All jobs near Europe
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- 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...
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- Switzerland
- Negotiable
- Posted 2 days ago
We are seeking a skilled CSV Engineer to join our team on a 6-month initial contract in Basel. The ideal candidate will have a robust background in Computer System Validation (CSV) and Automated systems within the pharmaceutical and biotechnology industries. This role involves leading validation ...
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- 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...
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- 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...
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- 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 ...
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- 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...
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- 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) ...
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- 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...
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- 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...
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- 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 ...