Cleanroom Technician

Aerotek; Guilford (CT); On-site; USD 39,000 - 45,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Short/long-term disability

Life insurance

Job summary

Aerotek is seeking a Cleanroom Technician (Consumables Assembly Technician) to join a regulated manufacturing team in Guilford, CT. The role focuses on assembling, inspecting, and packaging high-precision diagnostic consumables for medical devices in a controlled cleanroom environment.

Responsibilities include repetitive bench assembly, microscopic inspection, labeling, and adherence to SOPs, GMP, and ISO standards.

Qualifications

• 1 year or more of manufacturing, assembly, or production experience.
• Ability to read and follow detailed SOPs and work instructions.
• Experience with small parts and high-volume assembly environments.
• Comfort in a cleanroom or regulated manufacturing setting.
• Strong attention to detail and quality standards.

Responsibilities

• Assemble diagnostic consumables per written work instructions.
• Perform repetitive bench assembly and light mechanical tasks.
• Inspect components under magnification for defects and accuracy.
• Maintain GMP/ISO documentation and traceability.
• Package finished items with correct labeling and packaging.
• Follow gowning and cleanroom protocols.
• Operate basic production equipment safely.
• Record production data and report issues to supervisors.

Skills

Manufacturing experience

Detail oriented

Cleanroom environment

Read SOPs

Microscope inspection

Basic computer skills

High-volume assembly

Documentation

Tools

Microscope

Fixtures

Sealers

Benchtop tools

Job description

Job Title: Cleanroom Technician (Consumables Assembly Technician) Job Description

The Cleanroom Technician is responsible for assembling, inspecting, and packaging high-precision diagnostic consumables used in advanced testing platforms. Working in a clean, controlled manufacturing environment, this role directly supports the production of medical device components and plays a critical part in ensuring product quality, reliability, and compliance with regulated manufacturing standards.

Responsibilities

• Assemble small plastic and component-based diagnostic consumables in accordance with detailed written work instructions.
• Perform repetitive bench assembly tasks, including fitting, sealing, and light mechanical assembly operations.
• Inspect finished components under magnification or microscope for defects, quality issues, and dimensional accuracy.
• Follow GMP and ISO manufacturing practices and maintain accurate, complete production documentation.
• Package finished consumables for distribution, ensuring correct labeling and traceability.
• Maintain a cleanroom or controlled work environment by following proper gowning procedures and cleanliness protocols.
• Operate basic production equipment such as fixtures, sealers, and light automated tools safely and effectively.
• Record production data in designated systems and promptly report issues or nonconformances to supervisors or engineering staff.
• Support continuous improvement initiatives to enhance production efficiency, product quality, and workflow.
• Collaborate with team members to meet production targets while maintaining high quality standards.

Essential Skills

• At least 1 year of experience in manufacturing, assembly, or production, preferably in a regulated environment.
• Demonstrated ability to work with small parts or in high-volume assembly settings.
• Ability to read, understand, and follow detailed work instructions and standard operating procedures (SOPs).
• Strong attention to detail with a high level of quality awareness in all tasks.
• Comfort working in a cleanroom or other regulated manufacturing environment.
• Basic computer skills for data entry and documentation, including recording production information.
• Ability to stand or sit for extended periods and perform repetitive tasks with consistent accuracy.
• Capability to use microscopes or magnification tools for inspection of small components.
• Familiarity with cleanroom practices, assembly processes, and basic production equipment operation.

Additional Skills & Qualifications

• Experience in medical device, laboratory consumables, or diagnostics assembly environments.
• Background working under GMP and ISO quality systems in a cleanroom or controlled environment.
• Hands-on experience with plastic component assembly, including light welding or sealing processes.
• Previous exposure to continuous improvement or lean manufacturing initiatives.
• Comfort with documenting work in electronic or paper-based systems and maintaining traceable records.

Why Work Here?

You will join a highly regulated, quality-focused production environment where your work directly supports critical diagnostic technologies. The organization promotes a culture of precision, safety, and continuous improvement, giving you opportunities to develop specialized cleanroom and medical device assembly skills. You will work alongside a collaborative team, gain experience with industry-standard GMP and ISO practices, and build a strong foundation for long-term growth in advanced manufacturing and life sciences.

Work Environment

This role is based in a cleanroom or controlled manufacturing environment dedicated to producing medical device consumables. You will follow strict gowning procedures and cleanliness protocols, including wearing appropriate cleanroom attire and personal protective equipment. Work is primarily performed at a bench, involving repetitive assembly tasks with small plastic components, microscopes, fixtures, sealers, and light automated tools. The position requires the ability to stand or sit for extended periods while maintaining focus and precision. The facility operates under GMP and ISO standards, with an emphasis on accurate documentation, labeling, and adherence to standard operating procedures.

Job Type & Location

This is a Contract to Hire position based out of Guilford, CT.

Pay and Benefits

The pay range for this position is $28.00 - $33.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

Medical, dental & visionCritical Illness, Accident, and Hospital401(k) Retirement Plan Pre-tax and Roth post-tax contributions availableLife Insurance (Voluntary Life & AD&D for the employee and dependents)Short and long-term disabilityHealth Spending Account (HSA)Transportation benefitsEmployee Assistance ProgramTime Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Nov 6, 2026.

Workplace Type

This is a fully onsite position in Guilford,CT.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.