Pfizer Engineer Jobs in Michigan (NOW HIRING)

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide-ranging pharmaceutical products.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

Transforming Delivery of high quality products

Pfizer, We are one

PGS - Manufacture the Future

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 vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.

WHAT YOU WILL ACHIEVE

Working with Pfizer’s dynamic maintenance/engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment.

As a Senior Maintenance Compliance Engineer, your knowledge and skills will contribute towards the goals and objectives of the team. Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams.

It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

HOW YOU WILL ACHIEVE IT

Contribute to completion of projects, manage time to meet targets, develop plans for short-term and mid-term work activities on projects.

Provide engineering support to develop scope of work, project execution plans, and associated engineering studies for equipment and component installation, modification etc.

Provide necessary operational support as needed.

Review preventive and corrective work order activities, provide equipment maintenance history review and work on preventive maintenance improvements.

Manage technical writing and document review.

Ensure maintenance/engineering compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices.

Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans.

Partner with Production and Quality Team Leads on troubleshooting and scheduling.

Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture.

Actively participate in site & corporate initiatives.

Leads and participates in investigations, change controls and develops/implements Corrective and Preventative Actions (CAPA's) for the maintenance department.

Serve as a liaison between Quality Operations and engineering/maintenance departments to facilitate timely closure of investigations.

Technical support for standard operating procedure improvements and updates.

Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with more than 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.

Experience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM/PDM optimization, and/or Failure Modes and Effects Analysis.

Demonstrated experience in manufacturing / reliability engineering, plant engineering and/or project engineering.

Teamwork spirit, good communication skills and training abilities.

Excellent interpersonal effectiveness and communication skills (written and oral).

Working knowledge of MS Office Applications.

Strong knowledge and understanding of Current Good Manufacturing Practices.

BONUS POINTS IF YOU HAVE (Preferred Requirements)

Certificates, Licenses or Registrations: Certified Maintenance and Reliability Professional (CMRP) (or equivalent) desired but not required.

Experience with pharmaceutical manufacturing equipment and/or utility systems.

PHYSICAL/MENTAL REQUIREMENTS

This is an on-site role at a penicillin manufacturing facility. Candidates must not be allergic to penicillin.

Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and complex data analysis, problem solving.

Ability to work in clean room conditions.

Ability to write general correspondence and technical reports.

Requires good written, oral communication and presentation skills.

Requires good planning, organizing, time management and team participation skills.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Regular Work Schedule:

Standard (M-F) daytime. Overtime work may be required. Work requires on-site presence. Occasionalnational/internationaltravel for equipment factory acceptance testing, training seminars, vendor meetings, work progress meetings, etc.

At different times of the year, this position will work long hours for scheduled manufacturing shutdown periods and throughout the year may be required to work late with little notice as need arises when equipment is unexpectedly down.

Demonstrate proficiency in cGMP, GMP, software development life cycle, environmental, health and safety procedures to assure compliance with regulatory, policies and/or established guidelines.

Observe and notify any risk situation for the environment, health or safety. Assure that all automation engineering initiatives comply with all regulatory agency requirements.

OTHER JOB DETAILS

Last Date to Apply for Job:September 4, 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.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

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 for 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 www.pfizer.com/careers 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.

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

• Contribute to completion of projects, manage time to meet targets, develop plans for short-term and mid-term work activities on projects.

• Provide engineering support to develop scope of work, project execution plans, and associated engineering studies for equipment and component installation, modification etc.

• Provide necessary operational support as needed.

• Review preventive and corrective work order activities, provide equipment maintenance history review and work on preventive maintenance improvements.

• Manage technical writing and document review.

• Ensure maintenance/engineering compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices.

• Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans.

• Partner with Production and Quality Team Leads on troubleshooting and scheduling.

• Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture.

• Actively participate in site & corporate initiatives.

• Leads and participates in investigations, change controls and develops/implements Corrective and Preventative Actions (CAPA's) for the maintenance department.

• Serve as a liaison between Quality Operations and engineering/maintenance departments to facilitate timely closure of investigations.

• Technical support for standard operating procedure improvements and updates.

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 more than 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.

• Experience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM/PDM optimization, and/or Failure Modes and Effects Analysis.

• Demonstrated experience in manufacturing / reliability engineering, plant engineering and/or project engineering.

• Teamwork spirit, good communication skills and training abilities.

• Excellent interpersonal effectiveness and communication skills (written and oral).

• Working knowledge of MS Office Applications.

• Strong knowledge and understanding of Current Good Manufacturing Practices.

BONUS POINTS IF YOU HAVE (Preferred Requirements)

• Certificates, Licenses or Registrations: Certified Maintenance and Reliability Professional (CMRP) (or equivalent) desired but not required.

• Experience with pharmaceutical manufacturing equipment and/or utility systems.

PHYSICAL/MENTAL REQUIREMENTS

• This is an on-site role at a penicillin manufacturing facility. Candidates must not be allergic to penicillin.

• Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and complex data analysis, problem solving.

• Ability to work in clean room conditions.

• Ability to write general correspondence and technical reports.

• Requires good written, oral communication and presentation skills.

• Requires good planning, organizing, time management and team participation skills.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Regular Work Schedule:

• Standard (M-F) daytime. Overtime work may be required. Work requires on-site presence. Occasionalnational/internationaltravel for equipment factory acceptance testing, training seminars, vendor meetings, work progress meetings, etc.

Non-Regular Work Schedule:

• At different times of the year, this position will work long hours for scheduled manufacturing shutdown periods and throughout the year may be required to work late with little notice as need arises when equipment is unexpectedly down.

• Demonstrate proficiency in cGMP, GMP, software development life cycle, environmental, health and safety procedures to assure compliance with regulatory, policies and/or established guidelines.

• Observe and notify any risk situation for the environment, health or safety. Assure that a