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Job Details

PW-6961 Interim QMS Manager – London

Company: AXESS
Location: London
Reference: PW-6961
Closing Date: 13 Nov 17
Type: Permanent
Salary (£): Competitive
Benefits: Central London – Rolling Contract

Job Summary:

Opportunity for a QMS Professional to join a Global Pharma on contract – based in Central London – some home working.

Requirements:

BACKGROUND

Global Pharmaceutical (Top 20)

Office Based Role

Initially 6 Month Interim Role

 

PRIMARY DUTIES

Interim QMS Manager is responsible for ensuring that procedures, processes and resources for the Quality Systems and implementation of Quality compliance activities are communicated and implemented to meet the needs of GRA and conform to all applicable regulatory requirements. You’ll also be responsible for the ongoing development, maintenance and support of the global Quality Management System (QMS).

Act as subject matter expert and project lead for multiple projects to drive continuous improvement of systems.

Facilitate the process to reach harmonized and streamlined processes which meet business needs. Ensuring that personnel are aware and responsive to external guidelines and regulations as they pertain to quality management and compliance. Coordinate and participates in audits and inspections in GRA.

Work to ensure compliance for the Regulatory Organization, including internal and external teams and partners.- Participates in the creation, review, approval and lifecycle management of controlled quality documents (e.g. SOPs) and supporting documents within Global Regulatory Affairs.

Develop and delivers training materials describing system related business processes. Plan and ensures end-user training is conducted globally and locally.

Advises on the use of the global QMS in daily business work- Manages, maintains and implements QMS documents with RA functions, which reflects best regulatory practice focusing on factors such as business need, resources and methods.

 

QUALIFICATIONS / EXPERIENCE REQUIRED:

Bachelor's degree (or equivalent) / Masters preferred

Significant experience in Pharmaceutical industry, in Regulatory Affairs, research and development or quality assurance/compliance.

Strong QMS experience. Experience in the development, implementation and maintenance of a QMS

Demonstrated knowledge of pharmaceutical and regulatory affairs requirements and practices

Demonstrated knowledge of global health authorities, regulations, product approval and lifecycle processes for major markets.

Practical operational experience of working across disciplines and across multiple regions.

Experience working within a global team framework and a multi-cultural environment.

 

Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.

 

TO APPLY:

For a confidential discussion please telephone Sukhveer Gill at AXESS Limited on 020 8560 2300. To apply, please send your CV to jobs@axess.co.uk quoting reference PW-6961.

 

Keywords:

Quality Systems Manager / Auditor / Quality Partner / QMS Manager / Quality Officer / Pharma Quality Auditor / Quality Systems Lead / Quality Systems Manager / Regulatory Affairs QMS Manager / QMS Manager / Interim QMS Manager London / London QA interim Manager / QA Manager / Interim QA Manager / Interim Quality Manager / Interim Manager QA / London / Global QA Manager

 

ABOUT AXESS:

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

 

Apply for this job:  PW-6961 Interim QMS Manager – London

Contact Information:

Address:  Head Office
Isabella House,
12 Union Court,
Richmond upon Thames,
Surrey
TW9 1AA
England
Tel:  +44 (0)20 8560 2300
Fax:  +44 (0)20 8560 2033
Website:  Visit Our Web Site

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