Kaizen Pharmaceuticals Hiring Manager Regulatory Affairs, Apply Now!
Kaizen Pharmaceuticals (Pvt.) Ltd., a company with an advanced, high-tech manufacturing facility setting new standards in pharmaceutical care, is seeking a highly skilled and experienced professional to join its team as Manager Regulatory Affairs. If you have strong expertise in pharmaceutical regulatory submissions, compliance, and authority coordination, this is your opportunity to contribute to continuous improvement, excellence, and better patient care.
Position Available
Manager Regulatory Affairs
Qualification: Pharm-D
Experience: 7–8 years of relevant experience in Regulatory Affairs
Key Responsibilities:
- Manage regulatory submissions, registrations, renewals, and variations.
- Ensure compliance with DRAP and export market regulations.
- Liaise with regulatory authorities and manage queries/follow-ups.
- Coordinate with QA, QC, R&D, Production, and other stakeholders.
- Monitor regulatory changes and ensure timely compliance.
- Maintain regulatory documentation and ensure audit readiness.
Why Join Kaizen Pharmaceuticals?
- Growing Company: Be part of a dynamic organization setting new standards in pharmaceutical quality and care.
- Career Growth: Opportunity to develop your career in regulatory affairs.
- State-of-the-Art Facility: Work in an advanced, high-tech manufacturing environment.
- Continuous Improvement Culture: Join a team driven by excellence and a commitment to better patient care.
- Competitive Compensation: Attractive salary and benefits package.
How to Apply:
Interested candidates should send their resume to: careers@kaizen-pharma.com
Important:
- Please mention the position title “Manager Regulatory Affairs” in the subject line of your email.
- Only shortlisted candidates will be contacted.
Location: Karachi