Ref No.



UK ~ Reading

Data Verification and Documentation Group Scientist

Company Overview

Our growing and successful business comprises of over 850 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 Verification and Documentation Group Scientist. As Data Verification and Documentation Group Scientist, 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.  There is always a fresh challenge, offering you the chance to develop your expertise within the cutting edge of Pharmaceutical Science.

Key Responsibilities

  • Verification of laboratory data including lab note books, raw data packages, excel spread sheets
  • Verification of data in reports
  • Writing and checking of protocols, reports, test methods, certificates of analysis and specifications
  • Contribute to the writing of protocols, reports and specifications
  • Assess and write specifications/test methods for API, excipient and packaging release testing.
  • Coordinate API, excipient and packaging release testing at external laboratories or perform internally.
  • Performs job responsibilities in compliance with cGMP and all other regulatory agency requirements.
  • Work in compliance with documentation e.g. SOPs.
  • Carry out duties in accordance with the companies’ health and safety policies.
  • To maintain your own training record and to discuss needs with your line manager.
  • To employ the principle of continuous improvement and a basis of teamwork in day to day activities with colleagues.
  • Undertake any other duties as requested by management. This role is based at our Reading site.

The Candidate

Candidates requiring part-time or full-time hours will be considered. 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. Strong IT skills and experience of completing documentation with a high degree of accuracy is also a must.

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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