Contract jobs

• Visp
• Negotiable
• Posted 1 day ago

We are looking for a Deviation Manager to join a large-scale mammalian cell culture facility in Visp on a 6-month contract. This role offers the opportunity to work in a dynamic and regulated environment, ensuring compliance and quality in manufacturing processes. Key Responsibilities: Own, autho...

• Berlin
• Negotiable
• Posted 7 days ago

Freelance Medical Science Liaison Are you passionate about making a difference in the field of medical science? We are seeking dedicated candidates to join our team for a multi-project study. This is an exciting opportunity to work with a dynamic team and contribute to groundbreaking research. Ke...

• Berlin
• Negotiable
• Posted 7 days ago

Freelance Medical Science Liaison (MSL) Are you passionate about making a difference in the field of medical science? We are seeking dedicated candidate to join a multi-project study. This is an exciting opportunity to work with a dynamic team and contribute to groundbreaking research. Key Respon...

• Switzerland
• Negotiable
• Posted 10 days ago

We are seeking an experienced consultant for the validation of fill & finish processes for one of our client. The ideal candidate will have a strong background in the pharmaceutical industry and will ensure that production processes comply with regulatory standards and Good Manufacturing Practice...

• South Carolina
• Negotiable
• Posted 11 days ago

Our client is a leading organization in the pharmaceutical industry, committed to innovation and excellence. They are currently seeking a highly skilled and experienced Senior Manager/Associate Director - Statistician to join their team in New Jersey. Key Responsibilities: Lead and manage statist...

• New Jersey
• Negotiable
• Posted 11 days ago

We are seeking a highly skilled Computer System Validation (CSV) Engineer to join our client on a contract basis. This role is crucial for ensuring the validation and compliance of computerized systems in a regulated, GxP-compliant environment, contributing to the production of innovative oncolog...

• Limerick
• Negotiable
• Posted 11 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...

• Paris
• Negotiable
• Posted 12 days ago

My client is building the first universal AI Operating System to lay the foundation for Biological Artificial Superintelligence (BASI). This OS integrates a suite of AI agents that decode complex biology, accelerate research, and dramatically increase productivity. Acting as copilots,My clients a...

• Paris
• Negotiable
• Posted 13 days ago

Job Title: Senior Regulatory Affairs Specialist Location: France (Hybrid) Start Date: Within the next month Job Type: Full-time (Consultant, Freelancer, or Contractor) Industry: Medical Devices Key Responsibilities: Documentation Specialist: Lead and manage all regulatory documentation processes,...

• Marlborough
• Negotiable
• Posted 13 days ago

About the role: You will develop, negotiate, and finalise site agreements and budgets for medical device clinical trials in a variety of therapeutic areas by collaborating with internal key stakeholders and working with external health care institution staff. Your responsibilities will include: P...