Jobs in East of England
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Clinical Study Manager, responsible for UK and Ireland clinical trials and evidence to support new product launches in ostomy and continence care.
Clinical Data Reviewer required for minimum 6 month contract - Remote UK work - strong background in Oncology and clinical data review is essential
Permanent opportunity for a PV professional with post-marketing PV and QC'ing experience
Ongoing part-time contract for a full QP with UK GMP experience, ideally within generics - 1-3 days a week depending on capacity
Full-time opportunity for either life science graduate looking to move into PV OR someone with 1 years PV experience in post marketing PV
Full-time permanent position for a quality assurance professional with significant QMS development and management experience
Develop artworks to support European Regulatory applications (MRP, DCP, CP and Nationals)Develop print ready artworks to support all aspects of the pr
The Regulatory Affairs Regulatory Affairs Associate is responsible for providing regulatory support during the development of complex respiratory comb
The Regulatory Affairs Manager is responsible for providing regulatory support during the development of complex respiratory combination products and
As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 100 regulatory...
PPD is seeking a Regulatory Affairs Specialist to join our growing Regulatory Affairs department. This is a fantastic opportunity to further your...
If you’re a strategic thinker, planner and multitasker as comfortable working independently as you are on a team...
A fantastic opportunity to join a leading employer within the pharmaceutical industry.
International Pharmaceutical Manufacturer seeks an experienced Stability Analyst on a part time basis, 3 days per week 9 am till 5 pm.
International Pharmaceutical Manufacturer seeks experienced Biochemistry Analyst.
Pharmaceutical Manufacturer based in Hertfordshire requires an experienced Planning Co-ordinator.
International Pharmaceutical Manufacturer seeks an experienced Sterility Assurance Officer.
Leading Pharmaceutical Manufacturer requires an experienced Production Manager with experience working to a high level of GMP experience.
International Pharmaceutical Manufacturer seeks a Microbiology Lab Analyst working on a 24/7 shift pattern.
Pharmaceutical Manufacturer requires an experienced Pharmaceutical Quality Management Systems Manager.