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Quality Manager - Pharma/Lens

  • Salary: Negotiable
  • Job type: Permanent
  • Location: Waterford
  • Sector: Science
  • Date posted: 27/08/2018
  • Job reference: BBBH15518

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Quality Manager - Pharma & Contact Lens

A Quality Manager is required to join a leading med device manufacturing company. This position offers an impressive and unique opportunity for interested candidates. This position requires people who want to be challenged, have a passion for success, and a constant drive to exceed expectations.

This role will be responsible for managing the compliance within the dept. and ensure that the area is operating in accordance to GMP, assisting in any validation activities that may as the Quality representative within the project, and to oversee the product and process performance using appropriate metrics Quality representative on the sign off of change controls, documentation and validation activities

This is a perfect opportunity to join a select team that has already established itself as a frontrunner leading the way in the Pharmaceutical industry.


  • To liaise with other departments on the communication of the true failures and supply support for any further investigation or documentation required to close out the failures.
  • To approve all reports generated due to any investigational work that is requested due to a complaint or a potential issue within the manufacturing site. To ensure that the data generated is accurate and generated in a timely manner to help close out issues and potentially release product.
  • During validation activities support and risk manage process change initiatives to ensure appropriate level of validation and verification.
  • Lead projects for the introduction of new equipment within the site, ensuring that the correct level of validation is completed, that the relevant procedures are updated, and that there is a training plan in place.


  • Degree in chemistry, science or related technical discipline
  • Experience as a working QP required
  • Full understanding of the requirements of the Regulatory Standards
  • The ability to assess and evaluate information to determine appropriate risk and required actions that are critical.
  • Experience of scientific report writing including such documents as SOPs, protocols, deviations, reports etc.

Other preferred requirements

  • Have managed a QA department for 5 years
  • Ability to evaluate and assess information to determine appropriate risk and required actions is critical.
  • Knowledge of purified water and Environmental Monitoring systems

Contact Jack on 01-6455262 for more information!