-effective manner * Propose improvements to the area as appropriate * Make quality and timely decisions within the tasks under her / his responsibility * Gather relevant data to inform the decision makers regarding complex issues * Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others) * Undertake any additional tasks commensurate with the role as and when required * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. We are looking to recruit a Candidate:: * University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory) * Typically requires 3\-5 years of relevant experience in a QC laboratory environment, preferably under pharmaceutical cGMP (desired) * Training and experience of GMP and ICH standards (mandatory) * Experience of HSE rules and regulations (mandatory) * Experience of investigational analysis (desired) * Strong understanding and knowledge of GMP and ICH practices, analytical theory, and techniques * Knowledge of EU/US quality related pharmaceutical regulations * Competence in conducting quality\-based investigations and root cause analysis * Fluency in English is a requirement * Computer literate with good working knowledge of the MS Office package **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Indeed

Supply Chain Director

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: * Lead and develop the site supply chain team using servant leadership principles, promoting a culture of coaching, accountability, and alignment with corporate strategy and values. * Ensure execution of all end\-to\-end supply chain activities (transportation, warehouse, import/export, distribution, planning) with a focus on long\-term performance and creative problem\-solving. * Manage and execute supply chain projects that improve operational processes and systems across the site. * Drive standardization and best practice implementation across functions and sites by partnering with corporate and local teams, fostering continuous improvement and harmonization. * Promote cross\-functional collaboration and team performance management, including recruitment, onboarding, training, and fostering a high\-performance culture aligned with strategic goals. * Define and lead strategic initiatives to address complex supply chain challenges, working closely with production, R\&D, maintenance, and engineering departments. * Define, implement, and monitor inventory targets, KPIs, and metrics, ensuring strong governance and data\-driven decision\-making. * Support the creation and control of supply chain budgets and resource planning, including variance analysis and corrective action planning. * Ensure compliance with GMP, HSE, and internal quality systems, while maintaining accurate documentation and safe working practices. We are looking to recruit a Candidate:: * 10\+ years of supply chain experience within a manufacturing industry, ideally in the pharmaceuticals or fine chemicals. * Master’s degree in Business Administration, Logistics, Engineering, or related field (technical background preferred), with * Proven leadership and coaching capabilities, with a track record in developing people and achieving performance targets. * Deep knowledge of supply chain principles, tools, and best practices across Planning \& Control (e.g., S\&OP, materials planning, master data), Logistics, and Warehouse/Shipping. * Strong process and time management skills, able to drive continuous improvement and operational excellence. * Solid understanding of applicable regulations, international trade policies, and insurance in a global supply chain context. * Excellent communication skills (verbal and written), with fluency in both Portuguese English and the ability to work in compliance with internal procedures and external standards. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Drug Product Operations Process Engineer63822737146243129

Indeed

Drug Product Operations Process Engineer

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are **In it for life**. You will be responsible to:: * Support and mentor production teams to optimize drug product manufacturing processes, minimize downtime, and maximize productivity; * Identify and troubleshoot operational issues related to equipment and drug product processes, implementing innovative solutions to enhance efficiency and quality; * Monitor and analyze production data to ensure compliance with regulatory standards and quality control measures; * Participate in client visits as a technical expert, providing insights into our operational processes; * Prepare and review manufacturing process documentation, including batch production records, campaign reports, change controls, operating manuals/procedures, mass balance sheets, bill of materials, cost proposals, validation plans, validation reports, and other GMP\-related documentation for all processes run in operations; * Update Line Managers and team members on relevant occurrences and trends that may significantly impact Area KPIs; * Provide training and guidance to team members to achieve production objectives and enhance their skills and knowledge; * Coordinate tech\-transfers and process improvement projects for established and new processes, utilizing the best available technology, practices, and tools; * Act as a technical expert on operational activities; * Train, coach, and manage operational teams to ensure adherence to standards developed by Hovione and encourage individual ownership towards achieving overall team goals. We are looking to recruit a Candidate:: * Bachelor's degree in Chemical Engineering, Pharmaceutical Engineering, or a related field; * Proven experience and knowledge working within the pharmaceutical industry and/or or Drug Product (area of production) processes like compounding, coating, tableting, granulation or encapsulation; * Strong knowledge of GMP (Good Manufacturing Practices) and regulatory requirements; * Excellent problem\-solving skills and the ability to work under pressure; * Effective communication skills to collaborate with cross\-functional teams and represent the company to clients; * Experience in technical manufacturing support; * Strong interpersonal, team\-oriented skills, self\-motivation and direction, with strong bias toward timely performance and problem resolution; * Competent English (written and verbal); * Computer literate with good working knowledge of SAP Intermediate; * Availability to work in shifts. **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity. ***Notice to Agencies and Search Firms Representatives*** *Hovione does not accept unsolicited resumes from agencies or search firms for this job posting. Any resumes submitted to Hovione by a third\-party agency or search firm without a valid written and signed search agreement will become the sole property of Hovione. No fees will be paid if a candidate is hired for this position as a result of an unsolicited referral.*

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Quality Assurance Specialist638227371790111210

Indeed

Quality Assurance Specialist

Join a Market Leader: Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off\-patent drugs to market. Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites. Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. That is why we are In it for life. You will be responsible to:: Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual needs of each project. Implements policies, procedures and methods to evaluate and to continuously improve the quality of products and operations throughout the products lifecycle. Provides global supplier qualification services in support of new product introduction and existing products. Collaborates with suppliers and Procurement to assure the quality of their products, materials, components and/or operations. * Rigorously, accurately, efficiently and professionally manage all quality activities for the assigned projects and / or products in accordance with applicable cGMP, quality operational standards / procedures and legal regulations, ensuring the site is always “audit ready” * Promote the importance of high\-quality levels and the importance of a continuous improvement culture in relevant company activities * Act as a catalyst for change and improvement in performance/quality * Assigned projects may relate to any of the following (non\-exhaustive) areas: Raw Materials, Suppliers, Specifications, Production Processes, Change Control, Deviations, Quality agreements, Qualification and Validation, Stability Programs, Batch Release, Equipment Cleaning, Client Audits, Internal Audits, Customer Complaints, Customer requirements, PQR * Provide an example of professionalism and support the induction and training of new colleagues within the area * Efficiently, accurately and reliably ensure that project and / or product activities are delivered in compliance with cGMP requirements and maintenance of the company Quality Management System is assured * Manage and participate in Quality Product key activities for the assigned product / projects, and introduction of new products; including (but not limited to) preparation, review and approval of auxiliary documentation, protocols and quality related reports * To prepare for and support internal and external site audits and inspections, conducting regular reviews and periodically following\-up action plans as necessary. * Ensure inspection readiness in work completed and Act in an advisory capacity for all internal and external site audits * Periodic follow\-up of ongoing deviations and PdAs to assure timely closure of deviations and approval of PdAs, as appropriate * To close open deviations and propose CAPAs based on the outcome of periodic follow\-ups * Prepares SOPs, department IOPs, quality related reports, revision of executed batch documentation and change control documents (PdAs) as required and appropriate * Approves IOPs, process master documentation and product specifications as required and appropriate. * Ensures that SOPs and IOPs are up to date, compliant and supports efficient production * Review regulatory documentation and co\-ordination of site documentation to support regulatory requirements * Authorize the usage of production equipment/utilities when qualification required * Solve challenges related to compliance problems by providing collaborative and timely support to all areas and departments, escalating as required * Ensure the effective and proactive flow of information between stakeholders, representing the team as appropriate * To assure and promote compliance on Health, Safety and Environment in the area and activities for which is responsible, or in which participates * To maintain a regular presence on manufacturing floor, providing on\-the\-job support, developing a sense of collaboration with operational areas and performing a general oversight of activities, as required * To approve Validation Master Plans, Process Validation Protocols and reports as required * Accurately use and maintain all information systems * Support the generation / reporting of KPIs for the team. * Develop and accumulate strong QA expertise, sharing knowledge of new developments and methodologies within the area * Co\-ordinate and assist with the analysis and investigation of customer complaints that may arise; ensuring all complaints are investigated and closed out within specified timeframes * To provide relevant training to new colleagues, and to the other areas in applicable cGMP, internal procedures and quality systems in accordance with established training plans * Be an advocate for safe operating and high\-quality performance, alerting ascending colleagues to any potential risks, discrepancies, deviations or non\-conformance in accordance with Hovione internal procedures, suggesting optimizations or improvements * Ensure all assigned tasks are planned and delivered on time, safely, efficiently, reliably and in a cost\-effective manner * Propose improvements to the area as appropriate and solve problems * Make quality and timely decisions within the Quality Assurance tasks under her / his responsibility * Gather relevant data to inform the decision makers regarding complex issues * Execute professional activities in compliance with GMP and HSE guidelines, internal and external requirements as well as promote the implementation and maintenance of Hovione´s policies, systems and procedures (COPs, HBR, SOPs and others) * Undertake any additional tasks commensurate with the role as and when required. * Carry out assigned tasks and duties in a safe manner, in accordance with instructions, and to comply with environmental, health \& safety rules/procedures, regulations and codes of practice. We are looking to recruit a Candidate:: * University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar scientific field (mandatory) * Typically requires 3\-5 years of relevant experience in a QA GMP environment within the Pharmaceutical Industry (highly desirable) * Experience of working in a GMP operational environment (mandatory) * Training and experience of GMP standards (mandatory) * Experience of working with Regulatory Affairs and a basic knowledge of the function (desirable) * Strong understanding and knowledge of GMP practices * Fluency in English is a requirement * Computer literate with good working knowledge of the MS Office package * Strong documentation skills and attention to detail **Hovione is a proud Equal Opportunity Employer** Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

R. António Caetano Bernardo 6B, 2670-457 Loures, Portugal

Negotiable Salary

Analyst, Quality Control - H4 - Robot642789760152331211

Indeed

Analyst, Quality Control - H4 - Robot

Description: Founded over 40 years ago by Samih Darwazah in Jordan, Hikma's purpose is to provide high-quality, affordable medicines to people who need them. Built on strong foundations, we continue every day to innovate and find practical solutions to transform the lives of the millions of people we serve. In the late 1980s, we expanded our reach beyond the Middle East and acquired land in Portugal for the construction of a manufacturing facility for sterile injectable pharmaceuticals. This was a significant turning point for the company and our first step into a new region. Today, in Portugal, we have more than 900 employees and three manufacturing plants for injectable medicines. Hikma is seeking to recruit an **Analyst, Quality Control** (m/f) to join its **Quality Control** department, on-site. We value responsibility, enthusiasm for challenges, proactivity, motivation, and teamwork. **Desired Profile:** * Bachelor’s degree in Chemistry or Biochemistry; * Industrial experience and knowledge of GMPs are valued; * Good level of English; * Proficiency in Microsoft Office; * Ambition and team spirit; * Interpersonal skills valued: dynamism, time management, flexibility, assertiveness, and attention to detail; * Proactivity and autonomy are essential traits for performing the role. **Main Responsibilities:** * Qualification of the new Waters Andrew\+ Pipetting Robot equipment. * Validation of analytical methods using the new Waters Andrew\+ Pipetting Robot equipment, combined with HPLC techniques. * Daily documentation of collected data and verification of the accuracy of reported values. * Writing qualification and analytical method validation reports using the new Waters Andrew\+ Pipetting Robot equipment. * Ensuring data integrity and compliance with GMP regulations for all laboratory tasks performed. **We Offer:** * Competitive salary package aligned with the responsibilities * Opportunity to join a rapidly expanding group If you believe this is a great opportunity for your professional career, join us and contribute to *better health, accessible to everyone, every day.* Location: Sintra, Sintra, PT

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Assistente de Sala (m/f/d) | Restauração642266499937301212

Indeed

Assistente de Sala (m/f/d) | Restauração

Our culture is shaped by each one of us. We are passionate about everything we do and build. We are experts in every business area, and we believe that attitude, dedication, and the willingness to learn contribute to making us a standout company in the job market. Here, you will have a world of opportunities waiting for you! We are looking for Room Assistants. Below, check out what you will do with us, what we expect from you, and what you can expect from us. What will you do with us? * Delivering excellent service * Taking orders and serving guests at tables * Preparing, organizing, and cleaning the dining area What do we expect from you? * Minimum education level of 9th grade; * Willingness to learn; * Team spirit; * Availability for rotating days off; * Good communication skills; * Positivity and teamwork; * Dedication and sense of responsibility. What can you expect from us? * Initial and ongoing training tailored to the role; * Opportunities for development and career progression; * 3 extra vacation days if there are no unjustified absences; * Birthday leave or half\-day leave for your child(ren)'s birthday(s); * Medical center available to our employees; We also believe that with us, you will have the right opportunity to grow, develop, and share your experiences. Your application is only complete when you fill out our recruitment form! Link: https://lnkd.in/emuScAbF We have different stories, but a common purpose. Join\-us! \#juntosfazemoshistória Type of offer: Part\-time Expected hours: 25 per week Benefits: * Internet access

PV49+C7 Lisbon, Portugal

Negotiable Salary

Indeed

Promoters (m/f/d)

Our culture is shaped by each one of us. We are passionate about everything we do and build. We are experts in every business area, and we believe that attitude, dedication, and the willingness to learn contribute to making us a distinctive company in the job market. We are seeking a Promotion and Management employee whose main responsibility will be acquiring new customers for the El Corte Inglés credit card through direct customer approach within the store. Below you can find what you will do with us, what we expect from you, and what you can expect from us. What you will do with us? * Actively promote the El Corte Inglés card among potential customers visiting the ECI shopping center. This involves approaching customers, explaining the card's benefits, answering questions, and assisting them through the application process. * Achieve sales targets by working to meet and exceed the company's established sales goals. * Provide high-quality service and proper assistance to current and potential customers to ensure a positive experience at all times. * Represent and act as an ambassador of the company's brand image. What we expect from you? * High school diploma (12th year); * Availability for rotating shifts (between 9:00 AM and 11:30 PM); * Availability for rotating days off; * Determination and dynamism; * Communication skills and solution-oriented mindset; * Sense of responsibility; * Goal-oriented attitude; What you can expect from us? * Initial and continuous training tailored to the role; * Opportunities for development and career progression; * 3 extra vacation days if there are no unjustified absences; * Birthday leave or half-day leave for your child(ren)'s birthday(s); * Parental support measures; * Medical center available to our employees. We also believe that with us, you will have the right opportunity to grow, develop, and share your experiences. To complete your application, access our Employment Portal via the link: https://empleo.elcorteingles.es/ep/ We have different stories, but a common purpose. Join us! \#wemakehistory Job Type: Full-time Benefits: * Internet access

PV49+C7 Lisbon, Portugal

Negotiable Salary

Lyophilized Production Technician - 8H642266500366091214

Indeed

Lyophilized Production Technician - 8H

Description: Founded over 40 years ago by Samih Darwazah in Jordan, Hikma's purpose is to provide high-quality, affordable medicines to people who need them. Built on strong foundations, we continue every day to innovate and find practical solutions to transform the lives of the millions of people we serve. In the late 1980s, we expanded our reach beyond the Middle East and acquired land in Portugal for the construction of a factory to produce sterile injectable pharmaceuticals. This was a significant turning point for the company and our first step into a new region. Today, in Portugal, we have more than 900 employees and three factories producing injectable medications. Hikma is seeking to hire a **Technician II, Lint Free** (m/f) to join its **Production** department, working onsite in a fixed afternoon or night shift. We value responsibility, enthusiasm for challenges, proactivity, motivation, and teamwork. **Main Responsibilities:** * Prepare the production line; * Perform routine tasks related to cleaning the production line; * Operate machinery; * Carry out job-related tasks in compliance with internal and external regulations; * Conduct environmental monitoring in the production area. **Ideal Candidate Profile:** * Education: High school diploma (12th grade) * Professional experience in an industrial environment will be valued * Strong interpersonal skills * Proactivity and autonomy are essential traits for performing the role * Availability to work a fixed shift (afternoon or night) between 3:00 PM and 7:00 AM * Availability to work on rotating days off. **We Offer:** * Competitive salary package appropriate to the responsibilities * Life insurance * Health insurance * Opportunity to join a rapidly expanding group If you believe this is a great opportunity for your professional career, join us and contribute to Better Health, Within Reach of Everyone, Every Day. Location: Sintra, Sintra, PT

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Assistant, Documentation642154961418261215

Indeed

Assistant, Documentation

Description: Founded over 40 years ago by Samih Darwazah in Jordan, Hikma's purpose is to provide high-quality, affordable medicines to people who need them. Built on strong foundations, we continue every day to innovate and find practical solutions to transform the lives of the millions of people we serve. In the late 1980s, we expanded our reach beyond the Middle East and acquired land in Portugal for the construction of a sterile facility for injectable pharmaceutical products. This was a significant turning point for the company and our first step into a new region. Today, in Portugal, we have over 1,000 employees and three manufacturing plants producing injectable medicines. Hikma is seeking to recruit a **Documentation Assistant (m/f)** to join the **Quality Department**. **Main Responsibilities:** * Issuance of batch records and related documents; * Filing of production documents; * Perform job tasks in compliance with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs). **Ideal Candidate Profile:** * Completed 12th grade; * Proficiency in Microsoft Office (Word, Excel, PowerPoint, and Outlook); * Professional experience in an industrial environment is an advantage; * Strong verbal and written communication skills; * Proactivity, autonomy, and teamwork spirit; * Availability to work fixed shifts; * Valid driver's license and own vehicle. **We Offer:** * Temporary employment contract; * Competitive salary package appropriate to the responsibilities performed. If you believe this is a great opportunity for your professional career, join us and contribute to Better Health, Within Reach of Everyone, Every Day. Location: Sintra, Sintra, PT

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Analyst, Quality Control640891117384971216

Indeed

Analyst, Quality Control

Description: Founded over 40 years ago by Samih Darwazah in Jordan, Hikma's purpose is to provide high-quality and affordable medicines to people who need them. Built on strong foundations, we continue every day to innovate and find practical solutions to transform the lives of the millions of people we serve. In the late 1980s, we expanded our reach beyond the Middle East and acquired land in Portugal for the construction of a manufacturing facility for sterile injectable pharmaceuticals. This was a significant turning point for the company and our first step into a new region. Today, in Portugal, we have more than 900 employees and 3 manufacturing plants producing injectable medicines. Hikma is seeking to recruit a Quality Control Analyst (m/f) to join its Quality Control department, onsite, working in a 3-shift system: morning, intermediate, and afternoon shifts. We value responsibility, enthusiasm for challenges, proactivity, motivation, and teamwork. **Desired Profile:** * Bachelor’s degree in Chemistry or Biochemistry; * Experience in an industrial environment and with GMPs is valued; * Professional experience in the field will be preferred; * Good command of English; * Proficiency in Microsoft Office; * Ambition and team spirit; * Interpersonal skills valued: dynamism, time management, flexibility, assertiveness, and attention to detail; * Proactivity and autonomy are essential characteristics for performing the role; * Availability to work in shifts. **Main Responsibilities:** * Analyze raw materials, packaging materials, finished products, and stability samples according to specified testing requirements; * Perform analyses after cleaning production machine components; * Record daily collected data and verify accuracy of reported values; * Write SOPs and reports (investigation reports, vendor validations, among others); * Conduct analysis of materials supporting production. **We Offer:** * Direct employment contract with the company; * Salary package commensurate with the responsibilities; * Life insurance; * Health insurance; * Integration into a rapidly expanding group. If you believe this is a great opportunity for your professional career, join us and contribute to *better health, accessible to everyone, every day.* Location: Sintra, Sintra, PT

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Pharmaceutical Technician - Lourinhã640888940067871217

Indeed

Pharmaceutical Technician - Lourinhã

We are recruiting a Pharmaceutical Technician to join the team of a pharmacy located in Lourinhã. **Main responsibilities:** * Providing customer service and advising on health and well\-being; * Dispensing prescription and non\-prescription medications; * Stock management, ordering, receiving and checking products; * Assisting in the organization and daily operations of the pharmacy; * Supporting the delivery of pharmaceutical services and health promotion initiatives. **Profile:** * Bachelor's degree in Pharmacy; * Strong communication skills and enjoyment of direct customer interaction; * Sense of responsibility, accuracy, and teamwork; * Dynamism and motivation for professional development. **Offer:** * Integration into a stable, collaborative team with strong community ties; * Attractive salary conditions adjusted to demonstrated experience; * Opportunities for professional growth and development in a structured environment. Type of offer: Full\-time

Av. de Moçambique A, 2530 Lourinhã, Portugal

Negotiable Salary

Pharmacy Technician - Algés640888940267531218

Indeed

Pharmacy Technician - Algés

We are recruiting a Pharmacy Technician to join the team of a pharmacy located in Algés. **Main Responsibilities:** * Customer service and advising on medications and health products; * Assistance in receiving, storing, and stock control; * Collaboration in the organization and daily operation of the pharmacy; * Participation in pharmaceutical services and health promotion campaigns; * Support to the technical team in various tasks related to pharmaceutical activities. **Ideal Candidate Profile:** * Bachelor's degree in Pharmacy; * Experience in community pharmacy (valued), although candidates at the beginning of their careers will also be considered; * Enjoy customer service and have good communication skills; * Organizational skills, dynamism, and teamwork spirit. **Offer:** * Integration into a pharmacy with an experienced and collaborative team; * Salary package tailored to profile and experience; * Opportunity for learning and professional growth in a dynamic environment. Type of offer: Full-time/Full\-time

R. António Sérgio 5, 2780-199 Oeiras, Portugal

Negotiable Salary

Indeed

Pharmacy Technician

Farmácia Santa Marta is an establishment with 63 years of history, being a reference location in the Barreiro area. Currently, it is recruiting a Pharmacy Technician to join its team. **Main Responsibilities:** * Attend to customers and provide information regarding proper use of medications and/or health products * Perform tasks related to the pharmacy's operations **Requirements:** * Pharmacy Technician qualification * Strong sense of responsibility * Proactivity, friendliness, and dynamism * Team spirit and enjoyment in public interaction **Offer** * Opportunity to join a dynamic and experienced team * Immediate start * Employment contract * Participation in various pharmaceutical intervention projects * Continuous training and updates on brands sold in pharmacies * Competitive base salary commensurate with experience, plus meal allowance, holiday allowance, Christmas allowance, and performance bonuses Apply now! Send your CV to \- stamartabarreiro@gmail.com Job type: Full-time Benefits: * Meal card/Ticket Education: * Higher education (Preferred)

R. 1B 85, 2830-302 Barreiro, Portugal

Negotiable Salary

Pharmacist – Production Area (M/F)640888626522911220

Indeed

Pharmacist – Production Area (M/F)

**Required Profile:** Bachelor's degree in Pharmaceutical Sciences or equivalent field Minimum of 1 year of experience in the Pharmaceutical Industry (preferably in Manufacturing/Production) Knowledge of national and European regulations (GMP) **Valued:** Experience in statistical process control, manufacturing validations and Pharmaceutical Technology Good command of English and computer skills Planning, organizational and interpersonal skills **Main Responsibilities:** Support and report to Production Management Review documentation related to drug manufacturing Contribute to compliance with GMP standards and NP EN ISO 9001, 14001 and 45001 certifications Support manufacturing processes, validations and statistical control An opportunity to join a solid company in the pharmaceutical sector and develop expertise in production with high quality standards.

R. D.João IV 13, 2800-712 Almada, Portugal

Negotiable Salary

Indeed

Pharmacist (m/f)

Talent Formula is a Human Resources consulting company that supports Portuguese companies in the growth and development of their employees. We are currently recruiting a Pharmacist (m/f) for a client pharmacy located in Sintra. Main responsibilities: Customer service at the pharmacy; Advice on medications and health and wellness products; Pharmaceutical care follow\-up programs. Requirements: Integrated Master's Degree in Pharmaceutical Sciences; Excellent communication and persuasion skills; Proactivity and dynamism; Strong interpersonal relationship skills; Results and goal\-oriented; Passion for working in community pharmacy with a focus on customer service; Team spirit. We offer: Stimulating work environment; Traditional neighborhood community pharmacy; Continuous training; Ongoing professional development opportunities; Working hours \- Monday to Friday: 9:00 AM to 7:00 PM \- Saturdays: 9:00 AM to 1:00 PM \- Sundays and Holidays: Closed If you believe you have the right profile and are interested in this opportunity, apply here! Type of offer: Full\-time Educational qualifications: * Master's degree (Preferred)

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Barral Group Recruitment – PHARMACISTS & PHARMACY TECHNICIANS638229414577931222

Indeed

Barral Group Recruitment – PHARMACISTS & PHARMACY TECHNICIANS

**The Barral Group is hiring!** We are looking for **Pharmacists** and **Pharmacy Technicians** to join different teams in our pharmacies in Lisbon. If you enjoy caring, communicating, and growing in a dynamic environment, this opportunity is for you. Locations: * **Oriental Pharmacy** * **Barral Pharmacy** * **Jerónimos Pharmacy** * **Av. Ceuta Pharmacy** **Positions available:** * **Pharmacist** * **Substitute Pharmacist** * **Pharmacy Technician** **What we value in your profile:** * Integrated Master's Degree in Pharmaceutical Sciences or Professional Course in Pharmacy Technician completed or nearly completed; * Strong communication skills and empathy with customers; * Passion for personalized customer service; * Team spirit and desire to grow; * Proactivity and responsibility. **Main responsibilities:** * Personalized pharmaceutical care and advice; * Support for pharmacy operational tasks (orders, receiving, stock organization); * Participation in health campaigns, screenings, and internal projects. **What we offer:** * Innovative projects in health, dermocosmetics, and wellbeing; * Continuous training and opportunities for advancement; * **Flexible schedules** and a healthy work environment; * **Competitive compensation**, bonuses, and incentives; * Store discounts and favorable conditions on products and services. **Send your CV to**: rhfarmaciaoriental@gmail.com Indicate the pharmacy(s) of interest and your availability. We are looking for talent and motivation – even if this is your first challenge! Type of position: Full-time

PV49+C7 Lisbon, Portugal

Negotiable Salary

Pharmacist for Pharmacotherapeutic Monitoring (m/f)638229414736651223

Indeed

Pharmacist for Pharmacotherapeutic Monitoring (m/f)

Talent Formula is a Human Resources consulting company that supports Portuguese companies in the growth and development of their employees. We are currently recruiting a Pharmacist (m/f) for a client pharmacy located in Sintra. Main responsibilities: * Customer service at the pharmacy; * Counseling on medications and health and wellness products; * Pharmacotherapeutic monitoring programs. Requirements: * Integrated Master's Degree in Pharmaceutical Sciences; * Excellent communication and persuasion skills; * Proactivity and dynamism; * Strong interpersonal skills; * Goal and results orientation; * Passion for working in community pharmacy with a focus on customer service; * Team spirit. We offer: * Stimulating work environment; * Traditional neighborhood community pharmacy; * Continuous training; * Constant opportunities for professional development; * Working hours \- Monday to Friday: From 9:00 AM to 7:00 PM \- Saturdays: From 9:00 AM to 1:00 PM \- Sundays and Holidays: Closed If you believe you have the right profile and are interested in this opportunity, apply here! Type of offer: Full time

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Pharmacy Technician (m/f)638229414892831224

Indeed

Pharmacy Technician (m/f)

**The Talent Formula** is a human resources consulting company that supports Portuguese organizations in promoting and developing their employees. We are currently recruiting for a **client pharmacy located in Lisbon**, a **Pharmacy Technician (m/f)**. **Main responsibilities:** * Customer service in pharmacy * Pharmaceutical and health & wellness products counseling **Desired profile:** * Bachelor's degree in Pharmacy * High sense of responsibility, accuracy, and autonomy * Enjoyment of public interaction and team spirit * Proactivity and results orientation * Good interpersonal relationship skills * Computer literacy **What we offer:** * Integration into a solid project with sustained growth * Positive work environment within a cohesive and collaborative team * Competitive salary commensurate with demonstrated experience If you identify with this challenge and have the profile we are looking for, **apply here** Job type: Full-time Experience: * Pharmaceutical: 1 year (Preferred)

PV49+C7 Lisbon, Portugal

Negotiable Salary

Automation and Electrical Technician for Electric Vehicle Chargers (m/f/d)638228754140171225

Indeed

Automation and Electrical Technician for Electric Vehicle Chargers (m/f/d)

**Automation and Electrical Technician for Electric Vehicle Chargers (m/f/d)** **Siemens Smart Infrastructure** connects buildings and cities to make them smarter and more energy-efficient! We help our customers thrive, communities progress, and support balanced development to protect our planet for the next generation. Working together with our global customers and partners, we help build intelligent solutions and outstanding places across the entire spectrum of buildings where we live, work, and relax. Siemens SI has its global headquarters in Switzerland, with around 7,400 employees in the European region, and is responsible for solutions and services business, being the market leader in Europe. **Together, we build technologies that take society even further.** **Shape the future with us!** **Your mission will be...*** Conducting and validating final factory electrical tests on electric vehicle chargers; * Completing quality control documentation according to test instructions and procedures, drawings, and specific documentation, following customer requirements; * Performing functional tests, parameterization, and calibration of circuits and components to ensure perfect equipment/product functionality before delivery to the customer; * Supporting and executing test procedures aligned with Engineering during technical visits conducted by the customer; **We are looking for someone with...*** Professional Technical qualification (Level III/IV) in Automation (preferred)/Electrical/Electrical Installations, or similar, equivalent to 12th grade; * In-depth knowledge of Electricity, Electronics, and Automation; * General knowledge of instrumentation, process, and electrical measurement signals; * Skills in reading and understanding electrical schematics and technical specifications; * Proficiency in using computer systems from a user perspective; * Fluency in English and Portuguese; * Punctuality, responsibility, teamwork enthusiasm, autonomy, and dynamism; **What you can expect****...** A flexible hybrid working model to promote a better work-life balance, along with a home office support budget and the opportunity to perform 16 hours per year of volunteer work. Health insurance, access to our on-site medical center, as well as the possibility to join sports groups. Additionally, you will have access to online learning platforms, discounts with our partners, and the possibility of financial support for your studies. **What makes us proud as an employer...*** Best Companies to Work for in Portugal 2023 (by LinkedIn); * World's Best Employers 2023 \- 1st place in the Engineering and Manufacturing category (by Forbes); * Most Attractive Workplace in 2023 \- 6th place (Universum ranking); * Company with the best reputation in the Technology/Industrial sector in Portugal 2023 (according to Merco Empresas study); **\#Siemens \#PeopleAtSiemens** *Siemens is committed to creating a diverse environment and is glad to be an equal opportunity employer. We strongly encourage applications from a diverse talent pool!*

R. Q.ta do Conde 29A, 2855 Corroios, Portugal

Negotiable Salary

Technician II, Lint Free638228734410251226

Indeed

Technician II, Lint Free

Description: Founded over 40 years ago by Samih Darwazah in Jordan, Hikma's purpose is to provide high-quality, affordable medicines to the people who need them. Built on strong foundations, we continue every day to innovate and find practical solutions to transform the lives of the millions of people we serve. In the late 1980s, we expanded our reach beyond the Middle East and acquired land in Portugal for the construction of a manufacturing facility for sterile injectable pharmaceuticals. This was a significant turning point for the company and our first step into a new region. Today, in Portugal, we have more than 900 employees and three manufacturing plants for injectable medicines. Hikma is seeking to recruit a **Technician II, Lint Free** (m/f) to join its **Production** department, working onsite in fixed afternoon or night shifts. We value responsibility, enthusiasm for challenges, proactivity, motivation, and teamwork. **Main Responsibilities:** * Prepare the production line; * Perform routine tasks related to cleaning the production line; * Operate machinery; * Carry out duties associated with the role in compliance with internal and external regulations; * Conduct environmental monitoring in the production area. **Ideal Candidate Profile:** * Education: High school diploma (12th grade) * Professional experience in an industrial environment will be valued * Strong interpersonal skills * Proactivity and autonomy are essential traits for performing the role * Availability to work fixed shifts (afternoon or night) between 3:00 PM and 7:00 AM * Availability to work rotating days off. **We Offer:** * Competitive salary package aligned with the responsibilities of the role * Life insurance * Health insurance * Opportunity to join a rapidly expanding group If you believe this is a great opportunity for your professional career, join us and contribute to Better Healthcare, Within Reach of Everyone, Every Day. Location: Sintra, Sintra, PT

R. Conde Seisal 25, 2710-593 Sintra, Portugal

Negotiable Salary

Indeed

Vulnerability Analyst

At IRIUM we want you to always pursue your dreams! Here, get ready to achieve your goals while enjoying the journey. We are currently looking for a **Vulnerability Analyst** **Requirements:** * Bachelor's degree in Computer Engineering, Electrical Engineering or Information Systems and Technologies preferred, or professional technical training in relevant fields * Proven experience in: * Proven professional experience ≥ 5 years. * Conducting technical cybersecurity investigations across a wide range of assets and devices directly related to security infrastructure; * Conducting analyses of information systems to detect existing or potential vulnerabilities; * Evaluating and supporting the implementation and compliance of security controls; * Developing system design policies and selection of architectural components. * Additional requirements: * Certified Information Systems Security Professional (CISSP) * GIAC Cyber Threat Intelligence (GCTI) * Certified Information Systems Auditor (CISA) * CompTIA Security\+ or Linux\+ * MCSA **Location: Lisbon** **Work arrangement:** Hybrid What do we offer? An innovative and growing company with many opportunities for professional development. Competitive compensation based on your experience and performance. Access to flexible compensation and private medical insurance as social benefits. Unlimited access to self-paced technological training. IRIUM is a company made up of dynamic and proactive professionals. Our values are responsibility and commitment to work quality. This is the spirit we look for at IRIUM. If you identify with these values, this is your company! Together we can build the future. Shall we talk? Send your application to: recrutamento@irium.pt At IRIUM we support a world without stereotypes or limitations and believe in equality for all, principles we uphold in our Equality Plan and Code of Ethics, ensuring equal treatment and opportunities regardless of any personal, physical or social condition. Type of offer: Full-time/Integral

PV49+C7 Lisbon, Portugal

Negotiable Salary

Intern Back Office Assistant – Medical Devices (m/f/d) / Lisbon638228725213471228

Indeed

Intern Back Office Assistant – Medical Devices (m/f/d) / Lisbon

CODAN 11, S.A. sales and distribution of Medical Instruments and Accessories We are looking for a **Intern Back Office Assistant –** **Medical Devices (m/f/d) / Lisbon** -------------------------------------------------------------------------------------- ##### **Responsibilities:** * Assist in preparing and receiving national and international orders and monitor them; * Provide back office support to the sales team; * Help with stock management; * Filing; * Provide support on various back office matters. ##### **Requirements:** * High school diploma (12th grade); * Proficiency in Microsoft Office (advanced knowledge of Excel); * Fluency in English (mandatory); * Excellent communication and interpersonal skills; * Strong time and priority management abilities; * High sense of responsibility ##### **We Offer:** * Salary according to the candidate's profile; * Job stability; * Real career opportunities within an international group; * Adequate training for the role. If you meet the requirements, please send your CV (in Portuguese and in English) to the following email: recrutamentoCODAN11@codanportugal.pt CODAN 11, S.A. Rua Stig Husted\-Andersen, 4 P\-2675\-492 Odivelas Telephone: \+351 21 934 94 50 Telefax: \+351 21 932 71 95 www.codancompanies.com

Largo Dom Dinis 15B, 2675-368 Odivelas, Portugal

Negotiable Salary

Medical Sales Representative638228715521311229

Indeed

Medical Sales Representative

**MartiDerm, you are the formula** MartiDerm is a leading company in dermocosmetics, distinguished by having created the ampoule category. Since 1952, MartiDerm has experienced strong growth and is currently undergoing a full transformation process. MartiDerm stands out for having its own R&D team, placing us at the forefront of innovation. Additionally, we carry out our production at our headquarters in Cervelló and are committed to developing products with low environmental impact. We also believe in transparency: our products do what they say, and say what they do. Welcome to our world. Welcome to MartiDerm. Do you want to join the MartiDerm team? We are looking for a **Medical Sales Representative - Portugal** to join our Iberia Sales team, reporting to the SALES AREA MANAGER. **Position Mission** You will be responsible for the **medical promotion of MartiDerm products** to healthcare professionals (general practitioners, dermatologists, among others) within the assigned geographical area. **Responsibilities** * Visit doctors within the assigned geographical area, promoting MartiDerm product lines based on scientific evidence. * Develop and maintain trust-based relationships with healthcare professionals and key medical stakeholders. * Identify new prescription opportunities and reinforce brand positioning within the medical channel. * Manage your medical visit schedule, optimizing frequency and coverage of targets defined by the company. * Report all activities in the CRM (via iPad), ensuring accurate recording of interactions and clinical feedback. * Prepare a quarterly plan for medical activities, including in-person and remote training sessions, coordinated with the regional TSC. * Monitor regional performance indicators and propose corrective actions when necessary. * Participate in congresses, scientific training, and medical events, as applicable. **QUALIFICATION AND EDUCATION REQUIREMENTS:** * Degree in Pharmacy/Health Sciences * Minimum 3-5 years of experience in the role * Knowledge of dermocosmetics * Communication skills * Previous experience in a similar role or as a dermocosmetic specialist in a pharmacy * Familiarity with CRM systems and Excel * Valid driver's license **ASSOCIATED COMPETENCIES:** * Strong communication skills * Negotiation ability and commitment * Proactivity and management capability * Ability to analyze and measure results to make appropriate decisions in each situation * Problem-solving mindset to resolve any conflict or issue * Ability to listen, understand, and know both internal and external customers **As a MartiDerm employee, you will have access to:** * Our work philosophy values autonomy, responsibility, and flexibility. * You will have access to all necessary facilities, resources, and tools to perform your job effectively. * Private health insurance. * Employee discounts. * Access to MartiDerm's training programs. * We offer continuous development opportunities with diverse challenges that foster on-the-job learning and specific courses tailored to your needs. * You will become part of a young, enthusiastic, and dynamic environment. **OUR CORE VALUES AND BEHAVIORS** At MartiDerm, we uphold four essential values composed of a set of behaviors that guide everything we do—from our strategy to daily decisions—and define how we relate to others and interact with our customers, consumers, and partners. Our corporate culture is "The Formula," which forms the foundation of our success, purpose, and true DNA. It is our way of being and how we care for people inside and out. "The Formula" is present in all our values: * **INNOVATION**: Innovation is our passion. We act with enthusiasm and a positive attitude. We show passion for sustainable skin health and well-being. We take risks and strive to be leaders, not followers. * **TRUST**: We are approachable and do what we say. * **FLEXIBILITY**: We embrace change as improvement. We see changes as opportunities to progress, adapt quickly, and remain open to new perspectives. * **COOPERATION**: Together we are stronger. We go beyond teamwork, caring for our colleagues, customers, consumers, society, and the planet. **WANT TO KNOW MORE ABOUT US?** * Visit our website: https://martiderm.com/es * Follow us on LinkedIn: https://www.linkedin.com/company/martiderm/mycompany/ * Follow us on Instagram: https://www.instagram.com/martiderm/?hl=es **WANT TO BE PART OF THIS ADVENTURE?** If you believe you fit the profile and the responsibilities described match what you're looking for, this is your opportunity. We would love to meet you! And if you think someone else might be suitable for this position, don't hesitate to share it!

PV49+C7 Lisbon, Portugal

Negotiable Salary