Introdution

An exciting opportunity has arisen to work with one of the market leaders in the pharmaceutical packaging industry. They use cutting edge technology combined with extensive knowledge to develop tailored solutions to their clients.

You will be responsible for:

• The development of the quality and validation plan in conjunction with the customer

• creating of the validation and quality documentation such as FS, DS, IQ and OQ

• Carrying out machine testing based on the test documents such as IQ, OQ and FAT

• Participation in machine acceptance

• Being the contact person for the customer regarding quality and validation throughout the project

You will bring the following:

• 5+ years of hands on validation experience with the pharmaceuticals industry

• Experience with servers, sensors and schematics.

• Practical experience with the implementation of guidelines in accordance with GMP/GAMP

• Knowledge of FDA, EMA and WHO guidelines

• Experience with MS office, Jira and SAP

• Fluent English

If you want to be part of an innovative company where you can grow and expand your current knowledge, GET IN TOUCH by emailing me on isaac.murray@biotalent.com