Supv., Quality Assurance (i) in Bohemia, NY at The Bountiful Company

Date Posted: 4/23/2021

Job Snapshot

Job Description



Company Description

The Bountiful Company is a global leader in health and wellness, living at the intersection of science and nature. As a manufacturer, marketer and seller of vitamins, minerals, herbals, supplements, protein bars and powders, we are focused on enhancing the health and wellness of people’s lives. The brands of The Bountiful Company are some of the most trusted in the world including Nature's Bounty®, Solgar®, Pure Protein®, Osteo Bi-Flex®, Puritan’s Pride®, Sundown®, Body Fortress®, MET-Rx®, Ester-C® and Dr.Organic®.

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 Description

    Our Quality team is currently looking to hire a Quality Assurance Supervisor to lead the overnight shift.  If you are driven to build teams, share your drive for excellence and innovative spirit, and focused on results, The Bountiful Company is where you want to be! We are building an organization of passionate people committed to the health and wellness of our customers and to the success of our culture and company. This Quality Assurance Leader is a critical role within our Manufacturing site, responsible for leading/driving quality standards and productivity within a team of Quality Inspectors.

    PLEASE NOTE: SHIFT SCHEDULE & HOURS - SUNDAY - THURSDAY / 11PM-7:30AM

    Responsibilities include but are not limited to:

    • Adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced
    • Identifies issues effecting efficiencies and assists in developing solutions
    • Monitor productivity and motivate associates in production and/or distribution areas
    • Ensure that all paperwork is properly documented
    • Keep accurate attendance records; file proper reports (accident, probation, etc.)
    • Supervise, counsel and coach associates on a regular basis
    • Complies with company policies and procedures and maintains regular work attendance
    • Personal responsibility for following safety rules, SOPs and cGMPs guidelines
    • Reviews and approves production in-process deviations
    • Helps resolve quality issues on the production floor
    • Prepares investigations to determine cause of quality deficiencies
    • Training of QA floor inspectors on SOPs

    Job Requirements

    • Bachelor's Degree, Science related field preferred 
    • 3+ years working in pharmaceutical, dietary supplement, or food manufacturing facility in Quality or equivalent combination of education and work experience 
    • Prior supervisory experience in a manufacturing, packaging and/or warehouse environment 
    • High level of organizational skills, good written and oral communication skills 
    • Ability to work independently and meet deadlines 
    • Must be able to multi-task and follow-up when responses are needed 
    • Basic mathematical skills 
    • Physical ability to lift, stand, climb, bend, etc... within a manufacturing environment 
    • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
    • Ability to write routine reports and correspondence
    • Experience with Quality systems, auditing, Root Cause Analysis/CAPA 
    • Experience with Food Safety plans/HACCP, GFSI a plus 
    • Knowledge of FDA regulations for the GMP of Dietary Supplements and Foods

      All your information will be kept confidential according to EEO guidelines.



      Ref # POS000000786