QA Deviations Lead & Compliance Manager

Biopharma Careers; Dublin; On-site; EUR 76,000 - 103,000; Full time

Job summary

Biopharma Careers is seeking a QA Manager with a strong background in deviations to lead a team of Quality professionals and ensure GMP compliance, regulatory alignment, and continuous improvement across the site in Dublin. The role focuses on deviations, investigations, CAPAs, and risk management in a fast-paced manufacturing environment.

The ideal candidate will have 7+ years in pharma/biotech, demonstrated leadership, experience with regulatory inspections, and ability to influence across

Qualifications

• Degree in Science, Engineering, Pharmacy, or related discipline.
• Demonstrated leadership experience managing teams and improving performance.
• 7+ years of experience in pharmaceutical/biotech with increasing responsibility.
• Strong expertise in GMP quality systems including deviations, investigations, CAPA, change controls and risk management.
• Experience supporting regulatory inspections and leading audit readiness activities.
• Proven ability to influence and collaborate across functions and levels in a matrix environment.
• Excellent communication, stakeholder management, facilitation and decision-making skills.
• Strong analytical and problem-solving skills with focus on continuous improvement.

Responsibilities

• Lead and develop a high-performing team of Quality professionals through recruitment, selection, training and development to foster a culture of safety, quality, accountability, inclusion, and continuous improvement.
• Provide strategic and operational leadership for manufacturing deviations, ensuring compliance with cGMP, GDP, Amgen standards, and global regulatory requirements.
• Oversee the effective execution of Quality Management System processes, including deviations, investigations, CAPAs, change controls, and associated quality assessments.
• Provide quality leadership and risk-based decision-making for complex quality, compliance and operational issues, escalating significant risks as appropriate.
• Partner cross-functionally with Manufacturing, Engineering, Validation, Quality Control, Supply Chain, and other stakeholders to support compliant and reliable operations.
• Lead inspection readiness activities and represent Quality Assurance during audits, inspections, and governance forums, ensuring effective management of observations, commitments, and remediation activities.
• Monitor quality system performance and trends to identify risks, drive continuous improvement, and enhance operational effectiveness.
• Support implementation of site and global quality strategies, driving simplification, standardization, and optimization of quality processes and systems.
• Promote compliance with environmental, health, safety, and sustainability requirements while fostering a safe and compliant workplace.

Skills

Leadership

GMP knowledge

Regulatory inspections

Cross-functional

Communication

Education

Degree in Science/Engineering/Pharmacy

Job description

Biopharma Careers is seeking a QA Manager with a strong background in deviations to lead a team of Quality professionals and ensure GMP compliance, regulatory alignment, and continuous improvement across the site in Dublin. The role focuses on deviations, investigations, CAPAs, and risk management in a fast-paced manufacturing environment.

The ideal candidate will have 7+ years in pharma/biotech, demonstrated leadership, experience with regulatory inspections, and ability to influence across