Specialist, Quality Assurance

6 days ago

Dorval, Quebec, Canada Groupe Marcelle Full time
Located in Montreal, Quebec, the Canadian company Groupe Marcelle is a leader in the cosmetics industry.

With the highest standards of quality and excellence, Groupe Marcelle develops, manufactures, and distributes care and makeup products and accessories with a portfolio of four brands:
Marcelle, Watier, Annabelle and CW Beggs and Sons.


At Groupe Marcelle we believe in an environment where passion can be expressed, creative minds lead to exceptional innovation, audacity and focus are a pillar of great success and acts of empowerment, collaboration and humanity are widely encouraged.

Because our purpose is to "Cultivate beauty in the world", we strive to care for you, people and the environment.

We are looking for professionals who will exemplify these values and bring energy and commitment to results.


Join a company with more than 300 employees in the cosmetics field and play a key role in the organization.

Groupe Marcelle is looking for a Specialist, Quality Assurance for a permanent full-time position.


Reporting to Manager, Quality Assurance and Quality Control, the Specialist, Quality Assurance is responsible for the compliance of internal and external batch records, as well as processes related to good manufacturing practices.


WORK ENVIRONMENT

  • Workplace: 9200, CôtedeLiesse Road, Montreal, Quebec, with 5 days a week working at the office.
  • Growing company.
  • A dynamic team of professionals.
  • Benefits: Competitive base salary and generous benefits package (including flexible hours, medical and dental insurance, pension plan, bonus and holiday vacation).
  • Employee discounts on all Marcelle Group products.

YOUR RESPONSIBILITIES WILL BE

  • Approve DIN/NPN batch records according to regulatory requirements (Health Canada/FDA).
  • Write/review nonconformance reports related to quality.
  • Conduct regular literature searches.
  • Followup and implement CAPAs.
  • Participate/collaborate in Health Canada and FDA inspections.
  • Continuously improve processes.
  • Write/revise and/or verify internal standard procedures.
  • Train staff on GMP principles and current procedures and schedules.
  • Build and maintain a solid batch file in accordance with current regulations.
  • Establish quality agreements with suppliers and subcontractors and follow up as appropriate.
  • Follow up on action plans and deadlines resulting from inspections.
  • Collaborate on change controls and do the appropriate followup.
  • Assist employees with QA processes.
  • Evaluate the various trends resulting from the quality systems.
  • Participate in the updating of key performance indicators (KPI).
  • Other, as needed, related tasks.
WE WOULD LIKE TO MEET YOU IF YOU HAVE

  • Bachelor's degree or DEP in quality assurance or any other related field.
  • Minimum 5 years of experience in the pharmaceutical field or in the quality assurance process.
  • Very good knowledge of GMP, GMP and Canadian, European and American regulations.
  • Good computer skills: Word, Excel, Outlook, Visio, etc.

AND IF YOU ARE

  • Bilingual, French and English, as the person will be working with documentation from both the United States and Europe.
  • Well organized, methodical, and responsible.
  • Good at working in a team environment.
  • Good at taking initiative, good judgment and good objective and relational approach.
  • Good with analytics.
The task and responsibilities listed above are summaries and indicatives.

TO APPLY

DIVERSITY AND INCLUSION
Groupe Marcelle wants to offer equal employment opportunities to all. It invites women, members of visible and ethnic minorities, Aboriginals, and persons with disabilities to apply.

Groupe Marcelle is also committed to pursuing the integration of diversity and making it a source of enrichment and pride for all its employees.

The use of the masculine gender in this document refers to both men and women.

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