Closing Date: 20 Feb 17
Salary (£): Competitive
Global organisation – top 20 pharma
Highly visible role across global organisation
Brand new role
Author, edit, gain approval and deploy Quality Documents (QDs) [e.g. standard operating procedures (SOPs), and/or other working practice or associated guidance documents].
Support process improvement initiatives to address complex problems and provide solutions to EMEA affiliates.
Support process improvement activities within the Clinical Operations function of Medical Affairs-EMEA and across affiliates.
Support functional Medical Affairs-EMEA Operations objectives:
Work closely with company training groups to support development of training materials to affiliates.
Support the global initiatives as directed by Director.
QUALIFICATIONS / EXPERIENCE REQUIRED
For a confidential discussion please telephone Anette Gillan at AXESS Limited on 020 8560 2300. To apply, please send your CV to firstname.lastname@example.org quoting reference PW-6750
Senior Process Optimization Manager, Senior Process Optimisation Manager, Senior Process Optimisation, Senior Process Optimization Manager, Manager Global Medical Affairs, medical affairs. Change management, process change management, quality documents, quality, medical affairs management, medical affairs process, SOP, Standard Operating Procedure. Process improvement, GCP, GXP, clinical development, clinical, QA, Quality Assurance, SOP, SOPs, standard operating procedures
AXESS has been operating since 1990
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development
We match professional candidates to the best permanent, contract and interim roles in the market
Visit us at www.axess.co.uk
12 Union Court,
Richmond upon Thames,
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