Summary
A leader in pharmaceutical production is looking for a Quality Assurance Specialist to join their growing team. In this role you will play a critical role in maintaining quality and compliance throughout the manufacturing process. Working closely with operations and quality teams, you'll support batch record reviews, raw material inspections, investigations, and quality system activities that help ensure production of exceptional pharmaceutical products. This is a DIRECT HIRE position with a 1st Shift Schedule. Competitive pay is based on a candidate’s level of experience. Don’t miss out on this great opportunity apply today!
Responsibilities
- Review executed batch records to ensure accuracy, completeness, and compliance with cGMP requirements
- Perform inspection and disposition of raw materials according to approved specifications
- Author and support deviations, investigations, and change controls
- Execute shipping release procedures to support product distribution activities
- Provide administrative support for QA activities, including document control, training support, data compilation, and records management
Qualifications
- Bachelor's degree required; degree in a scientific discipline preferred
- 5+ years of Quality Assurance, pharmaceutical, biotechnology, or related industry experience preferred
- 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
- Excellent written and verbal communication skills
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