If you want to change the world, come and work for GE!

If you share our values,ambitions and put the customer at the forefront of everything you do, we can offer you a career where your knowledge and ambitions will be recognized and rewarded. You will be working in a dynamic, fast-paced, international environment with many possibilities to develop, both personally and professionally, together with likeminded people that share your attitude and passion to make the world a better place!

Role Summary:

Essential Responsibilities:

• Responsible for ensuring 100 percent quality and regulatory compliance in accordance with documented procedures for all aspects of functional responsibility.
• Responsible for the development, implementation, and continuous improvement of process effectiveness and efficiency at the site.
• Develops process improvement plans using a variety of Quality and Continuous Process Improvement tools, including but not limited to Six Sigma, LEAN, Manufacturing, 5S, SPC, engineering studies, DOE, Gauge R&R, etc.
• Ensures process efficiency and compliance effectiveness through the development and implementation of process verification and validation plans, including Master Validation Plans (Site Level), Validation Master Plans (Product or Process specific plans), and the development of simple yet detailed process flow diagrams that describe critical process interdependencies with respect to process inputs, outputs, risks and impacts.
• Supports continuous product and process improvement through detailed failure analysis for non-conformances, and investigates, develops and implements effective and compliant solutions for product or process corrections, retrospective and remediation action plans, and for corrective and preventive actions (CAPA Program).
• Develops risk management tools and aids for use by the organization in accordance with documented procedures, including but not limited to PFMEA, DFMEA, Fault Tree Analysis, Failure Mode Analysis, etc. 
• Supports design mitigation efforts. 
• Develops process mitigation plans and strategies that are designed to mitigate the risks identified through the Risk Management process.
• Ensures process compliance through the development of simple yet comprehensive procedures, work instructions, flowcharts, forms, templates, checklists, worksheets, and other product and process related documentation.
• Performs a broad variety of tasks in support of product and process design as assigned by the departmental manager.

Requirements:

• Bachelor’s degree in Engineering, Science, Life Sciences or the Clinical domain (or high school diploma/GED plus significant years working experience, preferably in engineering in the medical devices or pharmaceutical industry)
• Some years experience working in quality assurance, engineering, scientific or biomedical discipline, preferably in the medical device industry
• Strong technical aptitude (i.e. able to read and comprehend technical documentation, ability to comprehend and execute procedures, demonstrated understanding of system documentation)
• Ability to effectively communicate using English (or local language)
• Good communication skills and analytical skills.
• Ability to execute and deliver on commitments.
• Passionate about QA

The deadline for application is ASAP but not later than 15.03.2017. We encourage all interested candidates to apply online asap since all applications will be processed ongoing.

We look forward to receiving application from you!