Technical Manager, Global Supplier Quality - Elusav Recruitment
  • Cork, Munster, Ireland
  • via BeBee.com
-
Job Description

Technical Manager, Global Supplier Quality sought for leading Global Biopharmaceutical in Cork, Ireland. 12-month contract. Key responsibilities include Quality Assurance review and approval for Supplier related activities, compiling Supplier Performance metrics, and leading cross-functional meetings.

Job Description

Elusav Recruitment has an exciting opportunity for a Technical Manager, Global Supplier Quality with a leading Global Biopharmaceutical in Cork, Ireland.

  • Provide Quality Assurance review and/or approval for Supplier related activities impacting Gx P operations at the company, including Change Requests, Deviations, and associated documentation.
  • Compile Supplier Performance metrics; including metrics for supplier changes, deviations, and other measures of supplier performance.
  • Lead and participate in cross-functional Supplier Quality meetings.
  • Represent Global Quality in multi-departmental meetings & project teams.
  • Participate in inspection preparation and participate in internal audits and regulatory inspections.
  • Maintain current knowledge of industry standards and regulatory requirements for products developed or manufactured by the company and for Supplier related approaches utilized at the company.

Requirements

  • BA or BS in a technical discipline (physical or biological sciences).
  • Equivalent experience may be considered.
  • 5+ years experience in a GMP regulated environment, with exhibited knowledge and proficiency working within quality systems preferred.
  • Organizational and management skills, with ability to effectively plan, schedule, execute, and track complex projects.
  • Ability to speak, present data, and defend approaches in front of audiences and inspectors.
  • Ability to comprehend technical information related to regulatory expectations.
  • Experience with cross functional project management.
  • Experience in participation in regulatory inspections, with experience in presenting or defending departmental functions in audits or regulatory inspections preferred.
  • Experience with Track Wise and/or Veeva QMS desirable.
  • Experience working with international project teams desirable.

;