Sr. QC Associate I (P-4984) at 10x Genomics

Pleasanton, California, United States -

Full Time

Start Date

Immediate

Expiry Date

30 May, 26

Salary

50.91

Posted On

01 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Chemistry, Biochemistry, Analytical Methods, ISO-Regulated Manufacturing, QC Testing, Data Analysis, Assay Setup, NGS, Immunofluorescence, Flow Cytometry, PCR, qPCR, Spectrophotometry, Spectrofluorometry, HPLC, Risk-Based QC Strategy

Industry

Biotechnology Research

Description

10x Genomics is looking for a Sr. QC Associate I to join our Quality Control team. This role is responsible for the qualification of consumable products associated with Single Cell, Spatial, and In-Situ product lines. In addition to ensuring a reliable supply of quality consumables, you will be a key contributor to the development of manufacturing infrastructure required to support commercial products in the life science field. The ideal candidate will possess deep working knowledge of chemistry, biochemistry, and analytical methods. You must have extensive hands-on experience working within an ISO-regulated manufacturing environment. What You Will Be Doing: Execute QC Testing: Perform quality control operations according to defined procedures to ensure the integrity and quality of raw materials, intermediates, and finished goods. Data Analysis & Disposition: Complete QC testing in a timely manner and disposition materials based on established acceptance criteria. Product Development and Sustaining Support: Serve as the primary QC point of contact to oversee project completion, providing expert guidance on assay setup and assisting in the introduction and optimization of new products and processes. Assay Cross-Training: Cross-train on various inspections, including first article inspection, metrology, microscopy, analytical assays, and NGS. Documentation: Maintain quality control batch records and ensure Good Documentation Practices (GDP) under ISO requirements. Accurately track QC test data, calibration records, and inventory. Draft Work Instructions in collaboration with the Manufacturing Systems & Engineering team. Quality Compliance: Initiate non-conformance, deviation reports, engineering change orders (ECO) and follow up on necessary action items. Ensure that lab operations and workflow execution are compliant with ISO requirements. Problem Solving: Effectively identify and communicate complications arising from QC testing with minimal supervision. Work closely with scientists to establish and maintain technical solutions. Drive completion of investigations and minimize disruptions to QC operations. Minimum Requirements: Education: B.S. in Analytical Chemistry, Biochemistry, or a related field. Experience: 5+ years of laboratory experience specifically in a QC environment. Technical Skills: Strong hands-on experience with NGS and tissue-based assays (including immunofluorescence and flow cytometry). Proficiency in PCR, qPCR, spectrophotometry, spectrofluorometry, and HPLC. QC Strategy Setup: Experience collaborating with R&D and QA on risk-based QC strategy assessment including assay robustness, assay cost, and alignment of QC checkpoints to the manufacturing process. Operational Knowledge: A solid understanding of New Product Introduction (NPI) and manufacturing processes. Adaptability: Ability to manage and track diversified QC assays and projects in a rapidly evolving environment. Soft Skills: Strong critical thinking, logical problem-solving skills, and the ability to communicate effectively with stakeholders. Preferred Qualifications: Proficiency with data analysis tools (e.g. Retool, Tableau, GitHub, Snowflake). Direct work experience within an ISO 13485 environment. Proficiency with Lean Six Sigma tools and methodologies. #LI-ES1 #LI-onsite Below is the base pay range for this full-time position. The actual base pay will depend on several factors unique to each candidate, including one’s skills, qualifications, and experience. At 10x, base pay is also just one component of the Company’s total compensation package. This role is also eligible for 10x’s equity grants, its comprehensive health and retirement benefit programs, and its annual bonus program or sales incentive program. During the hiring process, your 10x recruiter can share more about the Company’s total compensation package. Hourly $37.64—$50.91 USD About 10x Genomics At 10x Genomics, accelerating our understanding of biology is more than a mission for us. It is a commitment. This is the century of biology, and the breakthroughs we make now have the potential to change the world. We enable scientists to advance their research, allowing them to address scientific questions they did not even know they could ask. Our tools have enabled fundamental discoveries across biology including cancer, immunology, and neuroscience. Our teams are empowered and encouraged to follow their passions, pursue new ideas, and perform at their best in an inclusive and dynamic environment. We know that behind every scientific breakthrough, there is a deep infrastructure of talented people driving the life sciences industry and making it possible for scientists and clinicians to make new strides. We are dedicated to finding the very best person for every aspect of our work because the innovations and discoveries that we enable together will lead to better technologies, better treatments, and a better future. Find out how you can make a 10x difference. Individuals seeking employment at 10x Genomics are considered without regards to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation, or any other characteristic protected by applicable law. 10x does not accept unsolicited applicants submitted by third-party recruiters or agencies. Any resume or application submitted to 10x without a vendor agreement in place will be considered unsolicited and property of 10x, and 10x will not pay a placement fee.

Responsibilities

This role involves executing quality control testing on raw materials, intermediates, and finished goods for consumable products across Single Cell, Spatial, and In-Situ product lines. Key duties include data analysis, material disposition, serving as the QC point of contact for product development, and maintaining documentation under ISO requirements.