Process Engineer III (m/w/d)

JOTEC GmbH 2016; Stein; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading medical devices company in Hechingen, Germany, is hiring a Process Engineer III to support and improve manufacturing processes. Candidates should have a Bachelor's degree in relevant engineering fields and over 4 years of experience in a regulated industry. The role emphasizes collaboration across Operations, Quality, and Regulatory, ensuring compliance with quality standards. Competitive compensation and hybrid working options are offered.

Leistungen

Flexible working conditions

Attractive compensation and benefits

Continuous learning and development

Qualifikationen

• 4+ years of relevant experience in a regulated industry (preferably medical devices).
• Expertise in development, qualification, and maintenance of manufacturing process equipment.
• Experience with design and execution of testing and documentation (test protocols and reports).
• Solid understanding of change control, validations, and continuous improvement of manufacturing processes.

Aufgaben

• Support and improve manufacturing processes and equipment.
• Collaborate with Operations, Quality, and Regulatory to implement tooling, equipment, and manufacturing process changes.
• Lead engineering changes, author technical studies, and conduct statistical analysis for process modifications.
• Act as SME for manufacturing equipment, including user requirements and qualification.
• Support maintenance and complex troubleshooting.
• Assist in audit deliverables, CAPA actions, and root cause investigations.
• Ensure compliance with quality and regulatory standards in all activities.

Kenntnisse

Fluent in English

Fluent in German

Strong technical communication skills

Problem-solving abilities

Documentation abilities

Ausbildung

Bachelor’s degree in biomedical, chemical, mechanical engineering, or comparable qualification

Jobbeschreibung

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

Process Engineer III (m/f/d) – Hechingen, Germany

Your Strength

• Bachelor’s degree in biomedical, chemical, mechanical engineering, or comparable qualification
• 4+ years of relevant experience in a regulated industry (preferably medical devices)
• Expertise in development, qualification, and maintenance of manufacturing process equipment
• Experience with design and execution of testing and documentation (test protocols and reports)
• Strong technical, verbal, and written communication skills
• Fluent in English and German
• Excellent problem-solving and documentation abilities
• Solid understanding of change control, validations, and continuous improvement of manufacturing processes

Your Contribution

• Support and improve manufacturing processes and equipment
• Collaborate with Operations, Quality, and Regulatory to implement tooling, equipment, and manufacturing process changes
• Lead engineering changes, author technical studies, and conduct statistical analysis for process modifications, validations, and engineering studies
• Act as SME for manufacturing equipment, including the user requirements, start-up, debugging, and qualification (IQ/OQ)
• Support maintenance and complex troubleshooting
• Assist in audit deliverables, CAPA actions, and root cause investigations
• Stay up to date on industry standards and technologies, and share insights with the team
• Ensure compliance with quality and regulatory standards in all activities

Our Strength

• A collaborative environment driven by purpose and innovation
• Cross-functional teamwork across Quality, Manufacturing, R&D, and Regulatory
• Continuous learning and development in a high-tech, regulated environment
• Flexible working conditions and hybrid options
• Attractive compensation and benefits (pension plan, EGYM Wellpass, etc.)

Contact

Apply now and join the Artivion Team. We are looking forward to receiving your application documents in English directly via our online system.
Brian Russo,T: [phone]
JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.,
Lotzenäcker 23, 72379 Hechingen
www.artivion.com