Analytical Data Reviewer - 12 month contract
Quotient Sciences: Molecule to Cure. Fast.
Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. With over 35 years of experience and a track record of success, we provide Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway, including formulation development, clinical pharmacology, clinical trials, and commercial product manufacturing.
Our proprietary and disruptive platform – “Translational Pharmaceutics®” – integrates Drug Product Manufacturing and Clinical Testing to eliminate silos in the drug development process. This in turn reduces costs, improves outcomes, and significantly accelerates drug development times.
Why Join Us
Because every day counts when bringing new medicines to patients. Our 1,000+ experts across the US, UK, and beyond are united by science, agility, and a culture that turns ideas into impact—fast.
Are you an experienced analytical laboratory professional with a strong eye for detail and a passion for data quality? This is an opportunity to use your analytical knowledge in a role where you'll play an important part in ensuring laboratory data is accurate, complete and compliant. You'll work closely with laboratory analysts and management, reviewing analytical results and documentation while helping to maintain high standards across the laboratory.
The Role
As an Analytical Data Reviewer, you'll be responsible for reviewing chromatographic and analytical data, laboratory documentation and associated records to ensure work has been completed accurately and in accordance with approved procedures, methods and specifications.
You'll review testing across a range of laboratory activities, including in-process and final product testing, raw materials and cleaning validation or verification. You'll also work closely with analysts to resolve queries, improve documentation and reporting standards, and support an efficient and compliant data review process.
Key responsibilities
In This Role, You Will
- Review chromatographic and analytical data, laboratory write-ups and reports in accordance with Standard Operating Procedures (SOPs).
- Review analytical testing to ensure it has been performed in line with approved protocols, analytical methods and sp...
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis.