QC Analytical Chemist
hace 3 días
Las Vegas
Job DescriptionDescription: 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 Schedule & Work Environment This is a full-time, on-site position in Las Vegas, Nevada working within our QC laboratory and manufacturing environment.