select * from applications_reporting where candidate_id = '' 4

Data Verification and Documentation Group Scientist

£24k to £30k | South East, Berkshire |  Manufacturing and Operations |  Permanent  | Ref:889272

The Role

Data Verification and Documentation Group Scientist - Manufacturing and Clinical - Reading - £24k to £30k


The Company

  • Global Manufacturing and Clinical Organisations
  • Work to accelerate the development of new drugs for patients around the world
  • Innovated new approach to drug development which reduces costs and shortens timelines
  • Provide formulation development, clinical pharmacology trials and clinical commercial manufacturing services to the pharma and biotech industry.


The Role

  • Role is open due to growth and an increased number of projects
  • Verification of laboratory data including lab note books, raw data packages, excel spread sheets
  • Checking of protocols, reports, test methods, certificates of analysis and specifications
  • Coordinate API, excipient and packaging release testing at external laboratories or perform internally.
  • To employ the principle of continuous improvement and a basis of teamwork in day to day activities with colleagues.
  • There is always a fresh challenge, offering you the chance to develop your expertise within the cutting edge of Pharmaceutical Science.



To apply for this role as Data Verification and Documentation Group Scientist our client is hoping for someone with the following skills and experience…

  • You will have analytical experience and experience using HPLC
  • Good working knowledge and experience of working within a GMP laboratory environment
  • You will be reliable, enthusiastic and a self motivator
  • You will have strong IT skills and experience of completing documentation with a high degree of accuracy
  • You will have excellent communication skills both written and verbally.


What should you do next?

This new and exciting role is one not to be missed; it encompasses the opportunity to use your scientific background and build upon your verification and documentation skills. To discuss further, please submit your current CV.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



Natalie Hough

Which team and area do you work/specialise in?

Drug Development Team. I specialise in R&D and Manufacturing roles.

What are some of the typical roles you cover?

CMC, Engineer & CSV Engineers, Manufacturing Specialists, Scientists, Process Engineers, and Technical Specialists positions. 

What are the hot issues in your sector currently?

Rising drug prices


More jobs like thisSee all