Analytical Chemist Job at Adept Life Sciences, Chandler, AZ

  • Adept Life Sciences
  • Chandler, AZ

Job Description

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.

•Organized and process-oriented, with good time-management skills and the ability to multi-task and change priorities quickly in a fast-paced environment.

•Clear spoken and written communication, and the ability to work independently or as part of a team.

•Positive attitude, punctuality, and dependability.

•Understands and follows laboratory safety rules and procedures.

PHYSICAL REQUIREMENTS

•Regularly involves standing, walking, and sitting at a lab bench or computer for extended periods.

•Frequent use of hands and fingers for precise work with pipettes, glassware, samples, and instrument controls.

•Occasionally involves lifting and carrying up to 25 pounds.

•Specific vision abilities required include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT

•Primarily an analytical and microbiology laboratory environment, with some time at a desk or computer.

•Exposure to laboratory chemicals, solvents, compressed gases, and microbiological cultures, handled under established safety procedures.

•Required to wear protective gear, i.e. lab coats, safety glasses, and gloves, in the laboratory.

PI23ed5ca4e754-38059-41834485

Job Tags

Full time, Contract work, Monday to Friday, Shift work

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