Vacancy expired!
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Morinda of American Fork, UT is seeking to hire a full-time Regulatory Affairs Manager that will be responsible for coordinating Regulatory aspects associated with product registration/legalization, labeling reviews, and communicating with manufacturers and department representatives to ensure regulatory projects and registration documentation deliverables meet established deadlines, with particular focus on the New Age Beverages Corporation line of beverages.
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Our Regulatory Affairs Manager will earn a competitive wage and receive medical, dental, and life insurance at a very reasonable cost. We also offer paid time off (PTO) and paid sick days Our employees also enjoy a 401(k) plan, 12 paid holidays per year and subsidized gym memberships. If this sounds like the opportunity that you've been looking for, apply today!
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ABOUT MORINDA
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In 1996, Morinda disrupted the health supplement industry with the introduction of Tahitian Noni Juice, launching a multi-billion-dollar industry virtually overnight. Today, we use our unquestioned noni expertise to drive our mission to help everyone obtain the three things they want the most: better health, better appearance, and financial freedom. That is how Morinda changes lives all over the world. As a driving partner with New Age Beverages Corporation, Morinda is focused on our goal to be a part of the largest healthy beverage company in the world.
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At Morinda, our senior leadership understands the importance of ethical business practices so that both our customers and employees know that they can trust us. Many companies espouse lofty mission and vision statements; Morinda is focused on caring for employees and providing a friendly and supportive workplace. We understand that our success comes from the hard work of our employees which is why we offer competitive compensation and are committed to keeping healthcare costs low.
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A DAY IN THE LIFE AS A Regulatory Affairs Manager
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As Regulatory Affairs Manager, you obtain documentation from manufacturers to assist in registering/legalizing products in foreign markets; communicate with vendors, manufacturers, and various internal department representatives regarding status of registration projects and documentation; develop working knowledge of registration documentation and learn to prepare, edit, or modify affidavits necessary for product registration. You also incorporate country specific label format and text changes to ensure compliance with domestic and foreign government regulations; develop working knowledge of foreign and US regulations governing the sale of food/dietary supplements, foods, cosmetics, and OTC cosmetics; review labels and marketing materials for accuracy of information and for compliance with local government laws and regulations. You meet with various internal department representatives to coordinate the strategy of launching products and organizing product campaigns with market-specific materials, as well as review master formulas and suggest ingredient replacements with safety data or effectiveness. You obtain working knowledge of ingredient acceptability, upper limit, heavy metal, and microbiological requirements and registration regulations for region, and you
serve as primary contact for obtaining registration documentation and expert legal/regulatory review.
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QUALIFICATIONS
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BA/BS degree in related field with 4-6 years' experience with regulatory affairs, or sciences.
Expert knowledge of chemical, health, science, pharmacology.
Experience in food industry with specific beverage industry experience a plus.
Ability to communicate both verbally and in writing and represent department in a professional manner; high level of professionalism in work ethic, deadlines/deliverables, overall demeanor, and while working with others; ability to create strong professional rapport with internal and external personnel and demonstrate assertive leadership.
Willingness to take responsibility for assignments and errors, develop an ability to take calculated risks and appropriate initiative, complete assigned tasks efficiently, and communicate assertively to meet deadlines.
Ability to travel either domestically or internationally when assigned.
Familiarity with government issued product registration documents
Familiarity with the U.S. Food & Drug Administration (FDA), U.S. Federal Trade Commission (FTC), and U.S. Department of Agriculture (USDA) regulations and guidelines and corresponding international regulatory agencies
Knowledge of national and international labeling rules and formats for ingestible and topical products
Knowledge of ingredients and nomenclature, and enough knowledge of formulations to advise and assist in product development
Knowledge of national and international rules governing product claims of function and effect, and ability to critically-review technical documentation in relation to claims substantiation
Ability to effectively and efficiently manage external counsel
Knowledge of Good Manufacturing Practices (GMP), Hazard Analysis and Critical Control P (HACCP), and Adverse Event Reporting (AER) regulations as enforced domestically as well as internationally
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Working Environment:
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Work is performed in a typical office environment.Â
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For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.Click Here to Apply or use the link belowhttps://morinda.applicantpro.com/jobs/1064697-366193.html
Vacancy expired!