(Urgent Search) Head- Regulatory Affairs
18 hours ago
About Our Client
This opportunity is with a global MNC recognized for its contributions to the life sciences industry.
Job Description
1. Regulatory Strategy Development- Define and drive the regulatory vision and strategy for CRM products, aligning with company's business goals.
2. Leadership and Team Management- Build and lead a high-performing regulatory team, fostering a culture of excellence, innovation, and accountability.
3. Regulatory Submissions and Approvals- Oversee the preparation, submission, and maintenance of regulatory dossiers.
4. Compliance Oversight- Ensure that the equipments meet the required regulatory standards as set by CDSCO.
5. Cross-functional Collaboration- Partner with Govt affairs, Quality, Business Areas, Marketing and Legal team to integrate regulatory requirements.
The Successful Applicant
Education:
- Bachelor's or Master's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or related fields. Advanced degrees (e.g., MBA, Ph.D.) are an advantage. *
Experience:
- Minimum 10-15 years of regulatory experience (preferably in IVD), with at least 5 years in a leadership role.
- In-depth understanding of India's Medical Devices Rules, 2017, CDSCO guidelines, and applicable standards (e.g., ISO 13485, ISO 14971).
- Familiarity with global regulations like FDA (21 CFR), EU MDR/IVDR, and other regional requirements for international market access.
- Proven track record of managing regulatory strategies for medical device company.
- Exceptional leadership, communication, and negotiation skills.
- Strategic thinker with a proactive approach to problem-solving.
- Ability to navigate complex regulatory landscapes while maintaining agility
What's on Offer
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Leadership opportunity to head regulatory affairs for imports, driving compliance and approvals for advanced life sciences technologies.
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Strategic exposure to regulatory authorities and global stakeholders, influencing market entry and product availability.
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Platform to shape and strengthen the organization's regulatory framework while working with cutting-edge healthcare innovations.
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