Job Description

The opportunity has arisen for an additional Qualified Person to join our client, a steriles manufacturer, and undertake the duties specified in Article 51 of Directive 2001/83/EEC. If you’re looking for a secure position in a leading pharmaceutical company with a family environment, this could be the opportunity for you.

Alongside releasing activities, you will drive site-wide compliance through audit co-ordination and validation duties. You will not hold direct line management responsibilities under the current organisational structure but experience in this area could provide benefit.

One thing to note is that our client’s facility is operation 7 days a week and you would be required to work some unsociable hours. In return you will receive excellent remuneration, benefits and a great team of colleagues.

If you are a contractor who isn’t necessarily interested in a permanent position right now, I would still like to speak to you.

For more information or to apply, please contact Ryan Kennedy.

Due to the volume of applications received on a daily basis, we find it incredibly difficult to respond to each and every one. Should you not hear back from us within two weeks, please assume your application was unsuccessful on this occasion.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

To be considered...

To be considered for this position you must have come directly from a pharmaceutical manufacturing environment where you were registered as the releasing Qualified Person on that UK MHRA licence. Experience in Radiopharmaceuticals or steriles would be ideal but isn’t necessarily a pre-requisite for the position.

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