Pfizer
All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Â Pfizer, a global leader in the bio pharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.
Job Title:Â Â Â Assistant Manager Manufacturing Quality
No. of Posts:Â Â 1
Job Description:
The Manufacturing Quality Supervisor is responsible for ensuring Sterilization, Visual Inspection, and Packaging are operating under a state of cGMP compliance. The Supervisor is directly responsible for managing and coordinating all quality functions within the area. The individual must communicate effectively and work with cross-functional teams.
Responsibilities
- Supervise a specific shift to ensure that Terminal Sterilization, Visual Inspection & Packaging areas are operating within a state of cGMP compliance
- Facilitate achievement and maintenance of quality goals and cGMP compliance
- Collaborate with manufacturing management to identify and correct product and/or process defects
- Accountable for ensuring products meet cGMP requirements
- Ensure that when quality related issues arise, these issues are quickly escalated, so that documentation of events, investigations, and corrective actions are performed in a timely manner
- Manage deviations and prevent future occurrences by identifying root causes, enhance the capture of data for investigations, and implement effective CAPAs
- Manage quality project initiatives
- Maintain regulatory compliance by building and sustaining quality concepts
- Conduct audits / walkthroughs to ensure procedures are being followed in accordance with cGMP
- Provides guidance and mentorship to direct reports on quality concepts
Qualifications:Â
B. Pharm/M. Pharma/M. Sc. plus a minimum of 5 years working in sterile dosage manufacturing facility
- Leadership and decision making abilities
- Strong interpersonal skills
- Analytical mind to grasp complex analytical issues and provide feasible, logical and scientific solutions
- Communication skills to provide feedback and mentoring to QA colleagues and internal customers
