Principal Manufacturing Process Engineer

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 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 Pfizer’s 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

The  Principal Process Engineer supports the execution of Commercial, Clinical, and / or Development production according to Standard Operating Procedures and Production Schedule for  mAb 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

Supports  manufacturing operations on the production floor for buffer / media make-up 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 Contact   for the execution and issue resolution associated with process equipment commissioning, qualification and validation.

Owns  troubleshooting, technical support / analysis and resolution of equipment, automation, and process issues on the manufacturing floor.

Delivers Right first time execution and continuous improvement; Monitor, Identify and / or Communicate process and compliance trends in real time.

Participate in the authoring role  for controlled documentation; SOPs, Manufacturing Batch / Formulation Records, Forms, etc.

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

Responsible for remaining current on assigned training.

Leads Lean Manufacturing, Sustainability and Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.

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

Generates   work requests when issues arise with facility / manufacturing equipment. Provides support to maintenance to facilitate resolution, when needed. Point of contact for emergency work orders.

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

Leads and coaches beginner and intermediate Process Engineers through complex troubleshooting, 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 associate's 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 problem-solving 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)

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 role is standard day Monday through Friday (8 hrs), but at times it will be necessary to work according to the manufacturing shift schedules (1st, 2nd or 3rd shift, weekends) to support execution of batch records when manufacturing batches that are manufactured outside.

Limited Travel 10%.

Other job details

Last Day to apply : December 9th, 2025

Work Location Assignment :  On Premise

The annual base salary for this position ranges from $96,300.00 to $160,500.00. In addition, this position is eligible for participation in Pfizer’s 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 life’s 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 | (uscandidates.mypfizerbenefits.com). 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.

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

Pfizer endeavors to make    accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and / or interviewing, please email   disabilityrecruitment@pfizer.com . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and / or interviewing. Requests for any other reason will not be returned.

Engineering