Principal Process Engineer (Secondment - 9 Months)

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 crucial to ensuring that customers and patients receive the medicines they need precisely when they need them. By collaborating with our forward-thinking engineering team you will contribute to delivering medicines to the world at an accelerated pace by envisioning new possibilities and taking decisive action. Your role in the design and development of manufacturing processes as well as in maintenance and reliability support is essential for providing timely access to necessary medications. Working alongside our innovative team you will help expedite the delivery of medicines globally by imagining what can be achieved and making it happen.

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

ThePrincipal Process Engineerwill lead effort for Decommissioning of Train 4 Assets and support Technical Transferincoming mAb products. The Principal Process Engineer will lead interdisciplinary and cross functional teams project manage the decommissioning of equipment and support Mabs Technical Transfer Teamfrom the System Owner perspective.

How You Will Achieve It

• Provide comprehensive testing and technical support for new manufacturing facilities and processes.

• Facilitate and manage process and component improvement projects as needed.

• Assess manage and report on the process capabilities of operational equipment and services.

• Point of Contactforthe execution and issue resolution associated with process equipment commissioning qualification and validation.

• Actively share knowledge within the team through established systems.

• Apply technical expertise in Operations Quality and Validation to recommend improvements considering business challenges.

• Lead cross-functional project teams through high-risk technical assessments and develop complex engineering solutions.

• Provide guidance and lead moderately complex projects managing time and resources effectively.

• Participate in the authoring and review rolefor controlled documentation; SOPs Manufacturing Batch/Formulation Records Forms etc.

• Leadsin the escalation process through various levels of management when operations personnel safety equipment functionality product supply and/or quality compliance are at risk.

• Apply skills and discipline knowledge to contribute to departmental work and make decisions to resolve moderately complex problems.

• Work independently review own work mentor colleagues and exercise judgment utilizing knowledge and experience.

Qualifications

Must-Have

• Applicant must have a bachelors degree with at least 5 years ofexperience; OR a masters degree with at least 3 years of experience; ORa PhD with 0 years of experience; OR as associates degree with 8 yearsof experience; OR a high school diploma (or equivalent) and 10 years ofrelevant experience.

• Demonstrated experience in product development manufacturing science and technology sterilization or process validation or Process Engineering within the pharmaceutical industry.

• Thorough knowledge of cGMP (current Good Manufacturing Practices) combination device regulations and design control.

• Strong history of problem-solving skills project and task management skills.

• Ability to manage priorities and lead others under pressure.

• Strong verbal and written presentation communication skills.

Nice-to-Have

• Relevant experience in the pharmaceutical industry.

• Experience in decommissioning equipment and facilities.

• Project Management Experience.

• Cross Functional Team Lead Experience.

• Proven ability to work collaboratively in a cross-functional team environment.

• Strategic planning and forecasting skills.

• Ability to facilitate agreements between various teams.

PHYSICAL/MENTAL REQUIREMENTS

• Position requirements are typical for an office-based work environment with some lab floor exposure and clean room gowning will be required.

• Ability to work on own initiative.

• Strong technical management and organizational skills.

• Good leadership and communication abilities.

• Strong problem-solving skills.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

This will be standard M-F (8AM-5PM) role. For Engineering and Validation runs some off shift work may be required.

Work Location Assignment:On Premise

Other Job Details

• Last Date to Apply for Job:July 11 2025

• Additional Location Information:NO

• Eligible for Relocation Package NO

• Secondment 9 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

Relocation assistance may be available based on business needs and/or eligibility.