Are you looking to grow your career in the fast-paced regulatory affairs industry? RegDesk, a leader in regulatory information management software, is hiring! We’re seeking a Regulatory Intelligence Associate to join our Mohali team. This position is ideal for driven professionals with expertise in global regulatory affairs, particularly for medical devices. Discover the role’s details, responsibilities, qualifications, and application process below.
About RegDesk: Powering Regulatory Success with AI-Driven Insights
RegDesk offers an advanced AI-enabled regulatory information management software (RIMS) designed for medical device, diagnostic, and pharmaceutical industries. Our platform empowers regulatory affairs teams to prepare, manage, and publish international submissions efficiently, allowing them to achieve approval within unprecedented timelines. Join us in transforming regulatory processes and setting new standards in global regulatory affairs!
Responsibilities of a Regulatory Intelligence Associate at RegDesk
As a Regulatory Intelligence Associate, you’ll play a critical role in our regulatory affairs department, working to streamline international submissions and ensure compliance with changing global regulations. Your key responsibilities will include:
- Medical Device Regulations: Managing and submitting documentation for global medical device registration.
- Regulatory Intelligence: Gathering, synthesizing, and summarizing complex regulatory data to support regulatory submissions.
- Dossier Submission: Preparing and submitting detailed dossiers for international markets.
- Monitoring Regulatory Updates: Keeping track of regulatory updates and changes worldwide, ensuring the company remains compliant.
- International Communication: Engaging with international affiliates and the regulatory intelligence team to provide clear, concise regulatory insights.
- Data Simplification: Presenting critical regulatory data in an easy-to-understand format for stakeholders.
Qualifications: Are You the Right Fit?
RegDesk values expertise, a proactive attitude, and the ability to work independently while supporting global teams. The minimum qualifications include:
- Educational Requirements: M.Pharm or MSc in regulatory affairs or an equivalent field.
- Experience: 1–3 years in medical device regulations or submissions.
- Regulatory Expertise: Strong familiarity with international medical device regulations and dossier preparation for global markets.
Essential Skills for Success
To excel as a Regulatory Intelligence Associate at RegDesk, you should bring:
- Multitasking Ability: Ability to manage multiple projects and deadlines effectively.
- Team Collaboration: Strong teamwork skills, with a cheerful, proactive attitude.
- Proficiency in English: Strong communication skills in English, both written and spoken.
- Regulatory Knowledge: In-depth understanding of international regulatory laws and submission requirements for medical devices.
How to Apply for the Regulatory Intelligence Associate Role
If you’re ready to join the dynamic team at RegDesk, apply now! Send your resume to apurva.bhardwaj@regdesk.co with the subject line “Application for Regulatory Intelligence Associate-Medical Devices.”
