The Lead-Regulatory Affairs will be managing all regulatory activities, support product transfer and formulation development processes, review product life cycle management applications, marketing authorization applications, and approval of packaging material artworks.

Bachelor’s degree in Pharmacy
Masters in any related field will be an added advantage
Registered Pharmacist with 5+ years of experience in a Regulatory Affairs role within in a pharmaceutical industry of which 2 years should be at supervisory level
Sufficient knowledge of regulatory regulations, standards and guidelines
Ability to work independently and collaboratively within a team
Ability to work under pressure and to deliver on the set deadlines
Ability to adhere to GMP and Quality Management Systems
High analytical mind, with exceptional problem-solving skills and attention to detail
Self-starter, flexible and with excellent communication skills, both oral and written
Proficiency in MS Office (Excel, PowerPoint presentations)