Senior Product QA Manager

https://www.teamhorizon.ie/job-search/1777-senior-product-qa-manager/quality/galway/job2026-04-16 17:25:432053-08-30Team Horizon
Job TypePermanent
AreaGalway, IrelandMayo, IrelandRoscommon, IrelandSligo, IrelandLeitrim, IrelandGalwayIreland
SectorQualityManagementOperations & Manufacturing
Start Date
AdvertiserAshling Guthrie
Job Ref3907
Job Views209
Description

Team Horizon is seeking a Senior Product QA Manager & QP to join our client’s team. This is a leadership role and is responsible for compliance with marketing authorisations, current Good Manufacturing Practices (GMP), and supporting New Product Introductions (NPIs).


 


 


Why you should apply:



  • This is an excellent opportunity to make an impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience.


 


 


What you will be doing:



  • Manage QP , Regulatory, Change Management and New Product Introduction teams, including annual goal setting, performance reviews, development, and talent management.

  • Ensure products (commercial and NPI/CTS) are manufactured and released in line with marketing authorisation, GMP, and company quality systems.

  • Lead batch review and release, documentation, checks, and test completion.

  • Oversee validation of manufacturing and testing processes and accurate record keeping.

  • Provide quality governance on deviations, planned changes, and exception reporting with proper authorisations and regulatory notifications.

  • Support NPI activities: change plan review, validation, documentation approval, and release of CTS batches

  • Execute regulatory requests and submissions, engage directly with regulatory agencies (FDA, HPRA).

  • Chair Change Review Boards, approve changes, oversee completion of QA tasks.

  • Conduct internal/external audits and participate in regulatory/customer inspections.

  • Manage complaint investigations, coordinate product recalls, and address quality defects.

  • Ensure compliance with FDA CFR Parts 210/211/Q7, EU GMPs (ICH Q7, Volume 4), and  QA Policies.

  • Review and approve Product Quality Reviews (PQRs) and track finished product data.

  • Provide QP oversight for SAP, LIMS setup changes, and manage site quality metrics.

  • Act as Designee for the Quality Director when required.

  • Lead department/site goals, provide technical leadership/guidance on QP/regulatory matters, and present technical data for decision-making.


 


What you need to apply:



  • MSc in Industrial Pharmaceutical Science (or a comparable course recognized for QP status per Article 49 of Directive 2001/83/EC).

  • Minimum 10 years' experience in the healthcare/pharma sector within FDA/EMA approved environments.

  • Demonstrated experience leading teams, with 7+ years in leadership roles Demonstrated attention to detail, strong problem-solving and innovative thinking abilities.

  • Results-driven mindset with proven prioritization skills and commitment to quality.

  • High integrity, strong work ethic, excellent verbal/written communication, and interpersonal skills.


 


 

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