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Pharmaceutical Manufacturing Technician

Eurofins BioPharma Product Testing · Groton, CT

Posted November 3, 2026

Entry levelProductionGMPCleanroomOn site
Pay not postedApply

Quick facts

Experience
1 to 3 years
Education
High school diploma or Bachelor's
Job type
Full-time
Schedule
Some weekend work
Skills mentioned
GMP, Change control, Batch record review, SOP writing, Cleanroom, Procurement

Pulled from the ad below. The full ad has the details.

Job Description

This role is a great fit for candidates with strong mechanical aptitude who are looking to translate their hands-on technical skills into a rewarding career in pharmaceutical manufacturing. You'll have opportunities to operate, troubleshoot, and support complex manufacturing equipment while contributing to the production of products that make a meaningful impact on patients' lives.

  • Execute documentation associated with manufacturing operations: Paper and Electronic Batch Records, Log Books, Protocols, Change control, QTS, etc.
  • Utilize SOPs and Operating Instructions to manufacture drug product in a controlled clean room environment.
  • Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate and patient ready products
  • Set up, operation, break down, and cleaning of complex manufacturing equipment, manage and check documentation generated.
  • Complete activities associated with cGMP operations in a clean room manufacturing space
  • Generate, manage and report operational performance associated data
  • Identify, own and lead continuous improvement based projects

Qualifications

  • High school diploma, Associate's, or Bachelor degree in the sciences
  • Must hold a valid driver’s license
  • 1-3 years of Pharmaceutical manufacturing experience; may be substituted with experience in a regulated environment such as GMP, ISO, etc.
  • Experience with quality systems
  • Experience completing complex manufacturing operational documents
  • Experience utilizing AI to enhance manufacturing operations
  • Experience with utilizing Operating Instructions to perform manufacturing tasks
  • Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required.
  • Must be able to wear appropriate PPE (daily uniform, gloves, safety glasses, respirators, and full protective suits)
  • Strong computer, scientific, basic math, and organizational skills
  • Ability to communicate effectively within a multi-functional manufacturing team

Additional Information

  • Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed
  • May be requested to work on weekends, overtime, and holidays based on business needs.
  • Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
  • Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
  • LinkedIn: #LI-EB1
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Source: Eurofins BioPharma Product Testing's career site. PharmoniQ shows this job as posted and links to the original. Check the employer's page for the latest details.