All jobs near Germany in the Quality sector

• 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...

• 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, ...

• 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...

• 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) ...

• 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...

• 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 ...

• 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...

• 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...

• 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-...

• 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...

• 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...