
Regulatory Affairs Officer
11 hours ago
Responsibilities
- Prepare and submit CTD / ACTD dossiers for international markets, handle queries and follow up till registration.
- Ensure that all product registrations and submissions comply with applicable laws, guidelines, and industry standards.
- Prepare other supporting regulatory documents as required by foreign regulatory agencies.
- Collaborate with QA, QC, Production, and Export departments to gather accurate and up-to-date technical and manufacturing data for dossier completion.
- Maintain clear and continuous communication with international stakeholders regarding dossier status and updates.
- Maintain accurate and updated records of all submitted dossiers, correspondence, and regulatory approvals.
Qualifications
- Education: Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences.
- 6 months to 1 year in regulatory affairs for the pharmaceutical industry.
- Proficiency in CTD format preparation and dossier compilation.
- Excellent written and verbal communication skills.
- Ability to work effectively under tight deadlines
Location:
18km Multan Road Lahore Pakistan
Email:
Job Type: Full-time
Pay: From Rs50,000.00 per month
Application Question(s):
- How much Relevant experience you have in Regulatory Affairs.
Education:
- Bachelor's (Preferred)
Location:
- Lahore (Preferred)
Work Location: In person
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