Job Overview:
This role ensures the smooth operation of manufacturing processes, prevents disruptions, and leads continuous improvement initiatives. Ensuring equipment redundancy, validation, and maintenance is key to maintaining high-quality standards.
* Manage equipment redundancy, validation, and best-in-class laboratory practices and training programs to ensure efficient processes that support manufacturing and prevent disruptions.
* Measure and communicate process efficiency and effectiveness, delivering improvement projects on time.
* Lead procurement efforts for goods and services, ensuring adherence to company policies and procedures.
* Facilitate technical problem-solving, CAPA processes, and decision-making within areas of responsibility.
* Co-lead Quality Assurance initiatives, regulatory audits, and manage specification changes.
* Collaborate with leadership, offering guidance and solutions while ensuring alignment with Global Quality teams.
* Monitor team performance across key metrics (Safety, Quality, Delivery) and drive continuous improvement efforts.
* Oversee people management, including development, feedback, and performance evaluations.
* Stay current with industry trends to keep our practices competitive and aligned with industry standards.
Key Qualifications:
* Bachelor's degree in Engineering or Science; postgraduate qualification preferred.
* 6 + years of experience in a highly regulated industry.
* Experience with audit management, process validation, CAPA systems, sterilization, and clean room environments.
* Strong project management and Six Sigma experience.
* Proficient in data analysis and reporting tools (Excel, Project, Minitab).
* Excellent leadership, communication, and interpersonal skills, with the ability to work independently and collaboratively.