Manufacturing Associate

TEKBERRY; Woodland (CA); On-site; USD 28,000 - 34,000; Part time

Job summary

Tekberry, Inc. is seeking a Manufacturing Associate to support on-site cleanroom production in Woodland, CA. The role requires aseptic processing, documentation, inspection, and packaging within a regulated environment under cGMP standards.

Responsibilities include batch record completion, material inspections, and adhering to quality and safety requirements. Requires HS diploma or GED; 1–3 years in FDA-regulated settings preferred; 100% onsite location.

Qualifications

• 1–3 years experience in FDA-regulated manufacturing preferred.
• Experience with aseptic techniques in a cleanroom environment.
• HS Diploma or GED required.

Responsibilities

• Ensure products are manufactured per company procedures and cGMP standards.
• Operate in Class 1,000 and Class 100 cleanroom areas and adhere to aseptic techniques.
• Perform quality inspections on incoming and outgoing materials and products.
• Complete batch records accurately and timely for each day’s production.
• Assist with equipment maintenance, cleaning, and basic readings from manufacturing equipment.

Skills

Aseptic techniques

Cleanroom operation

Documentation

Quality inspections

Education

HS Diploma or GED

Job description

Manufacturing Associate

• Pay Rate Range: $20.00 - 25.00/hr (DOE)
• Employment Type: Contract (6 Months, Potential Extension)
• Schedule: Monday Friday, 8:00 AM 4:30 PM
• Location: Woodland, CA 95776 (100% Onsite)

Tekberry is looking for a highly qualified and motivated Manufacturing Associate to work on-site with our client in Woodland, CA. This is a contract opportunity supporting cleanroom manufacturing operations within a regulated production environment.

Position Summary

The Manufacturing Associate will support day-to-day production activities within a cleanroom environment, ensuring products are manufactured in accordance with cGMP standards, quality requirements, and production schedules. This role involves aseptic techniques, documentation, inspection, and packaging in a highly controlled manufacturing setting.

Key Responsibilities

• Ensures all scheduled products are manufactured according to company procedures and cGMP's to achieve customer satisfaction and conformance to company schedule/deadlines
• Understands the concepts of aseptic technique to operate inside Class 1,000 and Class 100 cleanroom areas as well as other controlled areas
• Performs quality inspections on incoming and outgoing materials and products
• Sorts and places materials or items on racks, shelves, or bins according to predetermined inventory procedures needed
• Completes batch records in an accurate and timely manner following each days' production
• Formulates, finishes, manufactures and fills all products produced at the plant with minimal guidance
• Monitors equipment and completes basic equipment maintenance and cleaning activities
• Utilizes and records readings from laboratory and manufacturing equipment
• Closely follows work instructions provided in writing or verbally by supervisor/plant leadership
• Moves stacks of crates from freezer to packaging area with hand truck/dolly to complete work
• Inspects and packages product by checking for damaged bottles, labels and/or heat shrinks that do not meet established standards
• Labels, bags, boxes and palletizes finished product in accordance with plant deadlines
• Provide input to new, and revising existing, SOP's to ensure procedures are accurate, up to date and in compliance with current Good Manufacturing Practices
• Responsible for reporting quality and safety issues to immediate supervisor
• Ensures personal training documentation is up to date and aid in the training of others as needed
• Maintain organization and cleanliness of production areas
• Special assignments and other responsibilities as required
• Use of cleaning products in an industrial environment
• Familiarity with GDP (Good Documentation Practices)

Qualifications Required

• 1-3 years' experience preferred in the following:
• Experience in an FDA-regulated environment.
• Experience with aseptic techniques and working in a cleanroom.

Education

• HS Diploma or GED required

Tekberry, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Tekberry is a certified Minority Business Enterprise (MBE) and Disadvantaged Business Enterprise (DBE).

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