Consultant sap Jobs in Balingen

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

Design Quality Engineer II m / f / d

Your strength

• Minimum of a Bachelor’s Degree in an engineering or science field, or equivalent work experience
• Several years of hands-on experience; preferably in an FDA / MDR regulatory industry (i.e., pharmaceutical, biomedical, medical device field) with an in-depth knowledge of current good manufacturing practices, quality system regulations, and ISO standards
• Specific experience in medical device design controls for developing and preparing design specifications and effectively demonstrating that the design output fulfills the design input
• Specific experience designing, preparing, executing, and statistically analyzing validations as well as developing report packages to approve equipment, processes, methods and software
• Goal-oriented team player with an open mind and a high level of adaptability, eager to embrace new ideas quickly
• Ability to work independently with minimal supervision

Your contribution

Partner with R&D and other cross-functional groups to support the successful development and commercial launch of new products

Partner with R&D and other cross-functional groups to support the proper application of design controls, process validation, risk management, and the investigation / correction of design failures / challenges

Review and approve design input requirements as appropriate

Review and approve the translation of design input requirements into design output documents

Establish and / or maintain risk management files to support product lines and corporate projects

Review and approve design verification / validation protocols and reports that demonstrate the design output fulfills the design input requirements

Review, approve, and validate test methods

Conduct investigations, documentation, review, and approval of non-conformances, CAPAs and customer complaints as necessary

An exciting field of activity

Apply now and join the Artivion team. We look forward to hearing from you!

Apply now!

Maximiljane Tyrs, T :

JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.

Lotzenäcker 23,Hechingen,