Regulatory Affairs Associate Job at Capleo Global in Piscataway, New Jersey

Job Title: Regulatory Affairs Associate

Duration: 12 Months (Possible Extension)

Location: Piscataway, NJ 08854

30 hours/week

Remote Role

Required Cosmetic/OTC Drug NA (US + Canada) Regulatory knowledge/experience.

The primary role of the Regulatory Affairs Associate is to help ensure regulatory compliance and to support the maintenance of the Company’s marketed products throughout the product lifecycle in the Americas region. This support includes performing regulatory activities necessary to maintain and to grow the business. Responsible to perform regulatory activities to support product development and registration projects, including the launch of new and existing skin care cosmetic and drug products and other projects as assigned. The Associate will research product ingredients, review formulations, approve label ingredient statements Review and approve artwork to ensure product and ingredient claims are compliant with applicable regulations. S/he will also submit notifications and reports to federal and state governments to help assure ongoing compliance with regulatory requirements and will be supporting the Distributors registrations in the region. S/he may also draft procedures.

University degree required; a degree in Life sciences or Regulatory Affairs Certification is preferred (e.g., chemistry, pharmacy, biology) but not required. 5+ years experience in North America regulatory affairs, with focus on cosmetics, cosmetic-OTC drugs, NHPs and/or DIN drugs, sunscreens Understanding of Global Regulatory Landscape Project management and organizational skills.Good knowledge of Google tools for documents, spreadsheets and presentations.Sound analytical thinking: ability to analyze technical data, to interpret and recognize implication of results and to recommend next steps.Ability to successfully juggle multiple competing priorities while maintaining attention to detail and adherence to priorities.