Manufacturing Technician - Cleanroom in Manchester

Energy Jobline ZR; Manchester; On-site; GBP 30,000 - 40,000; Full time

Job summary

A global energy job platform in Manchester is seeking a Manufacturing Technician for a cleanroom environment. The ideal candidate will handle assembly, testing, and documentation of medical device components. Successful applicants will have at least 2 years of hands-on manufacturing experience and possess strong attention to detail and communication skills. This role offers a dynamic work environment with a focus on quality and continuous improvement.

Qualifications

• Experience with assembly, testing, and documentation of mechanical and electrical devices.
• Medical device manufacturing experience preferred.
• Working knowledge of medical device regulatory procedures and lean manufacturing.

Responsibilities

• Maintain Clean Room integrity using proper attire.
• Assemble components into medical devices according to procedures.
• Utilize documentation to assemble product and record results.

Skills

Assembly skills

Communication skills

Manual dexterity

Attention to detail

Education

Minimum of 2 years hands-on experience in a manufacturing environment

Tools

Small hand tools

Calibration instruments

Microscopes

Job description

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Manufacturing Technician - Cleanroom

• 1st, 2nd, & 3rd Shift
• Contract to Perm

Overview

Manufacturing Technician needs to be self‑sufficient in assembly, testing and documentation of mechanical and electrical assemblies.

Duties & Responsibilities

• Maintain Clean Room integrity by using proper attire and adherence to Clean Room environment practices and procedures as applicable.
• Assemble plastic and metal components into medical devices in accordance with approved manufacturing procedures.
• Utilize small hand tools (both manual and electric), manual presses, assembly fixtures, calibrated instruments, measurement equipment, microscopes, and test fixtures.
• Utilize documentation such as Bill of Materials, product flow charts, work orders, check sheets, visual aids, production reports and assembly drawings to assemble product and record results.
• May perform soldering, fabricating, crimping, mechanical assembly, sealing, ultra‑sonic welding, bonding and gluing with adhesives, Epoxy or RTV.
• Kitting assemblies using a parts list, scanner and inventory software as required.
• Participates in any routine start up or end of day equipment inspections or verifications.
• Inspects work throughout the assembly process and communicates any quality or operational issues to appropriate leader.
• Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management.
• Participate in continuous improvement activities as part of a cross‑functional team.
• Meet all quality, quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating procedures for specific products where training has been completed.
• Show constant attention to detail, and immediately inform supervisor of anything out of the ordinary, or anything which does not conform to the approved process sheets.
• Work with Engineers and line leads to resolve issues and correct procedures to ensure quality and efficiency.
• Maintain accurate records/documentation related to quality, work in progress, test results, labor (e.g. timecards), and special projects.
• Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations.

Qualifications

Qualifications – Minimum of 2 years hands‑on experience in a manufacturing environment

• Experience with assembly, testing and the documentation of mechanical and electrical devices
• Exceptional interpersonal, verbal, and written communication skills are required
• Willingness to undertake various tasks and adapt to unexpected situations within dynamic company environment
• Medical device manufacturing experience
• Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing processes
• Good hand eye coordination and manual dexterity required
• Small parts assembly and able to work under a microscope
• Utilize tweezers, torque drivers, magnifiers and microscopes