HAVE YOU EVER WANTED TO MAKE A DIFFERENCE?

At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.

QUALIFICATIONS AND EXPERIENCE

• Relevant third level qualification in Engineering/Manufacturing/Science is preferred.
• Minimum 2 years in the Engineering/Manufacturing/ Scientific field.
• 2 years working knowledge of process, equipment, facilities and or software validation either within Quality or Engineering departments
• Basic understanding of design controls, design transfer and validation lifecycle.
• Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations
  Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.
  Abbott is an equal opportunities employer.

• Work with R&D. QA, PMO and Global Engineering functions to define and document validation strategies for new product introductions
• Complete impact assessments of proposed changes and/or new products and determine scope of validation work
• Generate, execute and/or review validation protocols and associated reports for related Process & Software Validation Activities
• Identification of improvements to manufacturing process & software and assist with implementation of same
• Ability to manage multiple responsibilities at once while adhering to project plans and timelines and report on progress to management
• Provide direction and mentoring to junior engineers as required
• Responsible for compliance with applicable Corporate and Divisional Policies and performing other duties as assigned by management
• Knowledge of cGMP and industry regulations