At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting the upkeep of systems, engineering is crucial to ensuring customers and patients receive the medicines they need. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world.
What You Will Achieve
In this role, you will:
Collaborate with technical services to identify and confirm Critical and Key Process Parameters essential for Equipment and Process Validation.
General knowledge of scientific principles, technical knowledge of production equipment, automation control systems, processing requirements, and any related procedural requirements with emphasis on assign production area.
Report team progress, highlight risks, clarify issues, suggest recommendations, and present next stage development plans.
Operate various process equipment such as fermenters, recovery equipment, and depth filtration equipment, and coordinate daily activities of Good Manufacturing Practices (GxP) production to meet supply chain needs.
Facilitate effective project meetings with internal team members and customers, and develop SPC charts for continuous process monitoring and control.
Manage project finances, provide information to support financial reporting requirements, and ensure process adjustments are incorporated into final SOPs, Master Batch Records, and Compounding Records.
Provide troubleshooting and technical support to manufacturing groups, participate in process and cleaning validations, adhere to site safety standards, and enforce safety and biosafety requirements in the manufacturing department.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with 0+ years of experience;
OR an associate's degree with 6 years of experience; OR a high school
diploma (or equivalent) and 8 years of relevant experience.
Demonstrated knowledge of Good Manufacturing Practices and experience operating / troubleshooting both equipment and automation in a highly regulated pharmaceutical environment.
Proficiency in project-oriented admin, cost control, and management.
Demonstrated experience in at least some of the following systems: EAMS (Computerized Maintenance Management Systems), DeltaV, SAP, PDOCs (Document management systems), or KNEAT, SIMCA, or Pi
Demonstrated experience in at least some of the following processes: Change controls, risk assessments, Investigations, or tech transfers
Good leadership and communication abilities
Strong problem-solving skills
Commitment to safety and compliance
Bonus Points If You Have (Preferred Requirements)
Experience in automation including DeltaV and equipment validation
Knowledge of the manufacturing process and equipment, preferably mammalian cell culture, protein purification processes, and solution prep.
Commitment to safety and compliance with biosafety requirements
BA/BS in Chemical Engineering, Biomedical Engineering, Electrical Engineering / Science (or related fields)
Physical / Mental requirements
Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
This role is rotating 2/2/3 twelve-hour shifts to support execution of mAb manufacturing.
Limited Travel 10%.
OTHER JOB DETAILS
Last Date to Apply for Job: July 24, 2025.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
Work Location Assignment: On Premise
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.
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