Date Posted: 15/8/2017 Application Close: 31/12/2017 Location: Arcinova - Alnwick

The successful applicant will be a Qualified Person with extensive knowledge and experience of pharmaceutical development, and experience in the management of scientific staff.

The role will include:

The provision of scientific and administrative guidance to a team of analytical and microbiological scientists
Working directly with potential clients to formalise the scope of work requests and to maximise the number and value of awards
Ensuring that awarded work is progressed and reported to the expected quality standards/schedule. As required act as the client’s main point of contact for awarded studies.
Discharging the responsibilities of “Person responsible for Quality Control” on the site MIA(IMP) licence
Acting as Qualified Person on the site MIA(IMP) licence under the provisions of Directive 2001/83/EC and Directive 2001/82/EC
Supporting the conduct of client and regulatory audits, bringing wider regulatory/local system knowledge to bear
Excellent written and oral communication skills together with good interpersonal and organisational skills are essential.


To apply please email your letter of application, CV and any relevant supporting documents to enquiries@arcinova.uk FAO of Nikki Edwell, Human Resources.

See this post on the Arcinova website.