INTERNSHIP DETAILS

Intern, Manufacturing and Technical Services

CompanyLife Extension Foundation Buyers Club Inc
LocationFort Lauderdale
Work ModeOn Site
PostedMarch 5, 2026
Internship Information
Core Responsibilities
The intern will support the QA function by creating, maintaining, and controlling documentation according to QA procedures and cGMP standards. Key duties involve conducting technical research, assisting with QA activities like RFQs and data collection, and managing controlled documents such as SOPs and Certificates of Analysis.
Internship Type
intern
Company Size
477
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Life Extension® is the health solutions expert that is translating scientific research into everyday insights for people wanting to live their healthiest lives. For almost 40 years, Life Extension® has pursued innovative advances in health, conducting rigorous clinical trials and setting some of the most demanding standards in the industry to offer a full range of quality vitamins and nutritional supplements and blood-testing services. Life Extension’s Wellness Specialists provide personalized counsel to help customers choose the right products for optimal health, nutrition and personal care.
About the Role


General Description: The intern supports the QA function by creating, maintaining, and controlling documentation in line with established QA procedures and cGMP standards. The position conducts technical research, summarizes findings for project needs, and assists with QA activities such as RFQs, manufacturing specifications, technical data collection, and records management. Responsibilities include coordinating supplier-related communications and follow-ups, supporting incoming label inspection and approvals, and organizing Certificates of Analysis, SOPs, and other controlled documents. 

Core Duties and Responsibilities:

  • Create, maintain, and update documentation in accordance with Quality Assurance procedures
  • Conduct technical research as needed for projects and summarize findings
  • Support QA team activities, including RFQs, manufacturing specifications, technical data collection, and records management
  • Assist with supplier-related issues, ensuring timely and accurate communication and follow-up
  • Support the incoming label inspection and approval process
  • Organize and maintain Certificates of Analysis, SOPs, and other cGMP documentation
  • Assist QA Management with GMO documentation and product registration requests
  • Regular on-site attendance is an essential function of this role
  • Perform additional duties as assigned

Position Requirements:

  • Actively enrolled Junior/Senior or recent alumni from a fully accredited College/ University with concentration in Biochemistry, Biological Science, Nutritional Sciences/Dietetics, Industrial/Manufacturing Engineering or related field
  • Highly disciplined with excellent attention to detail, strong communication (written and verbal), and superior organizational skills
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook).
  • Self-motivated with strong analytical and problem-solving abilities
Key Skills
Documentation ControlcGMP StandardsTechnical ResearchRFQsManufacturing SpecificationsData CollectionRecords ManagementSupplier CommunicationLabel InspectionCertificates of AnalysisSOPsGMO DocumentationProduct RegistrationAttention To DetailCommunicationOrganizational Skills
Categories
Science & ResearchManufacturingEngineeringAdministrative