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Added 41 mins ago
O
Sales Manager, Canadian Armed Forces (CAF) / Directeur des ventes
Octasic
Ottawa, ON
- Full-time
Be part of a growing Canadian company. Thrive in an environment that invests in innovation, R&D, and manufacturing capabilities while offering opportunities for professional development and…
Added 57 mins ago
MP
Human Resources/Office Administrator (Spanish speaking)
Mastronardi Produce
Delta, BC
- Full-time
Support to the Grower and Operations Manager in verifying the daily time entries in pay system
Added 1 hour ago
TT
Quality Assurance Manager
Titan Trailers
Tillsonburg, ON
- Full-time
The Quality Assurance (QA) Manager ensures that quality standards and procedures are met and aligned with legislation and customer specifications. This individual is responsible for…
Added 1 hour ago
T
Senior Production Planner
Techo-Bloc
Longueuil, QC · Saint-Hubert, QC
- Full-time
…mentors planners. Working jointly with the Production Planning Manager, this role collaborates closely with production, procurement and sales, and influences best practices without formal…
Added 1 hour ago
T
Production Planner
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- Full-time
…priorities. Working under the supervision of the Production Planning Manager, the planner coordinates daily with production and procurement, tracks results against the plan and flags issues…
Added 1 hour ago
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Keep supervisor informed of all program issues
Added 1 hour ago
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Manager, 3D Printing & Clinical Engineering
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Vancouver, BC
- Full-time
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Added 1 hour ago
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Mechanical Engineer
RBR Ltd.
Ottawa, ON
- $100,000 to $150,000 CAD / year
- Full-time
🚴 Greener commuting incentive program (bike-to-work, carpool, or transit passes)
Added 2 hours ago
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Sensor Engineer
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Ottawa, ON · Greater Ottawa Metropolitan Area
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- Full-time
🚴 Greener commuting incentive program (bike-to-work, carpool, or transit passes)
Added 2 hours ago
JI
Assistant Store Manager - Back-end Ops
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Port Hawkesbury, NS
- Full-time
As an Assistant Store Manager – Back‑End Operations, you will play a critical leadership role in ensuring these business lines are supported through safe, efficient, and accurate…
Added 2 hours ago
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A/P Administrator
Husky Technologies
Bolton, ON
- Full-time
Husky TechnologiesTM Canadian manufacturing facilities and global headquarters are located in Bolton, Ontario on a large, beautiful campus located just 20 minutes north of Toronto’s Pearson…
Added 2 hours ago
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Proactive Monitoring Spec.
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- Full-time
…SME interacts with customer’s designated Champion, Husky’s Program Manager, Technical Support Team and…
Added 2 hours ago
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Manager, Internal Controls
Husky Technologies
Bolton, ON
- Full-time
Working with Internal Audit and the global Finance and Operations teams, the Manager, Internal Controls will play a critical role in Husky’s global financial reporting. This includes the…
Added 2 hours ago
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Customer Success Manager - Quebec
InnovMetric Software Inc.
QC
- Full-time
By joining our team as a Customer Success Manager, you will be responsible for proactive customer engagement, personalized guidance, and cross-functional collaboration to support customer…
Added 5 hours ago
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Marketing Coordinator
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Saskatoon, SK
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Added 7 hours ago
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Added 8 hours ago
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Manager, Internal Controls
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Bolton, ON
- Full-time
Working with Internal Audit and the global Finance and Operations teams, the Manager, Internal Controls will play a critical role in Husky’s global financial reporting. This includes the…
Added 8 hours ago
HT
Proactive Monitoring Spec.
Husky Technologies
Bolton, ON
- Full-time
…SME interacts with customer’s designated Champion, Husky’s Program Manager, Technical Support Team and…
Added 8 hours ago
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A/P Administrator
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Added 9 hours ago
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Mechanical Technician | Manufacturing
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Added 9 hours ago
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Marketing Coordinator
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Added 9 hours ago
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SALES SUPPORT- Fixed Term Contract
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…equivalent education and experience as judged by the hiring manager to their…
Added 10 hours ago
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Electrical Assembler
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Added 10 hours ago
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Lead, Manufacturing Engineer
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Toronto, ON
- Full-time
…Toronto, Ontario, Canada, this role reports to the engineering manager and is responsible for leading the manufacturing team to improve efficiency and yield in the production of ADCS…
Added 11 hours ago
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Paint Line Operator
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Eaton’s ES AMER PCS division is currently seeking a Paint Line Operator. Eaton Airdrie is a fully integrated manufacturing plant that has been serving Canadian businesses for over 44 years.…

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

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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

Not detected in the job text

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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