QC Analytical Chemist: Precision Testing & GMP Impact

Nature's Lab; Las Vegas (NV); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Flexible Spending Account

Health Savings Account

401(k) Plan with up to 6% Match

Paid Time Off

Paid Holidays

Voluntary Life Insurance

Short-Term Disability

Long-Term Disability

Employee Wellness Program

Job summary

DrVita, Inc. in Las Vegas, NV, is seeking a QC Analytical Chemist to join our Quality team in a fast-paced dietary supplement manufacturing environment.

You will perform analytical testing of raw materials, in-process blends, and finished products to ensure quality and regulatory requirements. The ideal candidate has hands-on experience with HPLC and ICP-MS, a solid understanding of cGMP laboratory practices, and the ability to independently troubleshoot analytical testing and instrumentation.

Qualifications

• 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.

Responsibilities

• 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.

Skills

HPLC

ICP-MS

Excel

Education

Bachelor's degree in Chemistry or related

Tools

HPTLC

FTIR

Job description

DrVita, Inc. in Las Vegas, NV, is seeking a QC Analytical Chemist to join our Quality team in a fast-paced dietary supplement manufacturing environment.

You will perform analytical testing of raw materials, in-process blends, and finished products to ensure quality and regulatory requirements. The ideal candidate has hands-on experience with HPLC and ICP-MS, a solid understanding of cGMP laboratory practices, and the ability to independently troubleshoot analytical testing and instrumentation.