Pfizer Singapore is recruiting permanent employees for manufacturing site expansion of PFIZER ASIA MANUFACTURING PTE LTD (PAMPL) in Singapore.

Why Patients Need You

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.

What You Will Achieve

Working with Pfizer’s dynamic engineering team, you will play a critical role in the management of manufacturing information systems to improve manufacturing success rates and ensuring zero down time.

As a Senior 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.

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

How You Will Achieve It

• Support global AMPS team to setup AMPS System and build up Master data
• Configure Recipes per site processes and priorities
• Provide training to the end user in terms of configuration, trouble shooting and maintenance.
• Will be responsible for leading product manufacturing campaigns from the start of production and providing technical supervision with respect to quality and EHS until completion and release of the material.
• Contribute to achieve our vision of being the best-in-class manufacturing site, production highest quality products in the safest way.
• Deploy and use the IMEx "way of working" for day-to-day operations, problem solving, escalations and continuous improvements.
• Support global AMPS team and AMPS SME to setup AMPS System and build up Master Data.
• Support AMPS SME to configure Recipes based on the site processes.
• Ensure seamless data flow through all interfaces (e.g. SAP, DeltaV) and hierarchies of system connectivity.
• Prepare and review system development lifecycle documents.
• Provide training to the engineer to configure recipes in AMPS.
• Provide day to day support for trouble shooting and mentoring support to personnel writing recipes.
• Develop documentation for supporting the operation of AMPS e,g, SO P's, Impact Assessment, Change Controls, Design Documentation, Verification Documents and Reports.
• Collaborate with cross-functional teams to drive flawless execution.
• Develop Manufacturing/Operating Instructions and Standard Operating Procedures.
• Develop, maintain and troubleshoot the process control system recipes/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 robust 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.
• Ensure adherence to approved procedures and update the procedures as required, including the principles and practices of good data management (ALCOA).
• Focus on safety and GMP compliance as operational priorities and as performance measures.
• Accountable for the Good Data Management and Date integrity understanding and performance.
• Report and investigate actions or behaviors that may negatively impact the desired outcome of the GMP process or activity.
• Own one 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, QO).
• 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.

Qualifications

• Degree in Chemical / Instrumentation and Control Engineering

Experience

• Knowledge and understanding of the material flow process and solvent management.
• Extensive knowledge and experience in process automation system and S88 Batch Standard, preferably in Emerson DeltaV
• Embrace the use of digital technology to scale and speed up every form of Interaction and action.
• A demonstrated ability to proactively solve problems and develop solutions to Engineering and Quality scenarios.
• Excellent people and communication skills working in a cross functional team environment.
• Will have the initiative and creativity to identify improvement opportunities and work to see the implemented.
• Strong planning and organizational skills and a proven ability to deliver against timelines,
• A proven know ledge of GMP procedures and the requirements of change controls, Standard Operating Procedures, document control, etc.
• An ability to deal with process change and to implement new and effective processes.
• Demonstrated applications of Lean and Six Sigma tools will be an advantage.
• Preferably, 5-6 years’ experience in a relevant manufacturing environment.

Core Competencies

Technical Skills, Analytical Skills, leadership, Communication Skills, Good team player, Project Management, Curiosity & Innovation, Self-motivated and independent.

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.