QA Supervisor
Our client is seeking a talented Quality Assurance (QA) Supervisor to oversee incoming QA dealing with receipt, sampling, testing, storage, and release activities related to drug product components and container closures, and maintain records and procedures per cGMP and company standards. The Supervisor will supervise QA group, assist GMP audits, report Quality metrics and prepare, review, approve and issue batch records. Specific duties include but are not limited to:
- Supervises activities and coordination of the receipt, sampling, testing, storage and release of drug product and containers.
- Develops and maintains operating specifications and change controls, sampling and batch record protocols and reports as needed.
- Investigates and reviews reports and participates in audits regarding the compliance with quality procedures, policies and regulations.
- Plans and schedules work, supervises staff, represents the team in meetings and provides support during product manufacture as necessary.
Requirements
- Bachelor's degree in related field and 3 plus years of related experience in pharmaceutical manufacturing; Supervisory or Lead experience preferred.
- Detailed experience in Aseptic processing.
- Strong problem-solving, team management and record keeping skills.
- Excellent verbal, written and interpersonal communication skills.
- High level of initiative and self-motivation.
- Strong computer skills and Attention to detail.
- Able to plan, prioritize and organize diversified workload.
This is an exciting full-time opportunity with a growing a contract development and manufacturing organization offering an attractive work environment and compensation/benefits package. Please contact tony.roig@azzur.com for immediate consideration.
