Regulatory Affairs Manager / NR7 Job in Northridge 91325, California Us
Pharmavite is a leading and growing US manufacturer, marketer, and retailer of quality vitamins, mineral and herbal supplements both domestically and internationally with a strong portfolio of brands such as Nature Made, (Cholestoff, Triple Flex, and SAM-e Complete), and SOYJOY. With over 30 years as a major force in the nutritional supplement business, Pharmavite was built on the premise of producing the highest quality nutritional products in the country and operates one of the most sophisticated, state-of-the art research and development facilities in the industry.
Position Description:
Pharmavite is a leading and growing US manufacturer, marketer, and retailer of quality vitamins, mineral and herbal supplements both domestically and internationally with a strong portfolio of brands such as Nature Made, SAM-e Complete, and SOYJOY. With over 35 years as a major force in the nutritional supplement business, Pharmavite was built on the premise of producing the highest quality nutritional products in the country and operates one of the most sophisticated, state-of-the art research and development facilities in the industry.
As a member of the Pharmavite team, employees enjoy competitive salaries and an exceptional benefits package featuring medical, dental, vision, 401K, life insurance, and long term disability coverage. In addition, employees enjoy educational assistance, credit union membership, substantial discounts on our products, and 11 paid holidays per year.
We currently are seeking a dynamic, strategic, and innovative Regulatory Affairs Manager. This key position will be based in our corporate offices in Northridge, CA (So. CA).
Position Summary:
Responsible for corporate-wide compliance with all applicable laws and regulations affecting the labeling, advertising and composition of products made for foreign and domestic markets.
Responsibilities:
- Assures that existing and new products comply with all laws, rulings and regulations affecting the use of ingredients, labeling and advertising.
- Provides guidance to Marketing on new product concepts, claims and formulations to assure compliance with FDA and FTC requirements.
- Monitors the development and assesses the impact of new and proposed changes in laws, rulings, regulations and enforcement activities impacting the use of ingredients, product safety, labeling and advertising. Submits comments on proposed changes to regulatory agencies as deemed appropriate. Communicates new requirements and changes within the organization, and assures compliance.
- Helps identify and address potential patent and trademark issues in conjunction with in-house legal counsel.
- Assures that exported products (non-Japanese markets) comply with appropriate international formulation, labeling, advertising and product registration requirements.
- Participates with the CRN Regulatory Affairs Committee.
- Assists Legal Affairs in researching and responding to issues related to litigation and other legal matters, as needed.
- Performs other related duties as assigned.
Minimum Qualifications:
Education:
Requires a four year college or university degree or its equivalent, preferably in the physical or life sciences.
Certification:
A certification from Regulatory Affairs Professional Society is preferred.
Experience:
Requires at least five years experience in regulatory affairs, with an emphasis on regulatory issues related to dietary supplements.
Knowledge/Skills/Abilities:
- Comprehensive knowledge of laws and regulations pertaining to the manufacture and marketing of dietary supplements
- Competent knowledge of nutrition and health sciences
- Good analytical, organizational, and oral and written communication skills
Supervisory Responsibility:
The incumbent has direct supervisory responsibility for one to five employees.
Pharmavite is proud to be an equal opportunity employer. M/F/D/V
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