GMP QA Process Specialist - Documentation & Validation

HTBA (HealthTech Bio Actives) in Murcia is seeking a Q&A Process Technician to oversee technical documentation and GMP-compliant processes. Your responsibilities will include leading risk assessments, participating in validations, and optimizing operating standards.

The ideal candidate holds a degree in Chemistry, Chemical Engineering, or Pharmacy with at least 2 years of experience in validation. The role includes providing internal training and identifying improvements based on data analysis, with a permanent contract and attractive compensation package offered.