Quality Systems Specialist — GMP, Audits & CAPA

PeopleBox

Fatih

Vor Ort

TRY 300.000 - 460.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Sanovel is seeking a Quality Systems Specialist to join the Quality Assurance team in Turkey. The role focuses on deviations, complaints, CAPA, risk assessment, audits, and regulatory compliance. Strong English and a proactive, quality-oriented mindset are required.

Responsibilities include coordinating CAPA activities, training staff, generating APRs, and supporting regulatory inspections. The candidate should have a relevant degree in Chemistry/Pharmacy/Biology and at least three years in QA

Qualifikationen

  • GMP knowledge and quality systems experience are required.
  • Strong analytical thinking with problem-solving skills.
  • Advanced English verbal and written communication skills.

Aufgaben

  • Manage deviations, customer complaints, CAPA, risk assessments.
  • Coordinate root cause analysis and CAPA effectiveness evaluations.
  • Lead internal audits and prepare audit reports with corrective actions.
  • Ensure compliance with SOPs, GMPs, and global regulations.
  • Support regulatory and quality training for personnel.
  • Prepare APR reports with cross-functional teams.
  • Assist regulatory inspections and customer audits with documentation.

Kenntnisse

GMP knowledge
Analytical thinking
English communication
Problem solving
Time management

Ausbildung

Chemistry degree
Chemical Engineering degree
Pharmacy degree
Biology degree

Jobbeschreibung

Sanovel is seeking a Quality Systems Specialist to join the Quality Assurance team in Turkey. The role focuses on deviations, complaints, CAPA, risk assessment, audits, and regulatory compliance. Strong English and a proactive, quality-oriented mindset are required.

Responsibilities include coordinating CAPA activities, training staff, generating APRs, and supporting regulatory inspections. The candidate should have a relevant degree in Chemistry/Pharmacy/Biology and at least three years in QA

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