Analytical Data Reviewer

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.

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.

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.

• 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 specifications.
• Review results from in-process testing, final product testing, raw material testing and cleaning validation or verification, checking for accuracy, completeness and compliance.
• Ensure associated laboratory data and documentation, including electronic data, notebooks, logbooks and worksheets, are complete and appropriately reviewed.
• Check documentation for accurate data reporting, transcription and referencing.
• Work collaboratively with analysts to identify and resolve required corrections to laboratory documentation.
• Support analysts in improving the quality and consistency of analytical data documentation and reporting.
• Escalate deviations, discrepancies or potential issues identified during the review process promptly to management.
• Communicate potential data-review delays and their causes clearly to relevant stakeholders.
• Work with management to prioritise review activities and assignments.
• Identify opportunities to improve the effectiveness and efficiency of the data review process.
• Support other appropriate activities aligned with the responsibilities of the role.

• Experience working within an analytical, quality control or laboratory environment.
• Experience reviewing analytical or laboratory data and associated documentation.
• Good understanding of chromatographic data and analytical testing.
• Ability to review detailed scientific data accurately and identify discrepancies or…