Key skills
Sketch
About this role
Medara is launching as a professional intelligence infrastructure for regulated industries, seeking experienced professionals in the FDA regulated ecosystem. The role involves engaging with companies directly for contract projects, fractional roles, and full-time opportunities in the medical device and healthcare sectors.
Responsibilities:
- Create and build your Medara profile around your real work history, credentials, and specializations
- Submit your profile for review by the Medara team
- Join the platform ahead of the Summer 2026 public launch with first wave visibility when companies start searching
- Maintain quality and credential integrity through the review process
- Get direct visibility into contract projects, fractional and part-time engagements, and full-time roles
- Build your credibility and visibility across the regulated industry ecosystem with a verified profile
- Engage directly with companies without recruiter gatekeeping or generic platform markups
Requirements:
- Experience in the FDA regulated industry ecosystem
- Demonstrated execution history in regulated work
- Ability to take products from napkin sketch to design freeze
- Experience building design history files that hold up under regulatory scrutiny
- Ability to diagnose and fix complex issues in product development
- Experience in Healthcare, MedTech, Biotech, Pharma, and Life Sciences
- Willingness to create and build a Medara profile around real work history, credentials, and specializations
- Ability to engage directly with companies without middlemen or recruiter markups
- Experience as an independent consultant or solo operator
- Experience as a fractional or interim expert
- Experience running a boutique consultancy or specialized firm
- Early career professionals serious about building a credential backed profile