Regulatory Affairs Specialist (Pharm‑D, 3+ yrs experience)
Recruit AI · Lahore
Job description
About the role
The Regulatory Affairs Specialist will manage regulatory processes, prepare and submit documentation to health authorities, and ensure product compliance throughout its lifecycle.
Key responsibilities
- Prepare, compile and submit regulatory dossiers to health authorities in line with regulations and company policies.
- Maintain and update regulatory submission tracking systems and document management platforms.
- Interact with health authorities, respond to queries and provide required documentation.
- Support quality assurance by reviewing regulatory documents for completeness and accuracy.
- Coordinate with R&D, quality control and manufacturing to gather information for submissions.
- Monitor regulatory changes and update internal procedures accordingly.
Required profile
- Pharm‑D degree.
- Minimum three years of regulatory affairs experience in the pharmaceutical or nutraceutical industry.
Required skills
- Proficiency with regulatory submission software.
- Experience using document management systems for controlled record keeping.
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Published 5 hours ago
Expires 1 month from now
2 views · 0 interested
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Lahore