Responsibilities

Previous experience as a validation engineer in an aseptic pharmaceutical fill/finish environment.

Prior experience executing validation protocols on a pharmaceutical fill/finish line. Specific line components include.

Lyophilizers.

Depyrogenation tunnels.

Autocalves.

Previous experience with the project management requirements of validation project in a GMP environment.

Requirements

Managing validation schedule.

Communication of delays and changes to timelines.

Coordinating and leading meetings with cross functional teams.

Maintaining documentation protocols.

Prior experience editing/updating validation protocols.

Prior experience supporting a validation project in a paper-based environment.

Should you be interested, please send me a copy of your resume in word format along with the following details ASAP.