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Quality Control Assistant Manager

$60k - $65k per year

Crystal Claire Cosmetics Inc

Our company has inspired the industry with our award-winning cosmetics  services since 2004. We embrace research and innovation - ceaselessly bringing advanced cosmeceutical technologies and ingredients into our creation.

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:  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: 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. 

We sincerely thank all applicants for their interest in joining our company and look forward to the opportunity of welcoming dedicated talent to our team.

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. 

Our company 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.

Vacancy posted 1 day ago
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