Posted 7 hours ago 55 views Report Job
PKR. 45,000 - 60,000/Month
Regulatory Documentation Management
- Prepare, review, and submit regulatory documents for product registrations and variations.
- Ensure documentation accuracy and compliance with regulatory standards.
- Coordination with Regulatory Authorities
- Communicate effectively with regulatory authorities, including DRAP, to facilitate approvals and address queries.
- Stay updated on regulatory changes affecting the industry.
Post-Registration Activities
- Manage post-registration variations and address deficiencies.
- Ensure timely responses to regulatory letters.
Interdepartmental Collaboration
- Collaborate with various departments within DRAP and the company.
- Ensure smooth communication and regulatory compliance.
- Central Research Fund (CRF) Coordination
- Coordinate the CRF approval process with DRAP.
- Implement strategies to expedite CRF approvals.
Compliance Oversight
- Ensure all regulatory activities align with current requirements.
- Monitor and maintain regulatory compliance processes.
Technical Skills
Proficiency in DRAP portal operations.
Strong Microsoft Office skills, including Excel and Word.
Job Details
Industry:
Functional Area:
Total Positions:
1 Post
Job Shift:
First Shift (Day)
Job Location:
Gender:
Male
Minimum Education:
Bachelors
Career Level:
Experienced Professional
Minimum Experience:
2 Years
Apply Before:
Dec 01, 2024
Posting Date:
Nov 15, 2024
Welmark Pharmaceuticals
Healthcare / Hospital / Medical · 51-100 employees - Rawalpindi
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