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 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.
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 · 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 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 technician is responsible for maintaining, troubleshooting, repairing, installing, and calibrating pneumatic, hydraulic, mechanical, and low voltage electrical control components and systems with minimal supervision. Key duties include performing field and bench calibrations, ensuring integrity tests are conducted, and maintaining all related maintenance and calibration documentation.
On-site · Montréal
The technician is responsible for maintaining, troubleshooting, repairing, and calibrating pneumatic, hydraulic, mechanical, and low-voltage electrical systems. They must also ensure all work complies with GMP, SOPs, and safety regulations while documenting maintenance activities.