Description
Quality Engineer required for a Market Leading Pharmaceutical Client. 50% in Dublin/Home Based and 50% based in Bangalore IndiaIt is a sterile injectable product launch project and the Quality specialist will be required to assist with a product launch by supporting a supplier in the final stage of manufacture.
6 month contract the person will be required to work in India for 50% of the time (2 weeks on, 2 weeks off). The remainder of the time can be based at home or in the Dublin office.
Role while in India
Support the product launch to the US
Hands on batch review and documentation review
Ensure the quality requirements are met
Role while at home
Reviewing CAPA's and deviations
Batch record review
Investigation into deviations.
Requirements
Quality experience
Aseptic/sterile processing knowledge
Validation experience a plus
Personality: need someone able to challenge the contract manufacturer, query results and dig deeper to any answers.
This person will be supported by permanent members of the company's global groups.