Validation Technician

Grifols, S.A; Parets del Vallès; Hybrid; EUR 32,000 - 44,000; Full time

Benefits offered by this job

Permanent position

1 day remote work

Job summary

Grifols, S.A. in Parets del Vallès, Cataluña, Spain seeks a Technical Validations professional to validate In Vitro Diagnostics systems and ensure compliance with GLP and quality standards. The role involves cross-functional collaboration, data analysis and maintaining laboratory resources.

You will contribute to the validation lifecycle, investigate deviations, and support continuous improvement while working in a diverse, inclusive environment at Grifols.

Qualifications

• Bachelor’s degree in Life Sciences or related field.
• 1–2 years in lab environments, preferably Diagnostics/Pharma.
• Experience or knowledge in validation/verification of analytical methods.
• Intermediate English proficiency.
• Proficient in MS Office, especially Excel; basic SAP knowledge.
• Experience in IVD validation and lab instrumentation management valued.
• Analytical, organized, quality-oriented and team-oriented.

Responsibilities

• Plan, execute and document IVD system validation activities and prepare technical reports.
• Investigate deviations, complaints and perform root-cause analyses for corrective actions.
• Evaluate design requirements, specs and risk assessments for compliance.
• Collaborate across functions to support development, validation and improvement of IVD systems.
• Manage laboratory resources, equipment and consumables for validation work.
• Ensure proper use, verification, calibration and GLP-compliant maintenance of lab equipment.

Skills

English

Lab data analysis

GLP knowledge

Excel

SAP basics

Quality systems

Team collaboration

Education

BSc Life Sciences

Tools

Excel

SAP

Job description

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 opportunity fostering an inclusive environment where diversity makes us be outstanding.

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

Role Mission

Ensure, through validation activities and other complementary studies, and in accordance with applicable guidelines and regulations, that In Vitro Diagnostic (IVD) systems meet their intended use and defined requirements.

What your responsibilities will be

• Participate in the planning, execution, and documentation of In Vitro Diagnostic (IVD) system validation activities, collaborating in protocol development, data analysis, and preparation of technical validation reports.
• Support the investigation and resolution of deviations, complaints, and root cause analyses, contributing to the implementation of corrective actions and continuous improvement initiatives to ensure the quality and reliability of IVD systems.
• Collaborate in the evaluation of design requirements, technical specifications, and risk assessments, ensuring compliance with applicable quality standards and regulatory requirements.
• Participate in cross-functional projects and meetings, working closely with different departments to support the development, validation, and continuous improvement of IVD systems.
• Manage laboratory resources required for validation activities, including instrumentation, reagents, and samples, ensuring their availability, traceability, and proper maintenance.
• Ensure the correct use, verification, calibration, and maintenance of laboratory equipment, in accordance with internal procedures and Good Laboratory Practices (GLP).

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).

• CFGS or Bachelor’s Degree in Life Sciences, preferably in Biology, Pharmacy, Chemistry, Biotechnology, or a related field.
• You have proven experience of 1-2 years in laboratory environments, preferably within the diagnostics, biotechnology, or pharmaceutical sectors.
• You have experience or knowledge in validation and verification of analytical, chemical, and/or biological methods, as well as working within regulated quality systems.
• You have intermediate english proficiency.
• You are proficient in Microsoft Office, particularly Excel, and are comfortable managing and analyzing technical data, and have basic SAP user skills.
• Previous experience in In Vitro Diagnostic (IVD) system validation, laboratory instrumentation management, and participation in investigations related to deviations, incidents, or root cause analyses will be highly valued.
• You are an analytical, organized, and quality-oriented professional with the ability to work effectively in multidisciplinary teams, manage priorities, and contribute to the continuous improvement of processes.

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.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Flexible schedule: Monday-Thursday 8:00h – 17:00h and Friday 8:00h 15:00h.

Benefits package

Contract of Employment: Permanent position

Flexibility for U Program: 1 day remote working