MAP Mod 1- Operations Technician (Prep, Formulation & Tank Assembly)

Pfizer • Kalamazoo, MI

1d • Onsite

About The Position

The MAP Mod 1 Operations Technician supports production of injectable drug products in the Modular Aseptic Processing (MAP) Mod 1 Prep, Manufacturing, and Tank Assembly unit. Technicians may specialize in prep, manufacturing, or tank assembly, but must cross-train and perform work across other processing steps in the unit. Work must comply with manufacturing procedures and applicable regulatory requirements, including GMP and OSHA standards. The selected candidate is expected to transition into the MAP role in January 2027 to support succession planning and coverage in the candidate’s current department.

The role performs and supports equipment setup and changeovers, production unit operations, facility and equipment cleaning, material handling, process monitoring, troubleshooting, and quality inspections. It also includes working with PLC and SCADA systems, collaborating with maintenance and engineering, supporting projects and continuous improvement, maintaining training and certifications, and completing GMP documentation. As a mid-level role, the technician is expected to meet all Operations Technician Assistant requirements and independently perform routine processes, handle advanced processes with limited assistance, support safety and quality activities, and provide subject-matter expertise when needed.

The second-shift MAP operations team will begin on an 8-hour day schedule (7:00 a.m.–3:30 p.m.) in January 2027 for training and project deliverables, then is expected to transition to second shift around July 2027 (3:00 p.m.–11:30 p.m.) to support departmental PPQ activities. Weekends, holidays, and overtime may be required. The position is onsite in Kalamazoo, Michigan. The hourly salary range is $25.66–$42.76, with eligibility for overtime, weekend, holiday, and other pay premiums depending on schedule and company policy. Relocation assistance may be available based on business needs and eligibility. Candidates must have permanent U.S. work authorization; work visa sponsorship is unavailable.

Requirements

• High school diploma or GED and 24 months of experience as an Operations Technician Assistant, or at least 48 months of relevant GMP experience in a classified environment (such as freeze dry, manufacturing, or prep).
• Ability to perform the role’s physical demands, including lifting or lowering up to 55 pounds; working at elevations above 6 feet; and reaching, standing, walking, stooping, and crawling.
• Ability to wear required safety PPE, including a hard hat, body harness, and face shield.
• Ability to work in Grade D and Grade C environments with appropriate gowning.
• Permanent work authorization in the United States; work visa sponsorship is not available.

Nice To Haves

• Mechanical experience or aptitude.
• Experience handling biologic substances, APIs, or drug products.

Responsibilities

• Set up and change over equipment according to approved procedures.
• Perform production unit operations using a variety of equipment.
• Wash, sanitize, and clean facilities and equipment.
• Handle, charge, and package materials.
• Monitor process parameters and batch-end reports for quality or equipment concerns.
• Use computer skills to operate and interact with complex PLC and SCADA systems.
• Collaborate with maintenance and engineers to troubleshoot equipment and perform total productive maintenance (TPM) tasks.
• Support the development and execution of capital projects, corrective actions, and continuous improvement ideas.
• Share best practices, demonstrate a growth mindset, and use downtime effectively.
• Work safely and in compliance with applicable SOPs and standards, including completing GMP documentation.
• Achieve and maintain required certifications for working in graded spaces.
• Complete and maintain required training on time.
• Take ownership and accountability for the production schedule and product quality.
• Perform in-process quality inspections.
• Develop and contribute to IMEx activities.
• Perform routine lockout points and initiate and complete routine Safe Work Permits.
• Conduct unit safety facility inspections and suggest or implement safety improvements.
• Perform basic daily and non-daily processes independently and advanced processes with minimal assistance.
• Complete GMP records with minimal errors and maintain aseptic behavior and certifications.
• Keep training current and work areas audit-ready according to GMP and 5S requirements.
• Respond to alarms and notify appropriate personnel; perform advanced alarm response as applicable.
• Perform equipment functional testing and scheduled operator care activities.
• Complete SAP and EMS entries when required.
• Review batch records within target time and contribute knowledge of production planning and scheduling.
• Assist with investigations and document updates, and provide subject-matter guidance when needed.
• Perform other duties as assigned by the supervisor.

Benefits

• 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.
• Medical, prescription drug, dental, and vision coverage.
• Potential relocation assistance based on business needs and eligibility.
• Eligibility for overtime, weekend, holiday, and other pay premiums depending on schedule and company policies.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED