Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.
Post : Assistant Manager Manufacturing Quality
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
Candidate Profile
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
Additional Information:
Location: Vizag
Qualification : B. Pharm/M. Pharma/M. Sc
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: Manufacturing Quality
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