All jobs near Europe in the Quality sector

• Spain
• Negotiable
• Posted 1 day 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 2 days 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 2 days 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 3 days 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 3 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, ...

• Dublin
• Negotiable
• Posted 4 days 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 5 days 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 6 days 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 8 days 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 8 days 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 8 days 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 11 days 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 11 days 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 11 days 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 11 days 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 11 days 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 15 days 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 15 days 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 15 days 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 15 days 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 15 days 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 16 days 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 16 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 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 16 days 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 17 days 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 17 days 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 18 days 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 19 days 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 19 days 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 23 days 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 23 days 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 24 days 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 24 days 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 24 days 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 24 days 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 25 days 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 25 days 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 25 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...

• Frauenfeld
• Negotiable
• Posted 25 days 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...

• Devon
• Negotiable
• Posted 27 days ago

We have a current opportunity for a Director Site Quality Manager - Ilfracombe, Devon on a permanent basis. In this role, you will have the opportunity to: Represent the Ilfracombe site as the Quality Management Representative and lead management reviews Responsible for the leadership & developme...

• England
• Negotiable
• Posted 27 days ago

United Kingdom - Newcastle / Remote Opporunity You will be a part of the Quality Assurance team and report to the Manager, Quality Assurance (Design). You will be responsible for applying in-depth knowledge, experience, expertise in multiple areas of medical device quality assurance, guiding the ...

• Germany
• Negotiable
• Posted 29 days ago

Freelancer Qualification Consultant - Large Pharmaceutical Company Contract Duration: 8 Months (February to November) Location: Germany (Onsite) We're looking for a team of 4x Qualification Consultant to join a global pharmaceutical company! Your main focus will be room, medium, and equipment qua...

• England
• Negotiable
• Posted 29 days ago

United Kingdom - Newcastle / Remote Opporunity You will be a part of the Quality Assurance team and report to the Manager, Quality Assurance (Design). You will be responsible for applying in-depth knowledge, experience, expertise in multiple areas of medical device quality assurance, guiding the ...

• Denmark
• Negotiable
• Posted about 1 month ago

Job Title: Freelance CQV Engineer Start Date: March 2025 Contract: 12 Months Location: Denmark - Onsite EPM Scientific is partnering with a leading pharmaceutical company to find an experienced CQV Engineer to be part of their commissioning, qualification, and validation of pharmaceutical manufac...

• Italy
• Negotiable
• Posted about 2 months ago

ABOUT US We are a European organization recognized as an official Notified Body under Regulation (EU) 2017/745, specializing in verifying the conformity of medical devices with the stringent requirements of the MDR 2017/745 regulation. Our work ensures that medical devices meet the necessary stan...