Quality Operations Specialist
Çerkezköy, TR
Job Purpose
Key Responsibilities
Key Responsibilites:
- Ensure the implementation and sustainability of GMP, hygiene, and quality system requirements.
- Manage product release processes by reviewing batch documentation and related records.
- Oversee deviation, customer complaint, product return, and CAPA processes, including reporting activities.
- Prepare Annual Product Quality Reviews, trend analyses, and quality performance metrics.
- Participate in internal and external audits and contribute to the continuous improvement of quality systems.
- Effectively manage risk assessments, training activities, and quality documentation processes.
Required Education
Required Skills and Experience
Qualifications:
- Bachelor’s degree in Chemistry, Chemical Engineering, or a related scientific discipline,
- 3-4+ years of Quality Assurance experience in the pharmaceutical industry,
- Strong knowledge of GMP regulations and quality documentation systems,
- Proficient in Microsoft Office applications,
- Analytical, systematic, and results-oriented mindset with strong teamwork and communication skills,
- Fluent or professionally proficient English preferred,
- Completion of military service required for male candidates,
- Residing in or willing to relocate to Çerkezköy, Kapaklı, Çorlu or Ergene within a short time frame.
Technical Competencies
Required Behaviours and Competencies
Required Languages
Travel required in %