QC Associate (Contractor) (P-4709)

10x Genomics is seeking a dedicated and detail-oriented individual to join our Quality Control team. As a QC Associate, you will be responsible for inspecting raw materials, intermediates, and finished goods. The role includes biological reagent, consumable testing plus instrumental quality control tasks such as interpreting technical drawings and inspecting the first article inspection report. This temporary position is based in our Pleasanton, California site. This is an exciting opportunity to be a key part of an innovative Quality Control team driving the next generation of life science technologies.

Success in this position requires strong initiative, adaptability, and teamwork within a fast-paced life sciences environment. Candidates should demonstrate a working knowledge of manufacturing workflows and ERP systems. We value individuals who are self-starters, quick learners, and effective collaborators.

Key Responsibilities

• Conduct quality control testing on raw materials, intermediates, and finished products according to established procedures.
• Perform molecular biology techniques, including PCR, next-generation sequencing, microscopy, cell and tissue handling, and HPLC.
• Participate in instrument QC workflows, including training to work with mechanical stages and read technical drawings and first article inspection report.
• Accurately follow work instructions and standard operating procedures, while proactively identifying and reporting discrepancies.
• Maintain comprehensive and accurate records, including QC batch files and Receiving Inspection Reports, in accordance with Good Documentation Practices.
• Execute QC workflows from sample submission to final batch closure.
• Efficiently communicate complications identified during QC testing and collaborate with engineers and scientists to resolve issues.
• Uphold clean room standards to ensure a compliant laboratory environment for life sciences manufacturing.
• Maintain precise, repeatable laboratory practices to ensure consistent and reliable experimental results.
• Support process and product development activities, including process optimization, guard band and stability studies, and gauge R&R.
• Assist in root cause investigations for non-conforming lots and contribute to continual improvement efforts.

Qualifications

• B.S. in Biological Engineering, Molecular Biology, Analytical Chemistry, Chemical Engineering, or related discipline.
• 1 year of relevant laboratory experience in manufacturing and QC of life science products (e.g., PCR, NGS, protein analysis, HPLC).
• Willingness to rotate through various laboratory and administrative tasks.
• Demonstrated ability to work both independently and as part of a team.
• Strong attention to detail, organization, and commitment to quality.
• Effective communication and observational skills.
• Ability to multitask, prioritize workload, and perform under pressure to meet strict deadlines.
• Excellent critical and logical thinking skills to analyze and troubleshoot issues.
• Familiarity with reading and interpreting SOPs and equipment user manuals.
• Proficiency in data entry using tools such as Excel, Oracle ERP and LIMS.
• Flexibility to shift priorities in response to new developments.

Preferred Skills & Experience

• Experience with data science tools and common programming languages.
• Basic knowledge of statistics.