Job Description
You will play a crucial role in leading the design, development, and deployment of the strategic procurement related compliance programs, processes, and initiatives across the global organization. You will work closely with cross-functional teams including Global Sourcing, legal, compliance, QA, IT and data management to ensure we have a ‘One Agilent’ program in place. This role requires a deep understanding of regulatory compliance, quality management and audit and supply chain management.
Key Responsibilities:
- Leads the design, development, management and execution of strategic compliance programs and initiatives aligned with legal requirements, industry standards and organizational objectives. (e.g RoHS, responsible minerals, modern slavery)
- Acts as a “Process Champion”, consultant and recognized expert to the management team on strategic procurement processes, methodologies and strategies.
- Maintains a broad knowledge of major industry best practices and stay informed about the industry specific regulations and standards, identify and close the process gaps to ensure the organization complies with all relevant laws and regulation.
- Identifies opportunities and drive for continuous improvement initiatives for the organization to enhance efficiency and improve productivity.
- Develop and manage process documentation, policies and training.
- Leading the internal/external QMS, process and compliance audit for the organization.
Qualifications
- Bachelor’s degree in relevant field preferably in Engineering or Quality.
- Minimum of 8 years of experience in procurement, quality, compliance management, audit or regulatory affairs.
- Excellent problem solving and critical thinking skills.
- Strong project management skills and ability to handle multiple tasks simultaneously.
- Excellent communication skills and ability to work collaboratively in a team
- Strong understanding of QMS (ISO9001/13485), regulatory compliance, including knowledge and of relevant laws and regulations in the industry.
- Hands on working experience on FDA, IVDR and MDSAP will be and added advantage.
