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Ivd Project Manager Jobs (NOW HIRING)

Meridian Bioscience International Limited

Job Summary The Project Manager leads cross-functional new product development projects for in vitro diagnostic (IVD) assays and diagnostic instrument systems in an FDA-regulated medical device ...

CorDx

Senior Project Manager (Atlanta)

Atlanta, GA · On-site

We are seeking a highly motivated and experienced Senior Project Manager to lead and support cross-functional projects within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This ...

CorDx

Senior Project Manager (Atlanta)

Atlanta, GA · On-site

We are seeking a highly motivated and experienced Senior Project Manager to lead and support cross-functional projects within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This ...

CorDx

Senior Project Manager (Atlanta)

Atlanta, GA

We are seeking a highly motivated and experienced Senior Project Manager to lead and support cross-functional projects within our In Vitro Diagnostics (IVD) and broader diagnostics portfolio. This ...

CorDx

Regulatory Affairs Manager - IVD

San Diego, CA · On-site

Demonstrated ability to manage regulatory projects independently and work effectively across ... Direct experience with IVD products and FDA 510(k) submissions. * Experience serving as the primary ...

CorDx

Regulatory Affairs Manager - IVD

San Diego, CA

Demonstrated ability to manage regulatory projects independently and work effectively across ... Direct experience with IVD products and FDA 510(k) submissions. * Experience serving as the primary ...

IQVIA LLC

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

## Clinical Project Manager- IVDApplylocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1556598**Job Summary**The Project Lead is ...

IQVIA, Inc.

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

CorDx

Regulatory Affairs Manager - IVD

San Diego, CA · On-site

Demonstrated ability to manage regulatory projects independently and work effectively across ... Direct experience with IVD products and FDA 510(k) submissions. * Experience serving as the primary ...

CorDx

Regulatory Affairs Manager - IVD

San Diego, CA · On-site

Demonstrated ability to manage regulatory projects independently and work effectively across ... Direct experience with IVD products and FDA 510(k) submissions. * Experience serving as the primary ...

CorDx

Regulatory Manager- IVD and 510(k)

San Diego, CA · On-site

$90K - $150K/yr

Regulatory Manager - IVD and 510(K) Location: Onsite - San Diego Salary Range: $90000-$150000 ... projects to ensure compliance from concept to commercialization. • Review and provide input on ...

CorDx

Regulatory Manager- IVD and 510(k)

San Diego, CA

$90K - $150K/yr

Regulatory Manager - IVD and 510(K) Location: Onsite - San Diego Salary Range: $90000-$150000 ... Provide regulatory guidance on product development projects to ensure compliance from concept to ...

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

IQVIA

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

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How much do ivd project manager jobs pay per year?

As of Sep 10, 2026, the average yearly pay for ivd project manager in the United States is $96,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $113,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Ivd Project Manager job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.

Project Manager

Cincinnati, OH • On-site

Meridian Bioscience International Limited
See more jobs at Meridian Bioscience International Limitedexternal

Other

Posted 5 days ago

Job description

About Meridian

Meridian Bioscience is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products. We are dedicated to developing and delivering better solutions that give answers with speed, accuracy and simplicity that are redefining the possibilities of life from discovery to diagnosis. We are looking for talented and passionate individuals who help drive our vision.Our innovative culture will allow interested candidates to discover and create, through collaboration, cutting-edge solutions to tough problems.

Job Summary

The Project Manager leads cross-functional new product development projects for in vitro diagnostic (IVD) assays and diagnostic instrument systems in an FDA-regulated medical device environment. This role is accountable for project planning and execution from concept through launch, with emphasis on design control compliance, schedule, risk, resources, budget, and clear decision-making. The Project Manager partners with R&D, Regulatory Affairs, Quality, Clinical Affairs, Operations, Marketing, and external development partners to achieve business and product objectives. The position may be based locally in Cincinnati or performed remotely, with travel as required to support project teams and key milestones.

Key Duties
  • Partner with R&D, Operations, Regulatory Affairs, Quality, Clinical Affairs, Finance, and Marketing and others to define project scope, goals and deliverables as well as successfully manage projects
  • Develops accurate, achievable project plans and timeline, consistently communicating the plans with team members and the leadership team
  • Drives team ownership and commitment to project plans and recommends changes when necessary to meet project outputs
  • Tracks and communicates project performance, specifically to analyze successful completion of short- and long-term goals
  • Ensures on-time completion of tasks as required by the project and/or company procedures
  • Facilitates cross-functional project team meetings
  • Other duties as assigned
Qualifications
  • Bachelor’s degree in science, engineering or business administration or related field required; advanced degree preferred.
  • At least 5 years of project management experience leading cross-functional product development projects.
  • Direct experience managing FDA-regulated medical device product development projects.
  • Working knowledge of medical device design control requirements and product development processes, including design planning, design reviews, risk
  • Preferred: Experience with in vitro diagnostic (IVD) products, including assay and/or diagnostic instrument development.
  • Preferred: Experience working within Quality Management Systems compliant with FDA 21 CFR Part 820 and applicable medical device regulations.
  • Preferred: Project management qualification (PMP) or equivalent.
  • Demonstrated Project Management skills with proven record of practical project management experience preferably in the diagnostic or related biotechnical field
  • Demonstrate successful management of product(s) from concept to launch
  • Must have the ability to perform critical path identification
  • Excellent problem-solving skills. Must be a self-starter, detail oriented and able to prioritize and balance workloads and timelines and ability to work on multiple projects simultaneously
  • Must be able to work independently as well as collaboratively with peers and colleagues in a cross functional setting
  • Must be well organized and have the ability to meet strict deadlines and perform under pressure in a fast-paced work environment
  • Excellent interpersonal, organizational and written and oral communication skills
  • Basic understanding of device development, engineering, and manufacturing activities is a plus
  • 20% travel
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