Regulatory Affairs Lead.

vivimed labs

12–18 Years

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Position: Regulatory Affairs Lead
Department: Regulatory Affairs
📍 Location: Genome Valley, Hyderabad
🎓 Qualification: B.Pharm / M.Pharm
💼 Experience: 12–18 Years
🕒 Employment Type: Full-Time

FYND Talent Solutions is pleased to share an exciting opportunity for experienced Regulatory Affairs professionals looking to lead global filing strategies across regulated and emerging markets.

Key Responsibilities:
* Lead regulatory strategy and filing execution across Europe, Canada, and emerging markets.
* Drive dossier planning, submissions, reviews, and lifecycle management.
* Manage regulatory responses, renewals, variations, and country-specific requirements.
* Collaborate with R&D, QA, QC, Manufacturing, and Business teams.
* Ensure compliance with global regulatory guidelines and submission timelines.

Required Skills:
* Strong experience with regulatory filings for Europe and emerging markets.
* Expertise in dossier strategy, submissions, and lifecycle management.
* Proven leadership and team management capabilities.
* Strong understanding of global regulatory requirements and compliance.
* Excellent communication, coordination, and stakeholder management skills.

Disclaimer: FYND Talent Solutions is an independent recruitment platform. This job is shared for informational purposes only and is not an official communication from the hiring company unless explicitly stated.

Apply Now-careers@vivimedlabs.com

To apply for this job email your details to fyndtalentsolutions@gmail.com

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