9 QC Analyst Jobs in England

A leading Chemical company are looking for a QC Analyst to join their team in the Durham area. Salary and Benefits of QC Analyst Salary up to £28,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP … Standards Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience HPLC and GC Experience Responsibilities of the QC Analyst The role of QC Analyst consists of Plan and prioritises own work with guidance from Senior Analyst or … customer requirements and to carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations Additional Responsibilities of the QC Analyst : Maintain the flow of documents within the department ensuring they are complete, accurate and compliant with procedures or guidelines Carry out more »

QC Analyst required, based in Cheshire West on a permanent basis. Requiring proven industrial experience of Quality Control testing in a fast-paced environment with HPLC and GC experience being advantageous. Title: QC Analyst Location: Cheshire West Salary: £25,000 - £28,000 (dependent on … with an international company who specialise in the creation of speciality chemicals for a range of markets. They are now looking to add a QC Analyst to their Technical team on a full-time basis at their site in Cheshire West. This role will allow the QC … will include analysing raw materials, intermediates and finished products. Using mainly HPLC and GC techniques, this is a busy role in a fast-paced QC laboratory and will suit candidates coming from a similar environment. Proven industrial experience of Quality Control testing is essential. Working hours: 11am – 7pm Monday 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 … 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 contact James Horne on 0191 370 6483 or email jhorne@ckgroup.co.uk. Please quote job reference 56808 in all correspondence. 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 »

CK Group are recruiting for two QC Analysts 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 … 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 … 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 contact Hannah Oakley on 01246 457711 or email hoakley@ckgroup.co.uk. It is essential that applicants hold entitlement to work more »

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 complete, accurate and compliant with procedures or guidelines n Ensure that OOS/OOT investigations are performed in timely manner in accordance with the procedural requirements n Carry out minor analytical method development to … 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 »

x QC Analysts required, based in Teesside on a permanent basis. Requiring proven industrial experience of analytical chemistry including HPLC or GC. Title: 2 x QC Analysts Location: Teesside Salary: £27,000 - £28,000 (dependent on experience) Employment Term: Permanent SRG are working with an international company who … specialise in the creation of speciality chemicals for a range of markets. They are now looking to add 2 QC Analysts to their analytical team on a full-time basis at their site in Teesside. These permanent roles will be supporting a recent increased workload and sample volumes, and … desirable but not essential for this position. Benefits: 28 days holiday plus bank holidays. Monday – Friday, 9am-5pm (with flexibility). Role/Description QC analysis of raw materials, in-process and finished product samples in support of production using a range of techniques including HPLC and GC. Provide more »

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 … Free access to the Headspace App Employee Assistance Programme Free on-site parking Main Responsibilities So, what's the role? Working closely with the QC Shift Manager and the wider team, the day-to-day will involve a wide variety of responsibilities and cover Instrumental and HPLC testing. You … ll have the opportunity to attend release-for-sale meetings and develop strong relationships with Supply Chain, Warehouse, QC and other departments. We're a friendly bunch and always welcome collaboration and a fresh perspective. Other responsibilities include: Initiating Laboratory Investigation Reports (LIRs), Deviations, Change Controls, CAPAs, Due Date more »