Join a dynamic team where you will play a crucial role in enhancing quality assurance processes in the biotechnology sector. This is an exciting opportunity for professionals looking to make a significant impact in the field of operational quality and environmental monitoring.
As the ideal candidate, you are a competent QA coordinator with a strong background in quality management and operational excellence. Your analytical mindset and problem-solving skills will be key to your success in this role.
You design and implement QA oversight procedures, ensuring planning and documentation.
You conduct inspection rounds within the production site to guarantee compliance and maintain associated documentation.
You review Environmental Monitoring documentation, verifying the adequacy of tests performed on the floor.
You support the execution of quality monitoring tools across multiple production buildings.
You harmonize QA activities to strengthen operational quality across all departments.
You draft necessary documentation related to Environmental Monitoring and QA processes.
You collaborate closely with cross-functional teams to ensure adherence to Good Manufacturing Practices.
What are we looking for?
You hold a university certificate with a scientific orientation (Bioengineering, Biology, Biotechnology, Pharmacology, or equivalent experience).
You have at least 3 years of experience in a cGMP environment.
You possess a good understanding of regulatory matters and Good Manufacturing Practices (GMP).
You are analytical and critical, with a global and pragmatic approach to problem-solving.
You display strong impact and influence skills.
You have excellent technical writing skills.
You are proficient in English (oral and written).