QC Supervisor
Pharma manufacturer seeks talented Quality Control (QC) Supervisor to oversee and coordinate raw materials (including inspection, sampling and testing) for manufacturing and ensuring compliance with protocols, CGMPs and other regulations. The QC Supervisor interacts with other functional departments to ensure services are provided in a timely and efficient manner. Specific duties include:
- 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 and batch record protocols/reports as needed.
- Conducts Investigations and participates in audits regarding compliance and quality procedures, policies and regulations.
- Plans and schedules work, supervises/represents staff, and provides support during product manufacture as necessary.
Requirements
- Bachelor's degree (Chemistry or related field) preferred and 3 plus years of related experience in pharmaceutical manufacturing; Supervisory or Lead experience needed.
- Strong QC experience with Raw Materials in an aseptic processing environment.
- Good 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 pharmaceutical manufacturing organization offering a state-of-ther-art facility, career stability/growth and attractive compensation/benefits package. Please apply online for immediate consideration.
