Job Description
Overview
Our client is looking to hire an experienced Validation Lead to join their biomanufacturing site in Lendava, as Validation Lead you will be responsible for developing, implementing and managing the site process validation, primary packaging validation, cleaning validation and revalidation strategies to meet cGMP and quality requirements on time and on budget to ensure that programs are compliant with Regulatory Authorities’ expectations.
Your Key Responsibilities
Your responsibilities include, but not limited to:
Ready to Apply?
Submit your application today and join our talented team at Cpl Life Sciences.
Submit ApplicationJob Details
- Location Budapest, Budapest
- Job Type FULL TIME
- Category Other Production Occupations
- Posted Date March 01, 2026
- Application Deadline April 10, 2026