Analytical Method Development Lead — QC & Validation

ProCaps Labs; Henderson (NV); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical, Dental & Vision

401(k) Match

Paid Time Off

Gym Membership

Life Insurance

Short Term Disability

HSA Contribution

Employee Referral Program

Pet Insurance

Job summary

ProCaps Labs is seeking a Quality Control Method Development Specialist to provide technical leadership in analytical method development, validation, verification, and transfer, aligned with ISO/IEC 17025 accreditation and cGMP. The role covers HPLC, GC, ICP-MS, HPTLC, UV/Vis, Protein Analyzer, and other lab technologies.

The candidate will lead validation studies, adapt methods for instruments, and support continuous improvement, ensuring scientific soundness and regulatory compliance across QC

Qualifications

• Bachelor’s degree in chemistry or related science.
• 3+ years in analytical method development, validation, or QC.
• Experience in regulated laboratory environments.
• Strong understanding of analytical chemistry principles and investigations.
• Familiar with USP, AOAC, ICH, ISO/IEC 17025.

Responsibilities

• Develop, optimize, implement, and troubleshoot analytical methods for materials and products.
• Design and execute method validation, verification, transfer, and equivalency studies.
• Prepare validation protocols, reports, and supporting documentation.
• Lead instrument qualification, verification, and integration of new technologies.
• Support audits, CAPA, data reviews, and continuous improvement.

Skills

Analytical method development

Validation

Laboratory quality control

Regulatory compliance

MS Office proficiency

Leadership / mentoring

Education

Bachelor’s degree in Chemistry or related science

Tools

HPLC

GC

ICP-MS

HPTLC

UV/Vis

Protein Analyzer

Job description

ProCaps Labs is seeking a Quality Control Method Development Specialist to provide technical leadership in analytical method development, validation, verification, and transfer, aligned with ISO/IEC 17025 accreditation and cGMP. The role covers HPLC, GC, ICP-MS, HPTLC, UV/Vis, Protein Analyzer, and other lab technologies.

The candidate will lead validation studies, adapt methods for instruments, and support continuous improvement, ensuring scientific soundness and regulatory compliance across QC