REGULATORY AFFAIRS SPECIALIST
Corepharma
Compensation
$
Hours Per Week
40
Number Of Positions
1
Job Description
REGULATORY AFFAIRS SPECIALIST (Middlesex, NJ) Review/approve pharmaceutical batch records; verify/approve analytical specifications/methods/protocols/method transfer docs; oversee QMS, change controls, deviations, incidents, CAPA, OOS; ensure compliance with pharmaceutical calibrations; develop guidelines/procedures on cGMP/SOP and quality assurance activities. Masters (or foreign equiv. deg.) in Pharmaceutics, Health Informatics, or rel. + knowledge of analysis of raw materials, in-process/finished product samples, validation of results, internal audits, SOP implementation, calibration of laboratory equipment, IQ, OQ, PQ, review, drafting of batch manufacturing/packaging records. Send resume: Mail resume to Core Pharma LLC, 215 Wood Ave., Middlesex, N.J. 08846.
Place of Work
On-site
Requisition ID
133181
Application Instructions
Send resume: Mail resume to Core Pharma LLC, 215 Wood Ave., Middlesex, N.J. 08846.
Vacancy posted 1 day ago
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