QA Officer

Highly Competitive
  1. Contract
  2. Good Clinical Practice (GCP)
  3. United Kingdom
Hurley, England
Posting date: 13 Jan 2020
QA.SF.27132
This vacancy has now expired

A well-known international pharmaceutical company with sites around the globe is looking to hire a QA Officer. The company specialises in developing and producing medicines and vaccines for a wide range of therapeutic areas including oncology, cardiology and immunology.

Job Responsibilities

  • Providing day-to-day assistance for commercial QA activities associated with the effective running of the site QMS to support batch disposition activities with relation to the companies BREXIT preparations.
  • Ensuring assigned tasks are performed in a timely manner to meet internal standards and all associated international GMP/GDP requirements.
  • Providing maintenance of quality systems primarily the creation of QP declarations and associated electronic system changes to support BREXIT preparations.
  • Supporting change management activities relating to BREXIT and site compliance activities.
  • Completing scheduled records and quality system tasks in a timely manner and in compliance with internal standards and EU GMP.
  • Supporting inspection readiness for BOH inspections and external vendor audits in relation to BREXIT changes.
  • Collaborating with internal and external stakeholders to resolve quality issues and ensure compliance to EU GMP standards.
  • Compiling and review Product quality review sets for completeness and compliance to EU GMP, Hospira internal requirements and regulatory dossier submissions.

Skills and Requirements:

  • Bachelors degree in a related scientific discipline with relevant experience (Preferably Biology / Chemistry/ Pharmacy/Life Sciences).
  • Basic experience in pharmaceutical manufacturing, distribution and control measures.
  • Experience in Quality administered systems. Previous use of Trackwise QMS beneficial.
  • Experience in preparing or supporting QP declarations.
  • Experience in raising and management of change controls.
  • Ability to apply technical knowledge and understanding to make appropriate and timely risk based decisions.
  • Attention to detail and accuracy - able to follow verbal and written instruction (SOPs).
  • Quality and process orientation and mindset.
  • Ability to accept responsibility and be pro-active within defined limits.
  • Enthusiastic, positive individual driven to meet targets and standards.
  • High level of self- integrity and ethical conduct Prior Experience Preferred.
  • Biotechnology / Biologics / Sterile injectable manufacture.
  • Manufacture of novel dosage forms.
  • Secondary / outsourced packaging activities.
  • Global manufacturer and supply chains.
  • New product launches & commercial supply chain.
  • 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.

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 contact Numhom Sudsok at 0203 871 8093 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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