MSS Jefe de Sección Laboratorio - Temporary

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.

We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a MSS Jefe de Sección de Laboratorio like you.

Role Mission

Organize, plan, and coordinate the activities carried out in the section, optimizing material and human resources, in accordance with the guidelines of the superior, to ensure the fulfillment of the tasks assigned to the different maintenance and improvement projects of the production processes, technology transfers between sites, design transfer, industrialization of new products, investigation of production incidents, as well as the management of changes and incidents involving raw materials, with the required quality and within the established deadlines.

What your responsibilities will be

• Monitor process indicators, analyze and identify opportunities for improvement, and implement the necessary actions to improve processes.
• Design, implement, and maintain laboratory operations, including testing procedures, quality control, validation, calibration, sample traceability, and release of results.
• Ensure compliance with applicable regulations for clinical diagnosis, transfusion biology, and medical device regulations where applicable (quality standards, safety, internal/external accreditations).
• Supervise the laboratory technical team: assignment of tasks in the area.
• Control laboratory resources: reagents, consumables, equipment, instrument maintenance, storage, biosafety, waste management.
• Implement and supervise internal and external quality control programs, audits, validations, and non-compliance management, proposing corrective actions or continuous improvements.
• Ensure that the production of reagents and diagnostics complies with corporate quality standards and applicable regulations.
• Validate and approve technical reports, analysis results, reagent batches, quality control reports, and release documentation. Be part of the teams that manage the projects when required.
• Collaborate with other areas of the company (development, production, quality control, regulatory, R&D) to optimize processes, scalability, and regulatory compliance.
• Represent the laboratory in internal/external audits, regulatory authorities, among others.
• Ensure compliance with safety, hygiene, biosafety, confidentiality, and biological sample protection policies.

Who you are

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).

• Bachelor's degree in Chemical Engineering, Biochemistry or related fields.
• English level B2.
• You have two years of experience in laboratory areas within the industrial sector - pharmaceuticals.
• You are dynamic, responsible, and proactive, as well as organized and methodical; you enjoy working in a team.

What we offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. 

Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! 

Grifols is an equal opportunity employer. 

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).

Benefits package 

Contract of Employment: Temporary Full-Time

Location: Parest del Vallès

www.grifols.com