QA Floor Inspector (I) in Leonia, NJ at The Nature's Bounty Co.

Date Posted: 11/18/2022

Job Snapshot

  • Employee Type:
  • Location:
    Leonia, NJ
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:

Job Description

Company Description

The Bountiful Company, a Nestlé 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 Description

The QA Floor Inspector is responsible for ensuring products are being produced in a manner that meets all cGMP and Product Specification criteria. This enables improved first pass quality and adherence to cGMP’s on the production floor at all times. The position is the Quality Unit on the plant floor. The QA Floor Inspector provides real time review of in-process test data and batch documentation in order to limit the need for later review or rework. The QA Floor Inspector is the Quality expert on the production floor and will guide and advise operations associates as necessary on cGMP’s and Good Documentation Practices to ensure timely release of product or reaction to issues.

Additional Responsibilities:

  • When required, conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks.
  • When required, performs in-process testing verifications of operations data to confirm consistency in testing methodology and test data.
  • Consistently reviews in-process batch documentation to ensure real-time compliance to product specifications, good documentation practices, company SOP’s and cGMP’s. Discusses errors directly with line personnel so corrections can be made if required.
  • Confirms reconciliation/yield data for adherence to specifications and ensures that deviation reports are generated by responsible personnel if out-of-specifications are observed.
  • Reviews Production logbooks for accuracy and compliance.
  • Provide real-time guidance to line operations personnel pertaining to compliance to cGMP’s by monitoring dress code, documentation practices, testing methods, and testing accuracy.
  • Collects data on FPQ and performs release of batch records.
  • Complies with company policies and procedures and maintains exceptional work attendance.
  • Performs daily compliance Audit for responsible areas within production.
  • Responsible for conducting duties in compliance with safety rules, applicable SOP’s, and cGMP Guidelines.
  • Performs other duties as assigned by Quality Management.

Job Requirements

  • Strong organizational skills 
  • High attention to detail 
  • Excellent written and oral interpersonal communication skills 
  • Intermediate to advanced computer knowledge of MS Office programs (Outlook, Excel, Word)
  • Understanding of mathematical functions, such as mean, median, average, and standard deviation is preferred.

Ref # POS000001779