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Ensure efficient processes to support manufacturing and prevent disruptions through managing equipment redundancy, validation, and best in class laboratory practices and training programs.
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Measure and communicate process efficiency and effectiveness, delivering improvement projects on time and within budget.
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Lead procurement efforts for goods and services, ensuring adherence to company policies.
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Facilitate technical problem-solving, CAPA processes, and decision-making within areas of responsibility.
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Co-lead Quality Assurance initiatives, regulatory audits, and manage specification changes.
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Collaborate with leadership, offering guidance and solutions while ensuring alignment with Global Quality teams.
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Monitor team performance across key metrics (Safety, Quality, Delivery, Cost, People) and drive continuous improvement efforts.
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Oversee people management, including development, feedback, and performance evaluations.
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Stay current with industry trends to keep our practices competitive.
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Participate in the hiring process for critical roles and be a key member of the Site Quality Leadership team.
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Bachelor’s degree in Engineering or Science; postgraduate qualification preferred.
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6 + years of experience in the medical device or highly regulated industry.
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Experience with audit management, process validation, CAPA systems, sterilization, and clean room environments.
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Strong project management and Six Sigma experience.
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Proficient in data analysis and reporting tools (Excel, Project, Minitab, Power BI).
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Excellent leadership, communication, and interpersonal skills, with the ability to work independently and collaboratively.