QA & Validation Lead

Competitive
Permanent
Dublin North
22 May 2020
BBBH760086

An excellent leadership position in a very reputable distribution company

THE ROLE

A market-leading distribution company are looking for a QA & Validation Lead to join their team in a leadership role. The ideal candidate will have a minimum of three years in QA & Validation in the medical device or pharmaceutical sector. This role is offering a competitive salary and a permanent contract.

THE RESPONSIBILITIES

  • Lead all operational and non-operational departments (within their area of responsibilities) on Validation including GAMP.

  • Support business growth and strategy around systems and equipment sourcing, implementation and qualification.

  • Support business growth by Leading on projects and advising on Validation Lifecycle requirements.

  • Ensure harmonisation of Validation best practices for GDP/ GMP is applied to all Supply Chain sites.

  • Create strong and effective working relationships with colleagues in all relevant operational and functional roles.

  • Compliance First - Prioritise full compliance with GMP, GDP and ISO 9001 requirements to ensure Patient Safety - SISPQ (Safety, Integrity, Strength, Purity & Quality).

  • Work with and support the Quality Management team in raising quality standards and awareness across all the business functions in Ireland.

  • To undertake qualification and validation activities across DHL Supply Chain Life Sciences and Healthcare Ireland sites in accordance with site procedures and corporate policies to meet regulatory requirements in maintaining the validated status of GxP systems/ equipment.

  • Lead the Quality function for computer system validation and ensure all systems are assessed for GxP criticality and validation is maintained, reviewed and Managed.

  • Lead all operational and non-operational departments (within their area of responsibilities) on Validation including GAMP.

THE REQUIREMENTS

  • A minimum of years experience in QA & Validation activities in Medical Device or Pharmaceutical sector.

  • Demonstrate strong knowledge of working within a Quality Management System associated with cGDP/ cGMP.

  • Demonstrated ability to successfully facilitate quality project work.

  • Experience on Validation/ Qualification and thermometric studies applicable to facilities and systems is preferable; however previous employment in Quality or Engineering will be considered .

  • The Quality Validation specialist should have knowledge and understanding of the pharmaceutical industry and thorough understanding of Supply Chain elements

  • Sponsorship will not be provided.

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.

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Consultant | Manufacturing, Automation, Process & Project Engineering Recruitment.
Cork 353 (0) 21 2300300 | kmoriarty@morganmckinley.com