IVD Validation Specialist - Flexible Schedule & Remote Day

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

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.