Assignment Description
We are looking for an experienced Validation Engineer
What You Will Work On
- Plan, execute, and document validation and qualification activities
- Perform validation of technical systems, equipment, and automation solutions
- Develop, review, and execute validation and test protocols
- Perform Computerized System Validation (CSV)
- Execute FAT, SAT, IQ, OQ, and other qualification and verification activities
- Develop and maintain traceability matrices and requirements documentation
- Document test results, deviations, investigations, and corrective actions
- Support validation of DeltaV and other automation systems
- Collaborate with process, automation, commissioning, and quality teams
- Ensure compliance with GMP, GxP, and regulatory standards
- Support commissioning and startup activities
- Prepare validation reports and technical documentation
What You Bring
- Experience with validation and qualification activities within the pharmaceutical industry or other GMP/GxP-regulated environments
- Hands-on experience creating, reviewing, and executing validation protocols
- Experience with Computerized System Validation (CSV)
- Experience performing FAT, SAT, IQ, OQ, and other verification activities
- Experience with traceability matrices and requirements management
- Experience documenting test results, deviations, investigations, and corrective actions (CAPA)
- Understanding of automation systems, preferably DeltaV
- Strong knowledge of GMP, GxP, and quality management principles
- Excellent technical documentation and reporting skills
- Strong collaboration and communication skills
If this sounds interesting, please send your CV to cv@veritaz.se
