Description Key Roles and Responsibilities:- Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures. Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues. Identify and escalate any identified cGMP areas of concern. 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, production and support functions as required. Be involved in the preparation for MHRA/FDA and other regulatory body audits. Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required. Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager. Act as the QA representative for the introduction of new products, being a key member of the multi-functional team including R&D, QC and manufacturing thus ensuring that all cGMP documents are appropriate and all cGMP requirements are satisfied. 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 Ability to follow instruction accurately Ability to escalate issues as appropriate Qualifications Essential Qualifications:- BSc in a relevant Scientific discipline or equivalent. Essential Experience:- A minimum of 3 years’ experience within a cGMP environment manufacturing Active Pharmaceutical Ingredients is required. A College/University qualification in a scientific subject is required. Experience in dea ling with quality assurance, analytical chemistry, development, and manufacturing groups is beneficial