
QA Senior Associate
- Dún Laoghaire, Co Dublin
- Contract
- Full-time
- Act as disposition manager ensuring that batch disposition activities are completed in line with the clients standards
- Manage and drive Quality records to closure including deviation records, investigation reports
- Initiate Quality records for supplier related changes.
- Collaborate with Complaints team to request assessments, reviews complaint report and have comments addressed
- Provide data to the networks to support Quality Management Processes)
- Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations.
- Take part in operational and quality improvement initiatives, programs, and projects.
- Communicate effectively with stakeholders, ensuring alignment on quality objectives and compliance needs.
- A degree in science, engineering, or a related discipline.
- Minimum of 4+ years experience working in QA in a cGMP manufacturing environment and a deep understanding of regulatory requirements.
- Direct experience in batch release activities and good working knowledge of SAP.
- Experience in investigations, project management, and trending/analysis.
- Relevant experience in Supplier Management (raw materials, packaging, devices) and understanding of manufacturing/testing processes (e.g., API, Drug Substance, Drug Product, Packaging, Device).
- Strong analytical, troubleshooting, and communication skills (verbal, written, presentation).
- Ability to work effectively with global, virtual teams and manage multiple priorities with high initiative.
- Team-oriented with a focus on achieving team goals.
- Proven ability to positively influence others.