Manufacturing Process Technician

Aerotek

California (MO)

On-site

USD 42,000 - 56,000

Full time

14 days+

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Job summary

Aerotek is seeking a Manufacturing Process Technician I to support cleanroom production and packaging in a regulated environment. You will help prepare supplies, verify components, and ensure SOPs and quality standards are followed to maintain regulatory compliance.

Work with a small team on the 1st shift (6:00am to 2:30pm), handling inventory control, documentation, and daily production tasks to support build plans while upholding safety and quality standards.

Qualifications

  • High school diploma or equivalent.
  • 1–3 years in a cleanroom environment, preferably medical device.
  • Experience with documentation and inventory records.
  • Ability to lift up to 40 pounds and bend.
  • Ability to follow SOPs, GMPs, QSR, GTP, ISO standards.

Responsibilities

  • Support formulation and build of products according to procedures and quality standards.
  • Prepare and verify components for production.
  • Follow SOP requirements for cleaning, labeling, and sealing processed units.
  • Support ERP material movements and ensure transactions are accurate and timely.
  • Adhere to all company policies to maintain regulatory and quality compliance.
  • Transfer and stock supplies for controlled areas and complete inventory system transactions.
  • Assist with final packaging activities, including kitting and prepping lots for shipment.
  • Assist with main cleanroom activities to support daily production operations.

Skills

Cleanroom experience
Documentation precision
SOP/GMP/ISO knowledge
Team player
Lifting up to 40 lbs

Tools

ERP systems

Job description

Job Description

Job Title: Manufacturing Process Technician

Job Description

  • The Manufacturing Process Technician I prepares and packages supplies to support the production build plan and forecasted demand.
  • This role assists in overseeing production activities to ensure that all operations comply with standard operating procedures (SOPs), current GMPs, QSR, GTP, ISO standards, and internal company procedures.
  • The technician works closely with the production team in a cleanroom environment to maintain accurate documentation, support inventory control, and uphold high quality and safety standards.
  • 1st Shift Schedule: 6:00am to 2:30pm.

Responsibilities

  • Support formulation and build of products according to established procedures and quality standards.
  • Prepare and verify components to ensure accuracy and readiness for production.
  • Follow SOP requirements for cleaning, labeling, and sealing processed units to maintain product integrity.
  • Support ERP material movements and ensure all material transactions are completed accurately and on time.
  • Adhere to all company policies and procedures to maintain regulatory and quality compliance.
  • Properly transfer and stock supplies for controlled areas such as autoclaves, cleanrooms, and quality areas, including completing system transactions for inventory control.
  • Assist with final packaging activities, including kitting and prepping lots for shipment or further processing.
  • Assist with main cleanroom activities as required to support daily production operations.
  • Organize delivered gowning supplies from approved vendors and stock gowning items in the Gowning Room.
  • Assist in performing wastewater treatment processes to ensure proper disposal in accordance with guidelines.
  • Assist with daily general cleaning of the production and cleanroom areas to maintain a safe and orderly environment.
  • Perform other job-related duties as assigned to support production and facility needs.

Essential Skills

  • High school diploma or equivalent.
  • 1 to 3 years of experience working in a cleanroom environment, preferably within the medical device industry.
  • Experience with documentation and paperwork, including accurate completion of production and inventory records.
  • Ability to lift up to 40 pounds and perform tasks that may involve regular lifting and bending.
  • Ability to follow SOPs, GMPs, QSR, GTP, ISO standards, and internal procedures consistently.
  • Comfort working in a cleanroom setting with strict gowning and cleanliness requirements.
  • Basic familiarity with production and packaging processes in a regulated environment.
  • Ability to work respectfully and professionally as part of a small team.

Additional Skills & Qualifications

  • Experience working with medical devices or in a regulated manufacturing environment.
  • Exposure to ERP systems for material movement and inventory transactions.
  • Attention to detail in handling components, labeling and sealing of processed units.
  • Ability to manage and organize gowning supplies and other controlled materials.
  • Willingness to perform wastewater treatment tasks following established procedures.
  • Strong sense of cleanliness and organization in support of cleanroom operations.

Why Work Here?

  • This opportunity offers a clear path for career growth within a regulated manufacturing environment, allowing you to develop valuable cleanroom and production skills.
  • You will work in a supportive, professional setting that values respect, reliability, and adherence to high quality standards, providing a solid foundation for long-term development.

Work Environment

  • The role is based in a cleanroom environment with a small, close-knit team focused on high-quality production.
  • Work involves regular interaction with controlled areas such as autoclaves, cleanrooms, and quality spaces, as well as the use of ERP systems for material and inventory transactions.
  • Team members are expected to maintain a professional and respectful demeanor, with a strong emphasis on collaboration and a positive work atmosphere. Cleanliness, proper gowning, and adherence to procedural standards are essential parts of the daily routine.
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