LifeMatrix is active in the fast-growing field of medical biomimetics and part of the Wyss Zurich accelerator. LifeMatrix has developed a unique bioengineering technology to produce biomimetic cardiovascular implants which transform into living tissue after implantation and have the capacity to grow and regenerate with the patient.
The Wyss Zurich is a joint accelerator of the ETH Zurich and the University of Zurich, which was made possible by a generous donation from the Swiss entrepreneur and philanthropist Dr. hc. mult. Hansjörg Wyss. The mission of Wyss Zurich is to drive the clinical translation and technology transfer of outstanding scientific discoveries into new therapies for patients and breakthrough innovations in the emerging fields of Regenerative Medicine and Robotics, and to promote hybrid technologies in these fields. Wyss Zurich brings together some of the world's leading experts to form multidisciplinary teams, pooling their knowledge and expertise.
You will be supporting the clinical translation of biomimetic cardiovascular solutions for life. Your responsibilities will include the production of our next generation-biomimetic implants for clinical use. You will be working in the clean room facilities (GMP class B / ISO 5) of the Wyss Zurich. You have an active role in the transition of our technology from R&D to manufacturing by driving optimization and harmonization of the GMP processes. Your main tasks include:
Independent production of biomimetic implants such as vascular grafts and heart valves for clinical use according to instructions
Working under hygienic conditions and ensuring the appropriate working conditions in GMP cleanrooms (GMP Class B / work with cleanroom overall)
GMP-compliant documentation of the working steps and used equipment performed in adherence to all relevant SOP's and working instructions.
Cleaning of production equipment after use in cleanroom.
Initiate, write and investigate production deviations and act as a catalyst for continuous improvement
Support for corrective actions and preventive actions (CAPA)
Author, review and edit internal protocols, reports and documents
Help solving problems, create added value by standardization and improvement of manufacturing processes
Provide technical review and assessment when qualifying new suppliers
You have an apprenticeship or university degree in Chemistry, Biology or another relevant discipline and 2+ years of experience within a biotech/pharmaceutical manufacturing environment (GMP). Strong knowledge and interest in manufacturing operations is required. Previous work experience with cell cultures, tissue engineering and/or biodegradable polymers is a big plus.
you are flexible, open and have a positive mindset
you are solution-oriented, reliable and stress resistant
you have an analytical and structured working style
you give strong attention to details
you are able to effectively work in a multicultural and multidisciplinary team
you have good verbal and written communication skills in English and German
What we offer
We offer the unique opportunity to be part of a multidisciplinary start up team of young scientists, world-leading experts in tissue engineering and entrepreneurs who share the vision to help children with a congenital heart defect to have a better life. As part of the Wyss Zurich family, you further benefit from the international university environment of the University of Zurich and the ETH Zurich. You are part of a selected community of translational researchers, entrepreneurs and industry experts.
Did this has spark your interest? If so, we are looking forward to receiving your application including a letter of motivation, CV and certificates of employment.