Ref No.



UK ~ Reading

Manufacturing Document Co-Ordinator

Company Overview

Our growing and successful business comprises of over 800 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

We have an excellent opportunity for a GMP Document Co-Ordinator working in the Pharmaceutical Scientific and Technical Services area.  You will take the lead in Clinical Trial Project Packaging and be responsible for providing project support for the Pharmaceutical Operations working alongside colleagues in Project Management. 

The key responsibilities of the role are outlined below.

  • Drafting & reviewing of batch manufacturing and packaging records
  • Drafting & reviewing associated controlled clinical product labels for the business
  • Assist in the progression of Investigational Medicinal Products, clinical trial labelling and manufacturing services within Quotient Sciences
  • Take Project Leadership responsibilities for assigned Clinical Trial Product packaging and labelling operations
  • Maintain your training record and to discuss any needs with your line manager in order to maintain your knowledge
  • Undertake such duties as are required for the smooth running of the company or as requested by the Vice President
  • Support Project Management project teams as required
  • Work safely within H&S guidelines and in accordance with company procedures.

The Candidate

The ideal candidate will be educated to a minimum BSc or MSc. in Pharmaceutics, Pharmacy, or other related science subject (also suitable for graduates) with experience in drug development and/or manufacturing of IMP products, have knowledge of GMP procedures or been involved in clinical trial product management.  Previous formulation development, process development and/or cGMP manufacturing experience in the pharmaceutical industry would be an advantage.  You must be an organised individual, have a high attention to detail and should be able to work towards strict and tight project deadlines.  The ability to juggle a wide range of tasks simultaneously and responding to client and internal demands is also essential for this role.

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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