Quality Analyst (I)

Company: The Bountiful Company
Location: Bohemia
Posted on: August 4, 2022

Job Description:

Company DescriptionThe Bountiful Company, a Nestl-- Health Science Company, is a pure play branded leader in global nutrition, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbal and other specialty supplements, and active nutrition products, we are focused on enhancing the health and wellness of people's lives. The Bountiful Company's portfolio of trusted brands includes Nature's Bounty -, Solgar -, Osteo Bi-Flex -, Puritan's Pride -, Sundown - and Ester-C -.Inclusion and Diversity in the workplace matters at The Bountiful Company. This includes being focused on retaining and recruiting a diverse workforce and building a culture of inclusivity. Our goal is to create a place where people feel respected, valued and able to bring their authentic selves to work each day. Did we mention that we also offer excellent benefits, competitive compensation and a progressive, healthy company culture? If you've ever spent your workdays watching the clock, you know how important a positive work environment is for a person's well-being. The Bountiful Company is committed to supporting wellness in all forms. And when it comes to wellness, nature is a pretty good place to start.Job DescriptionThe Quality Analyst is responsible for managing the document review group by creating, managing, and distributing quality analysis reports and making recommendations to improve the production process based on findings from quality assurance analysis of the quality management systems.Additional responsibilities include, but are not limited to:Monitor the compliance of processes and associated records to company standard operating procedure requirementsReport findings to Quality Manager and assist in problem solvingDevelop CAPA plans and lead continuous improvement initiativesManage on-time closure of assigned deviations and CAPA'sDocument results of new procedures after implementation to show quality improvementsWrite and implement test procedures to obtain the defect information needed for analysis and report findings from test and inspection data to managementAnalyze quality inspection data to identify all types of quality problems and perform root cause analysisAnalyze plant controllable consumer complaint data to identify all types of quality problems and perform root cause analysisInitiate investigations and support deviation documentation process utilizing the company's electronic database systemAssist in collecting and reporting weekly and monthly Quality reports, e.g., First Pass Quality, Complaints, NCR, Deviations, and others as assignedParticipate in employee quality improvement teams to reduce defects and quality issuesMonitor the improvement procedure to determine if changes significantly improve the process and the defect quantitiesMaintain documents for Audits.Create new processes or modify and improve current processes by setting up clear and definite quality systems and SOPsCollaborate across multiple disciplines and interface closely with our Operations, Distribution, Technical Services, R and Procurement teamsParticipate in multi-function team activities, support and maintain Quality Systems and perform other assignments as directed by ManagerQualifications2+ years of experience in the food, pharmaceutical and or dietary supplement industry preferredKnowledge of regulatory requirements that affect the dietary supplement and/or pharmaceutical manufacturing businessBachelor's Degree in Pharmaceutical, Food Science, Chemical Engineering, Chemistry or other Science related field preferred or other closely related discipline with extensive significant experience can be considered in lieu of a Bachelor's degreeASQ CQE or CQM preferredMust be proficient with PC programs, i.e. Microsoft Office (Word, Excel, PowerPoint, Visio)Problem solving and statistical skills using quality tools (Pareto analysis, statistical process control, multi-variant DOE, 8D, etc.)AS400 Knowledge desirableKnowledge of regulatory and GXP compliance requirements such as 21 CFR Part 111, HACCP, HARPC preferredSQF practitioner / FSSC/ BRC / ISO experience preferredStrong communication skills both verbal and written across all levels of managementSolid attention to detail to maintain audit records and audit reportsStrong interpersonal and collaboration skillsAdditional Information

Keywords: The Bountiful Company, Stamford , Quality Analyst (I), Professions , Bohemia, Connecticut