Senior Validation Specialist

JR Spain; Madrid; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A pharmaceutical manufacturing company is seeking a Quality Assurance Technician for the Greater Madrid area. This role involves leading process and cleaning validation activities, ensuring compliance with GMP standards, and supporting product line quality across both sterile and non-sterile sectors. The ideal candidate will have a degree in Pharmacy or Life Sciences and over 5 years of experience in pharmaceutical validation, particularly with sterile products.

Formación

• Degree in Pharmacy or Life Sciences.
• 5+ years of experience in pharmaceutical validation.
• Strong understanding of GMP requirements.

Responsabilidades

• Develop and execute Validation Master Plans for process and cleaning validation.
• Prepare validation protocols, reports, and supporting documentation.
• Work closely with Production, QC, and Projects teams to implement validation strategy.

Conocimientos

Attention to detail

Technical writing

Cross-functional collaboration

Educación

Degree in Pharmacy or Life Sciences

Herramientas

TrackWise

SAP

Descripción del empleo

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Quality Assurance Technician – Validations

? Location: Greater Madrid area

? Sector: Pharmaceutical Manufacturing

? Type: Full-time, permanent

About the Role

We’re looking for an experienced Quality Assurance Technician to take a leading role in process and cleaning validation activities at a well-established pharmaceutical production site. This is a key quality role supporting both sterile and non-sterile product lines, offering strong long-term career potential.

You’ll act as a technical reference within the Validation team, planning and executing validation protocols in compliance with GMP standards, working cross-functionally with Production, Quality Control, and Engineering teams, and supporting inspections and improvement initiatives across the site.

Key Responsibilities

• Develop and execute Validation Master Plans for process and cleaning validation
• Prepare validation protocols, reports, and supporting documentation
• Ensure validation activities meet GMP standards and internal quality policies
• Work closely with Production, QC, and Projects teams to implement validation strategy
• Perform risk assessments, contribute to CAPAs and change controls
• Support site audits and inspections (internal, client, and regulatory)
• Contribute to quality system improvement and revalidation of ISO certifications

What You’ll Need

• Degree in Pharmacy or Life Sciences
• 5+ years of experience in pharmaceutical validation (ideally with sterile products)
• Strong understanding of GMP requirements
• Experience with systems like TrackWise, SAP, or similar QMS tools
• High level of English (spoken and written)
• Excellent attention to detail, technical writing skills, and ability to work cross-functionally