About this opportunity
Merck & Co. lists this QA Documentation Lead: MasterControl & GMP Compliance opportunity in south brunswick, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Tris Pharma, Inc. seeks a Quality Assurance Documentation Lead to support QA compliance with SOPs, cGMPs, and FDA standards at our Monmouth, NJ site.
Under QA management, you will maintain Master Control docs, support stability programs and APR data, and collaborate with multiple departments to ensure timely, accurate records and change controls.
Fluency in English is required; background checks may be conducted. Wage: $77,522–$101,750 plus comprehensive benefits.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.