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Technology Transfer Scientist Jobs (NOW HIRING)

Natera

Design Transfer Scientist

San Carlos, CA · Hybrid

Join Natera's Bio Development Team as a Design Transfer Scientist to lead the transition of our ... technologies * Strong operational knowledge of Design Controls, Quality Management Systems (QMS ...

Natera

Design Transfer Scientist

San Carlos, CA · On-site

$116K - $145K/yr

Join Natera's Bio Development Team as a Design Transfer Scientist to lead the transition of our ... technologies * Strong operational knowledge of Design Controls, Quality Management Systems (QMS ...

Actalent

Tech Transfer Lead

Wilson, NC

Bachelor's degree in science, engineering, or equivalent experience. * 3-5 years of experience in product development, process scale-up, or technology transfer. * Minimum 2-3 years of experience ...

New

Phlow Corp.

Sr. Director, Tech Transfer

Richmond, VA · On-site

$190K - $230K/yr

This role requires strong collaboration with Manufacturing Science & Technology (MS&T), Operations ... Requirements: Tech Transfer Leadership: * Lead the planning and execution of technology transfer ...

FUJIFILM Biotechnologies

... in life sciences or engineering, with 6 years of direct experience, OREquivalent Military ... tech transfer experienceCore competenciesTechnical depth with practical, hands-on problem ...

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Technology Transfer Scientist information

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$50.5K

$111.3K

$137.5K

How much do technology transfer scientist jobs pay per year?

As of Aug 12, 2026, the average yearly pay for technology transfer scientist in the United States is $111,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,500.00 and $137,000.00 per year, depending on experience, location, and employer.

What is the difference between Technology Transfer Scientist vs Research Scientist?

AspectTechnology Transfer ScientistResearch Scientist
CredentialsTypically requires a PhD in a relevant scientific field, with experience in intellectual property and licensingUsually holds a PhD or Master's degree in a scientific discipline, focused on experimental research
Work EnvironmentWorks in industry or university tech transfer offices, collaborating with R&D and legal teamsPrimarily in laboratories or academic settings, conducting experiments and data analysis
Employer & Industry UsageCommon in biotech, pharma, and university tech transfer officesFound in academia, research institutes, and corporate R&D departments

While both roles require advanced scientific credentials, the Technology Transfer Scientist focuses on commercializing research, licensing, and intellectual property management, whereas the Research Scientist concentrates on conducting experiments and generating new scientific knowledge.

More about Technology Transfer Scientist jobs
What cities are hiring for Technology Transfer Scientist jobs? Cities with the most Technology Transfer Scientist job openings:
What states have the most Technology Transfer Scientist jobs? States with the most job openings for Technology Transfer Scientist jobs include:
What job categories do people searching Technology Transfer Scientist jobs look for? The top searched job categories for Technology Transfer Scientist jobs are:
Technology Transfer Scientist jobs near you
Infographic showing various Technology Transfer Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $111,343 per year, or $53.5 per hour.

Design Transfer Scientist

Natera

San Carlos, CA • Hybrid

Full-time

Re-posted 20 days ago

Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

59th of 120 rated laboratories

Job description

POSITION SUMMARY: 

Join Natera's Bio Development Team as a Design Transfer Scientist to lead the transition of our market-leading In Vitro Diagnostic (IVD) Next-Generation Sequencing (NGS) assays from R&D into scalable clinical operations. This role bridges molecular biology with manufacturing execution, requiring an ownership mindset to build robust, compliant production pipelines that directly impact patient care. The ideal candidate combines rigorous laboratory execution with robust data analysis and precise technical documentation to deliver production-ready protocols. 

PRIMARY RESPONSIBILITIES: 

  • Own and execute process validations, stability studies, and study protocols, translating raw experimental data into final technical reports
  • Support test method development, characterization, and Test Method Validation (TMV) to generate accurate manufacturing specifications
  • Lead risk management activities, including FMEAs, to identify and mitigate potential product risks early
  • Manage change control workflows to evaluate and document the operational impact of design changes on on-market products
  • Investigate product or process deviations, perform rigorous root cause analysis, and implement sustainable Corrective and Preventive Actions (CAPA)
  • Coordinate with multiple internal groups (automation engineering, laboratory operations, bioinformatics, statistics, project and product management) and serve as point person to ensure the successful identification and timely execution of projects
  • Partner directly with Supply Chain to establish reliable raw material and consumable pipelines
  • Communicate complex technical updates, data-driven proposals, and project status clearly to cross-functional stakeholders across the business

QUALIFICATIONS: 

  • BA/BS with 8+ years experience, MS with 5+ years or PhD with 3+ years experience in assay development and automation for the life science industry 
  • Experience with automated high-throughput NGS assays

KNOWLEDGE, SKILLS, AND ABILITIES: 

  • Hands-on expertise with Next-Generation Sequencing (NGS) workflows, including DNA/RNA extraction, targeted enrichment, or library preparation
  • Direct experience executing molecular biology techniques such as nucleic acid extraction, PCR, NGS library preparation, and hybrid capture technologies
  • Strong operational knowledge of Design Controls, Quality Management Systems (QMS), and regulatory standards (FDA, ISO 13485, CLSI) within regulated clinical diagnostic manufacturing environments
  • Proven track record authoring comprehensive study plans, validation protocols, and technical reports
  • Proficiency in statistical analysis with experience using specialized software such as Minitab or JMP
  • Prior experience in IVD product development, scale-up, manufacturing, or commercial Quality Control (QC) is highly preferred
  • Experience operating or optimizing automated liquid handling platforms (such as Hamilton or Tecan) is preferred
  • Exceptional organization skills to manage complex validation timelines and drive technical projects to successful completion

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