Our quality assurance and technical operations team will meet your challenging recruitment needs.
This is an excellent opportunity to advance your career and gain exposure to CMC Regulatory Affairs in a varied pipeline of products.
Regulatory Affairs Submissions Specialist required to coordinate regulatory submissions within the EMEA region. The successful candidate will be responsible for the planning, review and submission of regulatory documents.
The desired candidate will have experience with case processing, medical review and ensuring quality control and quality assurance.
Work is an adventure.
And we're here to take you where you want to go.
End-to-end recruitment solutions or individual stand-alone services, tailored to your specific requirements.
My focus lies in Quality Assurance and Technical operations positions for Pharmaceutical, Biotechnology, Medical Device and CMO companies.
+44(0)20 7002 0000
I place freelance consultants across Quality and Technical Operations for Pharmaceutical, Biotechnology, Medical Device and CMO companies.
I place Pharmaceutical and Biotechnology Quality and Technical Operations professionals into exceptional companies on a permanent basis.
81% of survey respondents want a job with some degree offlexibility. It's an absolute must for talent attraction and retention.
I was recently asked about the top skills needed to be successful in my specialist area of permanent recruitment, which is Quality Assurance in the Pharmaceutical / Biotech world. How long is a piece of a string?!
In my last post, I looked at the technical skills required to succeed as a Quality Assurance Recruiter in a market that’s very technical and which requires in-depth subject matter expertise and relationship building savvy. My thoughts this week turn to talent scarcity in the ‘new normal’ environment of increasingly stringent regulation.