process expert (process and cleaning validation).

​In the context of a multinational Pharmaceutical Company undergoing Site development, a new building for aseptic filling is currently under validation to support the production of parenteral products.

As part of the Manufacturing Science and Technology Fill and Finish department, you will participate to validation of manufacturing processes or cleaning processes related to product transferred to the new production lines. You will be member of the validation team which deals mainly with process changes and monitoring of current processes (through establishing Process Control Strategy (PCS) and Continued Process verification). You will also be responsible for the preparation, execution and reporting of documentation related to process and cleaning validation.

This project function will give you the opportunity to perform the changes from start to end. This role is an opportunity with large collaboration in several departments and multiples sites of the Company Network.

YOUR PROFILE

• Education level: Pharmacist, CTF, Biotechnologist

• 1-3  years of experience in the validation topic

• Experience working with GMP  

• Validation process and statistical knowledge, QbD approach is a plus

• English spoken and written fluently

• Product Tech Transfer knowledge

• Experience in Aseptic filling is a plus

• Regulatory knowledge is a plus

​The profile is completed by:

dynamism, organizational skills, good will, collaborative and team spirit, resourcefulness and adaptability.

Availability to work overtime and if necessary on holidays is required. 

Domicile in Bari and province required. 

We offer an initial full-time contract for 6 with possible subsequent confirmation.

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