Ref No.

QUO01240

Location

UK ~ Reading

Data Reviewer

Company Overview

Our growing and successful business comprises of over 900 talented individuals globally, in an environment where everybody counts and is instrumental to our success.  With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug development solutions around the globe saving our clients both time and money.

People join Quotient Sciences because we are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. We pride ourselves on the quality of our services and our engaged culture. We are passionate about helping our customers get new medicines to market.

The Role

Due to an increased number of projects within our Pharmaceutical Operations department we have a fantastic opportunity for a Data Reviewer to join our Analytical Development Team. As Data Reviewer, you will be responsible for the verification of laboratory data along with coordinating the writing and checking of project documentation to meet internal and external project timelines, releasing excipients and Analytical practical work. 

You will assess and write specifications/test methods for API, excipient and packaging release testing. You will also coordinate API, excipient and packaging release testing at external laboratories or perform internally

You will ensure work performed by the analysis team is compliant with applicable procedures and analytical methods, and verify all affiliated data including electronic data and respective notebooks, logbooks, and worksheets are complete and reviewed.

You will discuss with analysts when necessary to resolve all required corrections to paperwork and educate analysts to improve analytical data documentation & reporting.  You will communicate frequently with Management, keeping them informed of potential delays in data review, reasons why the delay is occurring and also provide immediate notification of any deviations/discrepancies.

There is always a fresh challenge, offering you the chance to develop your expertise within the cutting edge of Pharmaceutical Science.

This role is based at our Reading Site.

The Candidate

The successful candidate will have Analytical experience and experience using HPLC. You will have a good working knowledge of and experience working within a GMP laboratory environment, will be reliable, enthusiastic and self-motivated as well as having excellent communication skills both written and verbally. Experience of reviewing data in a Pharmaceutical Development environment would be preferred. Strong IT skills and experience of completing documentation with a high degree of accuracy is also a must.

Candidates requiring part-time or full-time hours will be considered.

Applicants must be eligible to work in the UK at the time of being offered employment.

Company benefits

In return you will receive a competitive salary, a generous benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.

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