Sr. Associate, Quality Control

SC Johnson Professional™; Brantford; On-site; CAD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a Sr. Associate in Quality Control to join their dynamic team. This role involves performing critical tests on raw materials and finished products, ensuring compliance with rigorous standards. You will lead analytical method development and contribute to laboratory investigations, making a significant impact on product quality. With a commitment to safety and excellence, this company values diversity and inclusion, providing a supportive environment for all employees. If you're passionate about quality assurance in a laboratory setting, this opportunity is perfect for you.

Qualifications

• 3+ years of experience in quality control and laboratory testing.
• Familiarity with GMP requirements in Canada and the USA.

Responsibilities

• Perform tests on raw materials and finished products to ensure compliance.
• Conduct investigations for out-of-specification results and write reports.

Skills

Analytical Method Development

Problem-Solving Skills

Good Laboratory Practices

Gas Chromatograph (GC)

High-Performance Liquid Chromatograph (HPLC)

Mathematical Skills

Verbal Communication Skills

Education

University Degree in Science

Tools

Agilent OpenLab Software

UV Spectrophotometer

Karl Fisher

Analytical Balance

Job description

Sr. Associate, Quality Control page is loaded

Sr. Associate, Quality Control

Apply locations CAN - Ontario - Brantford time type Full time posted on Posted 3 Days Ago job requisition id 29799

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

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. Perform Analytical Method development, lead Lab investigation and write final investigation reports.

KEY RESPONSIBILITIES

• Execute testing of raw materials according to GMP and all applicable SCJ Pro 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 Calibration and temperature monitoring
• Carries out work within Good Laboratory Practices Guidelines
• Performs investigations and follow up for OOS/ non-conformance investigations including investigation root cause analysis and written investigation reports
• Assist in preventative maintenance/ calibration of assigned laboratory equipment
• Performs qualification/validation of test methods and laboratory equipment including writing of validation protocols and reports
• 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.

REQUIRED EXPERIENCE YOU’LL BRING

• Hold a university degree or equivalent in science related to the field of work.
• 3+ years’ experience
• Experience with Canadian, USA & international GMP requirements

PREFERRED EXPERIENCES AND SKILLS

• Agilent OpenLab software
• 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
• Excellent writing skills as lab investigation reports write up are required
• Skilled in use of Gas Chromatograph (GC) and High-Performance Liquid Chromatograph (HPLC) (including test method development), IR, UV spectrophotometer, Karl Fisher, analytical balance.
• Work related experience in laboratory procedures and test methods.
• Knowledge of USP & other pharmacopoeia requirements
• Excellent writing skills
• 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.

JOB REQUIREMENTS

• F/T 40 hours per week
• Overtime available as required and pre-approved by manager
• This position is not eligible for remote work
• This position is not eligible for relocation

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.