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Westaff is hiring Assemblers in Quincy, MA to join a production team focused on assembling medical devices and kits. You will follow established processes, operate equipment, inspect in-process items, and help meet daily production goals while communicating clearly with teammates.
Candidates should be able to lift up to 35 lbs, stand, bend, and reach as part of daily tasks; prior GMP training may be provided. This is a full-time position with weekly pay and comprehensive benefits.
Westaff is hiring Assemblers in Quincy, MA
Benefits to our Westaff Associates:
Schedule:
Monday - Friday
11am - 7:30am
Under supervisory direction, functions as a member of a production team whose goal is to assemble required components, operate equipment, inspect in-process medical devices / kits, and maintain the quality and integrity of the products at all times. Primary focus is to build product by following processes to meet production goals. Must be able to communicate clearly with co-workers both in speech and in writing.
Builds product by following all processes and complete other assigned work while meeting production goals and metrics.
Responsible for quality and 100% adherence to manufacturing process requirements,
Proactively identifies and communicates quality issues and concerns.
Maintains accurate records including training and shop floor paperwork(DHR).
Willing to participate in shared responsibilities and tasks.
Champions the "flex strategy", rotates as necessary and works well with group members, both within the team and cross-functionally.
Demonstrates proficiency in all communication, including written and spoken.
Ability to use computers at a basic level.
Lifting up to 35lbs occasionally, Standing, Bending, Reaching required
Understand and apply Core 5 Metrics in relation to the daily tasks.
Must have working knowledge of all processes in assigned area.Understands and ensures compliance of site specific and regulatory policies and procedures.
Responsible for attending and passing all required core site specific training (i.e. QS Basics, GDP, cGMP).
Participate in team meetings.
Participate during site internal audits and third party inspections.
Other tasks as directed by the Production Supervisor, Production Manager,
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