Assistant Manager, Regulatory Affairs

HERE YOU ARE. Another day at the office. Time to go home. Remember how proud you were when you landed that great job in that illustrious organization. And now? Well, your work's ok, your colleagues are pretty nice and the office parties get pleasantly out of hands at times. Of course you're keeping your eyes open. You're still very ambitious. You have untapped talent and energy waiting to soar. You want a change. You want new challenges. A new organization. So if you fit the description below, then don’t miss this chance of a lifetime and open your doors to a rewarding career with us.

YOUR RESPONSIBILITIES :

• Designs, establishes and maintains an organisational structure and staffing to effectively accomplish the division’s goals and objectives.
• Directs and oversees the supervision of assigned personnel, which includes work allocation, training and problem resolution, evaluates performance and makes recommendations for personnel actions.
• Ensures that work production in the assigned division meets established objectives, specifications, and standards, and that all-applicable operating policies and procedures are adhered to.
• Recommends and participates in the development of company policies and procedures to ensure efficient and safe operation of the division.
• Establishes rapport and maintains an amicable and fruitful business relationship with existing as well as potential clients and Principals.
• Identifies, evaluates and recommends regulatory strategies in accordance with the company’s objectives for product lines.
• Ensures that new products are successfully registered.
• Reviews and ensures accurate completion and timely submission of governmental, company and other reports as required in respect of assigned areas of responsibilities.
• Participates in the development and management of annual operating budgets for the assigned division and regularly monitors expenditure.

WHAT WE ARE LOOKING FOR ?

• Possess a Bachelor's Degree in Pharmacy or its equivalent.
• At least 3 years of product registration experience preferably in the pharmaceutical line or related business.
• Knowledge of regulatory procedures & guidelines both local and in Asean countries.
• Possess analytical skills for interpretation of data and statistics.
• Possess time management skills.
• Proficiency in local languages.
• Ability to create, compose and edit written materials and deliver presentations.

Working Hours : Monday - Friday & Alternate Saturday.

Note: Only shortlisted candidate will be contacted for interview.