Description
A growing specialist biopharmaceutical organisation is looking for an experienced Validation Manager to support their engineering department.This is an exciting opportunity to play an important role in the expansion of the production site.
Location: North Rhine-Westphalia, Germany
Duration: 6 months +
Role and Responsibilities:
• Co-ordinate the planning, execution and documentation of the validation and re-validation of all processes, equipment (production and lab) and utilities on the site
• Managing equipment qualification projects for new equipment installations
• Supporting the engineering department in the generation of equipment specifications and commissioning protocols
• Writing, reviewing and approving risk analyses, SOPs and change control documents
• Ensuring that the validation strategy is kept up to date with industry guidelines
Requirements:
• Degree educated in Chemical Engineering, Process Engineering, Biotechnology, Chemistry or similar
• Fluent in German and English
• In depth experience in the coordination and execution of validation activities
• Technical knowledge of biopharmaceutical production processes and equipment
Apply now for further details.