Qualified Person, Senior Quality Special

Co. Tipperary
At the office
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A fantastic opportunity has arisen a Qualified Person supporting the Spray Dried Intermediate Drug Product and final formulated Drug Product Formulation Facilities.

What you will do:

Lead the Drug Product Intermediate and final Drug Product quality release activities;

  • Ensure that the batch has been manufactured and tested in accordance with current GMP Guidelines Directive 2003/94/EC, EC Guide to GMP for medicinal products and/or the FDA Code of Federal Regulations.
  • Ensure that the batch is released according to the relevant Annex to the Rules and Guidance for Pharmaceutical Manufacturers and Distributors. In particular Annex 13 – Investigational Medicinal Products and Annex 16 – Certification by a Qualified Person and Batch Release.

Work with the Quality Specialist team to ensure timely and effective completion of the Quality IPT core functions, including.

  • Application of Quality Risk Management to all process and systems.
  • Production support and quality compliance guidance to ensure the facility meets and operates to all GMP requirements for development, clinical and commercial supply.
  • Documentation preparation, review & approval to support operations.
  • Prepare Annual Process and System Reviews.
  • Drug substance, Spray Dry Intermediate (SDI), excipients & component release.
  • Deviation management process,
  • Ensure that all Laboratory Out of Specification (OOS) and process deviations are documented, assessed and associated CAPA identified.
  • Provide support to deviation investigations and process performance monitoring.
  • Perform trending on deviations raised as required to identify improvement initiatives.
  • Ensure that root cause is identified and corrective actions are completed.
  • Ensure changes controls raised are documented, assessed, and completed.
  • Participate in the generation and communication of quality metrics.
  • Participation in the internal audit program and hosting of external audits.
  • Participate in Quality and site projects that may arise.
  • Participate as a team member in the site new product introduction.

Previous Experience:

  • Qualified Person status achieved. Relevant working experience acting as Qualified Person named on a Manufacturing & Importation Authorisation (MIA) is desirable.
  • Proven experience within the Pharmaceutical industry in a QA/QC/Compliance role.
  • Excellent knowledge of regulations and sources of regulatory information.
  • Knowledge of Quality IT systems desirable (e.g. SAP, Trackwise, LIMS, QSAT).
  • Knowledge and demonstrated expertise in Lean / Continuous Improvement.
  • Experience in High potency manufacturing / continuous manufacturing / Spray drying / Laboratory GMP / Project Management is desirable.
  • Degree or post-graduate qualification in Science, Pharmacy or equivalent.

Important Dates
Posted on
08 September, 2023
Application deadline
25 September, 2023