On Site QA Supervisor

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.

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Responsibilities Oversee the functions of the Quality Assurance Team Develop and maintain quality procedures and documentation

Determine disputation of material and products

Coordinate and review deviations, investigations and CAPAsParticipate in audits and address audit findings as needed

Perform product releases and finished product assessments

Qualifications

Associates degree required, Bachelor’s degree or above preferred

Minimum of 5 years experience working in pharmaceutical production or GMP environment

Excellent communication and documentation skills

Knowledge of cGMP regulations, quality systems, and pharmaceutical manufacturing processes.

Experience reviewing batch records, performing material inspections, and supporting quality documentation

Strong organizational, analytical, and problem-solving skills#ind skilled