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FDA-Grade Manufacturing Operator - 1st Shift; Onsite

Job in Marlborough, Middlesex County, Massachusetts, 01752, USA
Listing for: Global-Technical-Talent-1
Full Time position
Listed on 2026-10-13
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Production QC/QA, Production Associate / Production Line, Machine Operator
Salary/Wage Range or Industry Benchmark: 17 - 23 USD Hourly USD 17.00 23.00 HOUR
Job Description & How to Apply Below

Machine Operator

Location: Marlborough, MA

Onsite Flexibility: Onsite

Contract Details
  • Position Type: Contract
  • Contract Duration: 5 months
  • Pay Rate: $20.00 / Hour (USD)
  • Shift / Schedule: 1st Shift — Monday through Thursday, 5:15 AM to 3:45 PM; potential overtime on Fridays
  • Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Job Summary

Under the direction of the Manufacturing Supervisor, the Machine Operator will operate manufacturing equipment according to established specifications, standard operating procedures, and work instructions. An operator must demonstrate steady progress in learning all equipment and jobs in the assigned manufacturing area. He or she must also exhibit the ability to follow instructions of the supervisor while observing the quality of raw and finished goods before, during, and after production.

Key

Responsibilities
  • Monitor functions of equipment and operate per documented procedures including maintaining operational logbooks
  • Provide technicians with symptoms of equipment failures, when required
  • Assist in Preventative Maintenance (PM) following procedures
  • Support material handling as necessary
  • Maintain segregation of materials and lot and/or receiving numbers
  • Maintain area in a clean and orderly condition
  • Adhere to and demonstrate compliance to all company and department standard operating procedures including but not limited to: GMP, device history record, hazard communication, and safety rules
  • Utilize written procedures and training to accomplish tasks noted above
  • Accept full accountability for product quality
  • Report to supervisor or management unsolved problems encountered during the workday
  • Maintain complete and accurate records of work-in-process, component inventories, and relative documentation
Required Skills
  • Strong attention to detail
  • Packaging/manufacturing background
  • Experience working in an FDA-regulated environment
Preferred Skills
  • Team-oriented mindset
  • Positive attitude
  • Ability to adapt and pivot to changing priorities
Work Environment / Physical Requirements
  • Facility operates on a 4×10 schedule (Monday through Thursday)
  • Candidates should be comfortable working in a regulated manufacturing environment
  • PPE required: Gloves, hair net, and safety glasses as needed
Benefits
  • Medical, Vision, and Dental Insurance Plans
  • 401k Retirement Fund
Important Notes
  • Onsite interview required
About the Client

This client is an innovative medical technology firm focused on women's health, developing solutions that serve patients and clinicians across this specialized area of care. The organization employs professionals in manufacturing, quality assurance, production operations, and engineering roles who support the development and production of FDA-regulated medical devices.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-13264

Industry: Manufacturing & Operations

#gttmf

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