Turkey Job Openings

AstraZeneca

Quality Assurance Specialist (Temporary)

Levent

FULL TIME

September 2, 2024

Quality Assurance Specialist (6 months fix-term contract)


REPORTING LINES

  • This position will report to Quality Assurance Executive and Responsible Manager.

QUALIFICATIONS
  • University degree (in Chemistry or chemical Engineer)
  • At least 2 years of experience in pharma industry,
  • At least 2 years of practical experience in production and/or quality assurance and/or quality control areas in a company authorized by Ministry of Health to manufacture medicinal products
  • Good command of written and spoken English,
  • Knowledge in MS Office applications,
  • High interpersonal, communication and presentation skills,
  • Able to effectively function in a cross-functional team environment,
  • Able to multitask and meets deadlines,
  • Knowledge of Quality assurance requirements such as deviations, complaints, CAPA, SOP, etc..
  • No military obligation for male candidates

JOB DESCRIPTION
  • Support QA operations in Warehouse
  • Review and approval of temperature data of incoming products
  • Support incoming product quality approvals & Batch release approval of the products
  • Support management of quality complaints:
  • Prepare and issue annual product review reports
  • Support development of QA operations and systems in Astra Zeneca in accordance with global and local SOPs/policies,
  • Follow up of all quality processes in all Gx P related areas and ensure that monthly reports are prepared by relevant responsible,
  • Support evaluation of all Gx P related areas and reporting to management team in accordance w/ key performance indicators,
  • Management of SOP library of Astra Zeneca Turkey,
  • Follow up of inspection plans and attendance to the inspections carried out by Distribution Supplier related to Gx P activities,
  • Support management of internal audits for Gx P related activities,
  • Follow up quality requirements for computed systems (validations etc.) related to Gx P activities,
  • Support management (documentation, coordination and tracking of all action items) of deviation and change control systems in AZ
  • Support recall process & performing recall simulation if needed
  • Support product destruction process from quality perspective
  • Support management counterfeit and suspected products

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