Engineer III, Validation - Process & Cleaning

Become part of our team as a Validation Engineer III, leading process and cleaning validation in sterile pharmaceutical manufacturing. Oversee validation activities, collaborate across teams, and ensure compliance. Ideal for candidates with validation experience in pharmaceutical or biotech manufacturing and strong protocol writing skills.

Skills

• process validation
• cleaning validation
• equipment qualification (iq/oq/pq)
• validation protocol writing
• validation documentation
• deviation investigation
• sterile pharmaceutical manufacturing
• aseptic filling
• cleanroom environments
• fda regulations
• ema regulations
• cgmp regulations
• audit participation
• regulatory readiness
• project management
• client interaction