Markets Supplier Quality Assurance Manager - LATAM Markets
Philips Lighting
Ciudad de Panama, Panamá, Panama
hace 1 día

You are responsible for

  • Applying Philips Excellence practices to identify and solve major supplier quality issues where simple analysis of Supplier Quality data is required
  • Multi-disciplinary approach and knowledge basic Supplier Quality principles, theories and concepts; including ASL Management, Auditing, SCAR Coordination, Performance Monitoring, APQP, and Quality Transition Plans
  • Formulating the Supplier Quality solution based upon Supplier Quality feasibility studies
  • Leading projects in Supplier Quality, managing a small number of people
  • Applying company policies and procedures to resolve a variety of issues
  • Frequently interacts with functional peer groups, demonstrating the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects or schedules
  • Leading teams, fostering collaboration to deliver tasks
  • Working on problems of moderate scope where analysis of situations or data requires a review of a variety of factors
  • Exercising judgement within defined procedures and practices to determine appropriate action
  • Building productive internal / external working relationships
  • Able to focus on the problem at hand, identifying impact to the value chain (customer, supplier, Philips) and affected stakeholders
  • Normally receives general instructions on routine work, detailed instructions on new projects or assignments
  • You are a part of

    A fast growing and innovative team, within an ever-changing environment - constantly striving for improvements and exceeding internal and external stakeholder expectations.

    To succeed in this role, you should have the following skills and experience

  • 0-3 years of relevant experience in a similar function
  • Quality Management Systems knowledge, including Application and Implications : Including ISO 9001, Standards and Regulations
  • Ideally knowledge of the following Medical Device standards : ISO 13485 & FDA (21 CFR Part 820), MDD / MDR
  • Personal Care Awareness : ISO 22000 / FSSC 22000, ISO Standards 97.020, 97.030, 97.040, 97.060, 97.080, 97.170
  • Good Documentation Practices and Manufacturing Practices
  • Supplier Corrective Action Request (SCAR) Ownership, Execution and Independent Review
  • Experience working with Supplier Sustainability
  • Knowledge of LEAN : Including Daily Management
  • Preferably Lead Auditor Qualification
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