Description

In this role, you will be at the forefront of vaccine production, collaborating on innovative processes and ensuring compliance with GMP standards. Your day-to-day responsibilities will include executing manufacturing activities, troubleshooting equipment, and training staff, while also contributing to the setup of new production areas.

Requirements

• •Completed chemical/biopharmaceutical education or corresponding training qualification
• •Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or several years of relevant professional experience
• •Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation, protein purification, or Bioconjugates
• •Excellent communication skills
• •Teamwork skills
• •Driven and solution-oriented attitude
• •Fluency in English
• •Fluency in German is considered a plus
• •Basic GMP understanding is a plus

Tasks

• •Support the project team in defining innovative vaccine production processes
• •Collaborate on qualifying and validating new production areas and processes
• •Execute manufacturing activities in Upstream Processing, Downstream Processing, or Bioconjugates according to cGMP and SOPs
• •Evaluate test results and troubleshoot manufacturing equipment
• •Make recommendations for resolving manufacturing issues
• •Prepare risk assessments for Safety, Health, Environment, and Environmental Monitoring
• •Assist in preparing documents like electronic batch records and SOPs for the production area
• •Review production documentation and address deviations and change requests
• •Implement CAPAs to maintain high-quality GMP standards
• •Engage in capital investment projects for new manufacturing units as a manufacturing expert
• •Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
• •Train manufacturing staff on specific equipment and standard operations

Benefits