Regulatory Science Project Manager - Hybrid/Remote

ITG Brands, LLC

North Carolina

Hybride

USD 119 000 - 159 000

Plein temps

14 jours+

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Un CV et une lettre de motivation personnalisés, prêts à envoyer.

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Avantages offerts par ce poste

Medical insurance
Dental insurance
Vision insurance
401k match
PTO
Holidays
Education assistance
Referral bonus
Hybrid workplace
Casual dress

Résumé du poste

ITG Brands, LLC is seeking a senior regulatory leader to guide strategy and ensure product compliance across the portfolio. You will drive regulatory initiatives, oversee complex projects, and coordinate with legal and R&D teams to support market readiness.

The role requires strong knowledge of FDA/regulatory frameworks, plus experience leading cross‑functional programs and preparing submissions. Hybrid work model offered with competitive benefits.

Qualifications

  • Bachelor’s degree in Life Sciences, Chemistry, Regulatory Affairs, Business, or related discipline with 5+ years of Scientific Project Management experience.
  • Advanced degree preferred with 10+ years related work experience.
  • Strong proficiency with Microsoft Office and collaboration tools.
  • Knowledge of regulatory frameworks and submission processes.

Responsabilités

  • Lead regulatory strategy and compliance initiatives across product development.
  • Manage cross‑functional projects and prepare regulatory submissions.
  • Collaborate with Legal, R&D, Supply Chain, Marketing, and Finance teams.
  • Provide guidance on regulatory matters and portfolio impact.

Connaissances

Verbal and written communication
Attention to detail
Problem solving
Time management

Formation

Bachelor’s Degree in Life Sciences or related
Advanced degree (preferred)

Outils

SAP
Project management software

Description du poste

ITG Brands, LLC is seeking a senior regulatory leader to guide strategy and ensure product compliance across the portfolio. You will drive regulatory initiatives, oversee complex projects, and coordinate with legal and R&D teams to support market readiness.

The role requires strong knowledge of FDA/regulatory frameworks, plus experience leading cross‑functional programs and preparing submissions. Hybrid work model offered with competitive benefits.

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