Job Description:

1. Oversees a group of Maintenance Technicians in an GMP environment. Ensure GMP and EHS compliance of all colleagues while in operation.

2. Develop, maintains and review of all Corrective, Preventative Maintenance, Good Manufacturing Practice work orders in the Computerized Maintenance Management System (EAMS).

3. Provides technical leadership in the development and utilization of Clean-Inspect-Lubricate (CIL) and Centerlines during TPM implementation

4. Ensures equipment is maintained at basic condition and deliver PM’s in the scheduled time frame

5. Ensures the proper functioning of the instruments and systems of instrumentation, measurement, control, to ensure measurement correct set parameters

6. Provides leadership in troubleshooting and problem-solving breakdowns and reliability losses with cross-functional team

7. Work with purchasing, contractors, outside firms, and suppliers to support the maintenance department

8. Become a subject matter expert for site quality investigations from Maintenance & Automation

9. Contact vendors for support and emergency repair items when required

10. Write QARs which relate to Maintenance and Automation part

11. Maintain user access records, backups and restores of PLC’s/Computer Systems/Vision Systems, Generate Audit trails and review for Data integrity in Pharmaceutical Manufacturing plants. Recommend upgrades and repairs to manufacturing lines and systems

12. Troubleshoot advanced PLC Controls systems, Preventive Maintenance and Repairs to Validated Manufacturing Systems.

13. Active participate in daily Tier 1 Engineering meetings to verify plant priorities daily

14. Perform electrical walkdown, startups, installation of new equipment and upgrades.

15. Able to re-program and changes to various VFDs and PLC software systems. Provide support and advice to the Equipment Installation, Qualification & Commissioning

16. Prepare functional procedures and documentation for technical detail on Maintenance and Automation area

17. Leading all the site Automation project such as ICS Cyber program, CLAN infrastructure & migration, Alarm Management, and other CAPEX project which relate to Automation.

Qualifications

Must-Have

• Bachelor's Degree
• 3+ years of experience pharmaceutical aseptic manufacturing experience
• Strong understanding in GMP
• Good experience in equipment automation, equipment maintenance management
• Direct supervisory experience and understands knowledge management
• Knowledge of Good Manufacturing Practices {also cGMP} OSHA, Food and Drug Administration and environmental regulations applicable to the pharmaceutical Industry
• Strong people management experience
• Strong English speaking and writing skills
• Good computer skills in Microsoft Office suite of products

Nice-to-Have

• Master's degree
• Relevant pharmaceutical experience
• Hands on experience with communication protocols
• Strong technical skills
• Certified Sig Sigma Yellow Belt
• Lean manufacturing trained

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.