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 Pfizers 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 companys 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.

Position Summary

Support plant operations in the end to end manufacture (inclusive of changeover) of Active PharmaceuticalIngredients (APIs) in compliance with Good Manufacturing Practices (GMP) and Standard Operating Procedures(SOPs).
Collaborate cross-functionally to ensure safety quality and operational investigations are thoroughly conducted andreported in a timely manner.
Contribute to continuous improvement initiatives including IMEX activities and the development implementationand periodic review of documentation that enhances operational effectiveness and regulatory compliance.

Position Responsibilities

Support all aspects of manufacturing operations while ensuring full compliance with environmental health and safety(EHS) regulations

Maintain a state of perpetual safety and GMP compliance on the shop floor ensuring audit-readiness at all times
Execute production pre-maintenance and post-maintenance intervention activities to meet manufacturing targetsand reduce equipment downtime
Ensure that pre-manufacturing checks are performed safely compliantly in order to meet manufacturing plan
Review operational tasks in alignment with Manufacturing Standard Work (MSW) and Operation Standard Work(OSW) to optimize workflow efficiency
Lead/participate in troubleshooting activities for processing issues and deviations collaborating cross-functionally todrive immediate and preventive actions to meet manufacturing targets and reduce equipment downtime
Lead/contribute to EHS and quality investigations generate reports and drive resolution of issues identified duringoperations batch record review cleaning instructions review and associated manufacturing documentation
Drive Continuous Improvement (CI) initiatives using the Plan-Do-Check-Act (PDCA) methodology to enhance safetyquality and productivity
Lead/support the development of risk assessments and job safety assessments (JSAs); participate in HAZOP reviews asneeded
Author and review Standard Operating Procedures (SOPs); ensure SOPs remain current and compliant
Assist in commissioning qualification and validation (CQV) activities to support new equipment and process readiness
Participate as a member of the emergency response team (ERT) when necessary.
Development and review of changeover cleaning documentation and maintaining cleaning validation status

Development of changeover cleaning schedule and communication with cross functional departments for timelyrelease of equipment for production
Support manufacturing campaigns and changeover cleaning on rotating shift basis as required
Provide technical guidance for management of alarm responses and ensure alarm response is timely appropriate andassessed as per SOP. Ensure that interlock bypass is performed safely and compliantly as per SOP
Conduct hands on training including Structured On the Job Training (SOJT) Instructor Led Training (ILT) Job SafetyAnalysis (JSA) SOPs
Perform structured gemba on operational activities for continuous improvement opportunities and activeparticipation in good save initiative

Accountable for:
Safe operation of plant and equipment
Safety cGMP GDP and SOP compliance
Ensuring delivery of production plan inclusive of manufacturing and changeover cleaning

Here Is What You Need (Minimum Requirements):

Education

Degree in Engineering preferably in Chemical Engineering or Degree in Science

Experience

Preferably 2-3 years experience in a relevant manufacturing environment. Fresh graduates considered.

Core Competencies

Technical Knowledge Communication Teamwork Leadership Project Management Curiosity and Innovation Self-motivated and independent

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