Siza Internationals Pvt. Ltd.
Verified
Manager Regulatory Affairs
- Lahore
- Full Time
- Travel required
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Browse live jobsThe essentials
- Experience7 Years
- Career levelNon-Managerial
- ShiftMorning Shift
- EducationBachelor's degree in Pharmacy, Pharmaceutics, Pharmaceutical Sciences, Chemistry, or related field; or equivalent experience in pharmaceutical regulatory affairs.
What you’ll be doing
Company: Siza Internationals Pvt. Ltd.
Location: Lahore, Pakistan (On-site)
Employment Type: Full-Time
Shift: Morning Shift
Role Summary:
Location: Lahore, Pakistan (On-site)
Employment Type: Full-Time
Shift: Morning Shift
Role Summary:
- Manage licensing and product registration activities for pharmaceutical products.
- Prepare and maintain regulatory documentation for registrations, renewals, and regulatory filings.
- Prepare and submit registrations for new products and new molecular entities.
- Manage new plant licensing processes and prepare required submissions.
- Correspond with DRAP for submissions, approvals, renewals, queries, and other regulatory matters.
- Ensure compliance with DRAP regulations and applicable pharmaceutical legislation.
- Produce regulatory writing and technical documents with accuracy and clarity.
What we’re looking for
Must-have:
- 5 to 7 years of regulatory affairs experience in the pharmaceutical industry.
- Strong knowledge of DRAP regulations and pharmaceutical legislation in Pakistan.
- Experience in new plant licensing and product registration processes.
- Regulatory writing, documentation, and submission preparation skills.
- Ability to manage correspondence and interactions with regulatory authorities (DRAP).
- Attention to detail and ability to maintain regulatory records and timelines.
Perks & benefits
- Incentive Bonus
About Us
Siza International (Pvt.) Ltd. is one of Pakistan's leading pharmaceutical manufacturers, established in 1985. The company is committed to delivering high-quality, affordable healthcare solutions through continuous innovation, advanced manufac
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