Quality Assurance Specialist C&Q / Validation, Dun Laoghaire, Dublin
Office/Project Location:Dun Laoghaire, Dublin
Employment Type: Contract
Work Location: Hybrid Onsite requirement is 3 days per week
Pay: €50 - €57 per hour
Experience: 7+ years
Visa: EU passport or Stamp 4 visa required
Our client is a leading international Biotechnology company with a state of the art aseptic manufacturing facility in Dun Laoighaire, South Dublin.
The plant is one of the most dynamic in Ireland and is currently undergoing rapid expansion and capital investment.
This is an excellent opportunity to get experience into Ireland's leading aseptic manufacturing plant.
We are seeking an experienced Senior Quality Assurance Professional to provide quality direction and oversight for activities related to the installation of new syringe and inspection lines at our facility in Dun Laoghaire.
This role requires a strong understanding of Quality requirements associated with aseptic manufacturing, as well as an excellent understanding of C & Q / Validation requirements.
The desired candidate should have a proven track record in QA leadership, and be comfortable working as part of a cross functional team.
Quality Oversight of new equipment qualification:
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.
Validation and Documentation:
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.
Risk Management and Compliance:
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.
Documentation and SOPs:
Write, review, and approve Standard Operating Procedures (SOPs) in alignment with policies.
Regulatory and Safety Compliance:
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.
Requirements
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.
Excellent organizational, communication, and collaboration skills.
Ability to work independently with minimal supervision and operate effectively across functional boundaries.
Critical thinking and problem-solving abilities.
Familiarity with Quality by Design (QbD).
Proficiency in statistical analysis tools (e.g., Minitab, JMP) is a plus.
Team-oriented mindset with the ability to thrive in a collaborative decision-making culture.
Package
Contract role - Hourly rate €50 - €57 per hour
Minimum 12 month contract
Onsite requirement is 3 days per week