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
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 with 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…