Production Specialist

Insulet Corporation•Acton, MA

3d•$18 - $27•Onsite

About The Position

Insulet is seeking a detail-oriented, safety-conscious Production Specialist to support the reconfiguration of mobile devices into Personal Diabetes Managers (PDMs) and the assembly of Starter and Controller kits. The role includes hands-on assembly and testing, inventory management, and collaboration with Quality, Engineering, and Supply Chain teams. It supports manufacturing operations by producing finished goods in accordance with approved procedures and documentation for medical device production, with a focus on patient safety and product integrity. The Production Specialist also contributes to Continuous Improvement initiatives and Lean methodologies to improve operational workflows and performance in safety, quality, efficiency, and cost. Cross-training opportunities may be available. This position requires on-site work.

Requirements

High School Diploma or GED.
Ability to distinguish red, green, and blue colors on handheld devices.
Proficient in English and able to follow verbal and written instructions.
Strong organizational skills and attention to detail.
Comfortable working with light assemblies and basic mechanical tasks.
Able to lift and transfer up to 50 lbs.
Able to stand for extended periods and perform repetitive tasks.
Able to safely operate electric and manual pallet jacks.
Able to follow electronic training instructions and manual demonstrations.

Nice To Haves

Experience in regulated manufacturing environments.

Responsibilities

Safely reconfigure mobile devices into dedicated PDMs according to production schedules.
Operate test fixtures, including USB interfaces, touchscreens, keyboards, and pneumatic RF-sealed enclosures.
Unbox, assemble, label, and transact light components and finished goods.
Identify and report discrepancies in quality, safety, or process execution.
Collaborate with Quality, Engineering, and management to resolve issues.
Follow current SOPs and applicable regulatory standards, including FDA 21CFR, ISO 13485, and cGMP.
Maintain a clean, compliant work environment suitable for medical device production.
Perform data entry, cycle counts, and inventory reconciliation.
Organize components into kits according to instructions and inspect them for quality and accuracy.
Maintain accurate inventory records and support floor stocking levels.
Participate in Lean initiatives and cross-functional problem-solving.
Work independently and collaboratively in small teams to troubleshoot and implement corrective actions.
Support process efficiency and contribute ideas to streamline operations.