Machine Operator

Creative Solutions Services, LLC; Marlborough (MA); On-site; USD 23,000 - 32,000; Full time

Benefits offered by this job

Medical Insurance

Vision Insurance

Dental Insurance

401k Retirement Fund

Job summary

Creative Solutions Services, LLC is seeking a Machine Operator in Marlborough, MA for a 5‑month contract. The role runs 1st shift Monday through Thursday, with potential overtime on Fridays. Pay rate is $20.00 per hour, onsite with no visa sponsorship offered.

The operator will run manufacturing equipment, follow SOPs, maintain logs, and support maintenance and material handling while ensuring quality and regulatory compliance in an FDA-regulated environment.

Qualifications

• Strong attention to detail and accuracy in documentation.
• Experience in packaging/manufacturing environments.
• Experience working in an FDA-regulated environment.

Responsibilities

• Operate manufacturing equipment per SOPs and work instructions.
• Maintain operational logs and report equipment issues.
• Assist in preventative maintenance and material handling.
• Keep the work area clean and adhere to SOPs and safety rules.
• Maintain records of work-in-process and inventories.

Skills

Detail oriented

Packaging background

FDA-regulated environment

Job description

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 4x10 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

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