Manufacturing Process Engineer
Becton Dickinson AG
Auf einen Blick
- Veröffentlicht:21 Januar 2025
- Pensum:80 – 100%
- Vertragsart:Festanstellung
- Sprache:Deutsch (Fortgeschritten), Englisch (Fliessend)
- Arbeitsort:Straubstrasse 12, 7323 Vilters-Wangs
Fähigkeiten
Lean ManagementLean MethodologiesManufacturing engineeringProcess EngineeringProcess Validation
Job Objectives
- Developand implement efficient manufacturing processes to improve efficiency and reduce costs
- Ensure that products meet quality standards through meticulous testing and quality control measures
- Identify and implement cost-saving measures without compromising on quality
- Work closely with multi-functional teams to identify areas for improvement and implement solutions
- Promote a safe working environment by following safety regulations and advocating for standard methodologies.
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.
- Completing current and developing new equipment and manufacturing aides, as well as detailing production procedures. Offering technical mentorship and collaboration with R&D and QE, and performing process characterization (e.g., through 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. Collaborate with both internal (BD Wangs & Corporate) and external parties on all aspects of production processes.
- Handling, 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.)
Your profile :
- University Degree in engineering or equivalent experience.
- Consistent track record in the field of medical device engineering of at least 3 years.
- Validated 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: Proven track record regarding Lean manufacturing. Strong background regarding Six Sigma philosophy.
- Proficiency 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.
Kontakt
Becton Dickinson AG