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Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a qualified candidate for the position of Manufacturing Quality Assurance Director.  Responsibilities include creating SOPs, documents and forms, reviewing documents and data, conducting process-focused audits and inspections, consulting on quality and compliance issues, and mentoring employees in quality and compliance matters.  The successful candidate will possess strong leadership skills, problem solving abilities, and a positive can do attitude.  The Manufacturing QA Director would be expected to serve as the primary quality representative for manufacturing/formulation, interfacing with clients, leading client audits, and supporting regulatory inspections. 

The ideal candidate will possess a college degree and a minimum of 3-5 years’ experience working in a cGMP Manufacturing Quality Assurance role.  Extensive knowledge of ICH, FDA, 21 CFR, and other guidance documents is preferred.  The Manufacturing Quality Assurance Director will work with Project Management, Business Development, Supply Chain, and Analytical Development Support while overseeing the Quality team.   

QCL offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company.

Qualified candidates should apply via our website or apply now to email resumes.

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Manufacturing Quality Assurance Director Located At Nc, Wilmington - Job Post By: Quality Chemical Laboratories

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