Regulatory Affairs

Qualification Must-Haves

• Graduate

• 2 to 4 years’ experience in Regulatory Affairs (Pharma industry preferred)

• Knowledge of medical device industry

• Computer literacy.

Key Responsibilities

• Maintain regulatory databases, licenses, registrations, and product files while ensuring accuracy and completeness of records.

• Support in Developing and implementing regulatory strategies to achieve business objectives.

• Support in Preparing, reviewing, and submit regulatory dossiers, applications, and supporting documentation to ensure timely approvals from relevant health and regulatory authorities.

• Support in Monitoring changes in national and international regulations and assess their impact on existing and new products.

• Collaborate with cross-functional teams to ensure compliance with regulatory requirements.

Your attributes and skills:

• You show a collaborative, inspiring working style, and you can accommodate different personalities in a functional team

• You have excellent written and spoken English communication skills

• You are a great communicator, collaborative, inspiring, and able to accommodate different personalities in a functional team