Job Information
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