Description

In this role, you will play a key part in validating production equipment and systems, ensuring compliance through thorough documentation and active participation in process teams. Your day-to-day responsibilities will involve executing various validation activities and supporting technical documentation efforts.

Requirements

• •Degree or equivalent in engineering, pharmacy, or related field
• •At least 5 years of professional experience
• •Knowledge of GMP
• •Operation skills
• •Good knowledge of document and project management
• •German language knowledge
• •Basic English language knowledge
• •Parenteral manufacturing experience
• •Strong analytical and synthesis skills
• •Excellent interpersonal and communication skills
• •Ability to work independently and in a team
• •Ability to coordinate teams without direct hierarchical power

Tasks

• •Instruct and support validation of production equipment and systems
• •Perform sterilization, cleaning, filter, and process validation
• •Prepare and review technical documents, including change controls and validation protocols
• •Participate in process functional teams to achieve TS/MS objectives
• •Initiate and coordinate validation protocols and reports
• •Complete required training on time

Benefits