Manufacturing and Validation Engineer in Bettlach

Jabil Healthcare is the world's largest manufacturer of healthcare design and manufacturing services. We help improve the health and well-being of people around the world. Become a part of it and contribute to the development, design and manufacturing of products and solutions on behalf of leading international healthcare brands to improve patient health.

We are looking for a Manufacturing and Validation Engineer (m/f) 100%.

SUMMARY

Define, lead and or overtake manufacturing process and inspection related validation activities. Implement and maintain manufacturing processes and inspection methods through work instructions and process flows definition.

Responsibilities & Duties

• Support internal projects with manufacturing engineering project leaders.
• Support the implementation of new products in our current production lines.
• Support the definition of new process flows for existing or new products.
• Support the transfer of products production between sites.
• Support CAPAs.
• Define manufacturing processes, equipment, tooling, fixturing, and methods.
• Define inspection methods and contribute to their validation.
• Create or support the creation of URS for new assets.
• Contribute to the elaboration of business cases.
• Define, write, review and update manufacturing documentation like:- Manufacturing flowcharts and process information- Production risks analysis- Work instructions- Inspection sheets- DTQP

• Define, write, review, update documentation and perform activities like:- Validation assessments/Validation plans- FAT&SAT protocols- IQ, OQ, PQ protocols and reports- CSV- Compliance analysis- Test method validation- Final inspection reports- Process risk management- Engineering studies- Process monitoring- FIR for registration- Biocompatibility assessments

• Manage in ERP/MRP (SAP) product and process information like:- Master data- Routers- BOM

• Store and maintain information/documents in PLM system.
• Initiate and manage change management operations (DCR/DCO).
• Maintain our CAQ system.
• Interface with our customer, suppliers, other Jabil sites and internal stakeholder on technical and organization issues.
• Actively seek opportunities for process improvement.
• Accountable to the execution on time and in the required quality of the requested activities.
• Maintain a structured and reliable activities scheduling (workload).

• Bachelor's degree or Associates degree + 2 years related experience preferred
• 2+ years' experience of validation in a medical regulated business (implants preferred)
• 2+ years of manufacturing engineering experience in machining environment.
• Proficient in MS Word, Excel, PPT
• SAP knowledges

• Validation experience in a regulated medical business
• Experience of manufacturing processes related to CNC machining
• Experience in inspection methods
• Able to interpret correctly customer requirements
• Experience of medical implants manufacturing
• Experience of validation processes in a highly regulated business
• Ability to effectively present information and support all stakeholders
• Adhere to all site safety and health rules and regulations
• Flexible, resilient, able to work in a team, proactive and analytic thinking
• Good communication and presentation skills
• Fluent German / Proficient in English

Are you determined, outgoing, exact, a team player, positive and interested in working in a team, have organisational talent and are you always open to new ideas? Then this is the right place for you.

Apply online now!