Regulatory Affairs Associate Job Vacancy in Vitaquest West Caldwell, NJ 07006 – Latest Jobs in West Caldwell, NJ 07006
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Company Name : Vitaquest
Location : West Caldwell, NJ 07006
Position : Regulatory Affairs Associate
Job Description : Great opportunity to become part of the Vitaquest team!Vitaquest is an industry-leading development and commercialization partner for consumer products in nutraceutical and functional foods. With over 40 years of history, Vitaquest has the market insight, global reach and scale of operations to support emerging and existing consumer brands from the idea to the store shelf with flawless execution in every phase. Today, Vitaquest creates and produces more than 4,000 customer formulas for more than 500 brands in over 40 countries.Vitaquest’s employees follow an internal communications plan to encourage productivity and engagement within the organization. This is known as Vitaquest PROUD. We believe that each employee contributes directly to the organization’s growth and success. We are looking for individuals who share our innovative spirit and will take pride in being a part of our Company.Title: Regulatory Affairs Associate IIDepartment: Regulatory AffairsReports To: Manager Regulatory AffairsRegulatory Affairs Associate Position Purpose and ObjectivesTo proofread essential documents and labeling materials; coordinate and complete reports required by federal agencies; answer customer-generated questions; maintain files; work with project teams to obtain approval for company products; and lead the company’s efforts in those subjects.Regulatory Affairs Associate Essential Job FunctionsKnow and provide guidance on current food and supplement labeling regulations.Seek ways to improve the speed and accuracy of completing documentation requests.Attend outside training in order to master specific certification regimes.Proofread formulas and finalize supplement facts information.Maintain and update raw material documentation.Compile information for and submit reports required by federal agencies.Maintain files and electronic document management systems.Work with and lead project teams.Prepare high quality, detailed regulatory documents.Perform other related tasks/duties as required.Regulatory Affairs Associate Knowledge, Skills, and Abilities RequiredMust be computer literate (Word, Excel, Outlook).Detail-oriented, well organized, driven to meet deadlines goals.Demonstrate good verbal and written communication skills.Supervisory ResponsibilityParticipate in training of, and prioritize the day-to-day workflow of, Regulatory Assistant(s) and new Regulatory Associate I-level coworkers.Working ConditionsA dynamic and fast paced technical environment.Minimum QualificationsCollege degree in a life science or related field.3 – 6 years relevant regulatory experience.Success FactorsWell organized, self-motivated team player.Job Type: Full-timePay: From $70,000.00 per yearBenefits:401(k)401(k) matchingDental insuranceFlexible spending accountHealth insuranceHealth savings accountLife insurancePaid time offReferral programRetirement planVision insuranceSchedule:8 hour shiftDay shiftMonday to FridaySupplemental Pay:Bonus payEducation:Bachelor’s (Preferred)Experience:Regulatory Documentation: 3 years (Preferred)Dietary Supplements Regulation: 3 years (Preferred)Work Location: One location
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