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.
If interested, please share your updated resume at
hr@dawarconsulting.com
/
lakshmi@dawarconsulting.com
.