Manufacturing Process Engineer
Key information
- Publication date:21 January 2025
- Workload:80 – 100%
- Contract type:Unlimited employment
- Language:German (Intermediate), English (Fluent)
- Place of work:Straubstrasse 12, 7323 Vilters-Wangs
Skills
Lean ManagementLean MethodologiesManufacturing engineeringProcess EngineeringProcess Validation
Job Objectives
- Develop and implement efficient manufacturing processes to enhance productivity and reduce costs
- Ensure that products meet quality standards through rigorous testing and quality control measures
- Identify and implement cost-saving measures without compromising on quality Work closely with cross-functional teams to identify areas for improvement and implement solutions
- Maintain a safe working environment by adhering to safety regulations and promoting best practices.
Responsibilities
- Specifying, reviewing, and revising methodologies and documentation for the fabrication of components, subassemblies, and final products. Identifying and driving continuous improvement activities in production.
- Improving current and developing new equipment and manufacturing aides as well as defining / updating / documenting production procedures. Providing technical guidance and liaison to R&D and QE and executing process characterization (i.e., via DoE, Ishikawa, etc.) and process capability analysis
- Providing consistent support to production lines, the development of new products and processes, and their transfer into production. Resolve equipment issues and respond to operator questions.
- Managing, performing and documenting of process validations and support of Test Method Validations (TMV)
- Process monitoring, data compilation and reporting as well as failure analysis (RCAs etc.)
- Leading and executing maintenance, repair, and revalidation work
Preferred Requirements:
- University Degree in engineering or equivalent.
- Professional experience in medical technology, materials science, and mechanical engineering.
- Industry experience in the manufacturing or prototyping of medical devices (preferably catheters or comparable).
- Experienced producing in a regulated environment (ISO 13485, 14971) in addition to FDA regulations.
- Preferred: Track record regarding Lean manufacturing and strong understanding of Six Sigma philosophy.
- Fluency in both German and English languages
Click on apply if this sounds like you!
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.