Technical Writing Jobs in Westport

The Validation Engineer plays a crucial role in ensuring the qualification and validation of all cGMP equipment systems and processes at the AbbVie Westport site. Reporting within the Validation Department this position also serves as a Subject Matter Expert (SME) for Computer System Validation (CSV...

We are currently hiring a Senior Manager Bio-Tox Analytical QA to join our team for a 23-month contract. The Senior Manager Bio-Tox Analytical QA is responsible for developing and overseeing a robust Quality Assurance strategy focused on the transfer of New Product Introduction (NPI) QC methods to m...

We are looking for a Manufacturing Technician at our site Westport in the mulitdose department. ( Weekend shift role 39 hours)ResponsibilitiesCarry out daily tasks as assigned by the Production Manager according to GMP and the quality system.Active involvement and management of batch related CAPAs a...

People. Passion. Possibilities. Its who we are what we do and what we stand for.We are currently recruiting a Manufacturing Technician (Documentation Support) as part of the overall Product Flow function within the Core 2/3 Business this role you will be actively involved and manage the batch relat...