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Manufacturing Supervisor - Sterile Injectables
Pfizer Healthcare India Private Limited - Vizag
Visakhapatnam, Andhra Pradesh, India · Full Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 1 week ago
- Work mode
- In office
- Education
- B.Pharma
- Eligibility
- Applicants must possess a B.Pharma degree in any specialization to be eligible.
- Resume
- Required to apply
Where you'll work
Job description
About Pfizer Healthcare India Pvt Ltd
Pfizer Healthcare India Private Limited in Visakhapatnam operates a manufacturing plant specializing in sterile injectables (SI), including vials, emulsions, and ampoules produced via terminal sterilization techniques. The facility ensures continuous medication supply with a commitment to quality, integrity, and compliance centered on patient safety.
Role Overview & Responsibilities
- Lead daily operations for assigned manufacturing lines such as solution preparation, emulsions, fill-finish, sterilization, visual inspection, and packing, ensuring strict adherence to standard operating procedures.
- Plan and coordinate activities to maximize resource efficiency and supervise real-time batch record execution within respective areas.
- Maintain the manufacturing environment to high standards by implementing rigorous cleanliness, organization, clean room, and personal hygiene protocols.
- Prevent cross-contamination or mix-ups through vigilant operational controls and participate in equipment and process qualification and validation activities.
- Observe Pfizer’s core values of Courage, Equity, Excellence, and Joy in all manufacturing stages and promptly report any safety, quality, or behavioral incidents to shift supervisors.
- Create a transparent and ethical team environment, support both internal and external audits, and motivate team members to achieve and surpass performance expectations.
- Monitor compliance with Good Manufacturing Practices (GMP), investigate any deviations, and uphold quality standards including the ALCOA principles for data integrity.
- Drive continuous improvement projects aiming for enhanced efficiency and quality improvements and ensure comprehensive documentation of all operations.
- Escalate deviations or exceptions appropriately and provide coaching and guidance to the team on manufacturing processes and procedures.
Eligibility Criteria
Candidates must hold a Bachelor of Pharmacy (B.Pharma) degree in any specialization.
Skills
Process Validation
Batch Record Management
Equipment Qualification
Team leadership and coaching
Manufacturing Operations Management
Cross-contamination control
Continuous improvement methodologies
Good Manufacturing Practices (GMP) compliance
regulatory audit participation
Sterile injectable processes
Aseptic processing knowledge
Data integrity (ALCOA) principles