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Quality Control Laboratory Technician

Job in Novato, Marin County, California, 94949, USA
Listing for: Tucker Parker Smith Group (TPS Group)
Full Time position
Listed on 2026-02-06
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below

Join a leading pharmaceutical company at the forefront of innovation! We’re looking for a QC Analyst to play a vital role in managing and overseeing the life cycle of critical reagents that power groundbreaking global commercial products. In this exciting, hands-on position, you'll be involved in everything from reagent preparation to inventory management, technical documentation, and ensuring materials are distributed across the global testing network.

You’ll make a real impact by supporting cutting-edge research and development, ensuring the quality and stability of materials that are key to successful product outcomes.

Key Responsibilities
  • Acquire, prepare, and aliquot critical reagents with precision and care.
  • Lead qualification testing coordination with lab teams to ensure top-quality standards.
  • Oversee the smooth distribution of reagents across a global network of testing sites.
  • Utilize LIMS to track reagent activities, testing progress, and to generate actionable insights through trend analysis.
  • Maintain and optimize inventories, forecasting future reagent supply needs to keep everything running seamlessly.
  • Develop and maintain comprehensive technical documentation, including detailed protocols and qualification reports.
  • Champion continuous improvement, bringing fresh ideas to enhance workflows and drive operational efficiencies.
Skills & Qualifications
  • Bachelor’s degree in a related field, or Associate’s degree with additional relevant experience
  • 1+ years of hands-on laboratory experience.
  • Exceptional documentation, written, and verbal communication skills.
  • Expertise in Microsoft Word, Excel, and analyzing complex data.
  • Experience with reagent preparation, inventory management, and LIMS.
  • Knowledge of Good Manufacturing Practices (GMP) and QC principles.

This is a unique opportunity to contribute to a highly impactful and global team while gaining invaluable experience in the heart of the pharmaceutical industry. Apply today to embark on a rewarding journey with a top pharmaceutical company!

Seniority level

Entry level

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing and Biotechnology Research

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