Full-Time

Supv – QC Reagent

Confirmed live in the last 24 hours

Natera

Natera

1,001-5,000 employees

Genetic testing and diagnostics solutions provider

Biotechnology
Healthcare

Compensation Overview

$105.1k - $131.4kAnnually

Mid

San Carlos, CA, USA

For California site.

Category
Lab & Research
Life Sciences
Medical Research
Required Skills
Data Analysis
Requirements
  • 4+ years of experience if degree is in CLS/MLS or 4.5+ years of experience if BS/BA degree (or equivalent) in Biological Sciences or related field is required
  • Current California State CLS or CGMBS license (Clinical Genetics Molecular Biologist Scientist) is required for California site
  • Current MT/MTS/CLS certification from ASCP, AMT, or AAB is required for Texas site
  • Relevant Molecular Biology and/or Cell Culture experience in a laboratory setting is strongly preferred
  • Experience with writing of SOP's and QC documentation is preferred
Responsibilities
  • 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.
  • Support and provide approvals for QC documentation updates.
  • Oversee and maintain training records for new hires.
  • Implement new process changes, tech transfers, planning workflow and reagent preparation and qualification.
  • Provide direction and guidance to employees.
  • Provide direction for planning meetings to meet Turnaround time (TAT) to ensure work is consistently completed according to department goals.
  • Assist with Audit preparation by compiling data and prepares reports as needed.
  • Lead Continuous Improvement Projects.
  • Participate in the preparation of investigations, summaries, and reports.
  • Assist in maintaining, updating, and approving documents pertaining to raw material specifications, reagent qualification, laboratory procedures, and department training.
  • Perform Record Review of Incoming Inspection, Manufacturing, Qualifications, Maintenance Log, etc.
  • Responsible for day-to-day operational staffing, including hiring/training of personnel.
  • Administer company policies and management guidance that directly affect employees.
  • Meet regularly with individual contributors to discuss goals and performance.
  • Keep team morale up and maintains professionalism of team members.
  • Able to take on own projects with little supervision.
  • Actively interacts with interdepartmental teams such as OPS, Accessioning, Engineering, Stats, R&D, Support and Product Development.
  • Follow/Ensure GLP (good laboratory practices) and GMP (good manufacturing practices) compliance.
  • Conduct self in a Professional manner.
  • Perform other duties as assigned.

Natera specializes in genetic testing and diagnostics, focusing on advanced testing solutions for various medical needs, including cancer detection, organ health, and family planning. Their main technology is cell-free DNA (cfDNA) testing, which analyzes small DNA fragments in the blood to detect molecular residual disease (MRD) in cancer patients, aiding in treatment decisions. They also offer the Signatera test for cancer patients and provide testing for transplant patients to monitor organ health. For women's health, Natera has tests for prenatal screening and hereditary cancer risk, including the Panorama NIPT, which has been widely used. Unlike many competitors, Natera combines testing services with genetic counseling, allowing patients to receive personalized guidance remotely. The company's goal is to enhance patient care through precise genetic insights and support healthcare providers in making informed decisions.

Company Stage

IPO

Total Funding

$149.9M

Headquarters

Austin, Texas

Founded

2004

Growth & Insights
Headcount

6 month growth

11%

1 year growth

21%

2 year growth

61%
Simplify Jobs

Simplify's Take

What believers are saying

  • Natera's continuous innovation, such as the launch of the Prospera Heart test with DQS, demonstrates its commitment to improving patient outcomes and maintaining market leadership.
  • The company's diverse product offerings across oncology, transplant health, and women's health provide multiple revenue streams and reduce dependency on a single market.
  • Significant investments from entities like Massachusetts Financial Services Co. MA indicate strong financial backing and confidence in Natera's growth potential.

What critics are saying

  • Allegations of deceptive sales and billing practices could damage Natera's reputation and lead to legal and financial repercussions.
  • The highly competitive nature of the genetic testing market requires constant innovation and differentiation to maintain market share.

What makes Natera unique

  • Natera's focus on cell-free DNA (cfDNA) technology for a wide range of applications, from oncology to prenatal screening, sets it apart from competitors who may specialize in only one area.
  • The introduction of unique features like the Donor Quantity Score (DQS) for transplant rejection detection enhances the accuracy and reliability of their tests, distinguishing them from other genetic testing companies.
  • Natera's extensive portfolio of over 200 peer-reviewed publications underscores its commitment to scientific validation and credibility, which is a significant competitive advantage.

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Benefits

Flexible medical plans

Investment options

Time off

Workplace perks