Process Engineer with Project Responsibility (m/w/d)

JR Germany; Hechingen; Vor Ort; EUR 60.000 - 85.000; Vollzeit

Zusammenfassung

A leading company in medical technology seeks a Project Manager for automation projects. The role involves planning, process validation, and cross-departmental collaboration. Candidates should have a relevant degree and experience in medical technology, along with strong communication skills and proficiency in MS Office.

Leistungen

Flexible working hours

Training and development opportunities

Regular team events

Qualifikationen

• Several years of experience in medical technology.
• Expertise in process validation and technical documentation.
• Excellent German and good English language skills.

Aufgaben

• Responsible for planning and monitoring automation initiatives.
• Conducting and documenting process validations.
• Collaborate with various departments to improve products.

Kenntnisse

Analytical skills

Solution-oriented approach

Communication skills

Team spirit

Ausbildung

Degree in Engineering, Medical Technology, or comparable technical field

Tools

MS Office

Jobbeschreibung

Bentley InnoMed GmbH

Hechingen, Germany

Start Your Mission with Bentley!

Join our international team and help us improve people's quality of life worldwide. Support us in our journey with innovative products for minimally invasive treatment of vascular diseases. We offer a diverse work environment with good career opportunities at an exceptional employer!

We are looking for a:

• Project Manager for automation projects, responsible for planning, steering, and monitoring cross-departmental automation initiatives from concept to successful production launch.
• Responsible for planning, conducting, and documenting process validations and changes, including material and process qualification (OQ, PQ).
• Coordinate engineering studies and testing activities, create test plans and reports, and evaluate results.
• Develop and maintain work instructions and technical drawings.
• Collaborate closely with Regulatory Affairs, R&D, Production, and Quality Assurance to continuously improve products and processes.
• Hold a degree in Engineering, Medical Technology, or a comparable technical field.
• Possess several years of experience in medical technology, with expertise in process validation, material and process qualification, and technical documentation.
• Adopt an analytical, solution-oriented, and structured work approach.
• Bring team spirit, strong communication skills, and a high degree of initiative.
• Be proficient in MS Office applications.
• Have excellent German and good English language skills, both written and spoken.
• Enjoy working in a team and actively contribute to interdisciplinary projects.

Our agile and appreciative company culture features flat hierarchies and short decision-making processes, fostering dynamic and efficient work. Responsibilities are autonomous, combining startup mentality with the structure and power of an established company. Flexible working hours, regular team events, training, and development opportunities allow you to advance your personal growth.