Description Key Roles/Responsibilities:- QA primary point of contact (internal and external) for designated projects. Collaborate with internal and external stakeholders to ensure quality of all product related activities. Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation. Participate in quality related investigations, assist in the development, approval and implementation of effective CAPA in order to resolve production, audit and customer issues. Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning procedures Participate in the audits of suppliers and self-inspection of internal production and support functions as required. Be involved in preparation for and successful completion of MHRA/FDA and other regulatory body audits. Coordinate quality disposition activities associated with designated materials and products. Verify manufacturing, laboratory and associated documentation prior to performing the relevant disposition of products. Where potential issues exist, these are to be highlighted to the QA manager. Promote and work to ensure compliance with all relevant GMP/GxP requirements. Support and lead as required, quality process improvements and quality management system improvements within the department and on site. Escalate any identified GMP/GxP areas of concern to Quality Management and QP. Key Competencies:- Attention to detail Good communication skills, both verbal and written Good organisation skills Ability to work effectively individually and as part of a team Ability to analyse data and information to make considered decisions The ability to identify root cause of problems to determine appropriate solutions Ability to prioritise workload to ensure timelines are met. Qualifications Essential Qualification:- BSc in a relevant Scientific discipline or equivalent. RELEVANT EXPERIENCE:- A minimum of 3 years’ experience within a GMP environment manufacturing drug products or biological drug substances/intermediates is required. At least 2 years Quality Assurance experience is required A College/University qualification in a scientific subject is required. Experience in dealing with drug substances for use in sterile products is desirable.