It’s a good feeling to know you’re doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together.
We are hiring a
Preclinical Analyst m/f/d

Your strength:

Bachelor’s or Master’s degree in Medical Technology, Biomedical Engineering, Material Science, or a closely related scientific discipline
Work experience in preclinical research at CRO or medical device manufacturer is an advantage
Experience with FDA-, ISO-, GMP- and design control regulations
Working knowledge of relevant sections of EU MDR and Standards (i.e., ISO 10993 and European GLP regulations) pertaining to medical devices in general and more specifically, biocompatibility regulations / standards and toxicology assessments
Formal biological safety training in ISO 10993 series preferred
Proficient at project management, with the ability and proven track record to plan, manage and develop multiple projects
Foundational knowledge to identify and interpret regulatory / legal documents and determine the required compliance activities
Ability to work with team members and other departments, as well as external customers, vendors, consultants and regulatory authorities
Good spoken and written English skills

Your contribution:

Supporting the preclinical program for all products manufactured and in the pipeline at the Artivion Hechingen facility
Maintaining biological safety records supporting approvals for commercially launched products
Collecting biological safety data to advance new product development
Management and development of timelines for all preclinical deliverables
Participation in budget planning for preclinical deliverables
Coordination of resources, project plans and testing within development projects
Supervision and participation in all phases of preclinical testing
Creating documentation and coordinating / performing tests for biological safety
Ensure clarity of assignment and accountability for critical project objectives
Providing technical expertise for biological safety of new and existing products

Our strength:

An exciting field of activity in a challenging preclinical environment
An independent area of responsibility
Active participation in an international team
Intensive training with a mentoring program

Apply now and join the Artivion team. We look forward to hearing from you!
Please send your English application to:

Apply now!
Daniel Weber, jobs.europe@artivion.com , T +49 (0)7471 922 353
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.
Lotzenäcker 23, 72379 Hechingen, www.artivion.com