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Vitality Works Inc QC Analyst/Chemist - Full Time - Days; Monday - Friday in Albuquerque, New Mexico

Position Summary:

As a QC Analyst/Chemist, you will be conducting routine and non-routine tasks according to SOPs. Responsible for Quality Control functions relating to raw material and product testing, lab formulation, and analytical testing.

Position Responsibilities:

  • Accurate data analysis and documentation

  • Ensure compliance of Quality Control SOP’s throughout all aspects of position and troubleshoot when a deviation from standard process occurs

  • Conduct analyses for materials utilizing equipment such as HPLC, ICP-MS, HPTLC, FT-IR, UV-Vis as required

  • Work closely with the Laboratory Manager and/or the QC Chemist to validate and qualify new methods for in-house testing

  • Conduct Environmental & Water Monitoring testing as required

  • Conduct other wet chemistry tests such as Specific Gravity, Jones Reagent, Solubility, and Fill Weight Verification.

  • Facilitate testing of raw materials and products by third party contract labs as needed

  • Assist in investigating non-conforming products and disposition

  • Review and approve batch records

  • Review and approve powders for encapsulation and finished cap products

  • Assist with drafting and creating Safety Data Sheets

  • Provide backup and support for QC functions as needed

  • Complete projects and other duties as assigned by QC Manager

Qualifications

Skills & Requirements:

  • BS degree in Chemistry or related field

  • Experience working in a GMP facility

  • Understanding of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs) for the Dietary Supplement industry; specifically, quality control.

  • Proficient in MS Office (Excel, Word, Outlook, PowerPoint)

  • Strong math and analytical skills

  • Strong verbal, technical writing and interpersonal skills are required

  • Must be detail oriented

  • Ability to multitask and work under pressure to produce positive outcomes

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