Secondment - Production Supervisor (Solid Value

5 months ago

Jakarta, Indonesia Pfizer Full time

Why Patients Need You

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.

What You Will Achieve

Your expertise in the manufacturing domain will help Pfizer with the operations required for the assembly and packaging of finished goods. You will manage product finishing scheduling, setting up, operating, maintaining, and adjusting processes or packaging equipment.

As a Team lead, you will be involved in leading work teams within a division, also managing the technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day to day activities. You will be relied upon to maximize quality and efficiency, completing batch records and associated documentation, and working in an integrated computerized manufacturing environment.

It is your dedication and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It
- Manage multiple projects and ongoing work activities within the team.
- Perform operational functions to meet daily and weekly production schedule activities, including product check-in and in-process tests.
- Train staff on good safety practices and enforce all safety regulations.
- Train employees in all departmental procedures, product inspection and (Current) Good Manufacturing Practices (part of GxP).
- Maintain and improve labor standards for the operating departments.
- Effectively coordinate activities by communicating with other operational departments.
- Write departmental procedures and batch records for the department.
- Assure appropriate communication and implementation of corrective/preventive actions to avoid reoccurrence.
- Support the Technical Service Specialist / Engineering in the coordination of any packaging validation activity.
- Execute or supervise data entry on required systems and monitor metrics indicators.

**Qualifications**:
Must-Have
- Bachelor's Degree
- 3+ years’ experience
- Strong people management experience
- Effective written and oral communication skills required
- Ability to communicate effectively not only within the department but cross functionally at the site and with outside customers and regulatory agencies
- Computer literate, with skills in managing Excel spreadsheets, and knowledge of Microsoft Applications

Nice-to-Have
- Master's degree
- Relevant pharmaceutical industry experience
- Strong background in Manufacturing, Technical Services, Materials Management, QA/QC and Engineering

Work Location Assignment: On Premise

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

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