Production Manager

  • Cybersecurity / Information Security
  • Visakhapatnam
  • 6 days ago
  • $ - $
  • Full Time
  • Lead and manage people, manufacturing investigations, Continuous Improvement of manufacturing processes and ensuring alignment with short-term goals.
  • Actively share knowledge and identify potential improvements in processes or products, taking risks to develop innovative ideas.
  • Solve moderately complex problems within the department and assist with issues outside the department when needed.
  • Oversee manufacturing investigation related activities and manage multiple CI projects, often involving cross-functional representatives.
  • Recognize development needs in others, collaborate on development plans, and manage direct reports through goal setting, coaching, and ongoing assessment.
  • Communicate effectively by soliciting input, explaining complex concepts, and persuading others to adopt a point of view.
  • Support the manufacturing Suite Lead with resource planning, measuring team productivity, and identifying issues or opportunities.
  • Ensure inspection readiness by maintaining processes, providing guidance to the manufacturing team and communicating & acting on key learnings from internal & regulatory audits.
  • Stay updated on regulatory trends and Pfizer Quality Standards, recommending modifications to procedures and processes as necessary.

Here Is What You Need (Minimum Requirements)

  • Experience in Good Manufacturing Practices (cGMP) for regulated industries i.e USFDA with a focus on manufacturing process investigations.
  • A successful track record of continuous improvement and the development/implementation of best practices in Quality Operations and manufacturing
  • Experience with electronic systems including MES system Application and eQMS
  • Highly motivated, organized, and able to work effectively in a demanding environment with flexibility to changing priorities
  • Demonstrated leadership capabilities along with Coordination / Collaboration in a matrix organization.

Bonus Points If You Have (Preferred Requirements)

  • Pharmaceutical experience, particularly in Terminal Sterilization / aseptic manufacturing
  • Six sigma Green Belt certified
  • Ability to adapt to a fast-paced and changing environment
Employment Type: Full Time, Permanent
Role Category: Operations, Maintenance & Support
Education
UG: Any Graduate