Job description
Join our team as a Specialist* Validation New iNeST and play a crucial role in ensuring the quality and compliance of our personalized cancer therapies. You will be responsible for planning, executing, and documenting validation activities for new products and process optimizations.
Requirements:
Degree in Pharmacy, Biotechnology, Natural Sciences, or Engineering.
2-3 years of relevant experience in a regulated GMP environment.
Proven track record in process validation of biotech products.
In-depth knowledge of US and EU regulations and experience in dealing with relevant authorities.
Excellent communication and organizational skills.
Detail-oriented, with strong problem-solving and critical thinking abilities.
Fluent in German and English.
Work conditions:
Flexible working hours.
Mobile Office option.
Company pension.
Childcare support.
Job ticket.
Company Bike.
Generous vacation policy.
Fitness courses.
Responsibilities:
Plan and execute validation activities for new products and process optimizations.
Prepare and maintain validation reports.
Ensure the validated state of processes and products within your area of responsibility.
Provide support for process validation activities.
Create and maintain process-relevant documentation (process risk analyses, process descriptions, etc.).
About company
0-20 employees
Worldwide