Life Science Jobs Astrix- Apply for QC Specialist Role

Life Science Jobs Astrix- Apply for QC Specialist Role

A top biotechnology company in San Mateo County, CA is seeking a QC Specialist (LIMS) to ensure product quality and regulatory compliance. This contract-hire role offers hands-on experience in LIMS management, QC workflows, and cross-functional collaboration with Quality Assurance, Manufacturing, and R&D teams. Candidates with experience in biotechnology, pharmaceutical, or biomanufacturing industries are encouraged to apply.

About the Company

Astrix is a leading biotechnology staffing and consulting firm that connects top scientific talent with cutting-edge life sciences companies. With a focus on quality, innovation, and career development, Astrix helps professionals advance in biotechnology, pharmaceuticals, and biomanufacturing industries while enabling companies to access specialized expertise for critical roles.

  • Job Title: QC Specialist
  • Location: San Mateo County, CA
  • Job Type: Contract-hire

Life Science Jobs Astrix- Role

The QC Specialist (LIMS) will perform routine and non-routine QC testing, maintain data integrity in the LIMS system, support product release, and drive continuous process improvements. This position collaborates closely with QA, Manufacturing, and R&D teams, ensuring compliance with cGMP, GLP, and ISO 9001 standards.

Life Science Jobs Astrix- Key Responsibilities:

  • Lead and support LIMS design, configuration, and implementation for QC workflows.
  • Collaborate with QC, QA, IT, and external vendors to define user requirements and functional specifications.
  • Author and execute IQ/OQ/PQ validation protocols following 21 CFR Part 11 and GxP compliance.
  • Develop and deliver training materials for QC users; provide ongoing post-implementation support.
  • Ensure LIMS integration with other lab systems (CDS, ELN, ERP) to streamline workflows.
  • Monitor system performance and lead continuous improvement initiatives.
  • Maintain change control documentation and participate in audits as the LIMS subject matter expert.

QC Specialist Role- Qualifications:

Required:

  • Bachelor’s degree in Biology, Chemistry, Biochemistry, or related discipline.
  • 2–4+ years of QC experience in biotechnology, pharmaceutical, or biomanufacturing.
  • Hands-on experience with LIMS for sample tracking and workflow management.
  • Solid understanding of cGMP, GLP, and ISO 9001 quality standards.

Preferred:

  • Proficiency in analytical techniques like HPLC, ELISA, PCR, spectrophotometry, or enzymatic assays.
  • Familiarity with ERP systems, Electronic Lab Notebooks (ELN), and digital documentation tools.
  • Experience in enzyme, protein, or biologics manufacturing environments.

Compensation & Work Type:

  • Contract-hire role
  • Pay rate: $45–$65/hour DOE

Why Apply:

This is an exciting opportunity to join a leading biotech company and play a critical role in QC operations and LIMS management, contributing to the quality and safety of cutting-edge biotechnology products.

CLICK HERE TO APPLY NOW

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