Quality Validation Engineer

at  Abbott Laboratories

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.

EDUCATION AND EXPERIENCE

• Relevant third level qualification. Engineering/Manufacturing/Science is preferred.
• Minimum 4 years in the Engineering/Manufacturing/ Scientific field.
• 5-6 years working knowledge of process, equipment, facilities and or software validation either within Quality or Engineering departments
• Experience working in a 21CFR820 and/or ISO13485 regulated industry. May consider experience in pharmaceutical validations.

• The development and maintenance of Quality System procedures.
• Ensuring the site delivers safe and effective products that meet customer needs whilst maintaining compliance.
• Monitoring and maintaining the quality and compliance status of associated quality records.
• Maintaining the quality and compliance status of associated Procedures, work instructions and training materials.
• Presenting and communicating status, report metrics, identify trends potential issues, improvement initiatives, as applicable.
• The review and approval of validation documentation in accordance with divisional policies.
• Basic understanding of design controls and design transfer.