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QA & Regulatory Affairs Associate (North Brunswick, NJ).

Pharmaceutical manufacturing and research co. seeks QA & Regulatory Affairs Associate to utilize knowledge of ICH/FDA and cGMP regulations and guidelines to review executed manufacturing batch records and certificates of analysis for APIs, raw materials and in-process materials and sterile products to ensure compliance with safety guidelines. Deal with quality management systems on daily basis and provide QA support during manufacturing and analytical operations. Prepare SOPs, specifications and STPs for raw materials, intermediates and finished products. Send resumes to: HRD, Apicore LLC, 685 US Highway 1, North Brunswick, NJ 08902