natera
Supervisor QC Reagent
At a Glance
- Location
- San Carlos, California, United States
- Employment
- employment_required
- Experience
- 4+ years
- Posted
- 2026-06-17T16:26:03-04:00
Key Requirements
Certifications
- GMP
Domain Knowledge
- Clinical
- Regulatory
- Supply Chain
Requirements
Experience in PCR and other Molecular Biology Techniques.
Understanding of Quality Control methods development and implementation.
Supply chain, document control, and regulatory compliance experience.
Experience in a regulated environment, GMP, ISO, CLIA, CAP, and Aseptic techniques
Compensation & Benefits
This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.
This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:
Annual performance incentive bonus
Long-term equity awards
401(k) with company match
Responsibilities
The Supervisor, QC Reagent will manage day-to-day operations of manufacturing and testing of consumable reagents to support production.
Provide direct supervision and follow up to individual contributors in a highly regulated environment (CLIA/CAP/ISO13485) to ensure adherence to SOPs and safety procedures.
Perform, troubleshoot and follow up incoming inspection, manufacturing and Quality Control tests for reagent release
Support and leads development of workflow troubleshooting and procedure improvements
Escalate issues/concerns and suggests possible solutions and collaborates with Manager to resolve issues
Knowledgeable & competent in Reagent Team Benchwork & Data Analysis