Senior Validation Specialist

KEYVAC BİYOLOJİK ÜRÜNLER SAN. VE TİC. A.Ş

General Qualifications:

Graduates of university pharmacy faculties or the biology, chemistry, or chemical engineering departments within science faculties,

At least 3 years of experience in validation operations in the pharmaceutical industry,

Strong communication skills and a team player,

High level of English language skills,

High level of MS Office knowledge,

Have knowledge of GMP practices,

We are looking for a “Senior Validation Specialist.”

Job Description:

Responsible for coordinating, organizing and execution of the Annual validation implementation process prepared in accordance with the procedure according to the plan.

Draft qualification and validation protocol and report as required by regulations, guidelines and company management documents.

Review Qualification and validation protocol and report.

On-site execution of qualification and validation, to confirm the reliability of data; and participate in the investigation and assessment of validation deviations.