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Alexion

Global biopharmaceuticals focusing on rare diseases

Senior Manager - Country Quality, Canada

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMississauga, ON, Canada$88.3k - $115.9k /yr

About the Job

Requirements

  • A Bachelor's degree in life science or pharmacy is required.
  • At least 6 years of hands-on Quality Assurance or Compliance experience in the pharmaceutical or biotechnology industry.
  • Experience in sterile and biological finished product manufacturing, packaging and labelling, testing, and distribution processes.
  • In-depth knowledge of Health Canada regulations and guidelines pertaining to GMP/GXP is required; experience with EMA, FDA, or PMDA is an asset.
  • Demonstrable computer skills.
  • Ability to work globally in a matrix environment.
  • Ability to influence management, peers, and collaborators.
  • Ability to work in a dynamic environment and redefine the scope of responsibilities in alignment with compliance and business needs.
  • Ability to multitask and prioritize work.
  • Strong organizational ability.
  • Ability to travel overnight occasionally as required.

Responsibilities

  • Maintain the quality management system in line with Corporate Quality and Health Canada GMP requirements, including deviation management, CAPA, complaint management, change control management, documentation management, training management, recall management, self-inspection management, and quality management review.
  • Manage QA-related tasks, including lot release activities, in compliance with Health Canada GMP requirements.
  • Coordinate with Supply Chain and relevant collaborators to prioritize lot release according to business needs.
  • Manage the rollout and ongoing compliance with Alexion’s global quality and compliance systems, procedures, and standards at the site level.
  • Support coordination and management of Health Canada GMP inspections.
  • Manage the review and implementation of quality improvement and remediation plans identified through Corporate or internal audits.
  • Ensure Alexion Policies and Global Quality Standards Operating Procedures are implemented in accordance with local GMP/GXP guidelines.
  • Support quality oversight and activities associated with new product launches.
  • Support and collaborate with other functions, including Pharmacovigilance and Regulatory Affairs, by providing Quality input and identifying risks to the QMS.
  • Authorize the return to saleable stock of returned medicinal products.
  • Support the qualification and approval of suppliers and customers.
  • Approve and maintain quality agreements with vendors relating to wholesale distribution or transportation of medicinal products.

Desired Qualifications

  • An advanced degree is preferred.
  • Experience with EMA, FDA, or PMDA regulations and guidelines is an asset.

About the Company

Alexion

Global biopharmaceuticals focusing on rare diseases

Alexion, now the rare disease group within AstraZeneca, develops and sells therapies for rare and ultra-rare diseases by targeting the complement immune system. Its drugs, such as Soliris and Ultomiris, inhibit the C5 component to slow or stop disease processes, while Strensiq and Kanuma address specific metabolic disorders. It differentiates itself through a deep focus on complement biology, pursuing first- or best-in-class therapies, and using a strategy that blends internal R&D with acquisitions to expand its pipeline. Its goal is to improve outcomes for patients with rare diseases and bring these therapies to a broader international market using AstraZeneca’s scale and capabilities.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1992

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