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Added 4 mins ago
TG
Senior Manager, Enterprise Risk Management
TMX Group
Toronto, ON
- $130,000 to $145,000 CAD / year
- Full-time
Risk Assessments & Scenario Analysis: Design, facilitate, and execute comprehensive periodic and ad-hoc risk assessments across business units and corporate functions; actively contribute…
Added 4 mins ago
NW
Economic Planning Specialist
Nuclear Waste Management Organization
Ignace, ON
- Full-time
…community office locations may be considered). Reporting to the Manager, Social and Economic Programs, the successful candidate will provide subject matter expertise in municipal planning…
Added 4 mins ago
KG
Manager, TMF and Earthworks Area
Kinross Gold Corporation
Red Lake, ON
- Full-time
The TMF & Earthworks Area Manager leads safe, compliant delivery of major civil works for the Great Bear Project in Red Lake, including tailings facilities, dams, roads, excavations,…
Added 4 mins ago
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Quality Manager
Ganotec
Clarington, ON
- Full-time
As a Quality Manager, you will lead the the Quality team and program on a projects in your assigned location.
Added 4 mins ago
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Communications Specialist
Glenbow
Calgary, AB
- Full-time
Hiring Manager: Manager, Marketing & Communications
Added 4 mins ago
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Manager, Events
Glenbow
Calgary, AB
- Full-time
Hiring Manager: Director, Commercial Services
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- Full-time
Integrates medical leadership into service design, policy development, and system planning across the continuum.
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Manager, Information Technology
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- Full-time
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EI
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- Contract
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Quality Manager
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- Full-time
As a Quality Manager, you will lead the the Quality team and program on a projects in your assigned location.
Added 4 mins ago
AL
Compliance Manager
ARAG Legal Solutions Inc. (Canada)
Toronto, ON
- Full-time
Reporting to the Director, Legal and Compliance, the Compliance Manager will support the day-to-day delivery of the Compliance program for a federally and provincially licenced Property &…
Added 4 mins ago
Senior Manager, Value Realization Office - Term position
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Scotiabank’s Global Wealth Management (GWM) Value Realization Office is looking for a Senior Manager to join its growing Finance team. This role sits at the intersection of finance,…
Added 4 mins ago
E
Geotechnical Field Technician
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- Full-time
…the Windsor, ON office. Under the leadership of the Project Manager, the successful candidate will participate in the conception and development of various residential, commercial,…
Added 4 mins ago
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Building Science Engineer
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- Full-time
design, specifications, and construction administration. You’ll work directly
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Consultant, Continuous Improvement
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Added 4 mins ago
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Press Team Leader
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Added 19 mins ago
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Orangeville, ON
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…efficient hiring journey. Reporting to the Human Resources Manager, you will coordinate recruitment and onboarding activities, keep processes moving smoothly, and provide responsive support…
Added 19 mins ago
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Senior Software Engineer, Core Product (Hybrid)
Homebase
Remote, Canada
- $130,000 to $200,000 CAD / year
- Full-time
- Remote
You ship fast, own what you ship, and make the people around you better. You’ll work alongside Product, Design, and Data, and you’ll build the AI-first way. As an E3, you’ll lead projects…
Added 19 mins ago
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Senior Manager, Visual Design
Dandy
Remote, Canada
- $140,250 to $170,000 USD / year
- Full-time
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We’re looking for a Senior Manager of Visual Design to lead and elevate Dandy’s graphic design team. This role will serve as the creative authority and steward of Dandy’s visual identity,…
Added 19 mins ago
UM
Mechanical Engineer
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- Full-time
The Ultra Mechanical Engineering function is responsible for the design, development, test, and documentation of mechanical assemblies for products, which includes new development, change…
Added 19 mins ago
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Mechanical Engineer
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- Full-time
The Ultra Mechanical Engineering function is responsible for the design, development, test, and documentation of mechanical assemblies for products, which includes new development, change…
Added 19 mins ago
PC
PwC Private, Manager Bilingual (EN/FR)
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Our team helps our clients design and implement personal and customized service plans that are unique to privately owned entities, entrepreneurs, and high net worth individuals. You’ll be…
Added 34 mins ago
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Specialist – Technical project integration
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- Full-time
…the Senior Director - Construction on technical, contractual, design, commissioning, and operational readiness…
Added 34 mins ago
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Manager, Sales Development Representative, Akai | Global
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The Manager, Sales Development Representative, Akai Global is responsible for leading a high-performing team of SDRs focused on generating qualified pipeline and supporting revenue growth…

GRIFOLS, S.A.

Change Control Manager 1

Mississauga, ON, Canada

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Job details

Experience: Typically requires a minimum of 10 years of general experience with 6 years performance quality audits in GMP environment within the pharmaceutical industry.
Posting language: English
Posted: Oct 26, 2026

Original job description

Souhaitez-vous rejoindre une équipe internationale qui travaille à l'amélioration des soins de santé ? Voulez-vous améliorer la vie de millions de personnes ? Grifols est une entreprise mondiale de soins de santé qui, depuis 1909, travaille à l'amélioration de la santé et du bien-être des personnes dans le monde entier. Nous sommes leaders dans le domaine des médicaments dérivés du plasma et de la médecine transfusionnelle et nous développons, produisons et commercialisons des médicaments, des solutions et des services innovants dans plus de 110 pays et régions.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Position title: Supply and Audit Director

Reports to: Quality Senior Director

Position Summary:

The Supply and Audit Director provides Quality Assurance leadership for GMP audit programs, supplier qualification, and regulatory inspections, ensuring compliance with Canadian regulations, cGMP requirements, FDA and European standards. The individual oversees risk-based audit strategies, auditor development, quality agreements, supplier performance, and quality system effectiveness to identify risks, drive continuous improvement, and maintain product quality and regulatory compliance.

Position Objective:

The Supply and Audit Director provides leadership and oversight for Quality Assurance (QA) GMP audit activities, including the development and maintenance of a risk-based audit program, as well as the training and ongoing development of GMP auditors within a matrix organization. This role is responsible for assessing and reporting GMP risks, quality trends, and the effectiveness of quality systems across Grifols Canada Plasma. As the primary Quality representative, the Supply and Audit Director supports and leads interactions during third-party audits and inspections conducted by Health Authorities. The role also evaluates critical suppliers in accordance with established procedures, using audit results and key performance indicators (KPIs) to assess cGMP compliance, product quality, and service performance. Through these activities, the position helps ensure continued supplier qualification, regulatory compliance, and overall quality excellence.

Key Responsibilities:

Develop, manage and oversee a global risk-based audit program to ensure effective QA oversight of Grifols Canadian Plasma GMP activities, internally and externally.
Participate in execution of risk-based GMP internal and external audits for Grifols Canadian Plasma activities, following the audit plan.
Lead the design and implementation of auditing and supplier qualification personnel training and development programs.
Oversee and provide feedback to Quality Audit specialists to discuss findings, emerging risks and identify actions to address identified risks, ensuring formal feedback is provided to senior management on a regular basis.
Provide quality direction in relation to regulatory updates as it impacts on the Grifols Canadian Plasma GMP audit program, ensuring continual compliance with policies and procedures.
Participate in the development and implementation of systems and processes required to support global audit processes and quality assurance requirements.
Participate in and support Regulatory inspections and aspect of notified body audits, as well as other external audits.
Establish an internal audit program to ensure that all areas in the company are in compliance with Canadian Regulation, cGMP requirements and in accordance with FDA and European standards, in order to ensure the quality and safety of final product according to the licenses approved by Health Authorities.
Ensure that supplier change notifications assessed with the support of each related areas.
Maintain and supervise Quality Agreements with critical suppliers.
Site certification (operational license, GMP, IQPP,…), new or renewal, management.

Required Skills, Qualifications and Experience:

Bachelor ‘s Degree in Health-related Sciences, preferably in Pharmacy.
Post-Graduate Certification in Quality Management.
Proven experience in GMP auditing within a Pharmaceutical Company is preferred.
Knowledge of GMP requirements preferred.
Auditor certification.
Typically requires a minimum of 10 years of general experience with 6 years performance quality audits in GMP environment within the pharmaceutical industry.
Proficiency with computers using Microsoft Office.
Organized and able to manage time effectively.
Ability to work within a highly regulated, labor-intensive environment.
Analytical and enquiring mind with the ability to interpret data and facts.
Excellent oral and written communication skills to produce clear and concise factual findings and the ability to present effectively to groups.
Effective organizational and planning skills with the ability to meet deadlines required.

The salary range for this position is currently being assessed and will be disclosed upon completion of the compensation review process, in accordance with applicable transparency requirements.

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Location: NORTH AMERICA : Canada : Mississauga:CAWINNIP - Winnipeg

Learn more about Grifols

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More about this job

Responsibilities

The Supply and Audit Director leads GMP audit programs, supplier qualification, and regulatory inspections to ensure compliance with Canadian, FDA, and European standards. This role oversees risk-based audit strategies, auditor training, and quality system effectiveness to drive continuous improvement across Grifols Canada Plasma.

Requirements

Candidates must hold a Bachelor's degree in Health-related Sciences, preferably Pharmacy, along with a post-graduate certification in Quality Management. A minimum of 10 years of general experience, including 6 years in GMP quality audits within the pharmaceutical industry, is required.

Skills

GMP Auditing
Quality Assurance
Regulatory Compliance
Supplier Qualification
Risk Management
Quality Systems
Audit Program Management
Regulatory Inspections
Data Analysis
Communication
Time Management
Pharmaceutical Industry Knowledge
Health Authority Liaison
Quality Agreements
Training Development

Visa sponsorship

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Keywords

GMP
Quality Assurance
Audit
Regulatory Compliance
Pharmaceutical
Plasma-derived medicines
Transfusion medicine
Supplier qualification
Risk-based audit
Health Authorities
FDA
European standards
Quality agreements
KPIs
IQPP
Operational license
Pharmacy
Quality management
Auditor certification
Microsoft Office
Continuous improvement
Matrix organization
Regulatory updates
Notified body audits
Internal audit program

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