Innovating for patients and society
Sant Cugat del Vallès, Barcelona
Grifols is a global healthcare company founded in Barcelona in 1909 committed to improving the health and well-being of people all over the world. A leader in essential plasma-derived medicines and transfusion medicine, we develop, produce and provide innovative healthcare services and solutions in more than 110 countries. Patient needs and our ever-growing knowledge of many chronic, rare and prevalent diseases, sometimes life-threatening, drive our innovation in plasma-based therapies and other biopharmaceuticals to enhance quality of life. Grifols is focused on treating conditions across six core therapeutic areas: immunology, neurology, pulmonology, hematology, hepatology and intensive care. With a workforce of over 25,000 employees in more than 30 countries and regions, we are committed to a sustainable business model that sets the standard for continuous innovation, quality, safety and ethical leadership in the industry. Our work has a positive social and economic impact in the countries where we operate, creating jobs and generating wealth. People are at the heart of what we do, and we strive to create an inclusive, diverse, fair and equal society. Maintaining and promoting a workforce that reflects this reality leads to enhanced professional relationships and helps us to give our best to patients, donors and customers. In 2024, Grifols was named one of TIME's 'World's Best Companies' for the second year in a row, reaffirming our commitment to excellence. We were also recognized by Forbes as one of the "Best Employers for Women 2023," reflecting our dedication to fostering an inclusive and supportive workplace for all. To maintain a positive community and overall respectful communication, please keep our community guidelines in mind.
On-site · Montréal
The specialist is responsible for coordinating and maintaining the site's document management system to ensure compliance with cGMP and regulatory requirements. They oversee the full lifecycle of controlled documents, including creation, review, approval, and archival, while supporting internal and regulatory audits.
On-site · Montréal
The Validation Technician supports engineering specialists by executing testing protocols, performing thermal equipment calibration, and analyzing data. They are also responsible for maintaining accurate documentation and managing test samples in compliance with quality standards.
On-site · Montréal
The Validation Specialist is responsible for designing, authoring, and executing qualification and validation studies for utilities, equipment, and processes. They also provide technical subject matter expertise for investigations, change controls, and regulatory audits to ensure compliance with GMP standards.
On-site · Montréal
The Manufacturing Technician is responsible for operating, cleaning, and maintaining production equipment within a regulated cGMP environment. They must accurately execute batch records, perform visual inspections, and assist with various manufacturing processes including purification and packaging.
On-site · Montréal
The Manufacturing Technician operates and maintains production equipment for albumin purification and packaging while adhering to cGMP and safety regulations. They are responsible for accurate documentation, equipment cleaning, and performing in-process testing to ensure product quality.
On-site · Montréal
The Manufacturing Technician is responsible for setting up, operating, and cleaning production equipment in a regulated environment. They must maintain accurate batch records, perform visual inspections, and ensure compliance with cGMP and safety standards.
Hybrid · Toronto
The Field Validation Specialist ensures adherence to cGMP and quality systems by executing validation protocols and testing at various donor center sites. They also analyze validation data, write reports, and provide training to donor center staff to ensure compliance and operational readiness.
On-site · Montréal
The technician is responsible for the operation, monitoring, and maintenance of critical clean utility systems in a regulated biopharmaceutical environment. They perform routine inspections, troubleshooting, and preventive maintenance to ensure system reliability and compliance with GMP standards.
On-site · Mississauga
The Director of Strategy & Transformation leads strategic initiatives, operational excellence, and business transformation programs to support Canadian self-sufficiency. This role oversees the Business Optimization function and partners with leadership to drive organizational performance and sustainable growth.
On-site · Kingsport
Perform physical examinations and establish medical histories to determine donor suitability while ensuring customer satisfaction. Manage donor injuries, provide health education, and assist with employee training programs.
On-site · Montréal
The Manufacturing Technician is responsible for operating, cleaning, and maintaining production equipment while adhering to cGMP and safety regulations. They must accurately document batch records and perform tasks such as sampling, weighing, and visual inspection to ensure product quality.
On-site · Montréal
The maintenance planner maximizes operational efficiency by analyzing work orders, scheduling resources, and coordinating maintenance activities with production requirements. They also develop detailed job plans, maintain equipment records, and optimize preventative maintenance programs to ensure plant reliability and safety compliance.
On-site · Toronto
The Validation Specialist ensures adherence to cGMP and quality systems by executing validation protocols and testing at various donor center sites. They also analyze validation data, prepare reports, and provide training to staff to ensure compliance and operational readiness.
Hybrid · Toronto
The Corporate Counsel provides strategic legal support for Canadian operations, managing commercial contracts, litigation, and regulatory compliance. They act as a primary advisor to business leaders while collaborating with cross-functional teams to mitigate legal risks.
On-site · Toronto
The Director of Regulatory Affairs is responsible for overseeing all regulatory compliance, submissions, and licensing for Plasma Operations in Canada. They serve as the Authorized Official for Canadian Health Authorities and lead regulatory strategies to ensure business objectives are met.
On-site · Montréal
The Automation Specialist is responsible for designing, developing, and implementing computerized process control and monitoring systems within a biopharmaceutical manufacturing environment. They will lead automation projects, provide technical troubleshooting support, and ensure compliance with cGMP regulations.
On-site · Montréal
The Senior Supervisor oversees the receipt, handling, storage, and distribution of human blood plasma to ensure compliance with cGMP and safety standards. They also manage inventory accuracy, supervise staff, and assist management with budget preparation and resource allocation.
On-site · Montréal
The Manufacturing Technician is responsible for operating and maintaining production equipment in a cGMP-regulated environment, including purification, filling, and packaging processes. They must also ensure accurate documentation of batch records and maintain the cleanliness of the facility to meet safety and quality standards.
On-site · Montréal
The Director of Site Engineering provides strategic and operational leadership for all site engineering, maintenance, facilities, and capital project execution. They ensure that site assets and utilities remain compliant, safe, and reliable while supporting uninterrupted manufacturing operations.
On-site · Toronto
The Field Validation Specialist ensures adherence to cGMP and quality systems by executing validation protocols and testing at donor centers. They also analyze validation data, write reports, and provide training to staff to ensure compliance and operational readiness.
