Use Your Power for Purpose

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 forwardthinking 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 Engineersupports the execution of Commercial Clinical and/or Development production according to Standard Operating Procedures and Production Schedule formAb products. The Principal Process Engineer will lead interdisciplinary and cross functional teams to own and implement process improvements and lead/participate in process troubleshooting.

How You Will Achieve It

• Supportsmanufacturing operations on the production floor for buffer/media makeup tanks glass washers autoclaves bioreactors / fermentors drug product filling filtration equipment inoculum preparation chromatography skids and/or UF/DF skids with varying levels of automation.

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

• Ownstroubleshooting technical support/analysis and resolution of equipment automation and process issues on the manufacturing floor.

• DeliversRight first time execution and continuous improvement; Monitor Identify and/or Communicate process and compliance trends in real time.

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

• Collaborates withthe Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.

• Responsible for remaining current on assigned training.

• LeadsLean Manufacturing Sustainability and Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.

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

• Generateswork requestswhen issues arise with facility / manufacturing equipment. Provides support to maintenance to facilitate resolution when needed. Point of contact for emergency work orders.

• Skilledin enterprise systems to support manufacturing operations including but not limited to SAP LIMS AMPS PDOCS and/or QTS.

• Identifies the need for escalation through various levels of management when there is a risk to operations personal safety equipment functionality product supply and/or to quality/compliance.

• Lead crossfunctional project teams through highrisk technical assessments and develop complex engineering solutions.

• Leads and coaches beginner and intermediate Process Engineers through complex troubleshooting initiatives investigations and projects.

• Oversee and conduct supplier technical audits and corporate audits.

• Actively share knowledge within the team through established systems.

Here Is What You Need (Minimum Requirements)

• BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associates degree with at least 8 years of experience or high School Diploma (or Equivalent) with at least 10 years of relevant 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 problemsolving skills project and task management skills

• Ability to manage priorities and lead others under pressure

• Strong verbal and written presentation communication skills

Bonus Points If You Have (Preferred Requirements)

• Experience in mentoring and/or coach others

• Relevant experience in the pharmaceutical industry

• Proven ability to work collaboratively in a crossfunctional team environment

• Strategic planning and forecasting skills

• Ability to facilitate agreements between various teams

Physical / Mental requirements

• The incumbent needs to take the necessary safety precautions when working with pressurized systems steam and corrosive chemicals.

• The incumbent is required to attain proficient knowledge of the operational equipment.

• The incumbent will be required to assist in solving problems regarding site assessment specific units used in Biopharmaceutical manufacturing.

• The incumbent must be able to follow SOPs MBRs and be proficient in a multitude of enterprise systems including SAP DeltaV etc.

NonStandard work schedule travel or environment requirements

• Train 5 works 24/7. The incumbent will work on a fixed 12hour night shift.

Other details

• Last day to apply: May 26th 2025

• No relocation support available

• Work Location Assignment:On Premise

The annual base salary for this position ranges from $96300.00 to $160500.00. In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver/parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.

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

Engineering