Process Engineer

Description

Caring for the world... starting with one person. This principle inspires and unites the people at Johnson & Johnson. The culture of caring is at the heart of our corporate philosophy, which is anchored in the Credo.

Cilag AG is an international production company of the Janssen pharmaceutical division of the Johnson & Johnson Group and produces pharmaceutical and medical technology products as well as active chemical ingredients (APIs) for the global markets at its production site in Schaffhausen. Thanks to our innovative products, processes and technologies, Cilag AG is now one of the leading pharmaceutical companies in Switzerland and is also a strategic launch and growth location.

Principal Engineer, Process Engineering (m/w)

main tasks

The Principal Engineer, Process Engineering is responsible for Engineering and Qualification; support Validation on process equipment, utilities & facilities and computerized systems in CM&T F2P2.

• Support the operation of the process equipment and production operation at the technical level in the Fill & Finish pilot plant
• Lead the annual Shut Down and Maintenance Groupe
• Substituted of Senior Manager by absence in CAPEX Projects
• Troubleshooting, rectification and documentation (troubleshooting, non-conformance management) in collaboration with production personnel, equipment suppliers and quality assurance
• Management of technical change and optimization processes(change control) systems and processes
• Supervision of the technical order system in cooperation with mechanics and Technical Services
• Instruction and training of employees on system and process level. Support in the evaluation and qualification of new technology-platforms/processes in the aseptic environment
• Cross-cutting project collaboration with other engineering functions at the local campus level and in the global engineering environment

Qualifications

your profile

• Specifications & design of process equipment and systems in the aseptic environment.
• Troubleshoot equipment failures and define optimization and / or changes to existing equipment. Root-cause analyzation , definition of corrective actions and follow-up of implementations.
• Building experience in process & facility engineering, support GMP-compliance of facility, utilities and process equipment (e.g. COC, events, deviations, NC, qualification, support validation, ...)
• Write procedures, protocols, analyse data and write summary conclusions in reports.
• Building experience and knowledge of Device Assembly and OI incl. HVAC, certification, monitoring - Additional experience in the aseptic field is welcome
• Identify projects, create project plans and participate in their implementation. Perform evaluations to drive efficiency and business results.
• Overall understanding of project budgeting processes and systems.
• Understanding of the own role and the role of the department within the broader organization (CSC/DPDS/IMSC).
• Readiness to lead a project team.
• Provides an opportunity to explore process proof-of-principles to build up of knowlage for commercial process. Plans, coordinates and oversees validation operations, including scale up and optimization processes, equipment assembly, in process sample analysis, use of reactors, and preparation of compliance documents.
• Evaluate analytical results to maintain and improve the quality of batches.
• Propose and determine new or improved technologies to enhance product quality, manufacturing cost efficiencies, personnel safety and regulatory compliance.
• Leadership Skills
• Managing of CAPEX Projects/Portfolio

“An internal pre-identified candidate for consideration has been identified. However, all applications will be considered”