Senior Validation Specialist

Quality Assurance Technician – Process and Cleaning Validation

Location:

Greater Madrid area

Sector:
Pharmaceutical Manufacturing

Type:
Full-time, permanent

We are recruiting a Quality Assurance Technician with deep, hands‑on experience in process and cleaning validation to join a pharmaceutical manufacturing site in the Greater Madrid area.

This is a manufacturing-focused quality role, supporting both sterile and non-sterile product lines. The position is designed for professionals who have built their careers around validating manufacturing processes and cleaning activities in GMP environments and who are comfortable owning these activities end to end.

• Lead and execute process validation and cleaning validation activities in accordance with GMP requirements
• Author and maintain process and cleaning validation protocols, reports, and supporting documentation
• Support and maintain the Validation Master Plan with a clear focus on manufacturing processes and cleaning
• Partner closely with Production, Engineering, and Quality Control to ensure validated processes remain in a state of control
• Perform risk assessments
  , manage change controls
  , and support CAPAs related to process and cleaning activities
• Support regulatory inspections and audits from a process and cleaning validation perspective
• Contribute to continuous improvement and revalidation activities across the site

• Degree in Pharmacy or Life Sciences
• 5+ years’ experience in pharmaceutical manufacturing xsgfvud , with a strong focus on process validation and cleaning validation
• Practical experience working in GMP production environments (sterile and/or non-sterile)
• Strong understanding of manufacturing process control and cleaning strategies
• High-quality technical documentation and report‑writing skills
• Experience using QMS tools such as Track Wise, SAP, or equivalent
• Fluent English
  , written and spoken,
  Fluent Spanish