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• Basel, Switzerland
• Posted 7 days ago

Senior Regulatory Affairs Manager (Medical Devices) Based in Basel     My client is a fast-growing SME and looking for a Senior Regulatory Affairs Manager to strengthen their team in Basel.       Tasks Ensuring that regulatory requirements for the approval of medical devices are met during the pr...

• Germany
• Posted 14 days ago

Qualified Person - Bavaria Responsibilities To maintain a robust quality system that fits the complexities of Company’s supply chain Perform certification of batches that are imported from outside the European Union in line with Directive 2001/83/EC Maintain QP certification register for all impo...

• Germany
• Posted 14 days ago

Job Description This position is responsible for writing the proposal between BAP Pharma and the client to detail the work to be performed by BAP Pharma to support the client’s clinical studies from a packaging, labelling, and distribution perspective. Close liaison with the client and interpreta...

• Germany
• Posted 14 days ago

Description This position is responsible for secondary packaging room activities, supervision of Packaging Room Associates and provision of support to the Clinical Project Manager and/or Project Associate. Responsibilities Executes batch records and manages the day-to-day secondary packaging room...

• Slough, United Kingdom
• Posted 15 days ago

Senior Quality Assurance Manager/ Responsible Person Slough, UK   Responsibilities To check ALL goods received are not counterfeit medicines, by looking for evidence of tampering or anything suspicious. Check product description, quantities, expiry dates, batch numbers are accurately recorded and...

• Munich, Germany
• Posted 15 days ago

Senior Strategist Clinical Regulatory Affairs (f/m/d) Munich, Bavaria   My client is developing a proprietary portfolio and growing pipeline of targeted treatments in various stages of clinical development addressing a range of cancers such as neuroendocrine cancers or bone metastases. Their main...

• Netherlands
• Posted 25 days ago

You will support the Regulatory Manager with activities including but not limited to IMPD/IND submission support, regulatory authority communications, regulatory strategy and project management. The Regulatory Specialist reports directly to the Regulatory Manager. Job Responsibilities Maintaining...

• United States
• Posted 30 days ago

Medical Writer (Senior/Principal) – Based in Durham, North Carolina, USA   Our client is looking for new Medical Writers (Senior/Principal) to join their ever-expanding team in Frankfurt. You will be given an opportunity like no other to grow and develop into the best writer you can be. You would...

• Germany
• Posted 30 days ago

Medical Writer (Senior/Principal) – Based in Cambridge     My client is looking for new Medical Writers (Senior/Principal) to join their ever-expanding team in Frankfurt. You will be given an opportunity like no other to grow and develop into the best writer you can be. You would be part of a gen...

• Germany
• Posted 30 days ago

Medical Writer (Senior/Principal) – Based in Frankfurt     My client is looking for new Medical Writers (Senior/Principal) to join their ever-expanding team in Frankfurt. You will be given an opportunity like no other to grow and develop into the best writer you can be. You would be part of a gen...