CQV Engineer

Posted Yesterday
Be an Early Applicant
San Carlos, CA, USA
In-Office
88K-110K Annually
Junior
Biotech
The Role
Provides Level 2 service and support for clinical laboratory equipment and instrumentation. Responsibilities include installation, troubleshooting, calibration, maintenance, repair, qualification, and validation of automation and sequencing systems. Develops equipment protocols, coordinates installations and MEP requirements, manages preventive maintenance programs, and ensures compliance with IQ/OQ/PQ, GDP, OSHA, CAP, CLIA, and quality-system requirements. Collaborates with laboratory, automation, process engineering, QA, equipment technicians, and vendors to minimize downtime and support new projects.
Summary Generated by Built In

POSITION SUMMARY:

The CQV Engineer is responsible for the service and support of laboratory equipment and instrumentation utilized in the Operations laboratory. The scope of support includes installation, calibration, maintenance, and repair of both simple (e.g., plate sealers) and complex (e.g., liquid handling robotics) instrumentation in the laboratory. The Instrument Service Engineer will be the primary point of contact for production lab personnel when equipment and instruments are not operating or not meeting operational specifications. 


PRIMARY RESPONSIBILITIES:

• Provides Level 2 support for all laboratory equipment,  troubleshooting hardware and software with some support from Level 3, Automation, and vendor.   

• Work with other Instrument Service Engineers, and the Automation and laboratory teams to respond to instrument failures and ensure proper instrument function, providing  Level 2 support for all laboratory equipment.

• Diagnose and troubleshoot any system concerns to minimize downtime, with the technical skills of a Level II, troubleshooting hardware and software with some support from Level 3, Automation, and vendor.

• Install new laboratory equipment (e.g., liquid handlers, sequencers, plate sealers, etc.) to support lab capacity or new projects

• Qualify all instruments are appropriately qualified, creating and updating equipment protocols as needed. 

• Support of new instrumentation and project deliverables.

• Develop and execute procedures for the cleaning and maintenance of  laboratory instrumentation

• Develop and revise instrument qualification protocols in accordance with design requirements, operational needs, and applicable standards

• Coordinate new automation equipment installations by reaching out to necessary groups to ensure necessary MEPs are in place

• Work with process engineering and QA teams to facilitate introduction of new equipment types into clinical laboratory

• Work with different departments to determine qualification (IQ/OQ/PQ), calibration and preventive maintenance requirements for new incoming instruments, as needed, to comply with regulations and meet process requirements.

• Maintain program for preventative maintenance (PM), routine maintenance, and calibration of all laboratory equipment.

• Perform troubleshooting activities and provide Level 2 service; coordinate with Level 3’s and vendors to address escalated service concerns.

• Recommend and implement changes to ensure ongoing high-quality performance of laboratory equipment.

• Perform all service activities in compliance with all relevant safety and regulatory bodies (e.g., OSHA, CAP, CLIA, etc.).

• Maintain and continuously develop knowledge and expertise related to the service of clinical laboratory equipment.

• Track all service activities utilizing system(s) developed in accordance with service procedures and laboratory policies.

• Ensure all service documentation is complete, timely, and accurate following Good Documentation Practices (GDP).

• Excellent verbal and written English communication skills.

• Adaptable, open to change, and the ability to work in ambiguous situations while responding to new information and unexpected circumstances.

• Strong interpersonal and teamwork skills; ability to easily convey concepts and priorities, as well as an ability to solicit feedback and inputs.

• Support and comply with the company’s Quality Management System policies and procedures.

• Coordinate duties with Equipment Technician

• Perform other tasks as specified by the supervisor/manager

• This role works with PHI on a regular basis both in paper and electronic form and have access to various technologies to access PHI (paper and electronic) in order to perform the job

• Employee must complete training relating to HIPAA/PHI

privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.

• Must maintain a current status on Natera training requirements.


QUALIFICATIONS:

• BS/BA in a biological science/biomedical engineering, similar field of study, or comparable industry experience

• 1-3 years industry related experience

• Experience supporting laboratory equipment required


KNOWLEDGE, SKILLS, AND ABILITIES:

• Ability to analyze and problem solve issues

• Excellent attention to detail and accuracy

• Ability to promote a positive team environment

• Candidate must be a self-starter who can independently drive projects and day-to-day work tasks to completion according to schedule

• Adaptability in a frequently-changing environment

• Maintain a high level of professionalism and responsibility

• Good technical writing and communication skills

• Must have strong interpersonal and organizational skills

• Computer skills (MS Word, Excel, PowerPoint, etc.)

• Familiar with DNA Isolation and Purification, PCR, Cell Culture, Sequencing, etc.

• Experience with automation and sequencing instrumentation

Compensation & Total Rewards 

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 skills considerations.

This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:

  • Comprehensive health benefits (medical, dental, vision)

  • 401(k) with company match

  • Generous paid time off and company holidays

  • Additional wellness and work-life benefits

Compensation Range
$88,300—$110,350 USD

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents. 

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:
- BBB announcement on job scams 
- FBI Cyber Crime resource page 

Skills Required

  • Bachelor’s degree in biological science, biomedical engineering, a similar field, or comparable industry experience
  • 1-3 years of industry-related experience
  • Experience supporting laboratory equipment
  • Experience with automation and sequencing instrumentation
  • Familiarity with DNA isolation and purification, PCR, cell culture, and sequencing
  • Computer skills, including Microsoft Word, Excel, and PowerPoint
  • Strong technical writing, communication, interpersonal, and organizational skills
  • Ability to analyze and troubleshoot hardware and software issues
  • Ability to independently complete projects and day-to-day tasks according to schedule
  • Ability to work in a frequently changing and ambiguous environment
  • Completion of HIPAA/PHI privacy, general compliance, and security training within the first 30 days

Natera Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Natera and has not been reviewed or approved by Natera.

  • Healthcare Strength — Medical plan choice, fertility support, and free Natera tests for employees and families are emphasized alongside dental, vision, and life/disability coverage. These elements indicate robust core health coverage.
  • Equity Value & Accessibility — An Employee Stock Purchase Plan is available, and equity is described as a significant part of compensation in some roles. This accessibility to ownership can meaningfully augment overall pay.
  • Leave & Time Off Breadth — A flexible, no‑accrual PTO policy and parental leave are positioned as part of the package. This breadth suggests meaningful time‑off provisions are included.

Natera Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Austin, TX
6,000 Employees
Year Founded: 2004

What We Do

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. Where some set out to build a test, we set out to achieve a mission: change the management of disease worldwide by using DNA testing to proactively inform treatment. Through a cfDNA technology platform approach, we've pioneered noninvasive testing in unlimited applications—each with their own potential to revolutionize care for patients. #TeamNatera includes clinicians, scientists, biostatisticians, researchers, and laboratory professionals from around the world. Our diverse teams blend a passion for patients with deep clinical, scientific, and technological roots. Natera’s tests are validated by more than 100 peer-reviewed publications that demonstrate high accuracy.

Similar Jobs

MMR Group Logo MMR Group

BIOPHARMACEUTICAL – Senior CQV Engineer

Energy • Chemical • Industrial • Renewable Energy
In-Office
San Francisco, CA, USA
4332 Employees

MMR Group Logo MMR Group

PHARMACEUTICAL – JR. CQV ENGINEER

Energy • Chemical • Industrial • Renewable Energy
In-Office
San Francisco, CA, USA
4332 Employees
80K-115K Annually

MMR Group Logo MMR Group

PHARMACEUTICAL – JR. CQV ENGINEER

Energy • Chemical • Industrial • Renewable Energy
In-Office
Los Angeles, CA, USA
4332 Employees
80K-115K Annually

MMR Group Logo MMR Group

PHARMACEUTICAL – JR. CQV ENGINEER

Energy • Chemical • Industrial • Renewable Energy
In-Office
Carlsbad, CA, USA
4332 Employees
80K-115K Annually

Similar Companies Hiring

Formation Bio Thumbnail
Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
New York, NY
150 Employees
SOPHiA GENETICS Thumbnail
Software • Healthtech • Biotech • Big Data • Artificial Intelligence
Boston, MA
450 Employees
Pfizer Thumbnail
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
New York, NY
121990 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account