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Ivd Product Manager Jobs (NOW HIRING)

Natera

Design Transfer Scientist

San Carlos, CA · Hybrid

... IVD) Next-Generation Sequencing (NGS) assays from R&D into scalable clinical operations. This role ... Lead risk management activities, including FMEAs, to identify and mitigate potential product risks ...

CorDx

Regulatory & Compliance Specialist

San Diego, CA · On-site

$90K - $95K/yr

... 510K) for IVD products. Requirements * Education: * Bachelor's degree in a related field (e.g., Life Sciences, Engineering, Regulatory Affairs, Quality Management) or equivalent experience.

BioFire Defense, LLC

Product Manager

Salt Lake City, UT · On-site

$110 - $150/hr

Description of Responsibilities Position Summary The Product Manager is a key marketing role within ... Experience working within a regulated medical device or IVD environment. Working Conditions and ...

BioFire Defense

Product Manager

Salt Lake City, UT · On-site

$94K - $108K/yr

Description of Responsibilities Position Summary The Product Manager is a key marketing role within ... Experience working within a regulated medical device or IVD environment. Working Conditions and ...

CorDx

Regulatory & Compliance Specialist

San Diego, CA · On-site

$90K - $95K/yr

... 510K) for IVD products. Requirements * Education: * Bachelor's degree in a related field (e.g., Life Sciences, Engineering, Regulatory Affairs, Quality Management) or equivalent experience.

CorDx

Program Director

Atlanta, GA · On-site

Lead cross-functional program teams across R&D, Regulatory Affairs, Clinical, Quality, Operations, and Commercial to deliver IVD/diagnostic products from feasibility to launch. * Develop and manage ...

CorDx

Program Director

Atlanta, GA · On-site

Lead cross-functional program teams across R&D, Regulatory Affairs, Clinical, Quality, Operations, and Commercial to deliver IVD/diagnostic products from feasibility to launch. * Develop and manage ...

CorDx

Program Director

San Diego, CA · On-site

Lead cross-functional program teams across R&D, Regulatory Affairs, Clinical, Quality, Operations, and Commercial to deliver IVD/diagnostic products from feasibility to launch. * Develop and manage ...

CorDx

Quality Manager

Atlanta, GA · On-site

Implement, manage, and improve the company's quality management system, with a primary focus on IVD products and equipment. * Conduct internal audits, compile audit reports, perform problem analysis ...

Natera

Senior Research Associate

San Carlos, CA · On-site

$108K - $135K/yr

The Senior RA will be working with internal cross functional teams to develop IVD products. The ... Ability to manage multiple priorities in a fast-paced, dynamic environment and to collaborate cross ...

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Ivd Product Manager information

See salary details

$51.5K

$159.4K

$197K

How much do ivd product manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for ivd product manager in the United States is $159,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,000.00 and $197,000.00 per year, depending on experience, location, and employer.

What is an IVD product manager?

An IVD (In Vitro Diagnostics) Product Manager is responsible for overseeing the development, marketing, and lifecycle management of products used to diagnose diseases or conditions through biological samples, such as blood or tissue, outside the human body. They work closely with R&D, regulatory, marketing, and sales teams to ensure products meet market needs and comply with relevant regulations. IVD Product Managers play a critical role in defining product strategy, launching new products, and ensuring customer satisfaction in the diagnostics industry.

What are the key skills and qualifications needed to thrive as an IVD product manager, and why are they important?

To thrive as an IVD Product Manager, you need a strong background in life sciences, product management experience, and knowledge of regulatory requirements such as IVDR or FDA, often supported by a bachelor's or advanced degree in a scientific field. Familiarity with product lifecycle management tools, CRM software, and regulatory documentation systems is typically required. Excellent communication, cross-functional collaboration, and strategic thinking are standout soft skills for this role. These skills and qualifications ensure that products are effectively developed, compliant, and successfully brought to market in the highly regulated IVD industry.

What are some common challenges IVD product managers face when launching new diagnostic products?

IVD Product Managers often navigate complex regulatory requirements, such as FDA or CE approval, which can lengthen timelines and require thorough documentation. Another challenge is coordinating cross-functional teams, including R&D, quality assurance, and marketing, to ensure product specifications meet both clinical needs and compliance standards. Additionally, staying updated with rapidly evolving technologies and competitor products is essential to position the diagnostic solution effectively in the market. Effective communication and agile project management are key to overcoming these hurdles.

What is the difference between Ivd Product Manager vs Ivd Quality Assurance Specialist?

AspectIvd Product ManagerIvd Quality Assurance Specialist
CredentialsBachelor's degree in life sciences, engineering, or related field; often an MBA or product management certificationBachelor's degree in biology, chemistry, or related field; quality assurance certifications like CQE are common
Work EnvironmentCross-functional teams, product development, market analysisLaboratories, quality control departments, compliance testing
Industry UsageUsed in medical device companies, biotech firms, and diagnostics manufacturersCommon in manufacturing, biotech, and medical device companies ensuring product safety

The Ivd Product Manager focuses on product development, strategy, and market success, while the Ivd Quality Assurance Specialist ensures product safety, compliance, and quality standards. Both roles are essential in the IVD industry but serve different functions within the product lifecycle.

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Ivd Product Manager jobs near you
Infographic showing various Ivd Product Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $159,405 per year, or $76.6 per hour.

Design Transfer Scientist

Natera

San Carlos, CA • Hybrid

Full-time

Re-posted 15 days ago

Natera rating

7.8

Company rating: 7.8 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

56th of 121 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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