2nd Shift Cleanroom Production Assembly

Aerotek; San Diego (CA); On-site; USD 26,000 - 27,000; Full time

Job summary

Aerotek is hiring a 2nd Shift Cleanroom Production Operator in San Diego, CA. The role focuses on high-volume assembly of insulin-contact cartridge components in an ISO Class 8 cleanroom, adhering to GMP and quality standards.

You will rotate across lines, operate semi-automated equipment, inspect batches, and document production activities while maintaining strict contamination-control practices. Overtime is possible on high-demand shifts.

Qualifications

• Experience in fast-paced production/manufacturing.
• Ability to follow SOPs with precision and consistency.
• Detail-oriented with strong quality focus.
• Reliable attendance and punctuality.

Responsibilities

• Assemble disposable cartridge components in ISO Class 8 cleanroom.
• Operate semi-automated equipment on a production line.
• Inspect, test, and document batch records per SOPs.
• Maintain GMP compliance and use PPE and cleanroom practices.

Skills

Attention to detail

Punctuality

Team player

Reading SOPs

Computer literacy

Mechanical aptitude

Cleanroom experience

Ability to follow GMP/Regulatory

Job description

2nd Shift Cleanroom Production Assembly - $19.76/hr

Job Description

As a Cleanroom Production Operator in the cartridge department, you will help manufacture a disposable cartridge component that stores insulin and integrates with an advanced pump system. This role centers on high-volume production in an ISO Class 8 cleanroom, following strict contamination-control and quality standards. You will work on a manufacturing line with a team, perform mechanical and medical device assembly, operate semi-automated equipment, conduct inspections and testing, and ensure all work meets Good Manufacturing Practice (GMP) requirements and documented procedures.

Responsibilities

• Assemble disposable cartridge components that come into direct contact with insulin, following detailed work instructions and standard operating procedures (SOPs).
• Work on a fast-paced manufacturing line as part of a team to complete mechanical and medical device assemblies accurately and efficiently.
• Monitor semi-automated manufacturing processes to ensure proper operation, product quality, and adherence to production targets.
• Operate production machinery and equipment safely and consistently, including automated machines used for sub-assembly, welding, inspection, and testing.
• Rotate through four different production lines: inspections, running automated machines, sub-assembly and welding, and testing of components.
• Review batch records and production documentation for accuracy, completeness, and compliance with quality and regulatory standards.
• Use computers to complete training modules, access SOPs, and maintain production and quality documentation.
• Follow cleanroom practices and contamination-control requirements at all times to protect sterile fluid-path components.
• Maintain a clean, organized, and safe work environment in accordance with cleanroom and safety protocols.
• Adhere to GMP and medical device manufacturing standards throughout all assembly, packaging, inspection, and testing activities.
• Demonstrate consistent attention to detail to identify defects, ensure product quality, and meet stringent inspection criteria.
• Show reliable attendance and punctuality to support continuous production in a high-volume environment.
• Be flexible and willing to be cross-trained and work in different departments or buildings as production needs change.
• Support packaging and related production activities when assigned, including work at nearby facilities as required.
• Follow all cleanroom dress code and personal hygiene requirements, including appropriate PPE, handwashing, and restrictions on personal items.

Essential Skills

• Previous experience working in a fast-paced production or manufacturing environment is highly desirable.
• Ability to follow SOPs and detailed work instructions from any industry with precision and consistency.
• Strong attention to detail for assembly, inspection, documentation review, and quality control.
• Reliable attendance and punctuality, with a strong sense of responsibility for meeting production schedules.
• Comfort working with computers for training, documentation, and production record-keeping.
• Mechanical aptitude for mechanical assembly, sub-assembly, and operation of production machinery.
• Ability to work effectively as part of a team on a manufacturing line and collaborate to complete assemblies.
• Trainable mindset with the ability to quickly learn new processes, equipment, and cleanroom procedures.
• Willingness to follow GMP and medical device manufacturing standards and quality requirements.
• Flexibility to work overtime and adjust to changing workloads and departmental assignments.
• Capability to work in a cleanroom environment and comply with strict contamination-control requirements.

Additional Skills & Qualifications

• Experience in disposable product manufacturing or medical device production is a strong plus.
• Background in cleanroom production, sterile manufacturing, or fluid-path components is beneficial.
• Familiarity with inspection processes, testing procedures, and documentation review in a regulated environment.
• Experience with packaging operations in a manufacturing or medical device setting is advantageous.
• Demonstrated good work ethic, including reliability, accountability, and a willingness to do what it takes to get the job done.
• Strong team player attitude with the ability to support colleagues and adapt to different roles.
• Openness to cross-training in multiple departments and learning new tasks across the production process.
• Comfort working in a high-volume environment where pace and priorities can change frequently.

Why Work Here?

You will join a large, established organization that maintains a close-knit, family-style culture within the production team. Colleagues care about each other and take pride in treating everyone with respect, regardless of employment type. The environment emphasizes teamwork, mutual support, and a strong sense of shared purpose. You can expect clear training, opportunities to be cross-trained in different areas, and the chance to grow your skills in a highly regulated, quality-focused setting. The company values flexibility, reliability, and a positive attitude, creating a workplace where your contributions are recognized and appreciated.

Work Environment

This role is based in the cartridge department within an ISO Class 8 cleanroom, supporting high-volume disposable product manufacturing. Work is performed on a manufacturing line and may involve rotation between different departments and buildings, including nearby packaging operations approximately 2.5 miles away. The pace of work will increase over time, and employees must be flexible with assignments and overtime as production demands grow over the next several months. Cleanroom dress code and hygiene requirements include wearing designated PPE such as hair cover, lab coat or gown, gloves, and side-shielded glasses; regular handwashing and glove use; and strict restrictions on fragrances, makeup, lipstick, fake or acrylic nails. Pants are required (no leggings or shorts), necklaces must be tucked into shirts, and all personal items must comply with contamination-control standards. Shifts operate Monday through Thursday on an AWS schedule, with one shift running from early morning to mid-afternoon and another from afternoon to late night. Overtime is provided for hours worked beyond 10 hours in a day or more than 40 hours in a week, and employees must be comfortable with varying workloads, cross-training, and working in different production areas as needed.

Job Type & Location

This is a Contract position based out of San Diego, CA.

Pay and Benefits

The pay range for this position is $19.00 - $19.76/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 position based out of San Diego, CA.

Application Deadline

This position is anticipated to close on Nov 8, 2026.

Workplace Type

This is a fully onsite position in San Diego,CA.

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.

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.