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.