Job Opportunity in Personalized Cell Therapy
We are seeking experienced professionals to join our client's innovative team, dedicated to advancements in cell therapy, oncology, and immune cell biology and engineering.
Key Responsibilities:
* Quality Engineer: Ensure adherence to GMP guidelines and quality standards in aseptic manufacturing facilities.
* Process Engineer: Develop and implement efficient production processes for cell and gene therapies.
* Supervisor: Lead teams in pharmaceutical or biotech environments, focusing on process optimization and staff development.
* CAR-T Specialist: Design and execute CAR-T cell production protocols, ensuring high-quality outputs.
* Data Management: Analyze and interpret complex data sets related to cell therapy production.
* Production Expert: Oversee daily operations in aseptic manufacturing facilities, prioritizing patient safety and product quality.
* Laboratory Analyst: Conduct experiments and analyze results in the context of cell and gene therapy research.
Requirements:
* Master's degree in a scientific field (PhD preferred)
* At least 2 years of experience in pharmaceutical or biotech environments, with a focus on aseptic manufacturing facilities.
* Experience with cell and gene therapy production, including GMP compliance.
* Excellent organizational skills, with ability to manage shifting priorities in fast-paced environments.
* Strong communication skills (written and oral) in English and Dutch.
* Detailed-oriented, with problem-solving abilities and critical thinking.
* Availability to work shifts.
What We Offer:
A chance to contribute to groundbreaking innovations, collaborate with experts in the field, and grow professionally within our dynamic organization.