Supervise packaging operations, ensuring compliance with GMP standards and safety. Develop procedures, manage personnel, and drive engagement on the production floor.
Position Purpose:
To provide direct support and guidance to operators, ensuring they perform packaging processes in a compliant, safe, effective and efficient manner. As our front-line leadership, your leadership presence on the Production Floor is fundamental to the success of your team and ensuring they deliver on their commitments. Your leadership presence will keep colleagues focused and engaged and is fundamental to your own success in the role.
Primary Duties:
• Supervising daily activities to ensure compliance in Quality, Safety, effective and efficient operations by:
- Ensuring packaging areas, machine, and facilities in good condition, tidy and safe.
- Verifying critical process in daily production (e.g. Line Clearance, Cleanliness Verification, Lot Start Up Verification, printing verification (Lot No./ Mfg. Date/Exp. Date/HET)).
- Reviewing all GMP documents (e.g., packaging (batch record/LHF, logbooks) to ensure that all activities were follow approved procedures/instructions and appropriated documented properly as per Data Integrity and Good Documentation Practices principles.
- Ensuring production personnel who performing packaging activities are qualified.
- Executing purchase manufacturing supplies based on budget availability.
• Developing GMP documents as follows:
- Master Packaging Instructions (MPI).
- Standard Operation Procedures (SOP) included working form of machine, cleaning, handling etc. to meet cGMP and PQS requirements.
• Actively involved on conducting gap assessment, any deviation/investigation, OOS/OOL/OOT result and product complaint (rework, complaint, recall) to find out the root causes, provide solution, and prevent the reoccurrence and conducting CAPA completion as the results of investigation, product complaint, or follow up audit. • Responsible for ensuring that PGS Jakarta delivers on customer expectations of supplying quality products. Schedule Adherence against the Production Plan, and delivery of committed production volumes is critical. • Actively involved in other activities as follows:
- Environmental, health & safety (EHS) program and activities.
- BPOM, RQA, and third-party quality audit.
- Validation/qualification activities.
- Integrated Manufacturing (IMEX) program and initiatives in packaging activities (e.g. Encouraging colleagues to rise up their ideas/innovative to find a better operation)
- Site projects
• Drive team engagement and effective communication within the team.
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements):
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Manufacturing
To provide direct support and guidance to operators, ensuring they perform packaging processes in a compliant, safe, effective and efficient manner. As our front-line leadership, your leadership presence on the Production Floor is fundamental to the success of your team and ensuring they deliver on their commitments. Your leadership presence will keep colleagues focused and engaged and is fundamental to your own success in the role.
Primary Duties:
• Supervising daily activities to ensure compliance in Quality, Safety, effective and efficient operations by:
- Ensuring packaging areas, machine, and facilities in good condition, tidy and safe.
- Verifying critical process in daily production (e.g. Line Clearance, Cleanliness Verification, Lot Start Up Verification, printing verification (Lot No./ Mfg. Date/Exp. Date/HET)).
- Reviewing all GMP documents (e.g., packaging (batch record/LHF, logbooks) to ensure that all activities were follow approved procedures/instructions and appropriated documented properly as per Data Integrity and Good Documentation Practices principles.
- Ensuring production personnel who performing packaging activities are qualified.
- Executing purchase manufacturing supplies based on budget availability.
• Developing GMP documents as follows:
- Master Packaging Instructions (MPI).
- Standard Operation Procedures (SOP) included working form of machine, cleaning, handling etc. to meet cGMP and PQS requirements.
• Actively involved on conducting gap assessment, any deviation/investigation, OOS/OOL/OOT result and product complaint (rework, complaint, recall) to find out the root causes, provide solution, and prevent the reoccurrence and conducting CAPA completion as the results of investigation, product complaint, or follow up audit. • Responsible for ensuring that PGS Jakarta delivers on customer expectations of supplying quality products. Schedule Adherence against the Production Plan, and delivery of committed production volumes is critical. • Actively involved in other activities as follows:
- Environmental, health & safety (EHS) program and activities.
- BPOM, RQA, and third-party quality audit.
- Validation/qualification activities.
- Integrated Manufacturing (IMEX) program and initiatives in packaging activities (e.g. Encouraging colleagues to rise up their ideas/innovative to find a better operation)
- Site projects
• Drive team engagement and effective communication within the team.
Here Is What You Need (Minimum Requirements)
- Bachelor's degree in pharmacy from a reputable university, with a minimum of 3 years' experience in pharmaceutical industry, specifically in manufacturing-packaging operations.
- Excellent interpersonal and communication skills
- Strong people management experience
- Proven record of problem-solving and decision-making skills
- Effective written and verbal communication skills in both local language and English.
- Ability to communicate effectively within the department, cross-functionally at the site, and with outside customers and regulatory agencies
- Strong organizational and project management skills
- Ability to work collaboratively in a team environment
- Demonstrated ability to manage multiple priorities and projects
Bonus Points If You Have (Preferred Requirements):
- Certified Six Sigma Green Belt
- Certified Lean Six Sigma
- Proficient in using SAP systems
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Manufacturing
Top Skills
SAP
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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