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Astrix Technology Quality Control Associate I in Fremont, California

Quality Control Associate I

Quality Control

Fremont , California, US

  • Added - 12/03/2026

Pay Rate Low: 26 | Pay Rate High: 28

Position Overview

We are seeking a detail-oriented Quality Control Associate I to support Microbiology and Environmental Monitoring operations within a multi-product pharmaceutical manufacturing facility. This role executes routine testing and sampling activities in compliance with GMP standards and is ideal for a science graduate looking to build hands-on laboratory experience in a regulated environment.

Location: Fremont, CA Schedule: Full-time, Monday–Friday, 1st Shift (8:00 AM – 5:00 PM) Duration: Approximately 6-month contract engagement Hours: 40 hours/week

Key Responsibilities

  • Execute routine Microbiology and Environmental Monitoring programs, including clean room sampling and raw materials testing of bulk drug substance and drug product.

  • Perform Raw Material sampling and microbiological compendial testing.

  • Develop proficiency in 1–3 analytical methodologies.

  • Conduct technical and quality review of laboratory data.

  • Maintain accurate sampling and testing records, equipment logs, and controlled documentation in both paper and electronic formats (LIMS).

  • Work with GMP and non-GMP databases to ensure samples are received, logged, stored, distributed, and tracked within defined timelines.

  • Coordinate with Sample Management, QC laboratories, and Raw Materials groups to prioritize samples and troubleshoot discrepancies.

  • Coordinate shipment of samples to contract laboratories and external testing sites.

  • Transfer samples from clean rooms to laboratories; perform and maintain clean room gowning compliance.

  • Support routine lab maintenance, quality, and compliance activities.

  • Assist other team members as needed and perform QC-related data entry.

Qualifications

  • Bachelor's degree in a scientific discipline; Microbiology preferred.

  • 1–3 years of GMP laboratory and/or clean room experience.

  • Proficiency with aseptic techniques and gowning procedures

  • Strong pipetting skills.

  • Familiarity with LIMS systems and standard laboratory documentation practices.

  • Willingness to support weekend shifts on an as-needed basis.

  • Strong attention to detail and ability to work under supervision per SOPs.

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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