Medtronic, a leader in global healthcare technology, offers a unique opportunity for aspiring professionals to join its dynamic team as an Apprentice in Regulatory Affairs. This role, based in Gurgaon, Haryana, India, provides a blend of hands-on experience, professional growth, and a chance to contribute to Medtronic’s mission of alleviating pain, restoring health, and extending life.
About Medtronic
With a team of over 90,000 passionate employees worldwide, Medtronic is dedicated to solving humanity’s most challenging health problems. From innovative R&D labs to efficient factory floors, Medtronic transforms ambitious ideas into practical healthcare solutions. The company thrives on a culture of experimentation, creativity, and collaboration to engineer the extraordinary.
Responsibilities in the Role
As an Apprentice in Regulatory Affairs, you will play a crucial role in supporting the Regulatory Affairs Specialist (RAS) and ensuring compliance with regulatory standards. Your responsibilities will include:
- Assisting RAS in implementing regulatory compliance systems.
- Downloading Standard Technical Documentation (STED) from Agile/Insight for GSR102 submissions.
- Naming, compiling, and organizing dossiers as per the checklist on the SUGAM platform.
- Maintaining an accurate track of received and pending documents.
- Uploading finalized documents for SUGAM submissions under RAS guidance.
- Archiving submitted dossiers and maintaining organizational records for all Operational Units (OUs).
- Providing administrative support for upcoming GSR 102 product submissions.
This role promises a combination of practical experience, document management expertise, and the opportunity to develop a deep understanding of regulatory compliance in the healthcare industry.
Qualifications and Skills
To excel in this role, candidates should possess the following:
Qualifications:
- A degree in a relevant field such as Pharmacy, Life Sciences, or a related discipline is preferred.
Skills:
- Strong organizational skills to manage documentation and track submissions.
- Attention to detail for precise dossier compilation and archival.
- Familiarity with regulatory platforms like SUGAM or Agile/Insight is an advantage.
- Effective communication skills to collaborate with team members and stakeholders.
- A proactive mindset and willingness to learn new systems and processes.
