My globally recognized client is looking for a stand out character to join them on a 12 month contract in San Diego, California!
What will be required:
A strong working experience working within the pharmaceutical/ biotechnology sector and a great background working with CAPA's and remediation projects. The location is San Diego - local candidates ideally - There will be no relocation expenses paid!
You will be responsible for carrying out day to day tasks over the QA department, with oversight of ensuring all activities are compliant and up to date with all regulatory requirements.
You will review batch records, both master production/packaging records and executed batch records ensuring compliance with GMP and registration requirements - as well as process product complaints, recording, contacting complaint, initiating manufacturing investigation and communicating conclusion/ summary to complaint.
- 6+ Years working in the pharmaceutical industry
- 3+ Years working in a QA environment
- B.S/B.H in a related life science discipline
So Why Would You be Interested?
This is the opportunity to work with a Globally recognized organization on a fantastic project! It is a 12 month initial contract based in sunny San Diego - you will be required to be on site the majority of the time to build relationships and credibility and then the opportunity to work remotely for a few days per week! You will be required to be an independent contractor, working on a 1099 basis with an LLC/ ESCORP.
What to do now...
Simply drop me an email/ application with your most up to date resume and give me a call! I am more than happy to explain this position in more detail on a personal level! firstname.lastname@example.org -- 646 415 8221
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