Qc analyst

CK Group are recruiting for a QC Analyst to join a leading pharmaceutical and chemicals CDMO, based at their site near Middlesbrough on a permanent basis. Your main responsibility will include testing intermediates, products and raw materials in line with demand and business requirements. Job Summary: Follow approved methods and procedures in accordance with cGLP GMP requirements. Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements. Ensure QC documents are complete, accurate and compliant with procedures or guidelines. Ensure that investigations are performed in timely manner in accordance with set procedures. Carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations. Identify ways to improve reduction in turnaround times and reduce costs, whilst still adhering to corporate quality standards. Assist in coaching and developing other members of the team. You will have the following experience/qualifications: Chemistry (or very closely aligned subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience. Experience of working in a GMP environment / method development experience / cleaning validation experience. To Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence