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Senior Process Technician/Tech ops 2

Pfizer
On-site
Andover, MA
Operations

Role Summary

Pfizer’s pharmaceutical manufacturing team enables breakthroughs to reach patients. You will contribute as a member of a manufacturing workforce that understands the critical impact of your role in delivering medicines to patients and physicians. You will help ensure timely access to medicines by maintaining quality and following established procedures in a dynamic production environment.

Responsibilities

  • Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.
  • Manage personal time and professional development, being accountable for results.
  • Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.
  • Identify and solve moderately routine problems.
  • Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.
  • Ensure work is reviewed for accuracy, quality, and adherence to standards.
  • Be responsible for the production of drug substances or active biological ingredients (ABI), assisting in various activities and functions within a manufacturing facility, and ensuring equipment functionality.
  • Support technical operations, maintain housekeeping standards, keep training status current, and assist in the implementation of new technology for process execution and analysis.

Qualifications

  • Required: High School Diploma or GED with 2+ years of relevant experience
  • Strong verbal and written communication skills
  • Proficiency in using standard manufacturing equipment and tools
  • Basic understanding of Good Manufacturing Practices (GMP)
  • Ability to follow detailed instructions and standard operating procedures
  • Strong problem-solving skills in a structured environment
  • Capability to work effectively in a team setting
  • Basic computer skills, including familiarity with data entry and reporting systems

Qualifications

  • Preferred: Experience in a pharmaceutical or biotechnology manufacturing environment
  • Knowledge of regulatory requirements and quality systems
  • Strong organizational skills and attention to detail
  • Ability to adapt to changing priorities and manage multiple tasks
  • Demonstrated ability to take initiative and drive continuous improvement
  • Strong analytical skills and the ability to interpret technical data

Additional Requirements

  • Physical/Mental Requirements: Include lifting (approx max of 50 lbs), sitting, standing, walking, bending, ability to perform mathematical calculations and complex data analysis.
  • Non-standard Work Schedule, Travel Or Environment Requirements: This is for a rotating second shift position (2pm to 2am).