Pfizer Singapore is recruiting permanent employees for manufacturing site expansion of Pfizer Asia Manufacturing Pte Ltd (PAMPL) in Singapore

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 in analyzing and designing a sequence of operations and workflow to improve the company's production facilities within regulations and Good Manufacturing Practices. You will be involved in activities, such as process monitoring, safety and environmental improvements, process reliability improvements, validation, and technology transfers. You will also conduct studies pertaining to cost control and reduction, inventory control, and production record systems. On the basis of these studies, you will develop and implement plans and programs for facility modifications and revisions to operating methods.

As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.

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

How You Will Achieve It

•  Develop Standard Operating Procedures related to the key support systems.
•  Develop, maintain and troubleshoot the key support systems.
•  Investigate, report and troubleshoot findings on both quality and EHS related issues in key support system.
•  Develop, implement and monitor robust preventive measures for key support systems.
•  Ensure the key support system meets the site safety and quality standards.
•  Monitor, identify, develop and implement improvements in support systems.
•  Communicate on a regular basis to the plant personnel on process updates.
•  Train the process technicians on the key support system procedures as required.
•  Ensure adherence to the key support system procedures and update changes as required.
•  Be the subject matter expert and system owner for key support system. Present the system to external and internal auditors.
•  Collaborate with cross functions to support manufacturing operations.
•  Participtate in the planning and execution of the annual shut down maintenance activities.
•  Assist in the budgeting, purchase and management of operation consumables.
•  Develop courses of action and drive implementation of solutions.
•  Uphold Pfizer’s code of conduct and values.

Accountable for:

•  Sustainability
•  Plant productivity
•  Safety performance
•  cGMP and SOP compliance
•  Yield and Quality

Qualifications

Must-Have

• Bachelor's Degree
• Demonstrated ability to lead people or processes
• Laboratory experience required (testing, data reviewing, or other supporting activities for laboratory operation)
• Basic functional and technical knowledge of the discipline
• Good organization skills and attention to detail
• Ability to document clearly and concisely
• Effective written and oral communication
• Knowledge of Microsoft Applications

Nice-to-Have

• Indirect leadership experience {e.g. testing/team Subject Matter Expert project lead, training lead)
• Demonstrate proficiency in computerized systems, experience and use of Laboratory Information Management System and Quality Tracking System

  
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.

Manufacturing

#LI-PFE