Company: Hobson Prior
Closing Date: 17 Dec 16
Salary (£): On Application
Benefits: £40 p/h
My client is a leading Pharmaceutical who specialises within clinical trials. They are seeking a QA Specialist to deliver global procedural document packages for Good Clinical Practice and /Good PharmacoVigalance Practice requirements.
My client is a leading Pharmaceutical who specialises within clinical trials.
They are seeking a QA Specialist to deliver global procedural document packages for Good Clinical Practice and /Good PharmacoVigalance Practice requirements.
The role provides an exciting opportunity to gain experience in a leading pharmaceutical working alongside global teams.
Key responsibilities include:
Implement the controlled document strategy for PDQ and the supported business partners.
Support implementation of GxP standards - specifically GCP.
Ensure that business partner expectations for SOP strategy, materials and deployment are met.
Qualifications and Experience:
5-7 years in the pharmaceutical industry.
Proven experience working alongside GCP & Pharmacoviglience standards.
Compliance and documentation experience within a QA role.
12 month contract.
Office based work is required.
If you have the required experience and interested in the role described, please email your CV to email@example.com.
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Hobson Prior International Ltd
7-9 Church Rd.
|Tel:||01892 612 612|
|Fax:||01892 612 613|
|Website:||Visit Our Web Site|
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