Regulatory Senior Specialist

A collective energy and ambition. A place where you can make a real difference. We’re a company that genuinely cares about our people, our products, our consumers and the environment. Our unique, informal culture champions courage, determination and collaboration. Knowing we have an open and supportive team means each of us has the freedom to take responsibility and ownership. We have a shared passion to work hard, innovate and push boundaries. United by the belief that when we strive for growth, anything is possible. While we might not be the largest company in our industry, we believe we can have the biggest impact because: Together We Have the Power to Win.

Church & Dwight   is   seeking a Regulatory Senior Specialist to join our team. This role is responsible for managing tasks to support regulatory processes and projects leading to the commercialization of OTC drug and cosmetic products across multiple business units.

The Regulatory Senior Specialist may lead medium-complexity projects or an appropriate scope project area.  This position carries out technical regulatory reviews, regulatory analyses and assessments, prepares regulatory summaries, makes conclusions, develops recommendations, and presents to cross-functional teams in support of a varied number of initiatives. Tasks will also include product label reviews and assessments, product listings with FDA, and facility registrations.  This position works with cross-functional partners in R&D, Quality, Legal, Marketing, and Supply Chain.

Remote : This role is performed on a remote basis and is open to candidates located anywhere in the United States who are able to work within the Eastern Time Zone (EST) business hours. Occasional attendance at in-person meetings may be required as business needs dictate.

Accountabilities and Responsibilities                                                          The Senior Regulatory Specialist manages tasks to support regulatory processes and projects leading to the commercialization of OTC drug and cosmetic products across multiple business units. This role Knowledge of FDA and CPSC regulations and general regulatory requirements related to products in the Health, Personal and Beauty Care categories, including OTC drug products and cosmetic products Knowledge of relevant State consumer product regulations, including the California Safe Cosmetics Program (CSCP) Proficiency in consumer product label reviews for cosmetics and OTC drugs Proficiency in product and facility registration and listing processes, including FDA Cosmetics Direct, CSCP, OTC Drug listings and reporting Knowledge and execution of relevant policies, procedures, and metrics Standard computer-based software knowledge Accurate documentation and submission of detailed reports High attention to detail, organization, and accuracy Ability to influence cross-functionally to deliver against project goals and objectives. Well organized and demonstrates forward-leaning and high initiative Delivers project tasks on time Works cross-functionally to identify and communicate regulatory requirements, regulatory risks and mitigation strategies Tests, confirms and/or improves processes Solves issues quickly and efficiently Ability to prioritize and handle multiple projects simultaneously Demonstrates agility and connectivity across the organization Actively builds connections and partnerships with others, internally and externally Ability to work with all levels of R&D, Marketing, Legal, Supply Chain, Technology teams to build relationships across functions Skills and Competencies Strategic and creative problem-solving skills Strong analytical skills Good oral and written communication skills Team-minded, detail-oriented, proactive self-starter Education and Experience        Required Qualifications: