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Pilot Plant Operator – GMP Manufacturing | Ridgefield, CT

Job in Ridgefield, Fairfield County, Connecticut, 06877, USA
Listing for: Sigma, Inc.
Full Time position
Listed on 2026-08-18
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA
Job Description & How to Apply Below

Pilot Plant Operator – GMP Manufacturing | Ridgefield, CT

Sigma Systems is seeking a Pilot Plant Operator to support pilot plant campaigns in a GMP manufacturing environment in Ridgefield, CT. The ideal candidate will have hands-on experience with bulk manufacturing, GMP procedures, manufacturing equipment, batch records, calculations, and process troubleshooting.

This position is well suited for candidates with experience as a Pilot Plant Operator, Manufacturing Technician, Process Technician, Production Technician, or Pharmaceutical Manufacturing Technician who are comfortable working in a regulated environment and following strict safety and quality procedures.

Key Responsibilities
  • Follow the direction of the Lead Client Technician during pilot plant manufacturing campaigns.
  • Work closely with plant technicians and campaign managers to identify and resolve process and equipment-related challenges.
  • Assist the BI Lead Technician with communicating batch status to chemists, Ch.D. Analytical, MAS, and other relevant teams.
  • Complete all required training within established deadlines.
  • Participate in daily team meetings, including 9:00 AM and 2:00 PM meetings.
  • Develop proficiency in pilot plant equipment operation, batch record entries, and manufacturing calculations.
  • Attend PSOR meetings, actively participate, and provide relevant input.
  • Follow all established GMP procedures, SOPs, safety requirements, and PPE guidelines.
  • Promptly report incidents, including spills, exposures, cuts, abrasions, or other safety events, to management.
  • Perform all manufacturing activities with safety as the highest priority.
  • Maintain accurate documentation and follow established manufacturing processes and procedures.
  • Assist with troubleshooting equipment and process issues as needed.
Required Qualifications
  • High school diploma/GED required;
    Associate degree preferred.
  • Previous experience working with GMP procedures.
  • Experience in bulk manufacturing, pharmaceutical manufacturing, chemical manufacturing, or a similar regulated production environment.
  • Technical knowledge of manufacturing systems, methods, and procedures.
  • Hands-on experience operating manufacturing or processing equipment.
  • Strong equipment and process troubleshooting skills.
  • Ability to accurately complete batch records, calculations, and production documentation.
  • Strong attention to detail and ability to follow written procedures.
  • Ability to work effectively as part of a cross-functional manufacturing team.
  • Commitment to maintaining a strong safety-first mindset.
Preferred Job Titles

Candidates with experience as a:

  • Pilot Plant Operator
  • Pilot Plant Technician
  • Manufacturing Technician
  • Process Technician
  • Production Technician
  • Pharmaceutical Manufacturing Technician
  • Biopharmaceutical Manufacturing Technician
  • Chemical Operator
  • Manufacturing Associate
  • Process Operator
  • Production Operator
  • GMP Manufacturing Technician
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