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Process Development Technician

Process Development Technician with Pfizer!
Andover, MA
1 Year-Perm
Max PR: $22.76
Shift- 06:00 AM - 06:00 PM

Job Summary
The Process Technician supports the execution of Commercial, Clinical, and/or Development production according to Standard Operating Procedures and Production Schedule. The Process Technician will work on interdisciplinary teams, to implement process improvements, participate in process troubleshooting.
Job Responsibilities
  • Supports manufacturing operations on the production floor for buffer/media make-up tanks, glass washers, autoclaves.
  • Supports the execution of SOPs for unit operations including but not limited to, CIPs, SIPs, Sanitization, etc.
  • Supports the execution and issue resolution associated with process equipment commissioning, qualification and validation.
  • Assists troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
  • Strives for Right first time execution, the timely review of daily documentation and supports data entry; Monitor, Identify and/or Communicate process and compliance trends in real time.
  • Implements any audit observation improvements.
  • View Role for controlled documentation; SOPs, Manufacturing Batch/Formulation Records, Forms, etc.
  • Assists the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
  • Responsible for remaining current on training programs in support of manufacturing processes.
  • Supports Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
  • Interacts with manufacturing asset in support of manufacturing campaigns.
  • Assists in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
  • Escalates the need for work requests when issues arise with manufacturing equipment.
  • Adequate in enterprise systems to support manufacturing operations including but not limited to, SAP, LIMS, AMPS, PDOCS and/or QTS.
  • Assists production sustainability through the performance of inventory accuracy, reconciliation and/or task prioritization to maintain metric adherence.
Education & Qualifications 
  • High School diploma or greater required.
  • 0-2 years of relevant experience
  • Experience in a GMP manufacturing environment is desired.
  • Ability to interpret and prioritize workflow to maintain the production schedule.
  • Effective verbal and written communication skills.
  • Position Comments visible to MSP and Supplier:              

PHYSICAL/MENTAL REQUIREMENTS
  • Requires the moving of heavy equipment and the ability to lift ~50 pounds. The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
  • The incumbent is required to attain detail knowledge of the operational equipment.
  • The incumbent will be required to solve problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
  • The incumbent must be able to express ideas into SOPs, MFRs and be able to use a multitude of programs including Excel, Word, Power Point, etc.


My aim is to connect with others who are (or have not yet realized they are!) open to opportunities in the biopharma industry. As a Randstad employee, I guide others into placements with only reputable, prestigious entities. That's because I wish to invest in the individual, always. Let me show you opportunities not readily accessible to the average job seeker. If you'd like to know more, or have someone in mind that would be a great fit, don't hesitate to reach out! samantha.nelson@randstadusa.com