Overview
On Site
Full Time
Skills
Pharmaceutics
Project Management
GMP
Management
Communication
Documentation
Editing
Job Details
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.
- 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.
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