Quality Control Assistant Manager
- Toronto, ON, Canada
- Scarborough, ON, Canada
$60,000 to $65,000 CAD / year · Full-time
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Job details
- Pay
- $60,000 to $65,000 CAD / year
- Job type
- Full-time
- Apply by
- Experience
- Minimum 3–5 years of relevant quality control experience in a GMP-regulated manufacturing environment, preferably in the cosmetics, pharmaceutical, or personal care industry.
- Posting language
- English
- Posted
Original job description
Crystal Claire Cosmetics Inc. has inspired the industry with its award-winning cosmetics services since 2004. We embrace research and innovation - ceaselessly bringing advanced cosmeceutical technologies and ingredients into our creation.
At Crystal Claire Cosmetics Inc., we take pride in our innovation, expertise, and excellence in creating the finest cosmetic formulas and packaging solutions for our clients. We partner with the world’s top leading cosmetics companies in providing full integrated turnkey solutions. We value and respect individuality and personal initiative where all employees can develop, grow, and achieve their career goals.
Join us, and be the sparkle of our team!
Job Title: Quality Control Assistant Manager
Department: Quality Control
Wage Category: Annual Salary with Benefits
Report to: Quality Control Manager
Location: 165 Milner Ave, Scarborough, ON, M1S 4G7
Annual Salary: $60,000 to $65,000
Duties and Responsibilities:
- Support in managing daily QC activities, including raw material and packaging component testing, bulk testing, filling and packaging line inspection, and product release activities.
- Ensure QC activities are performed in compliance with GMP/GLP requirements, established SOPs, quality standards, and applicable regulatory requirements.
- Supervise, train, and provide guidance to QC personnel to ensure proper execution of testing procedures, inspections, documentation, and quality control activities.
- Monitor QC workflow, assign daily tasks, and ensure testing and inspection activities are completed accurately and within established timelines.
- Assist in investigating deviations, out-of-specification (OOS) results, non-conformances, and customer complaints. Support root cause analysis and implementation of corrective and preventive actions (CAPAs).
- Coordinate with relevant departments to resolve quality-related issues and ensure timely communication of inspection and testing results.
- Supervise QC activities related to line trials, first production batches, label claim determinations, stability studies, and compatibility studies.
- Review testing results, inspection records, and QC documentation to ensure accuracy, completeness, and compliance with established specifications.
- Support the evaluation of product quality based on approved specifications and historical performance. Assist in reviewing range boards in collaboration with relevant departments.
- Monitor QC performance, identify opportunities for process improvement, and support the implementation of corrective actions to improve efficiency and quality.
- Ensure QC testing and inspection activities are completed within established cycle times and promptly escalate any delays or quality concerns to management.
- Assist in preparing, reviewing, and updating QC SOPs, test methods, protocols, and other GMP-related documentation.
- Ensure QC equipment and instruments are properly maintained, calibrated, and used in accordance with established procedures.
- Support internal and external audits by ensuring QC documentation, records, and practices meet applicable quality and regulatory requirements.
- Perform other related duties as assigned by management.
Qualifications and Skills Required:
- Bachelor's Degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline, or equivalent education and experience.
- Minimum 3–5 years of relevant quality control experience in a GMP-regulated manufacturing environment, preferably in the cosmetics, pharmaceutical, or personal care industry.
- Previous supervisory or team leadership experience is preferred.
- Proficiency in Mandarin and English, both written and verbal, is required.
- Good knowledge of GMP/GLP requirements, quality control procedures, and applicable regulatory standards.
- Experience with raw material testing, packaging component inspection, bulk product testing, and finished product quality control.
- Familiarity with deviation investigations, OOS investigations, CAPA processes, and quality documentation.
- Strong organizational, problem-solving, communication, and interpersonal skills.
- Ability to supervise daily operations, prioritize multiple tasks, and meet established deadlines.
- Proficiency in Microsoft Office and general computer applications.
- Ability to work independently and collaboratively with cross-functional teams.
- Strong attention to detail, adaptability, and commitment to continuous improvement.
We care for our employees:
- Convenient public transit (bus stop right outside the facility)
- On-site free parking
- On-site gym
- Employee Health Benefits
- Corporate Discount Program
- Group Retirement Saving Plan / Deferred Profit-Sharing Plan (GRSP/DPSP)
Please note: Qualified candidates are invited to apply by sending the resume via email to hr@crystalclaire.com . Only those selected for an interview will be contacted, and applicants who do not receive a response within a reasonable timeframe may assume their application was unsuccessful. Candidates who participate in an interview will be informed within 45 days of the interview, or the final interview if applicable, as to whether a hiring decision has been made, in accordance with Ontario legislation. For inquiries, please contact our Human Resources department at hr@crystalclaire.com. We sincerely thank all applicants for their interest in joining Crystal Claire Cosmetics Inc. and look forward to the opportunity of welcoming dedicated talent to our team.
For more information, please visit our Company Website or follow us on LinkedIn at https://www.linkedin.com/company/crystal-claire-cosmetics-inc/.
This posting represents an existing vacancy within our organization.
We affirm that our hiring process, including candidate screening, evaluation, and selection, does not involve the use of Artificial Intelligence (AI) or automated decision-making tools.
Crystal Claire Cosmetics Inc. is an equal opportunity employer. We are committed to providing a workplace that is inclusive, respectful, and free from discrimination. Accommodation is available for applicants with disabilities during all stages of the recruitment process.
More about this job
Responsibilities
Support and oversee daily quality control operations, including testing, inspections, product release, staff guidance, and review of quality records to ensure compliance with GMP/GLP requirements and applicable standards. Assist with investigations, CAPAs, audits, documentation, equipment maintenance, and process improvements while coordinating quality matters across departments.
Requirements
Requires a bachelor's degree in a relevant scientific discipline or equivalent education and experience, plus 3–5 years of quality control experience in a GMP-regulated manufacturing environment. Candidates must be proficient in written and spoken Mandarin and English and have knowledge of QC testing, GMP/GLP, investigations, CAPAs, and quality documentation; supervisory experience is preferred.
Skills
- Quality Control
- GMP/GLP Compliance
- Raw Material Testing
- Packaging Component Inspection
- Bulk Product Testing
- Finished Product Quality Control
- Deviation Investigations
- Out-of-Specification Investigations
- Root Cause Analysis
- Corrective And Preventive Actions
- Team Supervision And Training
- Quality Documentation
- SOP Development
- Equipment Calibration
- Microsoft Office
- Mandarin And English Proficiency
Benefits
- On-Site Gym
- Employee Health Benefits
- Corporate Discount Program
- Group Retirement Savings Plan
- Deferred Profit-Sharing Plan
- Free On-Site Parking
- Convenient Public Transit
Visa sponsorship
Not detected in the job text
Categories
- Manufacturing
- Management & Leadership
- Science & Research
Keywords
- Quality Control
- Good Manufacturing Practices
- Good Laboratory Practices
- Standard Operating Procedures
- Raw Material Testing
- Packaging Component Inspection
- Bulk Product Testing
- Finished Product Testing
- Product Release
- Line Trials
- First Production Batches
- Label Claim Determinations
- Stability Studies
- Compatibility Studies
- Deviation Investigations
- Out-Of-Specification Results
- Non-Conformances
- Customer Complaints
- Root Cause Analysis
- Corrective And Preventive Actions
- Quality Documentation
- Internal Audits
- External Audits
- Equipment Calibration
- Process Improvement
- Cosmetics Manufacturing
- Microsoft Office
- Mandarin
- English