MAP - Mod 1 Operations Technician (Prep, Formulation & Tank Assembly)
Use Your Power for Purpose
The MAP Mod1Technician role is responsible for supporting the production of injectable drug products in the Modular Aseptic Processing (MAP) Mod 1 sterile Prep, Dispense, Manufacturing and Tank Assembly unit. Although Techs may specialize in one specific area (i.e. prep, mfg, or tank assembly, they will be required to cross train and perform work in other processing steps run in that area).
The successful candidate will transition into their new MAP role in January 2027. This timeline is intended to support effective succession planning and ensure adequate coverage within the candidate's current department during the transition period.
What You Will Achieve
In this role, you will:
- Setting up and changing over the equipment per approved procedures
- Performing unit operations in the production area with a variety of different equipment types.
- Washing, sanitizing and cleaning facilities and equipment
- Handling, Charging and packaging materials
- Monitoring process parameters and batch end reports for quality or equipment concerns
- Utilizing computer skills to interact with multiple complex PLC and SCADA systems
- Collaborating with maintenance and engineers to troubleshoot equipment and perform TPM tasks
- Supporting development and execution of capital projects, corrective actions, and continuous improvement ideas
- Demonstrating growth mindset to share best practices & utilize downtime effectively
- Working safely and compliantly following all applicable SOPs and standards
- Achieving and maintaining appropriate certification to work within graded spaces
- Completing and maintaining all required training on time
- Demonstrating ownership and accountability of the production schedule and product quality
- Executing in-process quality inspections
- Developing and contributing to IMEx activities.
- Other duties as assigned by the supervisor
EHS
- Performs routine Lock Out Points
- Initiates & completes routine Safe Work Permits
- Unit safety facility inspections
- Suggests or Implements safety improvements for unit (Ongoing)
GMP
- Performs basic daily & non-daily processes without assistance
- Performs advanced processes with minimal assistance
- Exhibits good aseptic behavior (Certifications maintained)
- Maintains training requirements (up to date per unit goals)
- Maintains Working Areas Audit Ready (GMP/5S)
- Alarm response & notification awareness
DRUG PRODUCT OPERATIONS
- Appropriately display ability to troubleshoot and adjust production equipment
- Understanding of advanced processes
- Equipment Functional Testing
- Advanced Alarm response
- Complete Scheduled Operator Care activities
- Complete SAP / EMS entries when required
- Complete batch record review in target time
- Production planning / Scheduling knowledge
- Assist with investigations and document updates
- Provide SME guidance when needed
Here Is What You Need (Minimum Requirements)
- High School Diploma or GED.
- 4+ years of experience .
- Proficiency in Good Manufacturing Practices (GMP) and related systems.
- Ability to troubleshoot and resolve technical issues.
- Strong organizational skills and attention to detail.
- Capability to work independently and as part of a team.
- Ability to adapt to changing priorities and manage multiple tasks.
- Ability to communicate effectively across departments and follow written and verbal instructions.
Bonus Points If You Have (Preferred Requirements)
- Experience in pharmaceutical manufacturing or a related field.
- Knowledge of regulatory requirements and quality standards (cGMP).
- Experience with Lean Manufacturing principles
- Familiarity with Pfizer's Learning Solution and Quality Tracking System.
- Ability to train and mentor less-experienced colleagues.
- Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity.
PHYSICAL/MENTAL REQUIREMENTS
Physical Demands:
- Physical demands may include standing or walking for extended periods, lifting up to approximately 50–55 pounds, bending, kneeling, stooping, reaching, or working at elevated heights
- Able to wear safety PPE (Hard hat, body harness, face shield).
- Able to work under grade D and C environments with appropriate gowning requirements
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- Our MAP operations will start on a 8 hour shift schedule. We anticipate to run our operations on 1st with some occasional overtime.
- Weekends, holidays and overtime may be required to meet business or customer needs
Other Job Details:
- Last day to Apply: October 12, 2026
- Work Location Assignment: On Premise
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 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.
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 .
ManufacturingSource: the employer's careers page. Last checked 2026-10-06. Posted 2026-10-06.
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