R&D Regulatory Associate
Aequor
Piscataway, New Jersey
2d ago

Job Title : R&D Regulatory Associate (Vitamins, Minerals, Supplements)

Location : North Brunswick, NJ

Job Type : Fulltime

Description : This role is focused on supporting the compliance products / ingredients for our dietary supplement business.

This exciting position within the R&D organization will be accountable to support new product launches. This position provides ongoing regulatory maintenance of existing products, while striking a balance of driving compliance while simultaneously meeting business needs.

Cross-functional collaboration with colleagues within R&D and from other departments (e.g., Sourcing, Quality Assurance, Quality Control, Marketing, etc.

is required on daily basis. This role will be a great opportunity to make an impact to an exciting and emerging VMS category of product!

Essential Job Functions :

  • Works with sourcing team on Regulatory technical documentation in support of our raw materials / nutritional dietary ingredients / Finished product (botanicals / minerals / vitamins / specialty items)
  • Collect and collate regulatory documents from suppliers / vendors, internal Supply Chain group, QA, QC
  • Creates technical documents relevant to various finished dosage form such as Tablet, Capsule, Powder drink mix, Ingredients etc.
  • Manage from a Product development perspective the aspects of technical specifications and regulatory approval of dietary ingredients & finished product at customer requirement Perform detail review of New and existing product formulas to ensure accuracy of raw material ingredients & its technical documentation.
  • Develop Formula Specifications and Supplement Facts in collaboration with Product Development team, Marketing and Quality Assurance departments.
  • Maintain accurate project information & related Documentation in collaboration with the Senior staff members in department of proper documentation for new formula and product development projects.
  • Work with R&D Director to generate new formulation documents and New / Existing raw material.
  • Confirm feasibility of formulation and all relevant technical information
  • Ensure ail technical regulatory documentation align as per customer requirements with relevant project
  • Support all New Product Development regarding identifying and qualifying raw material suppliers and participates in supplier meetings Other duties as assigned.
  • Education and Experience :

  • Bachelor's Degree in Science & Regulatory Affairs with strong understanding of nutritional ingredients
  • Experience with managing projects of different complexities.
  • 1-3 years of experience in research and development involving new formulations
  • Familiarity with Good Documentation Practices and regulations for Food & Dietary Supplement industry
  • Knowledge, Skills, and Abilities;
  • Strong comprehensive written and verbal communication skills Proficient in a subset of basic tools : Excel, Word, Power Point Ability to work independently or collaboratively.
  • Must be able to lead projects that require cross- functional collaboration.
  • Must have the ability to learn quickly and excel in a fast-paced environment.
  • Must have attention to detail.
  • Apply
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