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Job Details

GCP Quality Specialist

Company: Hobson Prior
Location: London
Reference: AB000666
Closing Date: 23 Jan 17
Type: Contract
Salary (£): On Application
Benefits: Depending on experience

Job Summary:

My client, a large, global pharmaceutical company are seeking a GCP Quality Specialist to join their team. The experience required for the role include but are not limited to;

Requirements:

My client, a large, global pharmaceutical company are seeking a GCP Quality Specialist to join their team. The experience required for the role include but are not limited to;

Solid knowledge of GCP, PV and regulatory requirements.
Ability for problem identification / resolution in a complex environment or potential conflict.
Ability to analyse and simplify complex systems or processes into pragmatic solutions.

 

The key responsibilities for the role include:

Implement the controlled document strategy for PDQ and the supported business partners (gRED, pRED, PD, GPS and affiliates) for all relevant regulatory compliance standards and processes related to clinical development and safety/pharmacovigilance.
To develop Standards, Policies and SOPs, from identification of needs, to execution of development and deployment of outputs and materials.


If this position sounds like you, then please complete the form below. Alternatively, please recommend a friend using the following, refer a contractor.

 

 

 

 

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Contact Information:

Address:  Hobson Prior International Ltd
Wellington Gate
7-9 Church Rd.
Tunbridge Wells
kent
TN1 1HT
England
Tel:  01892 612 612
Fax:  01892 612 613
Website:  Visit Our Web Site

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