Analytical Chemist

2 days ago

Phoenix AZ, Maricopa County, AZ; Arizona, United States Adept Life Sciences Full-time

Accredited Labs is an Independent, ISO/IEC 17025 certified, 3rd party Analytical Laboratory in Chandler, Arizona. We provide chemistry and microbiology testing solutions for the Food, Nutraceutical, Cannabis, Personal Care Cosmetic Industries. As a full-service, 3rd party contract laboratory, we provide services to multi-national brands through the entire supply chain.

JOB TITLE:

Analytical Chemist REPORTS TO:

Laboratory Director LOCATION:

Chandler — Accredited Analytical Labs TYPE:

Full-time Exempt RATE:

From $65,000 per year SCHEDULE:

Full-time on-site; Monday through Friday, 7:00 AM to 4:00 PM, with occasional additional hours as testing demands require ABOUT THE ROLE The Analytical Chemist performs chemical and microbiological testing at Accredited Analytical Labs, the ISO/IEC 17025-accredited, independent third-party laboratory in Chandler. The lab tests raw materials and finished goods. This role runs analyses on advanced instrumentation (HPLC, UPLC, LC-MS/MS, GC-MS, ICP-MS, and FTIR), reviews and reports results, develops and validates methods, and helps the lab grow its capabilities. The lab is a modern, best-in-class facility built around its people, with a fast-paced, team-oriented culture, bright and comfortable workspaces. KEY RESPONSIBILITIES & DUTIES Analytical & Microbiological Testing

  • Prepare samples and conduct chemical and microbiological analyses of raw materials, in-process samples, and finished goods according to validated methods and standard operating procedures.
  • Operate HPLC, UPLC, LC-MS/MS, GC-MS, ICP-MS, FTIR, and other laboratory instruments following SOPs.
  • Perform microbiological analysis using Petrifilm and other approved methods.
  • Supervise and perform environmental monitoring and water testing.
  • Meet client and internal turnaround times by managing workload and shifting priorities quickly as needed. Data Review, Documentation & Reporting
  • Compile, document, review, interpret, and authorize testing results, following good documentation practices.
  • Prepare accurate data packages and support preparation of Certificates of Analysis (COAs).
  • Analyze and report data, including department KPIs such as turnaround time and testing backlog. Method Development, Validation & Investigations
  • Develop and validate testing methods, and verify compendial methods as needed.
  • Perform out-of-specification (OOS) investigations and report findings, including root cause and corrective actions.
  • Assist with writing and updating laboratory SOPs, and help design new SOPs as the lab adds equipment and capabilities. Instrumentation & Laboratory Operations
  • Perform routine maintenance, calibration checks, and troubleshooting of analytical instruments.
  • Maintain lab inventory, including supplies, reagents, and reference standards.
  • Take on assigned special projects, including implementing new equipment, methods, and testing services as the department grows. Quality, Compliance & Safety
  • Follow cGMP, ISO/IEC 17025 requirements, and laboratory quality procedures, and support internal, client, and accreditation audits.
  • Understand and follow laboratory safety procedures, including the chemical hygiene plan, safe chemical handling, and PPE requirements.
  • Keep the laboratory clean, organized, and audit-ready.
  • Perform other duties as assigned. QUALIFICATIONS & SKILLS

EDUCATION

  • Bachelor's degree in Chemistry, Biology, or a related science field required. EDUCATION & EXPERIENCE (PREFERRED)
  • More than five years of laboratory experience.
  • Familiarity with ISO/IEC 17025 laboratory accreditation requirements.
  • Experience in a dietary supplement, food, pharmaceutical, or contract testing laboratory.
  • Experience with LC-MS/MS method development and LIMS. REQUIRED KNOWLEDGE, SKILLS & ABILITIES
  • Laboratory experience, with three years or more preferred.
  • Hands-on experience with analytical instrumentation such as FTIR, UPLC, HPTLC, GC-MS, and ICP-MS.
  • Familiarity with cGMP requirements.
  • Excellent math, reading, and writing skills, and good technology and computer skills.
  • Meticulous attention to detail, with strong analytical and critical-thinking skills.