On Site QA Supervisor

The QTI Group

SummaryA local pharmaceutical manufacturer is looking to add a Quality Supervisor to their growing team. Candidates in this role would be responsible for leading and supporting the Quality Team. In this role you’ll also be supporting the team with different quality functions including on-site inspections, batch record reviews, raw material inspection/release, deviation reviews and supporting audits. This is a DIRECT HIRE role with a 1st shift schedule with competitive pay and benefits. Don’t miss out on this great opportunity, apply today to be considered!ResponsibilitiesOversee the functions of the Quality Assurance TeamDevelop and maintain quality procedures and documentationDetermine disputation of material and productsCoordinate and review deviations, investigations and CAPAsParticipate in audits and address audit findings as neededPerform product releases and finished product assessmentsQualificationsAssociates degree required, Bachelor’s degree or above preferredMinimum of 5 years experience working in pharmaceutical production or GMP environmentExcellent communication and documentation skillsKnowledge of cGMP regulations, quality systems, and pharmaceutical manufacturing processes.Experience reviewing batch records, performing material inspections, and supporting quality documentationStrong organizational, analytical, and problem-solving skills

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