QC Lab Analyst III

Our client, a leading Cosmetics manufacturing company is looking for QC Lab Analysts to join their growing team.

Location: Scarborough, ON,

Shifts: Day; Afternoon

Responsibilities:

Responsible for conducting complex analysis, evaluation and release of raw materials, mass and/or cosmetic finished goods in accordance with specifications and standards before being shipped or used in filling or manufacturing.
Will also conduct environmental monitoring testing and validation. Will evaluate improvement opportunities, propose solutions to management and lead/provide guidance to more junior QC Lab Analysts for OOS investigations as the QC technical subject matter expert.
When necessary, update SOPs and provide training on new technical procedures. As necessary, support the QC Lab Lead for a shift in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods/mass meet internal and external specification.

Key Roles & Duties:

Execution of QC Lab Testing

Support the QC Lab Lead for a shift (when necessary) in planning, organizing, implementing and controlling the daily activities of the QC laboratory to ascertain that both raw materials and assay of finished goods/mass meet internal and external specification. This could include management for lab workflow, sample analysis, sample retention, standards management, raw material qualification, TPM testing, outsourced testing, inventory management and document management.
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 complex routine and non-routine analysis of raw materials, mass and finished goods. 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.
Conduct environmental monitoring testing and validation.
Complete documentation as needed to support testing procedures
Work with Lab Coordinator to retain or discard sample, archive lab documents

Testing Data Review and Release - Data Reviewer role responsibilities (% will vary by site)

Revieof routine/non-routine supporting test data and results, including sample preparation records, chromatograms / graphs, 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

Investigation/Problem Solving

Evaluate improvement opportunities and propose solutions as the QC technical subject matter expert
Lead and/or provide guidance on Phase 1 OOS laboratory investigations
Conduct Quality Control evaluations of consumer complaints and Quality Inquiries

SOP Development & Training

Job Requirements & Qualifications:

Degree in Science preferably B.S./M.S. in Chemistry or Biochemistry or Microbiology equivalent experience
Minimum 3 years’ experience in Pharmaceutical/Cosmetic/Food industry.
Must have supervisory experience .
Experience in a microbiology, analytical chemistry or product evaluation laboratory in Quality Control for a global consumer goods or pharma company
Advanced physical product or Microbiology evaluation skills required with strong emphasis on color matching expertise & advanced fine fragrance odor evaluation ability, as applicable to role
Excellent awareness and practice of safe lab procedures
Excellent knowledge of laboratory testing techniques (GMP, GDP and Good Lab Practices) and proficient use of all laboratory equipment (e.g., Viscometer, ACS Color Computer, Vitek, Analytical Instrumentation)
Proficient oral and written communication skills and ability to appropriately communicate information to management
Experience with writing SOPs, deviations, change controls and OOS reports
Excellent problem solving skills
Knowledge of cosmetic ingredients & manufacturing procedures preferred
Proficiency in Microsoft Office Suite and SAP systems is preferred
Must be flexible to work different shifts and overtime as needed
Must be able to lift 35 lbs.

How to Apply:

Please send your resume to careers@gc-employment.com with the subject of "QC Lab Analyst III".