Are you passionate about medical device regulations and looking for an exciting career opportunity in Mohali, India? RegDesk, a leading name in the medical device regulatory domain, is hiring a Regulatory Intelligence Associate to join their on-site team. If you have expertise in global medical device registration, regulatory submissions, and a knack for staying ahead of regulatory updates, this could be your dream job!
Here’s everything you need to know about this opportunity, including how to apply, qualifications, and why this role stands out in the medical device industry.
Job Overview: Regulatory Intelligence Associate at RegDesk
- Position: Regulatory Intelligence Associate
- Location: Mohali, India (On-Site Only)
- Company: RegDesk
RegDesk is a trailblazer in providing regulatory intelligence and solutions for medical device companies worldwide. This role offers a chance to work in a dynamic environment, collaborating with international affiliates and driving compliance in the ever-evolving medical device regulatory landscape.
Why Join RegDesk? A Leader in Medical Device Regulatory Intelligence
RegDesk is renowned for its cutting-edge regulatory management software and expertise in navigating complex global regulations. By joining their team in Mohali, you’ll contribute to ensuring medical device companies meet international standards, making a real impact on healthcare innovation. This isn’t just a job—it’s a chance to grow with a company that’s redefining regulatory intelligence in the medical device domain.
Key Responsibilities: What You’ll Do as a Regulatory Intelligence Associate
As a Regulatory Intelligence Associate, you’ll be at the forefront of regulatory compliance and submissions. Here’s what the role entails:
- Global Medical Device Registration: Prepare and manage submissions for international medical device approvals.
- Regulatory Expertise: Stay updated on global medical device regulations and ensure compliance with the latest standards.
- Data Summarization: Analyze and summarize regulatory data clearly for stakeholders.
- Regulatory Law Synthesis: Source and synthesize regulatory laws from various regions.
- Track Updates: Monitor changes in regulatory frameworks and provide timely insights.
- Collaboration: Work closely with international affiliates and the regulatory intelligence team to streamline processes.
This role demands precision, proactive thinking, and strong communication skills—perfect for anyone passionate about medical device regulations!
Qualifications: Do You Have What It Takes?
RegDesk is looking for candidates who bring both experience and enthusiasm to the table. Check if you meet these requirements:
- Education: M.Pharm RA/MD or Masters in Medical Devices (or equivalent).
- Experience: 1-5 years in medical device regulations or submissions.
- Skills:
- Expertise in global medical device registration and submissions.
- Deep knowledge of regulatory compliance and international regulations.
- Ability to summarize complex regulatory data effectively.
- Mindset: Detail-oriented, proactive, and ready to collaborate with a global team.
If you’ve worked on regulatory submissions or tracked updates like MDR (Medical Device Regulation), you’re already a step ahead!
Location: Why Mohali, India?
This is an on-site only position based in Mohali, a thriving hub for technology and innovation in India. Known for its growing job market and vibrant community, Mohali offers a fantastic work-life balance. Joining RegDesk here means being part of a local team with a global impact.
How to Apply: Don’t Miss Out!
Ready to take the next step in your regulatory career? Send your resume to:
- Email: apurva.bhardwaj@regdesk.co / sandeep@regdesk.co
- Subject Line Suggestion: “Application: Regulatory Intelligence Associate – [Your Name]”
Applications are open now, so act fast—this is a hot opportunity in the medical device job market!
