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
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