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Astrix Technology Manufacturing Associate in South San Francisco, California

Manufacturing Associate

Manufacturing

South San Francisco, California, US

  • Added - 04/03/2026

Pay Rate Low: 25 | Pay Rate High: 30

ROLE DETAILS

Type: Contract Location: San Francisco Bay Area, CA (On-site)

POSITION OVERVIEW

We are seeking a detail-oriented Manufacturing Associate to join a fast-paced life sciences organization at a pivotal stage of growth. This contract role will directly support day-to-day manufacturing operations, with a primary focus on buffer formulation, material dispensing, and production kitting. The ideal candidate is a hands-on professional who thrives in structured, GMP-compliant environments and takes pride in executing procedures with precision and consistency.

KEY RESPONSIBILITIES

  • Prepare and formulate buffers and reagents in accordance with approved batch records and standard operating procedures.

  • Perform accurate material dispensing, weighing, and associated documentation within a controlled manufacturing environment.

  • Assemble production kits with attention to component selection, labeling accuracy, and full traceability.

  • Maintain thorough and compliant documentation practices consistent with GMP standards.

  • Support inventory management activities, including raw material staging and reconciliation.

  • Uphold cleanroom organization standards and adhere to all safety and contamination control protocols.

  • Collaborate cross-functionally with Manufacturing, Quality Control, and Supply Chain teams to support production goals.

REQUIRED QUALIFICATIONS

  • Bachelor's degree in Biology, Chemistry, Biochemistry, or a related life sciences discipline.

  • 1–3+ years of experience in a biotech, pharmaceutical, or medical device manufacturing environment.

  • Demonstrated experience with buffer formulation and reagent preparation.

  • Hands-on experience with material dispensing and/or kitting in a controlled or cleanroom setting.

  • Working familiarity with GMP documentation practices and compliance requirements.

  • Strong attention to detail with the ability to follow SOPs with consistency and rigor.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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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.

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