FDA-Regulated Medical Device Operator – 2nd Shift (Contract)

Global Technical Talent, Inc.; Marlborough (MA); On-site; USD 25,000 - 36,000; Full time

Benefits offered by this job

Medical, Vision, and Dental Insurance

401k Retirement Fund

Job summary

Global Technical Talent, Inc. is seeking a Machine Operator II for onsite work in Marlborough, MA. The role operates manufacturing equipment per SOPs under the supervision of the Manufacturing Supervisor, with a 2nd shift schedule (Mon-Thu 3:30 PM–2:00 AM) and potential overtime on Fridays.

It is a 3-month contract in a FDA-regulated manufacturing environment. Responsibilities include monitoring equipment, assisting with PM, ensuring product quality, maintaining logs and records, and adhering to

Qualifications

• Strong attention to detail.
• Packaging/manufacturing background.
• Experience working in an FDA-regulated environment.

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

Skills

Strong attention to detail

Packaging/manufacturing background

FDA-regulated environment

Job description

Global Technical Talent, Inc. is seeking a Machine Operator II for onsite work in Marlborough, MA. The role operates manufacturing equipment per SOPs under the supervision of the Manufacturing Supervisor, with a 2nd shift schedule (Mon-Thu 3:30 PM–2:00 AM) and potential overtime on Fridays.

It is a 3-month contract in a FDA-regulated manufacturing environment. Responsibilities include monitoring equipment, assisting with PM, ensuring product quality, maintaining logs and records, and adhering to