Senior Director Operations – Quality Solutions

Vantive
Castlebar, Ireland
Full-time
On-site
Senior

Key Responsibilities

  • Implement mid-long term strategy
  • Lead and direct quality resources for new product development, commercialized products, and manufacturing facilities
  • Manage multiple plants
  • Cascade Corporate Quality Goals at Entity level
  • Support Global and Regional leaders to accomplish business strategies
  • Integrate new businesses/acquisitions into Vantive Quality System
  • Sponsor, plan and conduct special projects
  • Communicate key measures, metrics and data
  • Escalate potential product quality or safety issues
  • Recommend risk mitigations/corrective action plans
  • Provide Quality input into Sub-Business Strategies and Planning
  • Ensure Quality Processes and Systems meet customer and regulatory requirements
  • Drive consistency with Corporate processes and standards
  • Monitor and meet key metrics and indicators
  • Continuously improve compliance, cost and talent
  • Monitor customer complaints
  • Identify potential quality or safety issues
  • Assess potential risks
  • Recommend mitigation strategies/actions
  • Effect field corrections, product removals, and corrective/preventative actions
  • Partner with development teams for quality support on new product development projects
  • Act as chief spokesperson and lead negotiator with Regulatory Authorities and Agencies
  • Partner with Manufacturing to drive operational efficiencies and technical change
  • Lead and direct Quality organizations
  • Conduct special projects to drive Quality and Compliance improvement

Requirements

Education

Bachelor's Degree in sciences, engineering, or related discipline

Experience

15 or more years in Quality and/or manufacturing operations

Required Skills

  • Technical experience in drug, biologics, and/or medical devices industry
  • Strong leadership experience
  • Global quality/manufacturing operations management
  • Ability to travel globally at least 25%
  • Expert in cGMP and ISO regulations
  • Passion for continuous improvement
  • Project management
  • Supplier Quality Processes management
  • Audit experience
  • Operational experience in Change Control, complaint handling, CAPA processes, Internal auditing, Product Quality reviews, and/or validation
  • Cross-cultural work ability
  • Relationship building with senior regulatory agencies

Required Certifications

  • Professional Project Management certification (preferred)

Interested in this position?

Apply Now

About the Company

Vantive

Castlebar, Ireland

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