Regulatory Affairs Intern

1w1 week ago

Pharmavite

West Hills, US · Internship · $60,000 – $60,000

About this role

Working at Pharmavite is an experience like no other, with a focus on complete nutrition for all. Each endeavor is urgent and every day counts. You'll work on the #1 selling national vitamin and supplement brand, Nature Made, and an exciting portfolio shaping healthy living.

The Intern – Regulatory Affairs develops regulatory acumen by supporting key projects to ensure compliance with federal and state regulations. This includes building process efficiencies and performing horizon scanning. The role reports to the Manager, Regulatory Affairs.

This hybrid role requires in-office work at West Hills, CA three days a week (Tuesday - Thursday), with remote work on Mondays and Fridays. Shadow the regulatory team to apply knowledge to activities supporting business priorities. Execute cross-functional projects within the Scientific and Regulatory Affairs Department.

Grow in educational and career development with training and mentorship. Career paths aren't predefined, and bureaucratic limitations don't exist. The environment fuels curiosity, encourages experimentation, and supports development from industry pioneers.

Requirements

Undergraduate (3rd or 4th year) in Biological Science, Nutrition Science, or other relevant field or Graduate student in Regulatory Affairs.
Available 8-12 weeks starting in June 2025.
Knowledge of federal regulations for conventional foods and/or dietary supplements.
Studied regulatory topics applicable to food, dietary supplements, or pharmaceuticals.
Ability to learn fast and effectively collaborate with internal stakeholders.
Proficient in Microsoft Office.
Excellent oral and written communication skills.
Strong analytical, organization and critical thinking skills.

Responsibilities

Develop or update records that help track regulatory compliance from raw material to formulation.
Optimize internal processes to support regulatory compliance from raw materials through to labeling.
Create or revise Job Aids and other reference guides.
Handle regulatory monitoring through various resources.
Shadow regulatory team to learn how to apply regulatory knowledge to activities that support business priorities.
Execute cross-functional projects within the Scientific and Regulatory Affairs Department.

Benefits

Hybrid role with in-office work three days a week (Tuesday - Thursday) and remote on Mondays and Fridays.
Training and mentorship for educational and career development.
Opportunity to grow, learn from industry pioneers, and develop as desired.
Environment geared to fuel curiosity and encourage experimentation.