Medical Device Production Operator – Dover, NH (Overtime)

Adecco Portugal; Dover (NH); On-site; USD 19,000 - 25,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Voluntary benefits

EAP program

Commuter benefits

401K plan

Paid leave including sick leave

Holiday pay

Job summary

Adecco is hiring a Production Operator for a leading medical device manufacturer in Dover, NH. This temp-to-hire position offers incentives and potential overtime, with a Monday–Thursday schedule from 6:30 AM to 5:00 PM and pay around $18 per hour.

Responsibilities include assembling, inspecting, labeling, and packaging medical devices, setting up jobs, and maintaining accurate production documentation while following GMP and safety standards.

Qualifications

• Strong attention to detail and commitment to quality.
• Ability to perform repetitive tasks while maintaining accuracy.
• Willingness to work overtime as needed.
• Ability to follow written work instructions and safety procedures.

Responsibilities

• Assemble and package high-quality medical devices.
• Perform visual inspections to ensure products meet quality standards.
• Count, label, cap, fill, and package products for shipment.
• Set up production jobs and monitor equipment performance.
• Complete production and quality documentation accurately.
• Troubleshoot minor equipment or product issues.
• Follow GMP, safety, and PPE requirements in a clean manufacturing environment.
• Communicate quality or safety concerns to supervisors promptly.

Skills

Attention to detail

Quality oriented

Repetitive tasks

Overtime flexibility

Follow written instructions

Job description

Adecco is hiring a Production Operator for a leading medical device manufacturer in Dover, NH. This temp-to-hire position offers incentives and potential overtime, with a Monday–Thursday schedule from 6:30 AM to 5:00 PM and pay around $18 per hour.

Responsibilities include assembling, inspecting, labeling, and packaging medical devices, setting up jobs, and maintaining accurate production documentation while following GMP and safety standards.