Licenced Quality Manager - QP (Qualified Person) – Sligo - Osborne
Job Summary
  • Sligo
  • Permanent
  • 11th December 2024
  • €60,000
  • Ref ID: #43445

Job Description

  • Location: Sligo, Sligo
  • Type: Permanent
  • Job #43445
  • Salary: €60,000

Licenced Quality Manager – QP (Qualified Person) – Sligo

The QP will be responsible for signing off on the final batches of medicines before they are released for sale. Work for a company that is a global manufacturer of medicated feed ingredients and solutions including vaccines. The QP will join the quality team and be an integral member onsite in Sligo, Ireland.

The candidate will have at least a level 8 academic qualification in Pharmaceutical Sciences and hold relevant licencing certificates. Knowledgeable of all GMP regulations.

Salary: €65000 – Monday to Friday (40 hours) –  8% bonus – 22 days AL – Healthcare – Pension contribution –  Educational Assistance

Experience:

  • Academic and practical experience working with veterinary medicinal directives.
  • Application procedures to manufacturing and testing.
  • Support and prep for agency inspections and audits.

Responsibilities:

  • Ensure all batches have been successfully fulfilled in compliance with Irish Law and EU Guidelines.
  • Follows and fulfils all legal and professional duties of the QP and maintaining a high ethical standard.
  • Responsible for the batch certification process so will have full knowledge of all the process for manufacturing.
  • Manage and confirm the supply chain process up to final batch sign off including the quality agreements.
  • Ensure compliance with all stakeholders included within the batch life cycle process.
  • Provide detailed information of all audits across all sites and ensure records are readily available.
  • Ensure post – marketing regulatory requirements have been met and addressed.
  • Manage the evaluation of changes to manufacturing and testing processes.
  • Ensure up to date veterinary medicinal directives are being followed in relation to the importation of substances.  
  • Review changes to all QMS and ensure new directives / regulation supporting documentation is recorded.
  • Work with all regulatory authorities and be in a position to co-operated with the assistance in exchanging information.
  • Review findings from audits.
  • Be up to speed with all regulations and guidelines and follow all legal requirements.

For more information please apply through the link provided for the attention of David McCoy or email David at david.mccoy@osborne.ie  call Osborne Recruitment on 01 5984334
If you are interested in finding out more about the above role and would like to be considered other suitable roles that we may have available for your skill set – please attach your CV via the link provided
Please submit your updated CV in Word Format
If you are living in Ireland and hold a valid work permit we would love to hear from you, if however you do not hold a valid work permit unfortunately we will not be in a position to assist you with your job search.

#INDMCCOY
#INDOSB1

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    Job Summary
    • Dublin
    • Permanent
    • Nov 17, 2022
    • Competitive
    • Ref ID: 123456