Quality Assurance Officer

3 weeks ago


Marlow, United Kingdom SRG Full time

  • Job Title: Professional - Quality Assurance Officer
  • Contract: ASAP for 5 months
  • Hours:37 hrs p/w
  • Location: Marlow (Hybrid)
  • Pay rate: £17.67


SRG are working with a global pharmaceutical company who are seeking a QA officer to join their Marlow site.


Role overview


Reporting to a Quality Manager you will provide day-to-day assistance for commercial QA activities associated with effective running of the site QMS supporting batch release. The QA Officer will ensure assigned tasks are performed in a timely manner to meet internal standards and all associated international GMP/GDP requirements.


Primary Duties:


  • To assist in maintenance of quality systems including deviations/ exception reporting, change control, supply agreements, document control, quality metrics reporting, training as determined by the QA Manager
  • Complete scheduled records and quality system tasks in a timely manner and in compliance with internal standards and EU GMP
  • To compile & review Product quality review sets for completeness & compliance to EU GMP, internal requirements and regulatory dossier submissions
  • Support in internal audits
  • Participate in Quality Risk Management (QRM) assessments
  • Project execution and support as required.
  • Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.


Experience and Education Required:


  • Experience from a quality-based job role
  • 2-3 years in a GMP environment
  • Basic experience in pharmaceutical manufacturing, distribution, and control measures
  • Basic experience in Quality administered systems. Previous use of TrackWise® QMS beneficial.
  • Ability to apply technical knowledge and understanding to making appropriate and timely risk-based decisions.
  • Able to demonstrate good planning and organisational skills
  • Attention to detail and accuracy – able to follow verbal and written instruction (SOP’s).
  • Quality and process orientation and mindset
  • Possession of good verbal and written communication skills
  • Sterile injectable manufacture/Manufacture of novel dosage forms is desirable


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