Qualified Person I am recruiting for a Qualified Person to join a global pharmaceutical CDMO based in Kent. My client is offering a competitive salary, 15% bonus, car allowance, private medical plus benefits. This person will be responsible for ensuring that all products released from the site comply with regulatory and quality standards. You will be working with operations team to ensure quality is embedded into their processes. Responsibilities Leads a Quality Operations value stream and team of quality officers and auditors to ensure quality and operations are aligned and quality culture is in built from the shop floor. Member of the Senior Quality Leadership Team, assisting in directing the Quality department strategy. Ensures excellent customer service and satisfaction in the QP value stream and swift resolution of issues. Contributes, and where applicable facilitates the resolution of operational problems in Pharmaceutical Production whilst maintaining compliance to cGMP and license commitments. Provides a day – to – day contact, aiming for consistency in approach for quality related issues for all departments through direct review of operational areas and practices. Assists in the handling of complaints, annual product review, periodic product reviews and failures investigations. Assist the QA Documentation and Compliance Group in ensuring site documentation is maintained to cGMP and agreed standards. Ensures that all packaging and raw materials manufactured products and bought in products have been processed and tested. Act as subject matter expert for GMP. Keep up to date with UK/EU/USA regulations. Requirements BSc or equivalent in a Pharmaceutical related subject A qualified QP is essential Extensive experience of working in a pharmaceutical manufacturing environment Strong people management and leadership experience Knowledge of US regulations If you a Qualified Person and have significant manufacturing experience then please apply now or contact Naomi Clarke at NES Fircroft.