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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.

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