Medtronic is hiring for the position of Associate Regulatory Affairs Specialist in Gurgaon, Haryana. This is an excellent opportunity for candidates looking to start a career in Regulatory Affairs, medical devices, healthcare technology, and regulatory compliance.
The official Medtronic job description classifies this as an entry-level individual contributor position and specifically states that 0 years of experience is required. Candidates need a Baccalaureate/Bachelor’s degree along with the theoretical knowledge required to perform regulatory affairs activities.
The selected candidate will support regulatory submissions, license renewals, registrations, labeling compliance, regulatory documentation, audits and inspections, and other activities required to maintain compliance with applicable regulatory requirements.
Key Responsibilities
As an Associate Regulatory Affairs Specialist at Medtronic, the selected candidate may be responsible for:
- Coordinating and preparing documentation packages for regulatory submissions.
- Supporting documentation required for internal audits and regulatory inspections.
- Compiling materials required for regulatory submissions.
- Assisting with license renewals and annual registrations.
- Reviewing and recommending labeling changes to maintain regulatory compliance.
- Supporting regulatory requirements related to manufacturing and marketing activities.
- Assisting with clinical protocol-related regulatory compliance.
- Monitoring and improving regulatory tracking and control systems.
- Staying updated with regulatory procedures, requirements, and changes.
- Supporting interactions with regulatory agencies on defined matters.
- Contributing to regulatory strategies for obtaining clinical trial application approvals.
- Working with internal stakeholders to gather, verify, and communicate regulatory information.
- Supporting smaller and less complex regulatory projects under supervision.
Qualifications & Eligibility
According to the official job description, candidates should meet the following requirements:
Education: Baccalaureate/Bachelor’s degree or equivalent qualification.
Experience: 0 years of experience required, making this an entry-level opportunity suitable for eligible fresh graduates.
Skills Relevant to the Role
Candidates interested in this Medtronic Regulatory Affairs job can benefit from knowledge of regulatory documentation, medical device regulations, regulatory submissions, quality and compliance requirements, labeling regulations, clinical trial applications, document control, regulatory intelligence, and effective stakeholder communication.
Freshers should emphasize relevant academic projects, internships, regulatory affairs certifications, medical-device knowledge, documentation skills, and familiarity with applicable regulatory frameworks on their resumes.
Why Join Medtronic?
Medtronic is a global healthcare technology company focused on developing medical technologies that help alleviate pain, restore health, and extend life. The organization operates across more than 150 countries and reports a global workforce of more than 95,000 employees.
Benefits highlighted in the job posting include:
- Competitive salary and compensation.
- Flexible benefits package.
- Career development and learning opportunities.
- Exposure to global healthcare technology and regulatory operations.
- Flexible work arrangement for this position.
- Eligibility for the Medtronic Incentive Plan (MIP).
- Opportunity to develop a career within the medical-device and healthcare technology industry.
How to Apply
