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CY partners are recruiting for an amazing opportunity as a CMC Regulatory Specialist and Project Manager for a growing pharmaceutical company based in Northumberland to join their team in the CMC department.
Key tasks of this position are:
· Coordinate, produce and review early clinical phase CMC regulatory documentation for submission to global regulatory agencies
· Act as project manager and client point of contact, for assigned CMC projects
· Participate in discussions with potential clients and assist in the preparation of regulatory documentation related work proposals
· Provide API and drug product related CMC regulatory advice to colleagues and clients
To be considered for this role you must have a minimum of BSc (Hons) (or equivalent) in a relevant scientific discipline and be able to demonstrate the ability to critically assess data.
Previous experience producing CMC regulatory documentation is essential and previous project management experience would be advantageous.
You will be working for a modern, forward thinking business; that believe trust and strong relationships are the key to their success.
You will receive a highly competitive salary and excellent company benefits.
For more information about the CMC Regulatory Specialist and Project Manager role or to apply send your CV now.
The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.
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