Validation Supervisor

KEYVAC BİYOLOJİK ÜRÜNLER SAN. VE TİC. A.Ş

Job Qualifications

Graduated from the relevant departments of Science or Engineering faculties of universities,

5 years of experience in the pharmaceutical industry, including at least 3 years in sterile production validation operations,

Has effective communication and management skills, good at teamwork,

Fluent in English,

Proficient in MS Office applications,

Experienced in GMP/GLP applications,

We are looking for a "Validation Supervisor".

Job Descrition

To draft the company's annual validation plan,

To coordinate, organize and supervise the excution of the annual validation plan,

To draft the annual validation summary report,

To prepare Qualification and validation protocol and report,

Responsible for supervising the implementation of qualification and validation on site,

Responsible for implementing Computerized System and Data Integrity Management within the scope of relevant procedures and supervising relevant departments,

Job-related GMP document drafting and revision,

Validation document management,

will be responsible for the tasks.