All jobs near Europe in the Quality sector

• Frankfurt am Main
• Negotiable
• Posted 5 days ago

Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? We have an exciting opportunity for you! Our Client a global leading German bank is looking for a Product Manager Tasks You use AI and LLMs to improve our chatbot and make customer i...

• Denmark
• Negotiable
• Posted 7 days ago

Project Coordinator / Junior Project Manager (Operational Readiness - Downstream) Duration: 12 months, possible extension Location: Denmark - on-site Start Date: ASAP -12month contract We are looking for an experienced Project Coordinator or Junior Project Manager with pharmaceutical industry exp...

• Copenhagen
• Negotiable
• Posted 7 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• Visp
• Negotiable
• Posted 8 days ago

We are currently seeking a highly skilled and dedicated Lab Scientist to join our client's Analytical Department. If you have a strong background in analytical chemistry and a passion for process optimization, we would love to hear from you! Responsibilities Provide analytical support for chemica...

• Visp
• Negotiable
• Posted 8 days ago

We are currently seeking a highly skilled and dedicated Lab scientist to join our client's Analytical department. Main tasks and responsibilities: Analytical support of chemical process development and process optimisation. Preparation, execution and documentation of analyses, method developments...

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• Cork
• Up to €50 per hour
• Posted 8 days ago

Responsibilities Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment. Conducts feasibility studies to verify capability and functionality. Develops new concepts from initial design to market release. Write an...

• Limerick
• Negotiable
• Posted 9 days ago

Acting as a Quality Lead for all phases of production realization including NPD, NPI, Commercialisation, Sustaining, End to Life. Monitor and drive compliance within the development process and/or operations to GMP and the requirements of the QMS within assigned area. Trouble shooting quality iss...

• Zurich
• Negotiable
• Posted 10 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Switzerland
• Negotiable
• Posted 10 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Switzerland
• Negotiable
• Posted 11 days ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Netherlands
• Negotiable
• Posted 12 days ago

Quality Engineer - Netherlands About the Role As a Quality Engineer, you will play a key role in ensuring compliance with industry standards, optimising processes, and driving a culture of quality throughout the organisation. You will work closely with cross-functional teams to maintain high-qual...

• Deutschlandsberg
• Negotiable
• Posted 15 days ago

Exciting Career Opportunity: Freelance CQV Consultant We are currently seeking an experienced Freelance CQV Consultant to join our client in Germany for a 12-month contract role. This is a full-time, on-site position with an immediate start. Key Details: Location: On-site, Germany Contract Durati...

• Valais
• Negotiable
• Posted 15 days ago

We are currently looking for a Project Engineer - Black Utilities to join the Global Engineering Team based in Valais, Switzerland! Summary: Your tasks will include developing and verifying ideas and requests, generating feasibility and conceptual studies, considering regulatory requirements and ...

• Stein
• Negotiable
• Posted 15 days ago

We are currently seeking a highly skilled and motivated GMP High Bay Warehouse Specialist to join our client's team in Stein. The Specialist will be driving the execution and coordination of the defined CQV activities in the warehouse for both cold and ambient temperatures and support building. R...

• Stein
• Negotiable
• Posted 15 days ago

We are seeking a skilled and motivated Instrumentation & Controls Engineer to join our client's team in Stein. Summary: The Instrumentation and Control (I&C) Engineer will report directly to the Automation Technical Lead and is responsible for providing hands on support to the commissioning and q...

• Bern
• Negotiable
• Posted 16 days ago

We are currently working with a leading pharmaceutical company looking for an MES Engineer to join their team in Switzerland. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Developing, testing, and optimizing ...

• Switzerland
• Negotiable
• Posted 16 days ago

We are currently working with a leading pharmaceutical company looking for an MES Engineer to join their team in Switzerland. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Developing, testing, and optimizing ...

• Zurich
• Negotiable
• Posted 16 days ago

We are seeking two skilled and motivated QC Analysts to join our client's team in Zurich. As a QC Analyst, you will play a crucial role in performing laboratory testing, ensuring the highest standards of quality control, and supporting the development of pharmaceutical products. Your expertise in...

• Visp
• Negotiable
• Posted 16 days ago

We are seeking a Process Analytics Technician to join a global leader in the specialty chemicals industry. This is a fantastic opportunity to contribute to cutting-edge projects and work in an innovative, sustainable environment. Key Responsibilities: Ensure the optimum availability of process an...

• Visp
• Negotiable
• Posted 16 days ago

Head of Process Analytics Engineering and Maintenance We are seeking an experienced and dynamic leader to head the Process Analytics Engineering and Maintenance function at a large-scale manufacturing site in the chemical or pharmaceutical industry. This position offers an exciting opportunity to...

• Germany
• Negotiable
• Posted 22 days ago

Seeking Freelance Automation Specialist - Large Pharma Project Location: Southern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are currently seeking an Automation Specialist to work exclusively with a large pharmaceutical company based in Southern Ger...

• Basel
• Negotiable
• Posted 22 days ago

We are currently searching for a Scientist QC Raw Materials to join our client's team in Basel, Switzerland on a 9-month contract. This is an exciting opportunity to become part of the Primary Packaging and Raw Material QC team, where you will play a critical role in ensuring the quality and comp...

• Basel
• Negotiable
• Posted 22 days ago

We are searching for a Scientist QC Raw Materials to join our team on a 9-month contract. This role plays a key part in the Primary Packaging and Raw Material QC team, ensuring the quality and compliance of raw materials used in drug product manufacturing. The successful candidate will be respons...

• Galway
• Negotiable
• Posted 22 days ago

Senior Validations Engineer The requirements of this role within the wider project are to cover the validation activities with respect to the testing and manufacture of the client's device. Role/ Responsibilities: Develop, and/or approve, validation documentation, including protocol, records, and...

• Belgium
• Negotiable
• Posted 23 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• Belgium
• Negotiable
• Posted 24 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• Belgium
• Negotiable
• Posted 24 days ago

We are currently working with a leading CDMO looking for a MSAT Packaging Engineer to join their team in Belgium. This is an exciting opportunity to build a long-term career in one of the fastest-growing CDMOs globally. You will be responsible for: Leading closure and shipping validation projects...

• Visp
• Negotiable
• Posted 25 days ago

We are seeking a Quality Assurance Manager to oversee compliance and customer Quality Agreement (QAA) activities for Drug Product manufacturing in Visp. This role involves collaboration with Drug Product Services and Drug Substance teams, acting as the primary QA contact for customer-related qual...

• Germany
• Negotiable
• Posted 26 days ago

I am working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender Manager, ...

• Deutschlandsberg
• Negotiable
• Posted 29 days ago

Job Title: Quality Control Team Lead Location: Germany Company Overview: Join an innovative Medical Device company dedicated to developing products that prevent fatalities from heart attacks. Position Overview: We are seeking a highly experienced QC Team Lead to join our dynamic team. The ideal c...

• Netherlands
• Negotiable
• Posted about 1 month ago

Job Title: Quality Management System (QMS) Specialist Location: The Netherlands About our client: Innovative medical device company focused on improving the lives of people with diabetes through our advanced insulin pump. Job Description: We are looking for a QMS Specialist to ensure top-quality ...

• Germany
• €100000 - €120000 per annum
• Posted about 1 month ago

Job Title: Associate Director - Qualified Person (QP) with Vaccine Expertise Location: Germany Job Description: We are seeking a highly qualified and experienced Associate Director to join our team. The ideal candidate will be a Qualified Person (QP) with a strong background in vaccines and holdi...

• Spain
• Negotiable
• Posted about 1 month ago

QARA Consultant - Diagnostics Software Specialist We are excited to announce a contract opportunity for an experienced QARA Consultant specialising in diagnostics software within the medical device sector. This role is fully remote and requires proficiency in Spanish, aligning with our commitment...

• Spain
• Negotiable
• Posted about 1 month ago

🚀 Exciting Opportunity - QARA Consultant - Software Diagnostics 🚀 📅 Contract Length: 12 Months 🌎 Location: Remote 💼 Hours: 20 Hours per week I am partnering with a leading medical device client who is looking for a QARA Consultant focusing on Software Diagnostics Compliance. 🔍 Key Skills & Experi...

• Germany
• Negotiable
• Posted about 1 month ago

Urgent Freelance Quality Assurance Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking We are working exclusively with a large pharmaceutical client to find a highly skilled Quality Assurance E...

• Germany
• Negotiable
• Posted about 1 month ago

Urgent Freelance CQV Engineering Consultant (Pharmaceutical Industry) Location: Northern Germany Duration: Immediate Start - 12-Month Contract Language: Must be German-speaking Company Overview: We are working exclusively with a leading pharmaceutical client to find a highly skilled CQV Engineeri...

• Deutschlandsberg
• Negotiable
• Posted about 1 month ago

I am currently working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender...

• Germany
• Up to €24000 per annum
• Posted about 1 month ago

I am working with a global leader in medical devices, dedicated to advancing healthcare through innovations in cardiology, orthopedics, surgical robotics, and diagnostics. They are currently looking for a GPO Tender Manager to join their expert team. Key Role Highlights: As a GPO Tender Manager, ...

• Dublin
• Negotiable
• Posted about 1 month ago

I'm currently looking for an experienced DeltaV Automation Lead with expertise in spray drying and a background in API manufacturing for a full-time, on-site role in the South of Ireland. The client is eager for an immediate start but is open to some flexibility for the right candidate. Ideal Can...

• Spain
• Negotiable
• Posted about 1 month ago

Estamos buscando un líder en Garantía de Calidad para unirse a nuestro equipo global y desempeñar un papel clave en el desarrollo y lanzamiento de nuevas moléculas, tecnologías y modelos de negocio. Reportando al Chief Quality Officer, esta posición será responsable de garantizar el cumplimiento ...

• Hesseneck
• Negotiable
• Posted about 1 month ago

The head of the QM & RA department leads the Quality Management and Regulatory Affairs team, ensuring adherence to regulatory standards and continuous development of the quality management system (QMS). This role encompasses management tasks, strategic oversight, and operational responsibilities,...

• Kaufering
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Quality Manager on a permanent basis. The position will be based in Kaufering. For further information about this position please apply. Your responsibilities include the management and coordination of cross-departmental quality management projects You also sup...

• Sweden
• Negotiable
• Posted about 1 month ago

About the Role: We are seeking an experienced CQV (Commissioning, Qualification & Validation) Consultant to support Factory Acceptance Testing (FAT) and commissioning for a key project. The successful candidate will play a critical role in ensuring that equipment and systems meet regulatory and o...

• Visp
• Negotiable
• Posted about 1 month ago

Our client is seeking a skilled Thermal Validation Subject Matter Expert to join their BIO Biologics Division Services (BDS) team for a 9-month contract in Visp. The successful candidate will be responsible for ensuring the qualification and validation of process and support equipment, including ...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Perform technical assessments of active medical devices, ensuring compliance with MDR 2017/745 and international regulatory standards. Conduct conformity assessments, design dossier reviews, and clinical evaluations for medical devices. Lead and participate in regulatory aud...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical evaluations of non-active medical devices. Perform conformity assessments and certification evaluations under MDR 2017/745 and related standards. Lead and participate in regulatory audits (ISO 13485, MDSAP, MDR) ...

• Visp
• Negotiable
• Posted about 2 months ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Visp
• Negotiable
• Posted about 2 months ago

Unser Kunde sucht einen qualifizierten Biotech Associate, der für einen spannenden 10-Monats-Vertrag dem Team der BIO Biologics Division Services (BDS) beitritt. Dies ist eine hervorragende Gelegenheit für eine detailorientierte Fachkraft, die im Bereich der Qualitätssicherung in einer hochmodern...

• Netherlands
• Negotiable
• Posted about 2 months ago

We are currently supporting a Quality Assurance Officer position for a client based in The Netherlands. Quality Assurance Officer Our client is an innovator in Global Health and is currently looking for a Quality Assurance Officer to join the team! Main Responsibilities of a Quality Assurance Off...

• Weybridge
• Negotiable
• Posted about 2 months ago

We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

• Weybridge
• Negotiable
• Posted about 2 months ago

We are currently supporting a Qualified Person and Responsible Person position for a client based in the London. Qualified Person and Responsible Person Our client is an innovator in the consumer health space and is currently looking for a Qualified Person and Responsible Person to join the team!...

• Oberhonnefeld-Gierend
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Head of QA/RA on a permanent basis. The position will be based in Oberhonnefeld-Gierend. For further information about this position please apply. Job Summary: The Head of Quality and Regulatory Affairs will oversee and manage all quality and regulatory functio...

• Norway
• Negotiable
• Posted about 2 months ago

Job Description: Medical Device Assessor & Lead Auditor - Non-Active Devices Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct technical file reviews, risk assessments, and clinical...

• Germany
• Negotiable
• Posted about 2 months ago

Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...

• Germany
• Negotiable
• Posted about 2 months ago

We are currently working with a reputable Solutions Provider in the pharmaceutical and medical device industry looking for an experienced Quality Management & Compliance professional to join the team in Germany. This is an exciting opportunity to work within a growing team, partnering with leadin...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Do you want to be a driving force in a rapidly expanding environment, making a tangible difference in the process? We have an exciting opportunity for you! Our Client is a market leader in the Biopharmaceutical Industry. They are looking to hire top QA Engineers. Tasks Run tests to make sure the ...

• Visp
• Negotiable
• Posted about 2 months ago

Our client is seeking a skilled Supplier & Material Qualification Specialist to join their BIO Mammalian team for a 6-Month contract to ensure the efficient and compliant supplier and material qualification process in line with regulatory requirements, corporate standards, and agreements with sta...

• Devon
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Director of site Quality Management on a permanent basis. The position will be based in Devon. For further information about this position please apply.

• Munich
• Swiss Franc80000 - Swiss Franc90000 per annum
• Posted about 2 months ago

Senior Quality and Regulatory Affairs Manager - Healthcare Technology (f/m/d) Responsibilities Conduct gap analyses of regulatory documents and QMS documentation, and implement necessary updates. Keep regulatory documentation, including laws, standards, regulations, and guidance documents, curren...

• City of London
• Negotiable
• Posted about 2 months ago

We are currently supporting a Process Engineer position for a client based in the London. Process Engineer Our client is an innovator in the Medical Device space and is currently looking for a Process Engineer to join the team! Main Responsibilities of a Process Engineer Facilitating the design, ...

• Luxembourg
• Negotiable
• Posted about 2 months ago

Role: Leasing Manager Location: Ireland (Homebased) About the Company: A global market leader in the Life Sciences testing space is searching for a Leasing expert to join their team. Responsibilities: Asset management - You will be fully responsible for the inventory, deployment and lifecycle man...

• Stuttgart
• Negotiable
• Posted about 2 months ago

Head of Non-Active Medical Devices - Leading Notified Body We are representing a leading Notified Body seeking an experienced Head of Non-Active Medical Devices to join their team. This is a pivotal leadership role within a globally recognized organization, providing regulatory expertise, strateg...

• Zurich
• Negotiable
• Posted about 2 months ago

My client are a leader in the medical device industry, dedicated to enhancing patient care with high-quality products and innovative technology. Position Summary: We are seeking a skilled Quality Engineer to maintain quality management systems, and drive continuous improvement in our manufacturin...

• Hamburg
• Negotiable
• Posted about 2 months ago

Your Responsibilities: Ensure compliance with the risk management process according to ISO 14971 for new developments and existing therapy products. Coordinate, create, and maintain risk management files for new developments, the existing portfolio, and change management in therapy products. Anal...

• Kaufbeuren
• £60000 - £80000 per annum
• Posted about 2 months ago

Senior Test Engineer - Digital Technologies Location: Bavaria, Germany Industry: Medical Devices Shape the Future of Digital Healthcare Join a pioneering team developing cutting-edge digital technologies that enhance surgical precision and patient outcomes. This is an opportunity to work on high-...

• Nyon
• Negotiable
• Posted about 2 months ago

Our client is seeking a skilled QC Validation Scientist to join their Product Innovation team for a 2-year contract. This position is ideal for someone with extensive experience in process, cleaning, and analytical validation within the pharmaceutical industry. As a QC Validation Scientist, you w...

• London
• Negotiable
• Posted about 2 months ago

A leading provider of certification, audit, and assurance services is seeking a highly skilled professional to join its Assurance Services team as a Lead Auditor. With over 70 years of experience in the UK, the organization ensures that products and systems are safe, reliable, and compliant by of...

• Tuttlingen
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a QA/RA Manager on a permanent basis. The position will be based in Tuttlingen. For further information about this position please apply. You can look forward to these tasks: * Evaluation, selection and continuous monitoring of suppliers in accordance with intern...

• Munich
• Negotiable
• Posted about 2 months ago

We are looking for a highly skilled individual to assist the quality management and touchpoints with regulatory bodies across various business units or subsidiary companies with a specific focus on Europe and other regions. Responsibilities Establish and maintain Quality System requirements effec...

• Vienna
• Negotiable
• Posted about 2 months ago

Job Title: Freelance eQMS Specialist Duration: 6 Months Industry: Pharmaceutical We are looking for a Project Quality Management Specialist to support the modernisation and update of our Electronic Quality Management System (eQMS) on a freelance basis. This is a contract position for six months, ...

• Switzerland
• Negotiable
• Posted about 2 months ago

I am on the search for a Quality Engineer for a key client of mine in Switzerland. The ideal candidate must meet the below requirements and expertise. Key Requirements: Proven experience with injection moulding and medical devices. Strong understanding of quality assurance processes and standards...

• Frauenfeld
• Negotiable
• Posted about 2 months ago

Job Description: This Exclusive mandate seeks a highly experienced and motivated Global Head of Quality and Regulatory with direct leadership expertise and hands on mentality to join a dynamic client in the medical device field. This leadership role is critical in ensuring our products meet the h...