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Quality Assurance Associate Consultant - Pharmaceutical

Offre en anglais

The Associate Consultant manages compliance projects, performs critical data assessments, and develops quality documentation such as SOPs and protocols. They are also responsible for releasing products to market and assisting with regulatory audits and self-inspections.

  • Hybride
  • Mississauga, ON
  • Publié 13 mai 2026
  • 1 poste

Résumé du poste

This Pharmaceutical Consulting role focuses on applying your GMP knowledge and experience to various projects, such that the client is confident in the approach and timing of execution of the project. Our consultants work independently within a team environment to ensure activities are undertaken in a timely manner. We are looking for consultants who want to apply their in-depth quality and compliance knowledge and out-of-the-box thinking to challenging projects with our clients. Our projects cover, but are not limited to: deviation investigations, auditing, management of quality systems, delivering of training, batch document review, product releases, equipment validation, computer validation (including data integrity): related to the fabricating, packaging and testing of pharmaceuticals, biologics, NHPs and Medical Devices. Depending on your experience and career goals, the successful candidate would be placed in one of the two operational companies : Q&C Services - focuses on supporting importing projects where importing experience is an asset OR QCR - supports various quality consulting roles. In this broad-based role, you will support the projects assigned to you, meeting the client’s needs. The role specifically prioritizes, plans, organizes and executes projects related to quality and compliance of health products to ensure smooth implementations. The role may involve coordinating/working with client personnel to meet project goals. Reporting to the Manager, Quality Services or Compliance Services the Associate Consultant is responsible for: Prioritizing and managing compliance projects Completing critical assessments of data and documents to identify gaps compared to regulatory requirements Communicating project milestones on a monthly basis Completing client assigned tasks: deviation investigations, review of importer documentation Developing documentation as required by the project: SOPs, protocols, reports, APQRs etc. Releasing product to market Assisting with hosting Health Canada audits, corporate audits, and self inspections If you are a Quality Assurance professional in the Pharmaceutical industry, we have the environment and exposure to the type of work you want to do. Education - Bachelors' degree in Science required 1 – 3 years industry experience in the following is an asset: Change/CAPA management Deviation investigations Master manufacturing/batch record review and lot release Annual Product Quality Reviews Stability review and assessment APQR review and assessment Exposure to Health Canada audits, corporate audits and self inspections Salary range: CAD 60,000 – 70,000 annually Annual salary will be based on candidate’s experience, skill, knowledge, and qualifications relevant to the role. This posting is for an existing vacancy. Learn about what makes our company unique at www.qualityandcompliance.com Q&C welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selections process.

Ce que vous ferez

The Associate Consultant manages compliance projects, performs critical data assessments, and develops quality documentation such as SOPs and protocols. They are also responsible for releasing products to market and assisting with regulatory audits and self-inspections.

Exigences

A Bachelor's degree in Science is required, along with 1 to 3 years of industry experience. Preferred experience includes CAPA management, deviation investigations, and exposure to Health Canada audits.

Compétences indiquées

  • Gestion de projetSouhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

  • GMP Knowledge
  • Deviation Investigations
  • Auditing
  • Quality Systems Management
  • Batch Document Review
  • Product Release
  • Equipment Validation
  • Computer Validation
  • Data Integrity
  • SOP Development
  • CAPA Management
  • APQR Review
  • Stability Review
  • Regulatory Compliance
  • Health Canada Audits
  • Project Management

Domaines d’emploi

  • Consulting
  • Healthcare
  • Science & Research
  • Manufacturing
  • Engineering

Renseignements supplémentaires

Formation minimale
Baccalauréat
Expérience minimale
2+ ans
Langue de l’offre
anglais
Heures de travail
40 heures par semaine
Exigences de lieu
Country, Canada