8 QC Analyst Jobs

CK Group are currently recruiting for a QC Analyst - Stability to join a patient focused pharmaceutical research company with Commercial, Discovery, Clinical and Manufacturing business units collated on a single site in Hatfield, Hertfordshire on an initial 12 month contract. QC Analyst Role: Your … to: - Qualify, maintain and calibrate all laboratory equipment according to procedures. - Maintain all laboratory Quality Systems and Quality Management Systems. - Write SOPs associated with QC Support. - Raise and support the investigation of deviations and associated CAPAs. - Support the collection of data for reporting Quality Assurance Performance Indicators. Your Background … professional with problem solving and decision-making capabilities. - Basic understanding of GMP Guidelines and Regulations. Apply: For more information, or to apply for this QC Analyst position please contact Hannah Oakley on 01246 457711 or email hoakley@ckgroup.co.uk. Please quote job reference 56706 in all correspondence. It more »

mRNA & DNA) · ex-vivo & in-vivo cell and genetic medicines · Gene therapy using viral vectors and gene editing · Autologous & Allogenic cell therapy Quality Control Analyst Touchlight is currently seeking … a QC analyst to join its Quality Control department. The Quality Control Analyst is responsible for supporting the Quality Control (QC) laboratory for day-to-day QC testing of manufactured dbDNA for our clients and internal pipeline. There will be a close interaction … with the other operational departments to support Quality and product needs. Key activities will include the day-to-day QC testing of finished product through molecular biology and biochemistry techniques , reagent preparations, goods receipt, sample receipt, procurement, good housekeeping activities, equipment and instrument verifications, and documentation. The QC 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 … 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 … 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/ more »

QC Radiochemist/Analyst Working exclusively with an international advanced pharmaceutical company, I am currently supporting multiple hires within their QC team for one of the UK facilities based in South Yorkshire. These positions are hands on production scientists within a significantly growing area of radiopharmacy … below or call Mark Bux-Ryan for further details. Key experience: Educated to degree (or equivalent level) in a Life Sciences subject Previous quality control (QC) chemistry or production experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. … to strict regulated procedures Flexible to work shifts Must have own transport to access the site due to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

QC Radiochemist/Analyst Working exclusively with an international advanced pharmaceutical company, I am currently supporting multiple hires within their QC team for one of the UK facilities based in South Yorkshire. These positions are hands on production scientists within a significantly growing area of radiopharmacy … below or call Mark Bux-Ryan for further details. Key experience: Educated to degree (or equivalent level) in a Life Sciences subject Previous quality control (QC) chemistry or production experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. … to strict regulated procedures Flexible to work shifts Must have own transport to access the site due to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

Hobson Prior are seeking a diligent QC Analyst to join a dynamic Quality Control team in the biotechnology industry. Responsibilities: - Perform environmental monitoring of the aseptic manufacturing facility and ensure all testing aligns with the Environmental Monitoring programme. - Maintain QC facilities to meet GMP requirements and more »

team. This would be performing critical lab-based tasks and maintaining high-quality standards. This is a permanent position based in Oxfordshire. Responsibilities: - Perform QC testing of various samples according to SOPs, including cell-based and ELISA-based assays. - Maintain cell lines, review testing data, and participate in QC more »

Practices for Electronic Data. Perform stability study programme activities, storage of in process, and final products samples and retention sample management System owners of QC equipment, assisting in equipment periodic reviews, monitoring and maintaining calibration status of equipment within the Quality Control department. Ownership and accountability of deviations, investigations … Integrity requirements Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives. Calibration of equipment and instruments used to perform QC testing and informing relevant personnel in a timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge … and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner. Attend internal and external scientific and technical more »