QA Project/Process Quality Manager

London  ‐ Onsite
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Keywords

Description

Ref. #:
4768SM
Location:
Greater London, UK
Industry:
Pharmaceutical Industry
Start:
ASAP
Duration:
6 months (with possible extension for additional 3 months)
Work load:
50%
Role:
We're looking for a QA Project/Process Quality Manager for a client mandate.
Tasks:
* Ensure proper implementation of global standards, policies and systems platforms
* Provide the framework, define and document information in the applicable internal and vendor-owned approved CMDBs/asset management tools (i.e., Service-Now, Remedy, Clarity, etc.) for the following:
- ISEC data classification and control criteria
- relevant compliance areas for data (e.g. GxP, ISEC / IT Security, Legal (e.g. Data Privacy), SOX)
- data protection and handling requirements
- data encryption requirements
- retention periods
* Interface with business and IT partners to ensure company practices are aligned with regulatory expectations and industry best practices
* Drive continuous improvement of the quality system to meet and sustain compliance with internal and external regulatory requirements
* Ensure the continuous improvement, rationalization and management of existing systems and operations
* Perform ITIC assessments to evaluate if processes and deliverables fulfill the requirements for quality, to uncover errors or deficiencies in processes and deliverables, and to identify strengths and opportunities for improvement.
* Ensure the review of the QMS for each of the vendors for compliance
* Follow up resolution of identified quality exposures and escalation to line management if critical situations are not resolved in due course
For assigned global services and vendors, effective alignment of IT investment to achieve the most efficient operations.
* Challenge business partners and push back when necessary to ensure the IT solution responds to their business needs while being cost-efficient at the same time
* Ensure key strategic IT Infrastructure services are delivered and implemented adhering to the company's IT quality standards
Additionally to the needed skills to perform the above tasks, you MUST also bring:
* Experience in global projects
* Experience in pharmaceutical industry
Language skills:
* Fluent in English (written and spoken)
Start date
03/2014
Duration
6 months (+)
(extension possible)
From
ITech Consult AG
Published at
08.03.2014
Project ID:
676387
Contract type
Freelance
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