Skipton, North Yorkshire, Yorkshire, United Kingdom
Dechra
Dechra is a growing, global specialist in the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high-quality products exclusively for veterinarians worldwide. It's a great time to join our modern Skipton facility and further investment for the Skipton site means … njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business. Quality Control Analyst Lates, 1400-2230 24-Month Fixed-Term Contract Every other Friday off Working within a close-knit and diverse team, you … ll be responsible for the analysis of Solid Dose Finished Products within a Quality Control environment. You'll become an integral member of the Dechra family and play an essential role in the testing process of solid-dose products. Package So, what's in it for you? An opportunity more »
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 … 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: For more information, or to apply for this QC Analyst position please more »
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: For more information, or to apply for this QC Analyst position please more »
requirements. Identify ways to improve material flow through the lab to aid reduction in turnaround times and reduce costs, whilst still adhering to corporate quality standards. Assist in coaching and developing other members of the team Main Tasks and Responsibilities n Follows approved methods and procedures in accordance with … cGLP & GMP requirements. n Plan and prioritises own work with guidance from QC Senior Analyst/QC Manager n Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements n Maintain the flow of QC documents within the department ensuring they are … commensurate with the post holder’s position in the company Skills & Qualifications Education 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/ more »
