QC Analytical Chemist

DrVita, Inc. is seeking a QC Analytical Chemist to join our Quality team in a fast-paced dietary supplement manufacturing environment. This position performs analytical testing of raw materials, in-process blends, and finished products to ensure they meet quality and regulatory requirements. The ideal candidate will have hands-on experience with HPLC and ICP-MS, a strong understanding of cGMP laboratory practices, and the ability to independently troubleshoot analytical testing and instrumentation. What You'll Do Perform analytical testing using HPLC, HPTLC, ICP-MS, FTIR, and wet chemistry techniques Prepare reagents, mobile phases, standards, and other laboratory solutions Operate, calibrate, maintain, and troubleshoot analytical instrumentation Review and interpret analytical data to ensure accuracy and specification compliance Conduct and document OOS/OOT investigations and support method verification, transfer, and validation Write and update SOPs, test methods, specifications, and laboratory documentation Support stability testing, reference standards, chemical inventory, and general laboratory compliance Maintain accurate records and follow cGMP, GLP, and laboratory safety requirements Why People Like Working with Us Collaborative team that values practical solutions and continuous improvement. Stable, full-time schedule with a focus on work-life balance. We offer a comprehensive benefits package to employees and their families. Flexible Spending Account & Health Savings Account options Voluntary Life Insurance Short-Term& Long-Term Disability 401(k) Plan with up to 6% Match Paid Time Off Paid Holidays (8 holidays) Quarterly Vitamin Allowance (up to $150) Employee Wellness Program Performance based spot bonuses Final candidate will be required to successfully complete a pre-employment background check and drug screening, as condition of employment in a GMP-regulated facility. Requirements What We're Looking For Bachelor's degree in Chemistry, Biochemistry, or a closely related physical science Minimum 2 years of hands-on analytical laboratory experience Hands-on experience operating and troubleshooting HPLC and ICP-MS Experience in a cGMP, GLP, ISO 17025, or other regulated laboratory environment Experience with OOS investigations and method validation/verification preferred Strong analytical, troubleshooting, and problem-solving skills Strong attention to detail and documentation Ability to work independently and keep pace with production demands Proficiency with Excel and general computer systems Ability to communicate effectively in English, both verbally and in writing This is a full-time, on-site position in Las Vegas, Nevada working within our QC laboratory and manufacturing environment. #J-18808-Ljbffr