QA Officer- GCP

£0.00 - £35000.00 per annum
  1. Permanent
  2. Good Manufacturing Practice (GMP)
  3. United Kingdom
London
Posting date: 05 Apr 2019
QA.LP.22616_1554461336

ProClinical is advertising a vacancy for a QA Officer - GCP position with a specialist contract research organisation (CRO). The company focuses on providing high quality analysis and consultation on Phase I-IV clinical trials across a variety of therapeutic areas for the new pharmaceutical industry. Based in London, this position offers an exciting opportunity to work with an organisation known for its innovative and high-quality solutions. The QA Officer will ensure that there is a focus on quality throughout all company activities.

Job Responsibilities:

  • Managing the Quality Management System, audit schedule, and CAPA process.
  • Reviewing all controlled documents related to quality (SOPs, policies, guidelines, forms).
  • Effectively monitoring compliance to processes.
  • Reviewing staff training records.
  • Coordinating and attending internal and client audits.
  • Updating the company and Management Team on quality related issues and initiatives.
  • Promoting good practice by challenging standards within the workplace and by suggesting areas for improvement.
  • Inspiring and driving the company to achieve and maintain quality values.
  • Reviewing lesson learned meetings, customer concerns, issues, and CAPAs for quality-related items and coordinating any resulting training or process updates.
  • Developing and coordinating training materials related to quality.
  • Performing work in full compliance with applicable internal policies, procedures, processes, and training.

Skills and Requirements:

  • Training in a variety of GxP areas by external training (MHRA/RQA).
  • At least 4 years of relevant QA experience, preferably within the life sciences sector.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

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 contact Leoca Powell at +440203 854 2624 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.

#HEOR

ProClinical is advertising a vacancy for a QA Officer - GCP position with a specialist contract research organisation (CRO). The company focuses on providing high quality analysis and consultation on Phase I-IV clinical trials across a variety of therapeutic areas for the new pharmaceutical industry. Based in London, this position offers an exciting opportunity to work with an organisation known for its innovative and high-quality solutions. The QA Officer will ensure that there is a focus on quality throughout all company activities.

Job Responsibilities:

  • Managing the Quality Management System, audit schedule, and CAPA process.
  • Reviewing all controlled documents related to quality (SOPs, policies, guidelines, forms).
  • Effectively monitoring compliance to processes.
  • Reviewing staff training records.
  • Coordinating and attending internal and client audits.
  • Updating the company and Management Team on quality related issues and initiatives.
  • Promoting good practice by challenging standards within the workplace and by suggesting areas for improvement.
  • Inspiring and driving the company to achieve and maintain quality values.
  • Reviewing lesson learned meetings, customer concerns, issues, and CAPAs for quality-related items and coordinating any resulting training or process updates.
  • Developing and coordinating training materials related to quality.
  • Performing work in full compliance with applicable internal policies, procedures, processes, and training.

Skills and Requirements:

  • Training in a variety of GxP areas by external training (MHRA/RQA).
  • At least 4 years of relevant QA experience, preferably within the life sciences sector.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

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 contact Leoca Powell at +440203 854 2624 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.

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