natera

Design Transfer Manager

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At a Glance

Location
United States
Employment
employment_required
Experience
6–8 years
Posted
2026-02-09T15:31:16-05:00

Key Requirements

Required Skills

Data Analysis

Certifications

  • GMP

Domain Knowledge

  • Biotech
  • Manufacturing
  • Medical
  • Regulatory

Requirements

Maintain audit-ready documentation for internal and external inspections

Advanced degree in molecular biology or related discipline. PhD is preferred; Master’s or bachelor's with equivalent industry experience considered

6-8 years of post-PhD biotech industry experience or >10 years of post BS/MS biotech experience

At least 4 years managing a team of scientists and research associates

Compensation & Benefits

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.

Responsibilities

We are seeking an experienced

Design Transfer Manager

to lead and coordinate the transfer of an early cancer detection assay from R&D into Operations. This role will plan, execute, implement, and document all design transfer activities for a next generation sequencing (NGS) IVD/PMA assay under Quality Systems Regulations and Design Control. The role will be managing a multidisciplinary group of scientists, providing technical mentorship, and ensuring timely delivery of project milestones. The manager also will ensure robust processes, documentation, compliance with regulatory requirements, and cross-functional alignment.

Design Transfer Leadership

Responsible for planning and managing activities and studies from late-stage development to launch

Team

Monitor performance, deliver timely feedback, and support career development of direct reports

Foster a culture of accountability, safety, compliance, and continuous learning

Cross-Functional Collaboration

Partner with Operations, R&D, Product Management, Quality Assurance, and Regulatory Affairs to ensure seamless design transfer and product launch

Serve as the primary liaison between development and operations, ensuring knowledge transfer and training of operational staff

Incorporate operational feedback into design improvements and refinements