A QA Specialist (Pharma compliance) role is available in Rutherford, NJ courtesy of Adecco Med/Sci. This direct-hire role is for a Quality (compliance/reg affairs) professional in the pharmaceutical with at least 4 years' experience and a strong background in in a lab/bench environment, as well as GLP, CLIA, CAP, SOP, etc. This person should have a broad range of compliance and QA experience and be comfortable interfacing with the labs.
This role will be a compliance resource that helps to manage the document control process and tracks SOPs. This person will also offer experience with GCP, OSHA, CFR Parts 21 and ICH guidance documents.
Bachelor's degree in Biology, Microbiology, or Clinical Laboratory Science preferred
1-3 years' experience in Compliance/Regulatory Affairs (with a small pharma or biotech preferred)
Experience in a clinical research lab
Knowledge of: CLIA; SOPs; CAP; GCPs, etc.
To be considered for this position, please APPLY NOW and submit your resume to email@example.com.
If you have questions about the position please contact Scott Shuman at 585.613.3028.
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