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QA Officer

Job LocationRuncorn, Cheshire
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Leading Pharmaceutical Manufacturer based in Cheshire seeks an experienced QA Officer to help administer the Quality Management Systems (QMS). The role holder will progress batch review (prior to QP certification), deviations, change controls and other qualitydocuments to the requirements of EU GMP and other applicable territories regulations.Duties may include:

  • Ensure batches are QA reviewed as required to support the business needs
  • Ensure deviations, CAPA and change control for which you are the owner are progress in a compliant and timely manner
  • Ensure deviations, CAPA and change control are review and/or approved in accordance with internal procedures
  • Ensure customer complaints are satisfactorily investigated and communicated
  • Participate and/or host internal audits and in risk assessments
  • Help support improvement of GMP knowledge across site
  • Help deliver Quality related improvements projects
  • Any other activity deemed quality related by the Quality Assurance Head/Director
Skills and experience:
  • Scientific degree or significant experience within a relevant role
  • Ability to read, write and follow written/verbal instructions
  • Good communication skills, and ability to write reports
  • Quality Management Systems performance ( CAPAs, deviations, and complaints)
  • Right first-time figure at QP release
  • Health and safety performance - accidents and lost time
  • Customer Audit performance
  • Understanding of quality management systems
  • Awareness of applicable GMP requirements
  • Ability to identify and raise deviations from above
  • Ability to root cause deviations
  • Ability to achieve set targets
  • React to shifting prioritys

Keyskills :
GMPManufacturingPharmaceuticalProductionQuality Assurance

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