Cleanroom Production Operator 2nd Shift

Aerotek

Carlsbad (CA)

On-site

USD 25,000 - 28,000

Full time

34 hours ago
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Job summary

Aerotek is seeking a Cleanroom Production Operator on the 2nd shift in Carlsbad, CA. The role involves assembling cartridges and reagent kit components in a regulated cleanroom, following cGMP and ISO standards, and operating line equipment.

You will adhere to SOPs, maintain documentation accuracy, and contribute to continuous improvement while ensuring safety. Ideal candidates have a High School Diploma and at least 6 months of manufacturing experience, with the ability to work independently or

Qualifications

  • High School Diploma required.
  • At least 6 months of manufacturing experience.
  • Experience in production, fast food, retail, or other high-volume environments.
  • Ability to follow SOPs and maintain cGMP/ISO standards.
  • Experience in cleanroom or medical device manufacturing environments.
  • Ability to safely operate manufacturing line equipment.
  • Strong attention to detail in reviewing records and orders.
  • Ability to work independently and on a team.
  • Commitment to a safe, compliant production environment.
  • Good organizational skills for floor area and supplies management.

Responsibilities

  • Follow cGMP and ISO guidelines in manufacturing activities.
  • Assemble cartridges and reagent kit components per procedures and quality standards.
  • Follow SOPs for all tasks and processes.
  • Organize and maintain the production floor, tools, materials, and supplies.
  • Work independently and as part of an assembly line team.
  • Maintain safety when handling chemicals and operating equipment.
  • Operate manufacturing line equipment in a cleanroom environment.
  • Adhere to schedules and complete work orders timely.
  • Review device manufacturing records and work orders for accuracy; submit documentation for release.
  • Serve as a role model for compliant manufacturing practices.
  • Troubleshoot line issues and suggest process improvements.
  • Assist with special projects and continuous improvement initiatives.
  • Perform additional duties to support production and team objectives.

Skills

High School Diploma
Manufacturing experience (6+ months)
Attention to detail
SOP adherence
cGMP awareness
ISO standards familiarity
Independent worker
Team collaboration
Safety consciousness
Documentation accuracy

Education

High School Diploma

Job description

Job Title: Cleanroom Production Operator 2nd Shift Job Description

This role focuses on assembling cartridges and reagent kit components in a cleanroom environment while following cGMP and ISO standards. You will operate manufacturing line equipment, follow detailed SOPs, and complete manufacturing work orders accurately and on time. The position requires strong attention to detail, the ability to work both independently and as part of an assembly line team, and a commitment to maintaining a safe and compliant production environment.

Responsibilities
  • Follow current Good Manufacturing Practices (cGMP) and ISO standards or guidelines as they apply to manufacturing activities.

  • Assemble cartridges and reagent kit components according to established procedures and quality standards.

  • Strictly follow manufacturing Standard Operating Procedures (SOPs) for all tasks and processes.

  • Organize and maintain the production floor area, ensuring that tools, materials, and supplies are properly stocked and arranged.

  • Work independently on assigned tasks and collaborate effectively as part of an assembly line team.

  • Maintain a safe work environment by handling chemicals and operating equipment in accordance with safety protocols.

  • Operate all manufacturing line equipment required for production in the cleanroom environment.

  • Adhere to the manufacturing schedule and complete manufacturing work orders in a timely and efficient manner.

  • Review completed device manufacturing records and work orders for accuracy, identify errors, correct them, and submit finished documentation for quality release.

  • Serve as a role model for cGMP-compliant manufacturing practices and support a culture of quality and compliance.

  • Resolve line issues as they arise, troubleshoot basic problems, and suggest process improvements to enhance efficiency and quality.

  • Assist with special projects as requested, contributing to continuous improvement and operational initiatives.

  • Perform additional duties as assigned to support overall production and team objectives.

Essential Skills
  • High School Diploma is required.

  • At least 6 months of manufacturing experience is required.

  • Experience working in production, fast food, retail, or similar high-volume, process-driven environments.

  • Ability to follow and adhere to Standard Operating Procedures (SOPs).

  • Familiarity with cGMP (current Good Manufacturing Practices) in a manufacturing setting.

  • Experience in cleanroom, packaging, assembly, or medical device manufacturing environments.

  • Ability to operate manufacturing line equipment safely and effectively.

  • Strong attention to detail for reviewing device manufacturing records and work orders.

  • Ability to work both independently and as part of an assembly line team.

  • Commitment to maintaining a safe work environment, especially when working with chemicals and equipment.

  • Good organizational skills to maintain floor area and manage supplies during production.

Additional Skills & Qualifications
  • Experience in medical device manufacturing or regulated manufacturing environments.

  • Previous exposure to ISO standards in a manufacturing or cleanroom setting.

  • Background in production, fast food, or retail that demonstrates reliability, teamwork, and ability to work in a fast-paced environment.

  • Ability to identify process issues on the line and propose practical improvements.

  • Comfort working on special projects and adapting to changing production priorities.

  • Strong documentation skills for accurate completion and review of manufacturing records.

Why Work Here?

This opportunity offers a contract-to-hire path in a large, modern facility with strong long-term prospects. From the first day of your temporary assignment, you begin accruing 401(k) benefits, and if you convert to a permanent role, your accrual dates back to your initial start date. Upon conversion, you can expect a pay increase and access to highly competitive benefits. The organization provides multiple pathways for growth and advancement, with significant opportunities anticipated in the coming year, including potential international opportunities once you become permanent. You will join a team that invests in its people, emphasizes stability, and supports professional development.

Work Environment

You will work in a cleanroom environment that supports medical device and regulated manufacturing activities. The role is on 2nd shift, with additional open positions on 1st shift, offering some flexibility in scheduling based on operational needs. The setting involves operating manufacturing line equipment, handling components and packaging materials, and following strict cGMP, ISO, and SOP requirements. You can expect a structured, process-driven environment with a strong emphasis on cleanliness, safety, documentation accuracy, and teamwork.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $18.00 - $20.16/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 jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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)

Job Type & Location

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

Application Deadline

This position is anticipated to close on Nov 17, 2026.

Workplace Type

This is a fully onsite position in Carlsbad,CA.

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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