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Pfizer Singapore is recruiting permanent employees for manufacturing site expansion of PFIZER ASIA MANUFACTURING PTE LTD (PAMPL) in Singapore. You will co-ordinate the manufacture of key API (Active Pharmaceutical Ingredients) Intermediate processes and provide appropriate technical support to process teams to sustain and improve the processes. You will ensure flawless execution throughout each assigned campaign, focusing on the fundamentals of safety, quality, supply and cost. Cost Improvement Projects (CIP) development will also be a key part of your role. As an Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams.
Job Responsibility:
Develop Manufacturing/Operating Instructions and necessary Standard Operating Procedures
Develop, maintain and troubleshoot the process control system recipe/Models
Investigate, report and troubleshoot findings on both quality and EHS related issues observed during manufacturing or during batch record review
Develop, implement and monitor extensive preventive measures for processing issues
Play a pro-active role in ensuring the site safety and quality standards are adhered to
Proactively monitor, identify, develop and implement improvements in processes and equipment
Communicate on a regular basis to the plant personnel on process updates
Train the process technicians on the process and procedures as required and practices of good data management (ALCOA)
Ensure adherence to approved procedures and update the procedures as required
Focus on Safety and GMP Compliance as operational priorities and as performance measures
Accountable for the Good Data Management and Data integrity understanding and performance
Report and investigate actions or behaviors that may negatively impact the desired outcome of the GMP process or activity
Own on or more multiple equipment/GMP systems in production and present the system overview with evidence compliance to internal and external auditors
Develop courses of action and drive implementation of solutions
Play an active and impactful role to deliver flawless execution for respective PCTs (e.g. API, MS, 00, Leadership, Engineering) by updating performance against metrics, highlighting & resolving issues with appropriate escalations
Work with the PCT to identify and drive improvement as per continuous improvement (Cl} goals of the PCT
Uphold Pfizer's code of conduct and values
Senior position is expected to perform coaching role to junior engineers and manage more complex manufacturing and operation issues
Also expected to lead working teams managing projects to support manufacturing processes
Collaborate with cross-functional teams to drive flawless execution
Requirements:
Degree in Engineering, preferably in Chemical Engineering or Degree in Science
5+ years of experience
Knowledge of Good Manufacturing Practices, Good Documentation Practices, experience in pharmaceutical environment
Experience of project orientated admin/cost control/management
Broad knowledge of theory and principles within a professional discipline or advanced knowledge of specific technical/operational practices
Strong technical, management and organizational skills