Technician, Quality Control- Fixed Term Contract

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

In this role you will perform day-to-day quality control and quality assurance activities.

KEY RESPONSIBILITIES

• Assist with Validation Activities
  • Cleaning validation/verification (sampling, testing)
  • Temperature mapping
  • Assisting with Calibration/PM program
  • Assist with execution of validation as projects arise
• Perform inspections and line clearances according to approved manufacturing and packaging records.
• Perform testing and releasing of packaging components.
• Perform testing and release of Bulk and Finished Product in the QC Chemistry lab.
• Review technical documents including packaging orders, batch records, QC testing (bulk and finished product), packaging components, stability and validation testing.
• Perform stability program activities including monitoring and mapping of stability chambers, placing and retrieving stability samples according to the established schedule.
• Assist in the generation and review of SOPs and associated controlled documents.
• Assist Lab Analysts with daily lab duties as assigned.
• Participates in investigation and follow-up for non-conformances (OOS and OOT)
• Assist in developing quality assurance policies and procedures, production capabilities and recommend improvements.
• Flexible to work different shifts as required to provide ongoing quality control support to Production.
• Work in a manner and with protective devices, measures and procedures required by the Occupational Health and Safety Act and the regulations.
• Use or wear protective equipment, devices or clothing that the company requires.
• Other duties as assigned.

ABOUT THE ROLE

The purpose of this position is to perform day-to-day quality control and quality assurance activities.

KEY RESPONSIBILITIES

• Assist with Validation Activities
  • Cleaning validation/verification (sampling, testing)
  • Temperature mapping
  • Assisting with Calibration/PM program
  • Assist with execution of validation as projects arise
• Perform inspections and line clearances according to approved manufacturing and packaging records.
• Perform testing and releasing of packaging components.
• Perform testing and release of Bulk and Finished Product in the QC Chemistry lab.
• Review technical documents including packaging orders, batch records, QC testing (bulk and finished product), packaging components, stability and validation testing.
• Perform stability program activities including monitoring and mapping of stability chambers, placing and retrieving stability samples according to the established schedule.
• Assist in the generation and review of SOPs and associated controlled documents.
• Assist Lab Analysts with daily lab duties as assigned.
• Participates in investigation and follow-up for non-conformances (OOS and OOT)
• Assist in developing quality assurance policies and procedures, production capabilities and recommend improvements.
• Flexible to work different shifts as required to provide ongoing quality control support to Production.
• Work in a manner and with protective devices, measures and procedures required by the Occupational Health and Safety Act and the regulations.
• Use or wear protective equipment, devices or clothing that the company requires.
• Other duties as assigned.

REQUIRED EXPERIENCE YOU'LL BRING

• Minimum College diploma.
• Quality Control/Assurance experience in a GMP environment

PREFERRED EXPERIENCES AND SKILLS

• Knowledge of validation/calibration of manufacturing equipment
• Experience performing physical/chemistry testing in a GLP laboratory
• Knowledge of applicable regulatory and industrial standards as it relates to cGMP and GLP is an asset.
• Ability to organize and manage multiple priorities
• Workplace Hazardous Materials Information Systems (WHMIS) training,
• Organizational skills to handle multiple tasks.
• Working knowledge of SC Johnson Professional product line.
• Strong interpersonal skills required to effectively liaise with manufacturing staff, administration staff and external contacts.
• Good Verbal and written communication skills in dealing/corresponding with outside contacts and internal staff.
• Good judgement and problem-solving skills are necessary when dealing with results that require modifications/resolving.

JOB REQUIREMENTS

• 5 hours per day as assigned by the Supervisor with a 30 minute lunch break, and two 15 minute breaks, Monday to Friday. 
• Must be available to work ALL shifts: days, nights, weekends. 
• Overtime available as required and pre-approved by manager
• This position is not eligible for relocation
• This position is not eligible for remote work

Other duties, responsibilities and activities may change or be assigned

at any time with or without notice as assigned by the Manager. The job description does not constitute a contract of employment.

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 – that enables all to bring their full contributions to the organization.

SC Johnson & Son Inc., SC Johnson Professional, and SC Johnson Lifestyle Brands is committed to accessibility in its workplace and recruitment processes for persons with disabilities. If you require accommodation in order to participate in this recruitment process, please contact Human Resources.