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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

Senior Quality Assurance Specialist


Reference:RK3854 Location: Dublin
Qualification:DegreeExperience:10+ Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: EHS Specialist, QA Specialist

Senior Quality Assurance Specialist
RK3854
18 Months
Dublin

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


Duties:

• Provide overall quality direction for processes and procedures associated with all aspects of new equipment introduction, including Computerised System Validation
• Act as the Quality point of contact and decision-maker c & Q / Validation execution activities, ensuring all activities comply with regulatory and company standards.
• Quality review and approval of validation documentation, including:
• Design Specifications (DS), User Requirements Specifications (URS), and Quality Risk Assessments (QRAES).
• Validation Plans, Protocols (IQ, OQ, PQ), and associated reports.
• Ensure robust and compliant validation documentation to support site activities.
• Conduct risk assessments and develop mitigation strategies for potential challenges in equipment introduction.
• Provide input and quality oversight for change control development and implementation.
• Ensure timely and robust implementation of change controls and CAPA records.
• Write, review, and approve Standard Operating Procedures (SOPs) in alignment with policies.
• Ensure all activities align with safety standards, SOPs, and regulatory expectations.
• Support a safe working environment by adhering to all environmental health and safety practices, rules, and regulations.

Education and Experience :

• University degree in a Science or Engineering-related discipline.
• Minimum of 10 years of relevant experience in the pharmaceutical or biotechnology industry.
• Proven expertise in new equipment introduction, technical transfer, PPQ execution, and lifecycle management.
• Strong understanding of validation principles and regulatory requirements for C & Q / Validation (FDA, EMA guidelines).
• Experience with change control, non-conformance resolution, and CAPA implementation.


If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.