3rd shift Manufactuing Assembler

3rd shift Manufactuing Assembler Top Prospect Group LLC•2.7 Manchester, NH Job Details Temp-to-hire | Contract $20•$28 an hour 12 hours ago Qualifications Press operation Computer operation Maintaining an organized workspace Inventory management ISO standards Safety standards in production Mid-level Inspection reporting and documentation Manufacturing standard operating procedures Microscope proficiency Electrical experience Quality control documentation Joining process implementation Cleanroom Computer skills Welding Quality assurance within manufacturing Manufacturing Clean workspace maintenance Hand tools Leadership Plastics Manufacturing company experience Communication skills Implementing lean manufacturing processes Electrical soldering FDA regulations Under 1 year Mobile devices

Full Job Description Cleanroom Manufacturing Assemblers Location:

Manchester, NH Type:

6-

Month Temp-to-Hire Pay Rates Cleanroom Manufacturing Assemblers:

$20•23/hr

DOE Team Lead Manufacturing Assembler:

$27•28/hr DOE Openings Available 22 Cleanroom Manufacturing Assembler Openings 1 Team Lead Manufacturing Assembler Opening Schedules & Shifts 3rd Shift (High Priority)

Hours:

11:00 PM•7:00

AM Schedule:

Sunday•Thursday Paid lunch and paid breaks Position Overview We are seeking reliable, detail-oriented Cleanroom Manufacturing Assemblers to support cleanroom and durable goods production operations across multiple shifts. This role is ideal for self-sufficient individuals with hands-on assembly experience or candidates looking to enter the manufacturing field with training provided. Cleanroom Manufacturing Assemblers play a critical role in assembling medical devices while ensuring quality, compliance, and efficiency in a fast-paced, regulated manufacturing environment. This is a cleanroom production environment where employees will assemble medical devices while following strict quality, safety, and documentation procedures. Key Responsibilities Assemble plastic and metal components into medical devices per approved manufacturing procedures Perform manual and automated assembly, testing, and documentation of mechanical and electrical assemblies Follow detailed electronic work instructions using a tablet/computer system Operate hand tools (manual and electric), presses, assembly fixtures, calibrated instruments, microscopes, and test fixtures Follow Bills of Materials (BOMs), work orders, check sheets, flow charts, and assembly drawings Perform soldering, crimping, ultrasonic welding, bonding, gluing, and other assembly techniques Conduct kitting using scanners and inventory management software Complete startup and end-of-day equipment inspections and verifications Inspect assemblies throughout the manufacturing process and report quality or operational issues Maintain accurate documentation for quality checks, WIP, test results, and labor reporting Maintain a clean, organized, and safe work area while participating in safety and 5S initiatives Work closely with Engineers and Line Leads to troubleshoot issues and improve processes Ensure compliance with

ISO, QSR, FDA

regulations, GMP, and company manufacturing policies Training Provided Training on the first day will be provided in the following areas: Good Documentation Procedures (GDP) Quality System Management (QMS) Safety procedures Foreign Object & Debris (FOD) Electronic tablet-based work instructions Online role-specific manufacturing training Cleanroom protocols and gowning procedures Quality standards and inspection processes Qualifications Minimum 2 years of hands-on manufacturing experience preferred Experience with assembly, testing, and documentation of mechanical and/or electrical devices preferred Strong attention to detail and ability to follow written procedures Strong verbal, written, and interpersonal communication skills Ability to adapt to a fast-paced, regulated manufacturing environment Comfortable using computers, tablets, scanners, and basic manufacturing systems No prior manufacturing experience required for select openings — training provided Preferred Experience Medical device manufacturing Cleanroom environments Familiarity with

ISO, QSR, FDA

regulations Lean manufacturing, GMP, or regulated production environments Work Environment Fast-paced, regulated medical device manufacturing environment requiring strict adherence to procedures, documentation, quality standards, and safety protocols. About Us Founded in 2010, Top Prospect Group is a technical staffing firm focused on aligning skilled professionals with industry-leading clients. In 2023, we joined HW Staffing Solutions, expanding our reach across manufacturing, logistics, and technology sectors nationwide. Interested Candidates•Apply Today Please submit: A clean copy of your resume Desired hourly rate Availability and at least one professional reference #INDTPGSHELTON