Job Description

Job Title: 2nd Shift Cleanroom Assembler

Job Description

This role supports the production of sterile, single-use surgical items, instruments, and kits used in hospitals and by healthcare product manufacturers. As a 2nd Shift Cleanroom Assembler, you work on a cleanroom production line to assemble, inspect, package, and prepare medical devices for sterilization, following strict quality and regulatory standards. You play a key part in ensuring that every product leaving the facility meets rigorous safety and quality requirements.

Responsibilities

• Count, cut, measure, fold, and otherwise modify raw materials according to instructions in the Device Master Record.
• Complete required inspections and documentation of quantities, control numbers, and other information in accordance with QS and GMP policies.
• Perform on-line inspection of each device as it is produced and promptly report any issues to the Production Supervisor for disposition.
• Seal products in their final packaging configuration, carefully following proper procedures and machine settings for the sealing equipment.
• Prepare packaged work in progress for sterilization, including completing all necessary documentation and assigning control numbers per QS and GMP requirements.
• Maintain proper inventory control procedures, including product staging, segregation, and rotation, to ensure accurate and efficient material flow.
• Perform and document scheduled facility cleaning tasks in accordance with QS requirements.
• Understand and consistently adhere to proper cleanroom etiquette and contamination-control practices.
• Operate basic production equipment safely and efficiently as required for assembly and packaging tasks.
• Communicate and collaborate effectively with production, purchasing, quality, and leadership to accomplish assigned goals and objectives.
• Support and help meet the objectives of the quality management system and recommend improvements to processes when needed.
• Identify and suggest improvements and modifications to departmental procedures to enhance efficiency and quality.
• Provide positive, enthusiastic support to team members and contribute to a constructive and high-morale work environment.
• Work as a cooperative member of the team to achieve company goals and production targets.
• Perform other duties as assigned by the Production Supervisor to support overall production and quality objectives.

Essential Skills

• Ability to follow detailed written instructions such as Device Master Records and work orders.
• Strong attention to detail with a focus on accuracy in counting, measuring, and documenting materials and products.
• Motivation to work in a fast-paced, production-oriented environment.
• Ability to lift up to 25 lbs as part of routine material handling and assembly tasks.
• Ability to operate basic production and packaging equipment safely and correctly.
• Good verbal and written communication skills, including basic English skills to read work orders and communicate with auditors and supervisors.
• Comfort working in a cleanroom environment and willingness to strictly follow cleanroom etiquette and gowning procedures.
• Ability to work effectively as part of a team on a production line.
• Capability to perform repetitive tasks while maintaining quality and consistency.

Additional Skills & Qualifications

• Preferred 1 year of experience in a cleanroom, medical device assembly, or warehouse environment.
• Experience with medical device production, medical assembly, or catheter-related assembly work.
• Familiarity with general production, packing, and assembly processes.
• Experience using hand tools and power tools in a production or assembly setting.
• Ability to work with microscopes or other inspection tools for detailed visual inspection.
• Ability to read and interpret simple blueprints or production diagrams.
• Demonstrated team leadership capabilities and the ability to contribute to a positive team culture.
• Ability to identify opportunities for process improvements within the department.
• Comfort working in an environment where many tenured employees primarily speak Spanish, while using basic English for documentation and communication with supervisors and auditors.

Why Work Here?

This opportunity offers a clear contract-to-hire path, typically around four months, providing stability and the potential for long-term growth. You contribute directly to products that support patient care and healthcare professionals, adding meaningful purpose to your daily work. The organization promotes teamwork, open communication, and continuous improvement, encouraging employees to share ideas and help refine procedures. Comprehensive benefits, including medical, dental, and vision coverage, support your overall well-being. The small-team environment in a new department allows you to build strong working relationships, have your contributions recognized, and grow your skills in a specialized cleanroom and medical device manufacturing setting.

Work Environment

This is a 2nd shift position, typically scheduled from 2:00 p.m. to 10:30 p.m., Monday through Friday, with potential overtime on weekdays or Saturdays based on production needs. You work in a cleanroom environment within a small team of about four employees in a new department. The role requires strict adherence to cleanroom gowning and hygiene standards, including wearing scrubs, a white coat, gloves, a hair net, and other protective gear, and refraining from wearing makeup, jewelry, artificial eyelashes, or artificial nails while in the cleanroom. You must fully gown and degown when entering or leaving the cleanroom, and you coordinate with the lead before taking water or restroom breaks to accommodate these procedures. The environment emphasizes cleanliness, organization, and compliance with quality system (QS) and Good Manufacturing Practice (GMP) requirements. Work involves using basic production equipment, hand tools, power tools, and inspection tools such as microscopes, as well as handling medical device components and packaging materials. Many tenured employees primarily communicate in Spanish, so you should be comfortable in a bilingual setting while using basic English to read work orders and interact with auditors and supervisors.

This is a Contract to Hire position based out of Placentia, CA.

The pay range for this position is $17.50 - $17.50/hr.

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 & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Placentia,CA.

This position is anticipated to close on Jun 26, 2026.

About Aerotek

Aerotek® Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions. To learn more, visit: Aerotek.com | 1-888-AEROTEK.

Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

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.

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