Posted 1 year ago in Biotech/Pharmaceutical
Perform various QC analyses on lab samples at mfg plants; Ensure compliance to cGMP’s and Safety & Health Programs. Analyze lab samples (raw material, in-process, finished product, stability, etc.)
Participate in lab investigations when required. Initiate and takes the lead role in Out-of-Specifications and Analytical Deviations of QC Lab investigations.
Ensure products are being tested strictly under cGMP conditions and disposition is taken on time as per committed Production Plan of every month, and/or procedural requirements.
Hands on experience in handling analytical instruments like HPLC, GC, IR, UV, AAS DSC, TGA, Malvern particle size.
Minimum of 3 years with BS in Chemistry, Pharmacy, Biochemistry or related field; MS/PhD preferred.
We have been been providing staffing services since 1996 to the Pharmaceutical, IT, and Financial Services industries. We do our best to find the right candidate for your team and corporate environment.
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