Study Director - In Vivo Biosafety

£26000 - £30000 per annum
05 Jan 2021
04 Feb 2021
Rachel Benjamin
Contract Type
Full Time
We are currently looking for a Study Director - In Vivo Biosafety to join a leading Research Institute company based in the Midlothian area. As the Study Director you will be responsible for conducting safety studies evaluating a range of biological medicinal products.


Your duties as the Study Director - In Vivo Biosafety will be varied however the key duties and responsibilities are as follows:

1. You will be responsible for the maintenance of equipment and facilities to Good Laboratory Practice Levels (GLP) / Good Manufacturing Practice (GMP).

2. As the Study Director you will compile/review SOPs and Validation Protocols.

3. You will process and analyse laboratory samples, where required.

4. The Study Director will also prepare and maintain stocks of laboratory consumables and reagents.


To be successful in your application to this exciting opportunity as the Study Director - In Vivo Biosafety we are looking to identify the following on your profile and past history:

1. Relevant degree in a Life Sciences related discipline plus industry experience.

2. Proven industry experience working in a GLP/GMP laboratory.

3. A working knowledge and practical experience of standard biological testing procedures,

Key Words: Study Director / In Vivo / Biosafety / Laboratory / Biologics / Biopharmaceutical / Life Sciences / GLP / GMP / Good Laboratory Practice / Good Manufacturing Practice / SOPs / Bio Safety / Bio-Safety.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

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