
Senior Manager
22 hours ago
About Us:
We are a leading pharmaceutical company with a presence in over 50 countries, recognized for our commitment to quality and excellence.
Job Description:
- Develop and implement strategic plans for global regulatory submissions and product lifecycle management.
- Ensure compliance with international regulatory guidelines and manage risk effectively.
- Liaise with cross-functional teams, external consultants, and health authorities to drive project success.
- Monitor evolving regulatory environments and assess impact on business operations.
- Collaborate with R&D, QA, QC, Manufacturing, Supply Chain, and Commercial teams to ensure project alignment and delivery.
- Drive efficiency in regulatory processes through digital tools, dashboards, and governance systems.
Key Skills & Qualifications:
- Expert knowledge of global regulatory frameworks (SFDA / GCC / PICs / BPOM / EAEU).
- Proven track record of successful regulatory submissions and project execution.
- Excellent leadership, stakeholder management, and communication skills.
- Ability to manage multiple projects under tight timelines and deliver results.
- M.Pharm / M.Sc. (Pharmaceutical Sciences, Regulatory Affairs, or related field) degree.
- 10–14+ years of experience in pharmaceutical regulatory affairs and project management.
- Demonstrated experience in global submissions and product lifecycle management.
Benefits:
We offer a dynamic work environment, opportunities for growth and development, and a competitive compensation package.
Others:
This is a challenging role that requires strong leadership skills, expertise in global regulatory affairs, and the ability to collaborate effectively with cross-functional teams.
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