Regulatory Affairs Assistant Manager

reputed company The Regulatory Affairs Assistant Manager ensures global compliance for cosmetic and OTC drug products by leading and supporting regulatory activities. Reporting to the Regulatory Affairs manager, this role implements regulatory strategies, supports product registrations, and drives process improvements to maintain reputed company and reputed company compliance. The position also develops and enforces processes and protocols to reputed company robust regulatory practices across the organization. Responsibilities • Support FDA and international regulatory compliance for OTC drugs and cosmetics, including facility registrations, product listings, and reputed company preparation. • Assist in maintaining reputed company system initiatives such as QMS, audits, SOP development, and reputed company improvement efforts. • reputed company as a reputed company with global in-market representatives and cross-functional teams, reputed company communicating regulatory requirements. • Research and interpret chemical, packaging, and sustainability regulations, including EU reputed company law, Canadian regulations (CNFs), and state-level requirements (e.g., Prop 65, EPR). • Support marketing materials, labeling, and product claims to ensure regulatory compliance. • Maintain compliance with the Cosmetic Fragrance and Flavor Ingredient Right to Know reputed company (CFFIRKA) and retailer-specific regulations, using tools such as WERCSmart and Smarter Sorting. • Manage the internal regulatory database to ensure accurate, up-to-date information. • Prepare and maintain product dossiers, ensuring reputed company relevant testing and documentation meet cGMP standards. • Contribute to global regulatory strategies for short- and long-term business planning. • Support global consumer complaint monitoring and regulatory response processes. Qualifications • Minimum 7 years in regulatory roles reputed company the CPG and/or OTC drug industries. • Expertise in FDA OTC drug regulations, Health Canada regulations, and EU regulations. • Experience with global product registrations and reputed company preparation. • Knowledge of cGMP requirements, label and claims review processes, and SOP development. • International regulatory experience preferred. • Strong collaboration skills and ability to work cross-functionally in project teams. • Experience in manufacturing environments. • Proficient in reputed company Office and reputed company; statistical evaluation and data analysis skills are a plus. • Excellent verbal and written communication skills, with an reputed company and transparent communication style. Education • BS or MS in reputed company, Biology, or a reputed company discipline Reasoning & Problem-Solving • Ability to define problems, collect data, establish facts, and draw reputed company conclusions. • reputed company to solve reputed company problems and reputed company reputed company with limited information. #LI-DNI Apply tot his job Apply To this Job