Quality Assurance Supervisor

KEYVAC BİYOLOJİK ÜRÜNLER SAN. VE TİC. A.Ş

Job Qualifications

Graduated from Chemistry, Biology, Chemical Engineering, Pharmacy Departments of universities,

5 years of experience in the pharmaceutical industry, including at least 3 years in sterile production quality tools management and GMP compliance,

Has effective communication and management skills, good at teamwork,

Fluent in English,

Proficient in MS Office applications,

We are looking for a "Quality Assurance Supervisor".

Job Descrition

Responsible for the deviation management

Responsible for the change control management

Responsible for the CAPA  management

Responsible for execute and coordinate  of internal and external inspection,

Drafting and revising GMP documents,

Responsible for Archive Management,

Responsible for the supervision of routine on-site audit,

Responsible for procedural verification,

Responsible for report of annual product review,

Responsible for OOS/OOT investigation,

Responsible for management of reprocessing,

will be responsible for the tasks.