Part of Phaidon InternationalProperty 1 Bull Dark

You are viewing the Switzerland [EN] site. to view your country site linked to your browser settings

Contract Go To Market Jobs

Get job alerts

Showing 40 results

Sort by:

Medical Writer
Irvine

We are seeking an experienced Medical Writer with a strong background in Health Economics & Outcomes Research (HEOR), Health Policy, and Market Access communications to support the development of high-quality scientific and technical deliverables. The successful candidate will have experience working within the pharmaceutical, biotechnology, or hea...

Software Quality engineer
Galway

Software Validation Engineer (Contract) | Galway | 12 MonthsA leading medical device manufacturer is seeking an experienced Software Validation Engineer to support manufacturing and quality systems within a highly regulated environment. This is an excellent opportunity to join a major organisation and play a key role in ensuring critical equipment ...

Senior CQV Engineer
Negotiable

Role Overview We are looking for a Senior CQV Engineer for a duration of 12 months, to support pharmaceutical manufacturing projects, with primary responsibility for commissioning and qualification of GMP manufacturing equipment. The role requires a hands-on engineering profile capable of independently driving CQV activities from planning and proto...

Elevate your career

Take the first step toward your next opportunity - submit your CV and get started today.

Register CV
Selby Jennings Start Your Career In Recruitment
DP MSAT Consultant
Negotiable

Senior Drug Product MSAT / Tech Transfer Consultant (Contract) Location: RemoteStart Date: November 2026Duration: 12 Months (to November 2027)Commitment: Approximately 25 hours per week Overview We are seeking an experienced Drug Product MSAT / Technology Transfer Consultant to support a high-profile CMC programme involving the transfer, scale-up a...

C&Q Engineer
Negotiable

We are seeking an experienced Commissioning & Qualification (C&Q) Engineer to support ongoing qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. The successful candidate will play a key role in coordinating qualification documentation, executing qualification activities, and ensuring alignment b...

Technical Support Specialist part-time
Negotiable

Our client is seeking a part-time Technical Support Specialist to support engineering and maintenance activities by managing SAP administrative tasks, updating technical documentation, and maintaining P&ID drawings. The objective of this role is to provide practical support to the engineering team by taking ownership of administrative and drafting ...