QA CSV Specialist Summary: Our client based in Dundalk has a greatopportunity for a QA CSV Specialist.
This role is responsible for overseeing all validation activities, ensuring compliance with current regulatory requirements, c GMP, and company SOPs.
It includes validation/qualification activities for facilities, utilities, equipment, computerised systems, cleaning processes, storage areas, controlled temperature units (CTUs) and shipping.
Responsibilities: Ensure the quality oversight of the qualification/validation activities of all facilities, utilities, equipment, computerised systems, cleaning processes, manufacturing processes, storage areas, controlled temperature units (CTUs) and shipping processes.
Ensure that all validation documentation and associated data, including but not limited to plans, URSs, quality risk assessments, protocols, and reports, are reviewed and approved by QA for conformance to SOPs, specifications and other applicable acceptance criteria.
Ensure that all events/deviations, investigations, and change evaluations that occur during qualification/validation activities have appropriate QA oversight, QA review and approval and adhere to SOPs and c GMP requirements.
Review SOPs relating to qualification/validation activities.
Provision of support in Regulatory inspections and Client audits.
Provision of QA Validations expertise to maintain the validation status of the facility.
Maintain an understanding of c GMP regulations and guidance in relation to all aspects of validation and/or qualification of facilities, utilities, equipment, computerised systems, cleaning processes, manufacturing processes, storage areas, controlled temperature units (CTUs) and shipping processes.
Coordinate all QA Validation activities to ensure schedule adherence and on-time delivery of project deliverables.
Manage and develop the QA Validations team, including, but not limited to, activities such as performance management, recruitment, and training.
Qualifications & Experience: B.
Sc or B. Eng in a Scientific or Engineering related discipline (e.g.
bchemistry, chemistry, engineering).
Minimum 5 years experience in a Quality Engineering/Quality Assurance/Quality Validations role for Biologics or related pharmaceutical/ medical device manufacturing in a FDA/ EU regulated environment.
Thorough understanding of the validation requirements associated with a c GMP manufacturing facility Knowledge of Gx P regulations applicable to biologics manufacturing (e.g.
EU-GMP, FDA, ISO) and the industry standards applicable to validation, including but not limited to; GAMP, ISPE, ISO, ASME and BPE.
Knowledge of trouble shooting and problem-solving skills.
Knowledge of formal root cause analysis methods and tools such as Ishikawa diagrams, FMEA etc.