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In Vitro Diagnostics Jobs (NOW HIRING)

Hologic Inc.

Trusted by many of the world's leading laboratories, hospitals and healthcare institutions, Hologic's in-vitro diagnostics portfolio helps clinicians deliver more accurate and timely diagnoses ...

Fujirebio

Finishing Technician

Malvern, PA · On-site

$24.05/hr

Our in vitro diagnostics (IVD) technology powers critical tests across the globe's leading diagnostic platforms. We are a biomarker and diagnostic content provider that strengthens diagnostics for ...

EKF DIAGNOSTICS INC

Regulatory Affairs Associate

Boerne, TX · On-site

$25 - $30/hr

Two (2) years proven quality and/or regulatory experience, within the medical device, In vitro diagnostics, biotechnology and/or pharmaceutical industries. * Knowledge of ISO 9001, ISO 13485, and the ...

New

EKF DIAGNOSTICS INC

Regulatory Affairs Associate

Boerne, TX · On-site

$25 - $30/hr

Two (2) years proven quality and/or regulatory experience, within the medical device, In vitro diagnostics, biotechnology and/or pharmaceutical industries. * Knowledge of ISO 9001, ISO 13485, and the ...

New

CorDx

Regulatory & Compliance Specialist

San Diego, CA · On-site

$90K - $95K/yr

Ensure compliance with regulatory requirements for In Vitro Diagnostic products, FDA 21 CFR Part 820, ISO 13485. * Provide regulatory guidance during the product development process, ensuring that ...

CorDx

Regulatory & Compliance Specialist

San Diego, CA · On-site

$90K - $95K/yr

Ensure compliance with regulatory requirements for In Vitro Diagnostic products, FDA 21 CFR Part 820, ISO 13485. * Provide regulatory guidance during the product development process, ensuring that ...

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All JobsIn Vitro Diagnostics Jobs

In Vitro Diagnostics information

See salary details

$27.5K

$129.2K

$248.5K

How much do in vitro diagnostics jobs pay per year?

As of Jun 10, 2026, the average yearly pay for in vitro diagnostics in the United States is $129,175.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,500.00 and $142,000.00 per year, depending on experience, location, and employer.

What are In Vitro Diagnostics?

In Vitro Diagnostics (IVDs) are medical tests performed on samples taken from the human body, such as blood or tissue, to detect diseases, conditions, or infections. These tests are done outside the body, usually in a laboratory setting, and are essential for diagnosing illnesses, guiding treatment decisions, and monitoring overall health. IVDs include a wide range of products like blood glucose monitors, pregnancy tests, and tests for infectious diseases. They play a crucial role in modern healthcare by providing timely and accurate information to both patients and healthcare providers.

What are the key skills and qualifications needed to thrive as an In Vitro Diagnostics (IVD) Specialist, and why are they important?

To thrive as an In Vitro Diagnostics (IVD) Specialist, you need a solid background in biology, chemistry, or biomedical sciences, often supported by a relevant degree and laboratory experience. Familiarity with diagnostic instruments, quality control systems, and regulatory standards (such as ISO 13485 or FDA requirements) is typically required. Strong analytical thinking, attention to detail, and effective communication skills help professionals excel in troubleshooting and team collaboration. These abilities ensure accurate testing, compliance, and the reliable delivery of diagnostic information crucial for patient care.

What is the difference between In Vitro Diagnostics vs Medical Laboratory Technician?

AspectIn Vitro DiagnosticsMedical Laboratory Technician
Required CredentialsCertification in IVD technologies, relevant degreesAssociate degree in medical laboratory technology, certification
Work EnvironmentManufacturing labs, quality control, product developmentHospital, clinical, or diagnostic labs
Industry UsageManufacturers, biotech firms, diagnostic companiesHospitals, clinics, diagnostic laboratories

In Vitro Diagnostics professionals focus on developing, testing, and manufacturing diagnostic devices and kits, often working in labs or production settings. Medical Laboratory Technicians perform tests on patient samples in clinical labs. While both roles require laboratory skills and certifications, In Vitro Diagnostics specialists are more involved in product development and quality assurance, whereas Medical Laboratory Technicians focus on clinical testing and patient diagnostics.

What are some common challenges faced by professionals working in In Vitro Diagnostics (IVD) and how can they be addressed?

Professionals in In Vitro Diagnostics often face challenges such as keeping up with rapidly evolving technologies, ensuring strict regulatory compliance, and troubleshooting complex instrumentation. Staying updated through continuous education and active participation in industry forums can help manage technological changes. Collaborating closely with cross-functional teams—including R&D, regulatory affairs, and quality assurance—can ensure compliance and effective problem-solving, while regular hands-on training supports effective instrument maintenance and troubleshooting.
More about In Vitro Diagnostics jobs
What cities are hiring for In Vitro Diagnostics jobs? Cities with the most In Vitro Diagnostics job openings:
What states have the most In Vitro Diagnostics jobs? States with the most job openings for In Vitro Diagnostics jobs include:
What job categories do people searching In Vitro Diagnostics jobs look for? The top searched job categories for In Vitro Diagnostics jobs are:
In Vitro Diagnostics jobs near you
Infographic showing various In Vitro Diagnostics job openings in the United States as of June 2026, with employment types broken down into 97% Part Time, 2% Temporary, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $129,175 per year, or $62.1 per hour.
Scientific Project Manager (In Vitro Diagnostics)

Scientific Project Manager (In Vitro Diagnostics)

INBIOS INTERNATIONAL INC

Seattle, WA • Hybrid

$88K - $125K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description

Description

Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.


About Us

InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.

  • Location: Seattle, WA
  • Employment Type: Full-time | On-site (Will consider hybrid work situation once established in position.) 
  • Position Salary Range (Annual): $88,000.00 - $125,000.00
    The starting annual salary offered will depend on the selected applicant's job-related knowledge, skills, and experience and internal equity.
What You'll Do

We're looking for a Scientific Project Manager to lead in vitro diagnostic (IVD) development programs in infectious diseases and oncology. The role requires strong technical project management experience across immunodiagnostic and molecular diagnostic platforms, with responsibility for managing government-funded programs from early development through GMP manufacturing, clinical validation, and FDA and CE regulatory submission. 


Key Responsibilities
  • Lead end-to-end project management for IVD programs, from proposal development through regulatory clearance.
  • Manage government-funded contracts and grants, ensuring compliance with technical, financial, and reporting requirements.
  • Develop and maintain project timelines, budgets, resources, and risk mitigation plans.
  • Coordinate assay development and validation across immunochemistry platforms (e.g., lateral flow, ELISA) and molecular diagnostics (e.g., PCR, nucleic acid-based methods).
  • Support cGMP manufacturing, technology transfer, and validation activities.
  • Support FDA and CE/IVDR regulatory submissions in collaboration with regulatory and quality teams.
  • Serve as primary liaison with internal teams, CROs, clinical sites, academic collaborators, and government agencies.
  • Oversee preparation of project documentation, protocols, reports, and sponsor communications.
What We're Looking ForRequired Qualifications
  • MS or PhD in relevant life science, or equivalent experience.
  • Demonstrated experience managing diagnostic development programs in infectious diseases and/or oncology.
  • Proven experience managing federally funded research or product development programs.
  • Working knowledge of immunochemistry-based and molecular diagnostic assay development.
  • Experience in cGMP-regulated environments.
  • Familiarity with FDA regulatory pathways; CE/IVDR experience preferred.
  • Strong organizational, analytical, and communication skills.
Preferred Qualifications
  • Proficiency with project management tools (e.g., Microsoft Project).
  • Experience supporting FDA submissions and/or CE marking for IVDs.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • 2 weeks paid vacation + 11 paid holidays , which includes the annual "winter-break" week (Christmas Day through New Year's Day).
  • Supportive, mission-driven culture
Apply Today

Be part of a team that's advancing science and improving lives.

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