Summary:
A 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!
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#indskilled
