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Manufacturing Associate I-Assembly & Packaging is sought for a contract-to-hire role in Fremont, CA. The position involves supporting drug product production in a cGMP environment, performing routine assembly, packaging, and SOP-driven tasks while ensuring quality and compliance.
The role requires high attention to detail, ability to follow written instructions, and basic computer skills. The shift is 1st shift, Monday–Friday, 6:00 AM–2:30 PM, with a pay rate of $22.15 per hour.
Manufacturing Associate I-Assembly & Packaging
Manufacturing
Fremont, California, US
Our client, a leading organization in the pharmaceutical and biotechnology manufacturing sector, is seeking a detail-oriented Manufacturing Assembly & Packaging Associate to support drug product production in a cGMP-regulated, multi-product facility. In this role, you will perform routine unit operations for assembly, packaging, and support troubleshooting efforts—all in strict compliance with standard operating procedures (SOPs).
Job Title: Manufacturing Assembly & Packaging Associate
Location: Fremont, CA
Terms: Contract-to-hire
Shift: 1st Shift | Monday–Friday, 6:00 AM–2:30 PM
Pay Rate: $22.15/hr
Responsibilities:
Assist in setting up automated and semi-automated equipment including autoinjector assembly, syringe assembly, and tabletop packaging systems.
Retrieve and prepare components, tools, and documentation prior to equipment setup.
Support equipment changeovers and minor equipment repairs or adjustments.
Identify and resolve operational issues during assembly and packaging processes.
Perform accurate documentation in controlled documents such as batch records, logbooks, and SOP attachments.
Execute assembly and packaging tasks and assist with visual inspection/filling operations as needed.
Ensure proper stocking of components, supplies, and materials before operations begin.
Transfer products and materials within the Controlled Non-Classified (CNC) manufacturing area.
Maintain cleanliness of production rooms, including waste disposal and sanitization in line with safety procedures.
Follow all safety protocols and report unsafe conditions immediately.
Participate in shift hand-off communications to ensure operational continuity.
Maintain 5S standards and ensure equipment used is properly calibrated and documented.
Complete required logbooks and maintain documentation compliance.
Qualifications:
High School Diploma or equivalent required; Associate or Bachelor's degree or biotechnology vocational training preferred.
Minimum 1 year of experience in a GMP-regulated manufacturing environment (pharmaceutical or biotechnology industry strongly preferred).
Basic computer skills (MS Office, Outlook, and other systems).
Strong organizational skills and ability to work in small teams.
Ability to read, comprehend, and follow written instructions.
Demonstrated math proficiency, including basic arithmetic and conversions.
Strong verbal and written communication skills.
Ability to stand for extended periods and perform physical tasks including lifting, bending, twisting, and climbing.
Must be fully vaccinated against COVID-19 or have an approved medical/religious exemption.
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We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.