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Medical Writer
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...
Hematology Account Manager Washington/Alaska | CONTRACT
Hematology Account Manager - Washington & Alaska (Contract)Contract Duration: 6-12 Months Compensation: $90-$110/hour + bonus Additional Compensation: Monthly car allowance providedPosition OverviewThe Hematology Account Manager will be responsible for building relationships with hematologists, oncologists, and key accounts to educate them on the p...
Software Quality engineer
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 ...
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Senior CQV Engineer
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...
DP MSAT Consultant
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
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...