Production Supervisor

KEYVAC BİYOLOJİK ÜRÜNLER SAN. VE TİC. A.Ş

Job Requirements:

- Graduated from Pharmacy, Chemical Engineering, Chemistry, Biology, Biotechnology and related departments of universities,

- At least intermediate level of English language skills,

-Proficient in MS Office Programs and ERP Software,

- Totally at least 5 years experiences but at least 2 years of experience in the Cell Culture, Virus Cultivation, Cell Bank and Virus Seed processes in the Pharmaceutical Industry,

- Good command of GMP practices and preferably has experienced the process from end to end,

- Sufficient technical knowledge and equipment about production equipment,

- Managerial competencies to organise a team or an established team,

- Prone to teamwork, strong communication skills,

- Completed military service for male candidates,

We are looking for a "Production Supervisor" position with specialities.

Job Responsibilities:

Responsible for preparing the culture group production plan in accordance with the Production Department’s production schedule,

Responsible for drafting and checking the HAV Bulk production order,

Responsible for monitoring the progress, yield, quality, and cost of the culture group, and for counting and analyzing them on a monthly basis,

Responsible for preparing the material requirement plan to meet production demand according to the culture group’s production plan,

Responsible for preparing the culture group documents in accordance with GMP regulations,

Responsible for review production records related to culture group,

Responsible for the monitoring of the culture group process, and continuously optimize the process procedures,

Responsible for supervising the implementation about the entry and exit of personnel and materials in cell area and virus area in bulk workshop,

Responsible for management of intermediate products, solution and materials related to culture group,

Responsible for regularly conducting the cell area and virus area production site management,

Responsible for management of workshop shutdown and restart in cell area and virus area in bulk workshop,

Responsible for overseeing the Cell Culture field processes of Equipment and Materials Management, GMP Training and Qualification Approval, Validation Management, Quality Management, and Occupational Health and Safety Management.