Senior Automation Engineer - AMPS

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals. Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products. Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. 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 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, troubleshooting, and maintenance. Lead product manufacturing campaigns from the start of production and provide 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, producing 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. 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 troubleshooting and mentoring support to personnel writing recipes. Develop documentation for supporting the operation of AMPS, e.g., SOPs, 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 proactive role in ensuring the site safety and quality standards are adhered to. Proactively monitor, identify, develop, and implement improvements in processes and equipment. Communicate regularly with plant personnel on process updates. Train process technicians on the process and procedures as required. Ensure adherence to approved procedures and update 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 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 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). Update performance against metrics, highlighting & resolving issues with appropriate escalations. Work with the PCT to identify and drive improvement as per continuous improvement (CI) 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. Initiative and creativity to identify improvement opportunities and work to see them implemented. Strong planning and organizational skills with a proven ability to deliver against timelines. A proven knowledge 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. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. #J-18808-Ljbffr