We have built this position for the CQV Biologics team. To support our qualification and re-qualification work in all areas of Biologics. A good level of training in GMP, cGMP, GDP and H&S as well as a general overview of pharmaceutical drug manufacturing can be provided here.

• General office duties including Document / Binder organizer with Project
• Coordinate with relevant departments to chase signatures for review and approval sign-offs
• Assisting with PQ (Performance Qualification) material from Black storage area to clean areas (Precise clean down is required for all material, training to be provided), Ross Shell storage and availability for new project - 92 Max load studies TCU
• Scan completed PQ documents and attachments into the Document Management System (DMS) for workflow approval
• Assisting with preparation of documents for availability to Vendors and collaborating closely with vendor for document completion and GDocP corrections.

• Bachelor’s degree in Biotechnology, Chemistry, Engineering, or a related field, or equivalent experience will be considered  
• Proficiency in Word and Excel, with strong computer, printer, and scanner skills
• Experience in Good Manufacturing Practices (GMP) is a plus
• Ability to work independently after training, with excellent communication skills
• Awareness of Health and Safety protocols or equivalent experience
• Demonstrated passion and eagerness to learn
• Excellent personal presentation and time management skills
• Fluency in English is required; German proficiency is a bonus.