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

Date Posted: 4/18/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Holbrook, NY
  • Job Type:
  • Experience:
    Not Specified
  • Date Posted:
    4/18/2019

Job Description

For more than 70 years, The Nature’s Bounty Co. has enriched the lives of consumers around the world and stood as the leader in health and wellness by introducing innovative products and solutions to the marketplace. Putting science and the highest quality standards at the heart of our business, the brands of The Nature’s Bounty Co. are some of the most trusted in the world. Always motivated by nature’s bountiful effects on people’s health, our vision for health and wellness has inspired leading brands such as Nature’s Bounty®, Sundown Naturals®, Solgar®, Osteo Bi-Flex®, Ester-C®, MET-Rx®, Pure Protein®, Balance®, Body Fortress®, Puritan’s Pride® and Organic Dr.®, among others. As a leading global manufacturer, marketer, distributor and retailer of vitamins, nutritional supplements, sports & active nutrition and ethical beauty products, The Nature’s Bounty Co. is committed to supporting wellness in all its forms.

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

Please note shift details: 1st shift 6:00 am - 6:30 pm (rotating weekly schedule)

Additional responsibilities include, but are not limited to:

  • When required, conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks. 
  • When required, performs in-process testing verification's 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.
  • Conducting duties in compliance with safety rules, applicable SOP’s, and cGMP Guidelines.

Job Requirements

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

Please note shift details: 1st shift 6:00 am - 6:30 pm (rotating weekly schedule)

Additional responsibilities include, but are not limited to:

  • When required, conducts approval of pre-start-up activities including line/room clearance, and initial equipment checks. 
  • When required, performs in-process testing verification's 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.
  • Conducting duties in compliance with safety rules, applicable SOP’s, and cGMP Guidelines.