MSAT Engineer 3

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 customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health.

What You Will Achieve

• Contribute to project tasks and milestones, ensuring work is organized to meet deadlines.
• Design and develop manufacturing processes for drug product in collaboration with Production and Technical Operations
• Provide drug product support and technical leadership in investigations to aid in determining root cause and implementation of appropriate corrective and preventive actions.
• Utilize small-scale production processes and use scaled-down lab processes to enable process troubleshooting.
• Assist in New product introduction, technology transfers, including Gap Analysis, Process Transfer Risk Assessments, process flow diagrams, and Drug Product Risk Assessment Life Cycle Management Program.                                                             
• Assist with drafting and updating drug product, material, and component specifications.
• Support Regulatory filing strategies through authoring and/or reviewing changes to drug product registrations
• Lead process, product and device improvements, create data packages by justifying recommendations for improvements in production processes and collaborate with the Production and Technical Operations to implement process technology initiatives.
• Broad knowledge of theory and principles within a professional discipline or advanced knowledge of specific technical/operational practices. Serving as a key scientific and technical representative for process-related issues at the facility.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelor's degree, in Chemical Engineering, Materials Science, Biomedical Engineering and Biomanufacturing Sciences preferred, 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
• Process Engineering or operational excellence experience in a pharmaceutical or medical device setting
• Demonstrated knowledge and experience with Good Manufacturing Practices and Process Monitoring systems.
• Strong communication skills
• Self-motivated attitude with the ability to work with minimal direction
• Flexibility and adaptability to changing priorities
• Ability to meet deadlines and perform well under pressure
• Proficiency in troubleshooting and problem-solving

Bonus Points If You Have (Preferred Requirements)

• Five or more years of experience in product development, manufacturing science and technology, sterilization or process validation or process engineering within the pharmaceutical industry.
• Experience with aseptically filled or terminally sterilized small volume and / or large volume parenteral products.
• Experience with technology transfer and scale-up processes
• 3+ years of experience in a pharmaceutical manufacturing site
• Strong attention to detail
• Ability to navigate complex challenges and opportunities
• Experience in a structured, process-driven environment
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

PHYSICAL/MENTAL REQUIREMENTS

Some standing, sitting, and basic lifting activities associated with an office-based support role for manufacturing is required.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• This role is standard day Monday through Friday(8am-5pm) work shift; some off-shift support to work 2nd or 3rd shift on occasion.

• The position may require working on the floor in manufacturing or within our lab which will require a heightened safety awareness and gowning will be required. 

Work Location Assignment: Hybrid

OTHER JOB DETAILS

Last Date to Apply for Job: November 27th, 2026

The annual base salary for this position ranges from $82,700.00 to $137,900.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. 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.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Engineering