Quality Consultant

PE Global; Limerick; On-site; EUR 110,000 - 150,000; Full time

Job summary

PE Global are currently recruiting for a QA Quality Risk Management Lead to be based onsite at a biologics facility in Limerick. The role focuses on redefining and embedding a risk-based quality management approach for a digitally enabled plant.

You will embed QRM across processes, systems and operations, address operational resiliency, data integrity and paperless manufacturing, and partner with Quality, Manufacturing, IT and Engineering to ensure regulatory confidence.

Qualifications

• Extensive experience in Quality Risk Management within GMP-regulated pharma or biologics manufacturing.
• Strong knowledge of ICH Q9, digital manufacturing concepts, and system-enabled operations.
• Proven ability to operate at a strategic level, influencing site design, operating models, and quality governance.
• Experience addressing operational resiliency, data integrity, and business continuity in digital or paperless environments.

Responsibilities

• Design and implement a modern, facility-wide Quality Risk Management (QRM) framework, aligned with ICH Q9(R1), supporting a fully digital plant.
• Embed risk-based thinking into all aspects of facility startup, including manufacturing processes, digital systems, automation, data flows, and quality oversight.
• Assess and manage risks related to dependency on digital and corporate systems, including DCS, MES, eBR, ERP, data historians, and network infrastructure.
• Define and govern business continuity and contingency strategies to ensure GMP compliance during system outages (e.g., network failures, cloud unavailability), including controlled fallback for paperless operations.
• Partner with Quality, Manufacturing, IT, Automation, and Engineering to ensure risks are proactively identified, mitigated, and owned.

Job description

PE Global are currently recruiting for a QA Quality Risk Management Contracotr to be based in our clients site in Limerick – fulltime onsite

QRM Lead– Digital Core implementation

Summary

The QRM lead is responsible for redefining and embedding a risk-based quality management approach for a new, digitally enabled biologics manufacturing facility. The role ensures that quality risk management is systematically applied across processes, systems, and operations, with particular focus on operational resiliency, digital system dependency, and paperless manufacturing continuity.

Essential Duties and Responsibilities include, but are not limited to, the following:

• Design and implement a modern, facility-wide Quality Risk Management (QRM) framework, aligned with ICH Q9(R1), supporting a fully digital plant.
• Embed risk-based thinking into all aspects of facility startup, including manufacturing processes, digital systems, automation, data flows, and quality oversight.
• Assess and manage risks related to dependency on digital and corporate systems, including DCS, MES, eBR, ERP, data historians, and network infrastructure.
• Define and govern business continuity and contingency strategies to ensure GMP compliance during system outages (e.g., network failures, cloud unavailability), including controlled fallback for paperless operations.
• Partner with Quality, Manufacturing, IT, Automation, and Engineering to ensure risks are proactively identified, mitigated, and owned.
• Ensure risk decisions are science-based, documented, and inspection-ready, supporting regulatory confidence in a highly digital operating model.

Education and experience

• Extensive experience in Quality Risk Management within GMP-regulated pharma or biologics manufacturing.
• Strong knowledge of ICH Q9, digital manufacturing concepts, and system-enabled operations.
• Proven ability to operate at a strategic level, influencing site design, operating models, and quality governance.
• Experience addressing operational resiliency, data integrity, and business continuity in digital or paperless environments.