Herbalife

Scientist, Document Control

Herbalife$80K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3+ years in Quality Assurance or Quality Control in FDA-regulated industry
  • Bachelor’s degree in a scientific field
  • Laboratory testing experience in relevant areas like Food or Pharmaceuticals
  • Strong customer service and relationship skills
  • High attention to detail and analytical abilities
  • Effective written and verbal communication skills
  • Proficient with Microsoft Office and Agile systems

Responsibilities

  • Perform technical review of raw material documents to ensure compliance
  • Collaborate with Document Sourcing for inquiries related to raw material specifications
  • Guide on raw material Agile processes for Corporate and Regional teams
  • Develop and revise raw material specifications in collaboration with multiple departments
  • Route and implement raw material change requests in Agile
  • Review raw materials for new formula assurance and supplier approval
  • Maintain all documents related to raw material specifications

Benefits

  • Collaborative work environment focused on safety and regulatory excellence
  • Empowerment to contribute ideas that influence product development
  • Be part of a tight-knit team committed to improving lives through nutrition
  • Opportunities for professional growth and development
  • Engagement with cross-functional teams and suppliers
Full Job Description
Overview

POSITION SUMMARY STATEMENT:

 

The Scientist, Document Control will be responsible for assuring that the existing as well as the proposed raw material specifications are in accordance with the Herbalife Nutrition and current regulatory requirements. The position will collaborate with cross functional teams to achieve timely approval of raw material changes.

 

DETAILED RESPONSIBILITIES/DUTIES: 

  • Perform technical review of raw material documents for acceptability for Inner Nutrition
  • Collaborate and provide guidance to Document Sourcing (Corporate and Regional) group when there are inquiries related to raw material specifications and documentation.
  • Collaborate and provide guidance to Document Sourcing (Corporate and Regional) group when there are inquiries related to raw material Agile processes.
  • Develop, review and revise raw material specifications in Agile based on current requirements and regulations by collaborating with Research and Development (Tech Ops, Developer, Sensory), Global Regulatory Affairs and Product Compliance (Corporate and Regional), Quality Control (QC), Product Science, and Transportation to assure appropriateness.
  • Route and implement raw material change requests and change orders in Agile by gathering approvals from different departments in a timely manner.
  • Review raw materials used in a new formula or formula revision assuring that the raw material and suppliers are approved for the contract manufacturers
  • Discuss specific country testing requirement with Global Regulatory Affairs and Product Compliance (Corporate and Regional), as needed.
  • Work with raw material suppliers or contract manufacturers (as needed) to resolve issues related to raw material specifications.
  • Inform contract manufacturers when there is a raw material specification change
  • Maintain all documents related to raw material
  • Perform other responsibilities as assigned

What makes the Team Special

 

Our Document Control team is a tight-knit group who are united by a shared commitment to product safety, regulatory excellence, and the belief that precision science truly changes lives. Here, you won't just execute processes — you'll be trusted, heard, and empowered to contribute ideas that shape the future of how we bring world-class nutritional products to people around the globe.

 

Qualifications

REQUIRED QUALIFICATIONS:

 

As a Scientist in Document Control, you will be empowered to make a real impact across the organization. Your day-to-day work will include:

 

Skills:

  • Basic knowledge in raw material documents and processes
  • High degree of attention to details to identify document acceptability
  • Results oriented to meet set expectations
  • Strong customer service and relationship
  • Excellent written and oral communication skills when collaborating with cross-functional teams
  • High analytical skills to execute changes
  • Excellent in planning and organization to manage multiple tasks
  • Proficiency in Microsoft Office
  • Team player
  • Flexible, comfortable adapting to changes

Experience:

  • 3 year experience in Quality Assurance or Quality Control in an FDA regulated industry (21-CFR- Food, Dietary Supplement or Drug)
  • Laboratory testing experience in (Food, Dietary Supplement, Pharmaceutical, Environmental)

Education:

  • Bachelor’s degree in a scientific field

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About Herbalife

Herbalife Nutrition is a global multi-level marketing corporation that develops and sells dietary supplements. The company was founded in 1980 by Mark Hughes and is headquartered in Los Angeles, California. Herbalife operates in over 90 countries and has over 8,900 employees worldwide. The company's products include weight management, targeted nutrition, energy, sports and fitness, and outer nutrition products. Herbalife has been the subject of controversy over the years, with some critics alleging that the company operates as a pyramid scheme. The company has denied these allegations and has implemented changes to its business model in response to regulatory scrutiny.
Learn more about Herbalife
Size
10,800 employees
Market Cap
$1.4 billion
Industry
Net Income
$372.6 million
Founded
1980
5 Year Trend
+5.3%
Revenue
$5.5 billion
NASDAQ

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