Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients.
As a growing and successful business, we employ more than 1,100 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA.
Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.
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 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.
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.
Our Commitment to Diversity & Inclusion
Quotient Sciences are advocates for positive change and conscious inclusion.
We strive to create a diverse Quotient family by remaining committed to the development of our culture, equality, mindset, diversity & inclusion in the workplace.
As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. All applicants welcome.
If you have any questions or need some support with your application, we’d love to hear from you so contact our friendly team at firstname.lastname@example.org.