380 Math Stats Info Sciences in Lisbon lowest at $14000.0+

Indeed

Software Developer

**Are you ready to revolutionise the world with TEKEVER?** At **TEKEVER,** we lead innovation in Europe as the European leader in unmanned technology, where cutting\-edge advancements meet unparalleled innovation. **Digital \| ️ Defence \| Security \| ️ Space** We operate across four strategic areas, combining artificial intelligence, systems engineering, data science, and aerospace technology to tackle global challenges — from protecting people and critical infrastructure to exploring space. We offer a unique surveillance\-as\-a\-service solution that delivers real\-time intelligence, enhancing maritime safety and saving lives. Our products and services support strategic and operational decisions in the most demanding environments — whether at sea, on land, in space, or in cyberspace. The future of autonomous aviation starts here At **TEKEVER UAS**, we build the future of autonomous systems that protect our oceans, support emergency response, and enhance global security. If you're passionate about engineering innovation, real\-world impact, and working with cutting\-edge aerial technologies, join us and help shape the next generation of Unmanned Aerial Systems **What will be your responsibilities:** * Implement / Integrate new sensors * Debug already existing software and implement fixes as needed * Suggest software solutions for product requirements * Develop Interface control documents (ICD) to align with other teams **Profile and Requirements:** * Higher education degree in Computer Science, Aeronautical Engineering, Aerospace Engineering, Electrical Engineering, or similar * 2\+ Years experience in C\#, Rust, C\+\+, C. * Familiarity with CI/CD pipelines and version control systems (e.g., Git). * Strong analytical skills and problem identification * Ability to work in a multidisciplinary team * Autonomy, initiative, curiosity, resilience, and customer orientation * Language Requirements: Advanced proficiency in English, with proven fluency at the C2 level. **Great to have:** * Knowledge of video pipelines (ffmpeg / gstreamer) is a plus. * Knowledge of messaging protocols (mavlink / dronecan) * Knowledge of networking protocols At **TEKEVER**, we believe in a dynamic, supportive work culture where innovation thrives. **Here’s what we offer:** * **Comprehensive Benefits**: Health insurance, meal allowances, and more. * **Competitive Compensation:** Salary based on your experience and qualifications. * **Opportunities for Growth:** Develop your career in a fast\-paced, mission\-driven environment.

CW56+2P Salir de Matos, Portugal

Negotiable Salary

Quality Assurance Trainee64731742437506121

Indeed

Quality Assurance 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:: 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. * Support quality activities for assigned projects and products while learning compliance with cGMP, operational standards, and legal regulations. * Assist in promoting high\-quality standards and a culture of continuous improvement across company processes. * Help with audits and inspections by preparing documentation and reviewing procedures to ensure the site remains "audit ready." * Participate in the management of change control, deviations, validation, and other quality\-related processes. * Learn to prepare, review, and update quality documentation, such as SOPs, reports, and regulatory files. * Support investigations related to customer complaints and compliance challenges, collaborating with stakeholders. * Assist with data reporting, including KPIs and information system updates, while developing expertise in Quality Assurance. * Maintain a presence in manufacturing areas, providing on\-the\-job support and oversight. * Ensure compliance with Health, Safety, and Environment (HSE) regulations in all assigned activities. 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

Indeed

Associate 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. * Follow the daily priorities in order to accurately and promptly perform the allocated sample analysis, to meet the requirements of the 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. * 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 (strong preference) * Relevant work experience * Proven practical pharmaceutical or related industry experience in a GMP regulated QC laboratory environment (preferable) * 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 * Must have the Knowledge, Experience and Skills to conduct their tasks in accordance with the rules and procedures set down. AJ372 **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

Indeed

QC Associate

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. * Apply and develop knowledge of Quality Control and participate in area processes, procedures and projects with the guidance of more senior colleagues * Rigorously, accurately, efficiently and professionally manage, execute and support all assigned projects in accordance with applicable GMP, quality operational standards / procedures and legal regulations, escalating as appropriate * Propose new methodologies taking into consideration project demands and requirements * Execute project specific analytical tasks and act as a stakeholder liaison * Provide an example of professionalism and support the induction of new colleagues within the area * Ensure that all assigned analytical tasks, including (but not limited to) method development, method creation, method transfer, method validation, protocol preparation and report preparation, in any analytical project is well managed and delivered on time, safely, efficiently, reliably and in a cost\-effective manner by performing and planning * Solve analytical problems relating to assigned projects by providing collaborative and timely support to all areas and departments, initiating the problem\-solving escalation process when unable to solve occurrences within the established period * Ensure the effective and proactive flow of information between the Analytical team and the internal and external (if applicable) stakeholders, representing the team (with support from senior colleagues) as appropriate * Reviews work generated by the team as required ensuring all procedures are followed * Creation, investigation and evaluation of CAPAS, incidents and deviations * Perform equipment maintenance, internal calibrations and internal qualifications on designated laboratory instruments * Accurately use and maintain all laboratory information systems * To maintain good hygiene and housekeeping within the laboratory * To maintain all laboratory records, project and general logbooks and notebooks to an acceptable GLP standard and in accordance with Hovione internal procedures * Fulfil and promote all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities * 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 * Assist with audits / investigations as required, following the instruction of QC Management * Support the reporting of KPIs for the team, if required \- Develop and accumulate strong analytical chemistry expertise * Maintain high standards in the QC Laboratories * Use analytical techniques and instrumentation, such as gas and high\-performance liquid chromatography (HPLC) amongst others * Interpretation of data and analysis to ensure meeting strict guidelines on documentation and recording data * Work collaboratively in cross\-functional teams and understand each departments function and role in delivery of tests and products * Perform to ensure all assigned tasks are delivered on time, safely, efficiently, reliably and in a cost\-effective manner * 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). * 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) * Requires educational / training experience in a QC laboratory environment * Hands\-on experience in Analytical Chemistry and QC procedures (desirable) * Training and experience of GMP and ICH guidelines standards (desirable) * Knowledge on HPLC and GC, and familiarity with Empower Software (desirable) * Technical understanding of GMP practices, analytical theory and techniques * Documentation skills and attention to detail \- 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. ***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

Global Senior Project Manager64294662199555124

Indeed

Global Senior Project 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. **Hovione** are seeking an experienced Pharmaceutical **Senior Project Manager** to lead cross\-functional teams in the delivery of cost\-effective, timely, and high\-quality project outcomes. Operating within a collaborative and structured environment. As the **Senior Project Manager** you will ensure alignment across all key stakeholders—including customers, suppliers, sponsors, and internal teams—through clear communication and effective coordination. The role involves planning, setting priorities, monitoring progress, and making informed decisions to deliver projects in line with defined scope, budget, and timelines. A commitment to optimizing customer satisfaction and enhancing financial performance is essential to supporting the long\-term success of the organization You will be responsible to:: **Key Responsibilities:** * Manage medium \- to high \- complexity pharmaceutical projects, ensuring alignment with business priorities * Take full ownership of project scope, budget, timelines, and quality across all assigned initiatives. * Lead cross\-functional project teams, fostering accountability, decision\-making, and stakeholder engagement. * Oversee team composition, clarify roles, and optimize use of technical and leadership capabilities. * Communicate effectively with internal and external stakeholders to build trust and maintain alignment. * Drive project delivery using structured methodologies and best practices tailored to CDMO environments. * Monitor and manage risks, proactively addressing roadblocks to ensure project continuity. * Support team performance through regular, constructive feedback and motivation strategies. * Apply advanced project management tools, methodologies, and decision\-making based on robust data analysis. * Ensure compliance with GMP, HSE, and internal policies while upholding a culture of safety and continuous improvement. We are looking to recruit a Candidate:: * Bachelor's degree required; Science, Engineering, or related field preferred. Or MBA with client\-facing experience is a plus. * Minimum 5 years of relevant experience in operational or scientific Project roles within the pharmaceutical industry, ideally in a CDMO environment. * Hybrid working with an on\-site presence required in Lisbon, Portugal. * Project Management certification (e.g., PMP, PRINCE2\) or formal PM training is highly desirable. * Strong technical background or proven experience in spray drying, drug development and manufacturing. * Demonstrated mastery of project management tools, methodologies, and best practices. * Proven leadership experience in cross\-functional project teams. * Comfortable working in dynamic, fast\-paced environments with change and uncertainty. * Strong decision\-making, risk management, and stakeholder communication skills. * Fluent in English with strong written, verbal, and presentation abilities. **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

Modelling & PAT Scientist64088809446403125

Indeed

Modelling & PAT Scientist

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:: Assures the maintenance of process analytical tools (PAT) methods and performance in the manufacturing assets in compliance with legislation and regulatory standards of Quality, HSE and cGMP policies. Promotes the scientific excellence and innovation in the area of PAT and contributes with technical expertise to optimize PAT applications.* Provide technical support (process analytical and statistical) in commercial projects; * Monitor and maintain successfully PAT tools and practices * Participate in the Technology Transfer and scale\-up of projects to Pilot Plant and Manufacturing Areas * Write reports and relevant documentation related with the use of PAT and related methods; * Promote, continuously, best practices, innovation and knowledge sharing within the company; * 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 Modelling \& PAT 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) * 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 Engineering or scientific field (mandatory) * Typically requires 1\-3 years of relevant experience in a production environment, preferable within the Pharmaceutical Industry * Strong understanding and knowledge on PAT and statistical tools (including chemometrics) * Fluency in English is a requirement * Computer literate with good working knowledge of the MS Office package and relevant modeling software (Matlab, Simca) * 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

Regulatory Affairs Manager63822690730369126

Indeed

Regulatory Affairs Manager

Requirements: ➡ Excellent understanding of medical devices to ensure our products fulfill all regulatory directives; ➡ Compile, review, submit, and follow up any applications for use \- CE marking, FDA, ISO 13485, INFARMED, UKCA, MDSAP; ➡ Registration of medical devices in various countries ➡ Actively research and analyze scientific data; ➡ Cooperate on new projects; ➡ Perform and manage audits; ➡ Collaborate on strategic planning together with top management; ➡ Work closely with partners, consultants, manufacturers, scientists, health professionals, and others; ➡ Lead and manage regulatory audits; ➡ Liaise with regulatory officials and consultants; ➡ Good communication and interpersonal skills; ➡ Proactive and action maker; ➡ Proficient English (written and spoken). ⠀ What we offer: ✅ Positive work environment ✅ Salary commensurate with proven experience ✅ Work\-related training ✅ Health insurance and other employee benefits ✅ High\-responsibility position ✅ Integration into a growing company ✅ Full\-time job ⠀ Schedule: Monday to Friday, from 8:30 am to 5:30 pm. ⠀ Apply now! Send your resume to: p.figueiredo@astrolabe\-medical.com Tipo de oferta: Integral/Full\-time Benefícios: * Cartão/Ticket refeição * Estacionamento gratuito * Seguro de vida * Seguro saúde

VW88+JM Vialonga, 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) * HPLC chromatography \- 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

Indeed

Web designer (m/f)

Company based in Caldas da Rainha Our company is recruiting a Web designer with knowledge in the field; seeking a challenging experience, and possessing a dynamic and proactive profile. Responsibilities: Development and maintenance of website Design of layouts for various types of pages; Manage and operate multiple audiovisual systems for sound and image recording (photography, video and sound); Image editing; Creation from scratch or adaptation of HTML, CSS files. Programming and database solutions such as PHP and MySQL Responsive Design (Preparing the site to be correctly viewed on various types of devices with different screen resolutions: desktop computers, tablets and mobile phones); Content placement (texts, images, videos, databases, advertising, others); Installation of tracking codes for statistical analysis, such as Google Analytics; Performing tests, corrections and adjustments, among other tasks. Requirements: \- Academic background in WeDesign; \- Proven professional experience (minimum 4 years); \- Knowledge of website analysis tools (Google Analytics); \- Strong analytical, organizational and proactive skills; \- Creative profile; \- Demonstrate determination in problem solving, decision making and identification of priorities; \- Good knowledge of English; \- Knowledge of MANAGEMENT SOFTWARE: preferably PHC We offer: \- Attractive remuneration according to proven experience. If you meet the requirements, please send an email to rh@americoalves.pt Type of offer: Full-time/Integral

R. 16 de Março 8, 2500 Caldas da Rainha, Portugal

Negotiable Salary