Lab Analyst II

Estée Lauder Companies•Melville, NY

14h•Onsite

About The Position

The Lab Analyst II is responsible for conducting basic analysis, evaluation, and release of raw materials, mass and/or cosmetic finished goods using HPLC, UPLC, GC, ICP and other wet chemistry techniques in accordance with the prescribed approved analytical test method before being shipped or used in filling or manufacturing. Will also conduct a peer data review of completed test data and validation testing. Perform OOS lab investigations and inform management of critical issues and suggest improvement opportunities. When necessary, update SOPs and provide training on new technical procedures.

Requirements

A minimum of three (3) years of experience in an analytical chemistry laboratory in Quality Control for a global consumer goods or pharma company
Advanced analytical evaluation skills required with a strong emphasis on instrumentation ability (HPLC, UPLC, GC, ICP), as applicable to the role
Proficient in troubleshooting laboratory instruments, with a focus on HPLC and GC
Solid awareness and practice of safe lab procedures
Advanced knowledge of laboratory testing techniques (GMP, GDP, and Good Lab Practices) and proficient use of all laboratory equipment (e.g., Viscometer and Wet Chemistry techniques)
Proficient oral and written communication skills and ability to appropriately communicate information to management
Ability to write SOPs, deviations, change controls, and OOS reports
Problem-solving skills
Must be able to lift 35 lbs.

Nice To Haves

Knowledge of cosmetic ingredients & manufacturing procedures preferred
Proficiency in Microsoft Office Suite and SAP systems is preferred

Responsibilities

Monitor Critical Control Parameters (lab process water, pH, balance) through daily equipment verification checks and alert QC lab manager of any out of trend events.
Conduct basic routine and non-routine analysis of raw materials, mass and finished goods using HPLC, UPLC, GC, ICP and other wet chemistry techniques in accordance with the prescribed approved analytical test method. This includes responsibility for sample preparation, sample analysis, sample reporting, processing of test results, entering results into SAP/LIMS, preparation of CoA, and sample disposition.
Proficient in troubleshooting laboratory instruments, with a focus on HPLC and GC, and work with Empower chromatography acquisition database software.
Complete documentation as needed to support testing procedures, including sample preparation records, logbooks, calculations, and data sheets.
Work on deviations, change controls, CAPA’s, investigations, SOP’s and other related tasks as required.
Work with Lab Coordinators to retain or discard samples, archive lab documents.
Flexible to do any task as requested by Management to meet business demand.
Review routine/non-routine supporting test data and results, including sample preparation records, logbooks, calculations, and data sheets. Enter results in SAP/LIMS, as needed.
Release of raw materials, non-OTC mass, and cosmetic FGs in the laboratory.
Identify quality problems and suggest improvement opportunities.
Perform Phase 1 OOS laboratory investigations with guidance from Supervisor.
Conduct Quality Control evaluations of consumer complaints and Quality Inquiries.
Create and update SOPs.
Provide training in new technical procedures when necessary.