Job Details:
Responsibilities
A vacancy has arisen within the Manufacturing Engineering department for a permanent Senior Manufacturing Engineer working in the
structural heart PDP space. Applications are invited from Medtronic employees and agency employees onsite. External candidates will also be considered. Medtronic is an equal opportunities employer.
Duties & Responsibilities
*.Lead Operations deliverables through the various phases of PDP Projects.
*.Support development and qualification of equipment and processes to support new product introduction as required
*.Lead the introduction of new products, in line with marketing plans
*.Lead the effort in terms of setting up pilot area capabilities for verification/validation builds.
*.Drive process validation activities
*.Co –ordinates troubleshooting and technical support of process, materials and equipment operation
*.Liaise cross functionally and with other Medtronic sites regarding technical issues, PDP deliverable transfers and onloads as applicable etc.
*.Utilise DRM tools where applicable to assist the project in achieving all it goals
*.Engineering lead for Audit activities for product family with corporate and regulatory bodies.
*.Ability to identify process improvement/cost saving opportunity.
*.Lead project planning and co-ordination.
*.Plan the technical aspect of process improvement projects. Drive continuous process improvement and equipment upgrades. Guide the conceptualization of new methodologies, materials, machines, processes or products.
*.Demonstrate complete understanding of relevant engineering systems and understanding of how they interact with relevant corporate policies.
*.Ability to develop technical capability of group to achieve business strategy through mentoring/coaching.
*.Demonstrate engineering leadership in corrective/preventative action procedures and NCMR closure.
*.Knowledge of Cell Operating System desirable.
Qualifications/Experience
*.A minimum of 5 years relevant manufacturing experience in a related engineering disciplinewith aBachelor Degree (BSc/B.Eng in Mechanical, Manufacturing or related engineering) is required.
*.Proven record of successful project and people management experience and of providing effective leadership.
*.Experience of working in a changing environment within the medical devices sector, preferably with familiarity of FDA regulations.
*.Strong technical engineering knowledge with problem solving experience using DMAIC methodology.
*.Statistical skills (basic and minimal advanced statistics) together with knowledge of statistical software.
*.Excellent verbal communication, presentation and technical writing skills, plus advanced computer literacy.
*.Experience in process development and introduction of new technology within the medical device industry desirable.
*.Experience in Drug devices or DES manufacturing an advantage.
*.Flexibility to travel frequently required.
Skills & Competencies
Competencies
*.Executes: Takes accountability for and delivers consistent decisions, actions and results. Aligns team, allowing people to move quickly in a coordinated fashion.
*.Clear Thinking: Translates complexity into simplicity and articulates clearly. Creates and communicates a clear strategy/plan and demonstrates good judgment...
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