Senior Director of Supplier Quality and Compliance

hace 3 días

Madrid, Madrid, España Gsk A tiempo completo
{"Job Title": "Supplier Audit and Compliance Senior Director", "Job Description": "Job Summary

We are seeking a highly experienced and skilled Senior Director to lead our Supplier Audit and Compliance team. The successful candidate will be responsible for providing strategic direction and oversight to ensure that all material and service suppliers within our scope are audited and managed appropriately regarding compliance with applicable external regulatory requirements and expectations and GSK requirements.

The ideal candidate will have a strong background in quality assurance and compliance, with experience in managing teams and developing strategies to mitigate risks. They will be responsible for maintaining a robust supplier audit program, defining and endorsing audit standards, and providing support and oversight to audits.

The Senior Director will also be responsible for collaborating with senior stakeholders to identify risks and potential risks, and working together to devise strategies to mitigate any such risks or potential risks. They will ensure that decisions regarding marginal suppliers are appropriately documented, communicated, controlled, and managed in accordance with applicable standard operating procedures.

The successful candidate will be a strong leader, with excellent communication and interpersonal skills. They will be able to motivate and develop their team, and ensure that the team is focused on delivering high-quality results.

Key Responsibilities
  • Provide strategic direction and oversight to the Supplier Audit and Compliance team
  • Maintain a robust supplier audit program
  • Define and endorse audit standards
  • Provide support and oversight to audits
  • Collaborate with senior stakeholders to identify risks and potential risks
  • Ensure that decisions regarding marginal suppliers are appropriately documented, communicated, controlled, and managed
  • Motivate and develop the team
Requirements
  • BA/BS degree or equivalent in experience (Chemistry, pharmacy, biological sciences, science related)
  • Detailed knowledge of world-wide cGMPs, associated regulatory guidances and expectations, and Quality Management Systems for pharmaceuticals, APIs, biopharmaceuticals, medical devices, and steriles
", "Language": "en"}

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