Specialist TAG in Bayport at The Bountiful Company

Date Posted: 9/1/2022

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    10 Vitamin Drive
    Bayport
  • Job Type:
  • Experience:
    5 years
  • Date Posted:
    9/1/2022

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 Technical Applications Group (TAG) is currently recruiting for a Sr. Specialist to support soft gel formulation and technology initiatives.  This is an exciting opportunity for candidates that are in a Process Development role supporting softgels and/or liquids manufacturing.

The Senior Specialist will work closely with multi-functional teams to help improve current products, address manufacturing issues, evaluate new technologies and/or ingredients, seek cost savings and maintain networks of external partners.  Project goals are accomplished with the supervision of the support Supply Chain technicians and scientists.  

Additional responsibilities include, but are not limited to:

  • Gather and analyze data on processes to determine recommendations for improvement; generate conceptual equipment designs, process flows, productivity models
  • Create standard operating procedures, user requirement specifications, basis of design, qualification documents, and work flows
  • Provide project status and update reports to management and customers to ensure visibility; maintain project plans and other project documentation in an organized and secure fashion; conduct toll gate meetings with management in response to major scope changes to a project, or prior to major milestones being met
  • Inform management in a timely manner of risks to product revenue generation; review the revenue forecast and work with Finance to ensure the forecast for all billed items are accurate and up to date
  • Leading and managing projects for the introduction of new products, equipment and processes to meet all safety, quality, regulatory and operational requirements.
  • Process mapping, gap analysis/identification for new and existing pharmaceutical manufacturing processes.
  • Process development (as part of technical transfer), troubleshooting and optimization.
  • Executing process and equipment trials and verifications.
  • Leading cross functional teams as part of project planning and deployment including collaboration with supporting departments such as Production/Operations, Quality, Safety, Regulatory Affairs, Facilities and Engineering, Supply Chain and Finance, Project scoping and gap analysis.
  • Assist with equipment specification/design/procurement/installation and validation.
  • Optimization of existing processes to achieve product output targets.
  • Coordinating changes using the approved change control procedure to ensure that cGMP is adhered to.
  • Generation, review and approval of project documentation (Scope, User Requirement Specifications etc), trial reports and Standard Operating Procedures.
  • Provide technical support to troubleshooting technical issues and assisting with process investigations.
  • Involvement in Continuous Improvement activities including but not limited TPM and six-sigma.
  • To facilitate and participate in meetings and workshops as part of Project and Continuous Improvement activities.
  • Develop user materials (e.g. SOPs + training aids) and provide training on equipment/process functionality.
  • Perform technical review of updates to Standard Operating Procedures (SOPs) related to the equipment/process.

Job Requirements

  •  Bachelors in Engineering or physical sciences, including, but not limited to: Chemistry, Biology, Chemical, Mechanical, Electrical, or Civil Engineering, or Pharmacy
  • 5+ years of relevant work experience preferable in solid dose manufacturing (softgels, tablets, 2-piece capsules, granulation, coating)
  • Working knowledge of project management principles and concepts in a cGMP environment; at least 2 years of project management experience or other experience that demonstrates successful team leadership and project completion
  • PC skills, including proficiency with Microsoft project and standard tools in project management; proficiency in CAD software, Autocad, Solidworks, etc
  • Good project management skills.
  • Ability to communicate and collaborate with external partners and scientific experts.
  • Ability to lift approximately 40 pounds.



Ref # POS000001573