Sr Specialist Quality in Bohemia, NY at The Bountiful Company

Date Posted: 11/2/2022

Job Snapshot

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 Quality Specification Specialist provides support, coordinates and manages specifications for raw materials, bulks (in-house and contract), turnkey finished products for all manufacturing sites and affiliates to meet applicable domestic and international regulations and compliance.

PLEASE NOTE - This position offers a hybrid work scheduled 

Responsibilities include:

  • Preparing, developing, executing review, and generating specifications and documents to assure compliance to meet internal customer requirements (such as technical services, quality, procurement, regulatory teams, RD, and business teams), manufacturing capability, applicable compendial monographs or market regulations using the company's PLM system.
  • As specification change analysts, determining appropriate reviewers/approvers for change requests to ensure specification completeness and integrity including claims to support label requirements.
  • Providing technical assistance to internal departments and manufacturing sites on issues related to specifications.
  • Ensuring generated specifications (manual and electronic) are maintained controlled, updated and communicated to all appropriate levels.
  • Participating in cross-functional teams as new products and new raw materials are evaluated. 

 

Job Requirements

  • Experience / knowledge of FDA regulations and industry standard monograph system as they relate to food and dietary supplements is preferred.
  • Bachelor’s degree in science required.
  • Ability to work independently and meet deadlines on a multitude of concurrent tasks.
  • Excellent verbal and written communication skills.
  • Computer literacy in a Windows environment (Word, Excel, and Outlook).
  • Attention to detail and ability to work well under pressure.
  • Effective interpersonal skills to interact with various levels of internal and external customers.
  • Working knowledge of Current Good Manufacturing Practices (cGMP).
  • Strong organizational and analytical abilities.


Ref # POS000007776