Quality Risk Manager

Headcount Solutions Polska Sp. z o.o.; Limerick; On-site; EUR 90,000 - 120,000; Full time

Job summary

Headcount Solutions Polska Sp. z o.o.

seeks a Quality Risk Management Lead to establish and embed a risk-based quality management program for a new digitally enabled biologics manufacturing facility based in Limerick, Ireland. The role will ensure that QRM is applied across facility start-up, operational resilience, digital system dependency, and paperless manufacturing continuity, partnering with Quality, Manufacturing, IT, Automation and Engineering to mitigate risks and ensure inspection

Qualifications

• Extensive QRM experience in GMP-regulated pharma or biologics manufacturing.
• Experience with ICH Q9(R1), digital manufacturing and system-enabled operations.

Responsibilities

• Establish and manage the facility QRM program in accordance with applicable regulations and internal procedures.
• Select appropriate risk assessment methods and facilitate the completion, periodic review and communication of risk assessments.
• Embed risk-based decision-making across facility start-up, manufacturing, automation, data flows and quality oversight.
• Ensure risk decisions are science-based, documented and inspection-ready.
• Partner with Quality, Manufacturing, IT, Automation and Engineering to identify, mitigate and assign ownership of risks.
• Develop and maintain the risk management plan for digital and corporate systems, including DCS, MES, eBR, ERP, data historians and network infrastructure.
• Support project quality and business objectives relating to GxP risk management.

Job description

Quality Risk Management Lead – Digital Core Implementation

An opportunity has arisen for a QRM Lead to establish and embed a risk-based quality management program for a new digitally enabled biologics manufacturing facility based in Limerick The project QRM subject-matter expert will ensure that quality risk management is systematically applied across facility start-up, operational resilience, digital system dependency, and paperless manufacturing continuity.

Responsibilities

• Establish and manage the facility QRM program in accordance with applicable regulations and internal procedures.
• Select appropriate risk assessment methods and facilitate the completion, periodic review and communication of risk assessments.
• Embed risk-based decision-making across facility start-up, manufacturing, automation, data flows and quality oversight.
• Ensure risk decisions are science-based, documented and inspection-ready.
• Partner with Quality, Manufacturing, IT, Automation and Engineering to identify, mitigate and assign ownership of risks.
• Develop and maintain the risk management plan for digital and corporate systems, including DCS, MES, eBR, ERP, data historians and network infrastructure.
• Support project quality and business objectives relating to GxP risk management.

Education and experience:

• Extensive QRM experience in GMP-regulated pharmaceutical or biologics manufacturing, including use of multiple risk assessment methods and facilitation of complex risk assessments.
• Strong knowledge of ICH Q9(R1), digital manufacturing and system-enabled operations.
• Demonstrated ability to influence site design, operating models and quality governance.
• Experience managing operational resilience, data integrity and business continuity risks in digital or paperless environments.
• Strong communication and leadership skills essential