Senior Quality Manager, NPI

Stryker

  • Cork
  • Permanent
  • Full-time
  • 1 day ago
Work Flexibility: OnsiteWe’re seeking a Senior Manager, Quality –NPI to lead a high-performing team at the forefront of innovation in medical device manufacturing.In this hands-on leadership role, you’ll play a pivotal part in our Product Transfer Quality team—mentoring engineers, guiding cross-functional collaboration, and ensuring every product transfer meets the highest standards of quality, safety, and regulatory compliance. Your work will directly shape the future of life-changing medical technologiesWhat You Will Do:
  • Sets direction: Drives the execution of Product Transfer strategy, with the goal of developing highly capable processes, that result in high yield and enable scalability.
  • Builds organizational capability: Promotes the optimization of inspection strategies for launch through technology, automation, and supplier certification. Enables the development of lean inspection strategies, enabling lower inspection cost per unit.
  • Inspires others: Coaching and development of staff who champion quality assurance during the product transfer process, ensuring product transfers meet or exceed established metrics.
  • Delivers results: Oversight and responsibility to ensure appropriate production and process controls are identified, qualified, and implemented throughout the manufacturing process.
  • Fosters collaborative internal/external professional relationships across Divisions and functions, associated with Product Transfer.
  • Collaborate with Regional QA Leaders to share and harmonize best practices, leverage lessons learned, and drive partnership and consistency within the global QA team.
  • Collaborate with Regional NPI QA Leaders to share and harmonize best practices, leverage lessons learned, and drive partnership and consistency within the global NPI QA team.
  • Ensures effective processes in selection of competent talent and supports the development of future potential experts and leaders. Ensures effective training and performance management processes are in place and executed.
  • Communicate effectively with all internal customers, stakeholders, and project teams to deliver successful Product Transfers that meet the project goals as well as the regulatory requirements. ·
  • Oversight and responsibility to ensure adherence to product quality performance indicators (supplier DPM, right first time, manufacturing loss, manufacturing complaints per million, units recalled, product escapes and use-as-is), in conjunction with other targets. Continuously monitors to assess opportunities for improvement.
  • Drives competency in metrology within the quality assurance NPI team including interpretation of complex engineering drawings and understanding of geometrical dimensioning and tolerance.
  • Guides the team to onboard suppliers with demonstrated quality, process capability and validation. Ensures robust supplier pFMEA, PPAP, supplier certification and inspection methods where appropriate.
  • Influences processes towards validation versus manual verification, where possible. · Drives competency in metrology within the quality assurance team including interpretation of complex engineering drawings and understanding of geometrical dimensioning and tolerance.
  • Ensures compliance to Stryker Corporate, GQO and external regulatory requirements.
  • Drive process development, optimization, and validation in a regulated medical device environment
  • Lead continuous improvement efforts and share best practices across global teams
What You Need:
  • Bachelor’s Degree in Engineering, Science discipline or equivalent. Business Management or MBA is an advantage.
  • Minimum of 10+ years’ experience in a Medical, Pharmaceutical, Bio-Medical/Pharma, Automotive or regulated manufacturing environment.
  • Minimum of 6+ years’ experience and a proven track record of successfully creating and managing a highly talented, engaged and performing team.
  • Experience in multiple areas / sites/ positions in the quality organization is advantageous.
  • Expert working knowledge of regulatory requirements, standards, and regulations, with experience of managing inspections/audits by the FDA and other bodies.
  • Working knowledge of quality tools such as SPC / Process Control, FMEA, Problem Solving / Root Cause Analysis, Poka-Yoke, and other Six Sigma tools.
  • Demonstrated leadership ability to develop and implement organization and functional strategy.
  • Initiates, sponsors, and implements change with a demonstrated track record.
  • Must be able to work in a team & individual environment, influencing effectively at all levels, and across all functions with ability to develop organizational relationship and build trust.
  • Demonstrated ability to make timely and sound decisions, through effective approaches for choosing a course of action or developing appropriate solutions. Works with a sense of urgency always.
  • The candidate must be highly organized and disciplined and be able to demonstrate their ability to meet deadlines.
Travel Percentage: 20%

Stryker