Use Your Power for Purpose

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

The annual base salary for this position ranges from $80 300,00 to $133 900,00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus tar