Regulatory Affairs Manager – Medical Devices / IVD

Dawar Consulting; Indianapolis (IN); Hybrid; USD 100,000 - 135,000; Full time

Benefits offered by this job

Medical

Paid Sick Leave

401 (k)

Job summary

Dawar Consulting in Indianapolis, IN is seeking a Regulatory Affairs Manager for Medical Devices/IVD on a long-term contract with hybrid work options (2 days remote/3 onsite).

Responsibilities include leading regulatory submissions, US 510(k)/PMA, EU IVDR, and coordinating global regulatory strategies with cross-functional teams.

Qualifications

• 5+ years of regulatory affairs experience in medical devices or IVD.
• Experience with submissions and regulatory strategy.
• Strong project management and stakeholder management skills.

Responsibilities

• Lead regulatory submission activities for medical device and IVD products.
• Support U.S. regulatory pathways including 510(k), PMA, and FDA Pre-Submission activities.
• Support European regulatory activities, including IVDR requirements.
• Contribute to regulatory strategies and submission planning for new and existing products.

Skills

Regulatory affairs

Project management

Stakeholder management

Job description

Regulatory Affairs Manager – Medical Devices / IVD

Indianapolis, United States | Posted on 09/16/2026

Our client, a world leader in biotechnology and life sciences, is looking for a “Regulatory Affairs Manager – Medical Devices / IVD”.

Location: Indianapolis, IN (Hybrid - 2 Days Remote/ 3 Days Onsite)

Job Duration: Long-Term Contract (Possibility Of Extension)

Company Benefits: Medical, Paid Sick Leave, 401 (k)

About the Role

You will work closely with cross-functional teams to support regulatory submissions, product compliance, and regulatory strategies across key global markets, including the United States, European Union, and China. The ideal candidate will have hands-on medical device or IVD regulatory experience and a strong understanding of regulatory pathways involving software, hardware, systems, and cybersecurity.

Key Responsibilities

• Lead and coordinate regulatory submission activities for medical device and IVD products.
• Support U.S. regulatory pathways including 510(k), PMA, and FDA Pre-Submission activities.
• Support European regulatory activities, including IVDR requirements.
• Contribute to regulatory strategies and submission planning for new and existing products.
• Compile, review, and coordinate technical and regulatory documentation.
• Partner with engineering, software, hardware, quality, product development, and other cross-functional teams.
• Manage activities across assigned product portfolios and identify and coordinate with key stakeholders.

Required Qualifications

• 5+ years of relevant regulatory affairs experience;
• Experience with medical device regulatory submissions and/or regulatory strategy.
• Strong project management and stakeholder management skills.

Preferred Skills

• Experience supporting both new product development and post-market/on-market compliance.
• Experience with global regulatory strategies and technical documentation.

Regulatory Submission, Medical Device/IVD, 510(k)/PMA/Pre-Sub/IVDR