Analyst, Quality Control

at  SC Johnson Professional

Joining the team at SC Johnson Professional® makes you part of a family company with a deep history in the professional market as a leading manufacturer of skincare, cleaning and hygiene products, and smart technologies. We provide solutions to Healthcare, Clean Industrial, Industrial, Office & Institutional, Hospitality & Travel, and Retail & Entertainment markets.
SC Johnson Professional®
is a business unit within SC Johnson, a family-owned and led company and leading manufacturer of quality, trusted products since 1886.
Position Summary
To perform chemical, physical and other tests of incoming raw materials /packaging components, in-process and finished product to ensure each meets company, customer and government standards and regulations.

Key Responsibilities

• Execute sampling and testing of raw materials according to GMP and all applicable DWHI SOPs.
• Perform testing on stability samples, when required.
• Perform inspections & tests of in-process, bulk and finished product.
• Perform logbook; lab book review
• Records test results in appropriate laboratory logs/records.
• Accountable for the accuracy and validity of testing results.
• Perform equipment temperature monitoring.
• Carries out work within Good Laboratory Practices Guidelines.
• Participates in investigations and follow up for OOS/ non-conformance investigations.
• Assist in preventative maintenance/ calibration of assigned laboratory equipment
• Assist in qualification/validation of test methods and laboratory equipment
• Must become familiar with the rules and safety programs applicable, follow prescribed health and safety policies and procedures and participate in the process of identifying, reporting and assisting in eliminating risks to health and safety in the workplace.
• Recognize and report typical out-of-specification or out-of-trend test results, instrument malfunctions and methodology problems.
• Review QC Analytical records and production batch records
• Purchases Lab supplies, keeps inventory in the QC Lab
• Any other duties as assigned by Supervisor.

EDUCATION AND SKILLS REQUIRED:

• Hold a university degree or equivalent in science related to the field of work.
• 1-3 years experience.
• Skilled in use of Gas Chromatograph (GC), High Performance Liquid Chromatograph (HPLC), IR, UV spectrophotometer, Karl Fisher, analytical balance.
• Good judgement and problem solving skills necessary when dealing with test results that require investigation.
• Ability to work independently in both technical and time management skills.
• Work related experience in laboratory procedures and test methods.
• Knowledge of Canadian, USA & international GMP requirements
• Knowledge of USP & other pharmacopoeia requirements
• WHMIS or other chemical safety training in relation to handling of chemicals.
• Accuracy required in recording test results.
• Mathematical skills to perform measurements & basic statistical analysis.
• Motor skills and co-ordination to operate hot plates, weigh scales, burettes, pipettes, viscometer, micrometer, photocopier
• Knowledge of laboratory and office equipment as noted above under motor skills.
• Analytical ability to assess test results.
• Care-taking skills to maintain a clean and safe laboratory area.
• Verbal communication skills in dealing with manufacturing, laboratory and office staff.
• Knowledge of company product line and packaging to ensure quality control.
• Proficient in the English language
• Experience, education or knowledge of microbiology testing an asset.

• Execute sampling and testing of raw materials according to GMP and all applicable DWHI SOPs.
• Perform testing on stability samples, when required.
• Perform inspections & tests of in-process, bulk and finished product.
• Perform logbook; lab book review
• Records test results in appropriate laboratory logs/records.
• Accountable for the accuracy and validity of testing results.
• Perform equipment temperature monitoring.
• Carries out work within Good Laboratory Practices Guidelines.
• Participates in investigations and follow up for OOS/ non-conformance investigations.
• Assist in preventative maintenance/ calibration of assigned laboratory equipment
• Assist in qualification/validation of test methods and laboratory equipment
• Must become familiar with the rules and safety programs applicable, follow prescribed health and safety policies and procedures and participate in the process of identifying, reporting and assisting in eliminating risks to health and safety in the workplace.
• Recognize and report typical out-of-specification or out-of-trend test results, instrument malfunctions and methodology problems.
• Review QC Analytical records and production batch records
• Purchases Lab supplies, keeps inventory in the QC Lab
• Any other duties as assigned by Supervisor