Lab Analyst Ii Fixed Term Contract Until June 2025

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.

ABOUT THE ROLE

The Lab Analyst II will perform chemical, physical, and other tests of incoming raw materials, in-process and finished product to ensure each meets company, customer and government standards and regulations. Assist on performing tests for Method Validation/ Verification/ Transfer or special projects as assigned. Troubleshoot analytical equipment such as HPLC and GC

KEY RESPONSIBILITIES
- Responsible of Raw material program which involves, but not limited to: review of receiving documents, coordinating sampling of raw materials, update related tracking databases, testing, and Releasing 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 and lab book review;
- Records test results in appropriate laboratory logs/records.
- Accountable for the accuracy and validity of testing results.
- Perform equipment temperature monitoring 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
- Any other duties as assigned by your Supervisor/Manager.
- 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
- 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
- Creating and updating of lab related SOPs as required
- 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.
- Any other duties as assigned by Supervisor.

REQUIRED EXPERIENCE YOU’LL BRING
- Hold a university degree or equivalent in Chemistry or other science related field
- 3+ years’ experience of working in a pharmaceutical Chemistry lab, including experience with chromatographic test methodology (HPLC & GC)

PREFERRED EXPERIENCES AND SKILLS
- 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
- Skilled in use of Gas Chromatograph (GC), High Performance Liquid Chromatograph (HPLC), IR, UV spectrophotometer, Karl Fisher, analytical balance.
- 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.
- Good judgement and problem-solving skills necessary when dealing with test results that require investigation.
- Knowledge of company product line and packaging to ensure quality control.
- Proficient in the English language

JOB REQUIREMENTS

8 hours per day. Normal working hours are 8.5 hrs as assigned by the Quality and Compliance Manager with a 30 minute lunch break, and two 15 minute breaks, Monday to Friday. 40 hours per week with overtime if and when required with prior approval by manager.

Inclusion & Diversity

We believe Inclusion and Diversity is more than a program. We embed inclusive practices in our day-to-day work, the way we relate to our colleagues, collaborate, and make decisions.

We value the collective richness of the differences people bring to the organization, including style, personality, thoughts, race, ethnicity, culture, religion, gender, gender identity, sexual orientation, age, and disability - th