► Cosmetic Manufacturing Industry
► Office Hour
► Working Location: Tuas

Responsibilities:

• Maintain comprehensive understanding and updated knowledge of the regional and international regulations and standards applicable to the company products and upkeep the relevant regulatory databases
• Implement regulatory-related policies and standard procedures that are in accordance with applicable regulations and standards
• Collaborate and maintain good relationships with external customers (including regulatory agencies, certification bodies, service providers, distributors, etc.)
• Provide regulatory advice, develop, and maintain links to other teams (including quality, production, HQ’s regulatory affairs) so that appropriate development and quality plans may be established
• Responsible for obtaining certification and compliance of the manufacturing site (eg. ISO22716, GMP, Halal, etc.) on a timely basis
• Maintain business licenses and other authorities’ licenses for business operation
• Assess the impact of regulatory changes on the company; monitor, perform gap analysis and ensure timely and appropriate reactions to regulatory changes
• Assist in the implementation of optimal regulatory strategies to ensure regulatory and commercial success in the most effective and timely manner
• To provide regulatory collaboration or undertake specific tasks in the project initiatives with cross-functional teams on technology transfer, CMC (Chemistry and Manufacturing Control), or other datasets for timely compilation
• Responsible for tracking and supporting departmental QMS and related SOP, periodic reports, surveillance of new regulatory changes, etc

Requirements:

• Degree in Science, preferably in Chemistry / Biochemistry / Biomedical Science / Cosmetic Science or similar
• 3 years of experience with the regulatory environment and in the Cosmetic, Health Food, Dietary Supplement, Pharmaceutical or other FMCG industry
• Good understanding of global regulation – ACD, USFDA, TGA, EMA, ISO22716, PICs GMP, Halal, etc
• Technical skills to guide cross functional teams on development requirements from a regulatory perspective

To apply, please visit to www.gmprecruit.com and search for Job Reference: 18189

To find out more about this opportunity, please contact Summer at summer.thung@gmprecruit.com

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Summer Thung | Registration No: R1871138