Ref No.

QUO00528

Location

UK ~ Nottingham

Temporary Analytical Scientist

Company Overview 

Our growing and successful business comprises of over 700 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 Clinical 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

Quotient Sciences has significantly expanded its technical and analytical capabilities with a capital investment of £1.3M to establish a new state of the art laboratory facility at its Ruddington site. The laboratory is fully operational and due to an increased number of projects within our Pharmaceutical Operations department we have a number of requirements for temporary Analytical Scientists.  

The Analytical department consists of 2 teams; Quality Control and Method Development. Therefore, we have temporary/ ongoing opportunities for QC Analytical Scientists and Development Analytical Scientists.

As the QC Analytical Scientist, you will be responsible for analytical testing to support generation of stability data for regulatory submissions and also QC testing for release of drug products to the clinic. Routine cleaning and general laboratory maintenance duties will also be required.

As the Development Analytical Scientist, you will be responsible for developing, optimising and qualifying analytical methods to support testing of a wide range of dosage forms for clinical dosing. This will include writing analytical method qualification protocols and reports and documenting laboratory activities in write ups.

Within Pharmaceutical Operations, no day is ever the same. There is always a fresh challenge, offering you the chance to develop your expertise within the cutting edge of Pharmaceutical Science.

Our unique business model means that Drug Formulation, Clinical Testing and GMP Manufacturing is all on one site. Communication is essential in this role to communicate the progress of projects effectively within your departments.

The Candidate

The successful candidates will have a good working knowledge of HPLC and dissolution methodologies and have experience of working within a laboratory environment. You 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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