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Sr. Manager QA APL & GEM EMEA

Skills

corrective actioniso 13485root cause analysis

Description

  • BSc Degree in a Scientific or Engineering discipline or related field

    5 years’ experience in the medical device or pharmaceutical industry

    3 years of QA management experience including comprehensive knowledge of ISO13485 or similar

    3 Years people management experience

    Any other specific local country qualification requirements must also be met

    Preferred Qualifications:

    Supply Chain or finished product distribution experience

  • HOW YOU CAN THRIVE AT ALCON:

    ● Manage your own workload and schedule while hitting your set targets

    ● Collaborate with teammates to share best practices and learnings as work evolves

    ● See your career like never before with focused growth and development opportunities

  • Alcon Careers

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