Eric Mattessich Email & Phone Number

Skillman, New Jersey, Us

* Develop regulatory strategies in support of the US Dietary Supplement portfolio as well as support Global expansion of the Kenvue supplement business.* Providing timely input to proposed guidelines, regulations and laws and participating at trade association meetings and working groups.* Providing regulatory intelligence and insights to internal teams to proactively prepare for changing regulatory requirements.* Approve promotional materials and product claims in accordance with internal procedures and external guidelines.* Lead the technical team responsible for creation and maintenance of the Dietary Supplement Core Labelling documents.* Liaise with external consultants on complex matters related to Dietary Supplement advertising and product development.* Develop and maintain procedures for key regulatory processes.

Laval, Quebec, Ca

- Provide regulatory strategy in the development, revision, review, and approval of labeling content as well as any post marketing labeling changes- Work with multidisciplinary project teams to ensure the accuracy of all information to be included in the labeling- Serve as the regulatory labeling liaison in tech transfer and reformulation projects with internal R&D and contract manufacturers- Train and delegate sub-projects to new team members and oversee respective projects- Lead the review process timelines and coordinate with other regulatory functions for the submission,approval, and notification of new/revised labeling content- Develop and manage tools, SOP’s, and archives/databases that support the coordination with other internal functions and private label owners to make certain only approved labels are produced for appropriate products- Research and implement ongoing changes in the regulatory landscape such as the bioengineered disclosure and sesame allergen inclusion

Ronkonkoma, Ny, Us

- Researched and implemented CFR regulations for FDA compliance for new and existing supplement, food, cosmetic, and OTC drug products- Created and updated label manuscripts and facts boxes for domestic and international labels according to marketing, regulatory, or quality needs- Communicated with cross-functional teams to find solutions for lawful structure/function claims- Calculated formulas to establish active ingredients, other ingredients, and excipient amounts for preciseclaims and placement on labels- Researched medical device regulations and provided decision-driving insights to management on possible DNA-test product for vitamin deficiency- Initiated changes for final product specifications according to Quality testing results using PLM software- Collaborated with internal departments including Legal, Quality, and Technical Services to obtain rawmaterial specifications and trademark attributions- Organized and documented relative formula attributions such as Gluten-free, Non-GMO, USP, and Organic as well as analyze raw materials specifications for allergens to mitigate risk

Ronkonkoma, Ny, Us

- Documented consumer feedback including adverse reactions and quality complaints- Compiled raw data for adverse event reports through consumers and at times medical professionals via phone, which were then reviewed by the Product Vigilance team- Technical writing and organization of trending inquiries and comments- Provided quality assistance for consumers through various modes of communication, with an average of 60-70 outgoing and incoming calls per day- Critical thinking and knowledge of products needed to provide consumer service and comprehension of product function or usage