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Job Details

Senior Quality Coordinator

Company: ProClinical Ltd
Location: Scotland
Reference: SC.NS.10842
Closing Date: 24 Feb 17
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

An attractive quality assurance job opportunity has arisen at a leading multinational pharmaceutical company who is seeking a Senior Quality Coordinator to work at their site in Scotland. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory.Job Role:The Quality team exists to deliver compliant, effective and efficient services in the area of Quality to the company's site in Scotland. ...

Requirements:

An attractive quality assurance job opportunity has arisen at a leading multinational pharmaceutical company who is seeking a Senior Quality Coordinator to work at their site in Scotland. The company employs 100,000 personnel across 150 countries, working across multiple therapy areas including cardiovascular, oncology, and respiratory.

Job Role:

The Quality team exists to deliver compliant, effective and efficient services in the area of Quality to the company's site in Scotland. The purpose of this role is to provide Quality function support to the site's quality improvement program. This Senior Quality Coordinator role will support delivery of key improvement initiatives on site and be part of the Quality Improvement Team.

The key features of this role includes:

i) Ensuring that day-to-day improvement challenges are resolved in a compliant, effective and timely manner;

ii) Ensuring that relevant teams within Quality are involved in improvement activities;

iii) Interfaces with other Departments to ensure they are effective for all parties and

iv) Ensuring that significant issues are escalated through the appropriate management lines and/or management processes.

Key Responsibilities:

  • To ensure site activities associated with the Quality Improvement Plan are in compliance with the company's quality management system requirements, including relevant GMP requirements (e.g. EU GMP, US GMP, Japanese GMP).
  • To participate in all aspects of improvement activities for the site, as directed by the Site Quality Improvement Leader.
  • Actively manage and ensure delivery of key initiatives supporting delivery of the sites Quality Improvement Plan.
  • Support implementation of a Gemba with Purpose approach to review high risk processing activities and deliver improvements.
  • To embed GPS in the management and delivery of the Quality Improvement Plan.
  • Support the Site Quality Improvement Leader in delivering a cultural change at site focusing on mindsets and behaviours and embed best practices.
  • Where required, to support teams in Root Cause Analysis.
  • To deliver training related to the Quality Improvement Plan to site based teams (e.g. eDM, Human Factors, DI awareness).
  • To support day-to-day activities associated with maintaining QMS compliance, particularly in the area of Quality Improvements for the site.
  • To coordinate and chair Quality Improvement meetings.
  • Maintain the Quality Improvement GPS Performance Boards.
  • Participate in the Quality Improvement communication and engagement plan.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Numhom Sudsok on +44 203 8718 093 or upload your CV on our website www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Apply for this job: Senior Quality Coordinator

Contact Information:

Address:  ProClinical Ltd
Eldon House Eldon Street London
EC2M 7LS
England
Tel:  0800 988 4437
Fax:  +44 (0)207 834 9470
Website:  Visit Our Web Site

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