Pharmaceutical CSV Tech Writer (Data Integrity)
Pharmaceutical CSV Tech Writer (MES)
The client is seeking a computer systems validation resource to perform technical writing for the implementation of a new MES system.
Day to Day Responsibilities:
This person will be responsible for authoring requirements/documentation as it relates to MES. This individual must have technical knowledge of this system as well as strong technical writing skills. They will primarily be responsible for assisting in the pre-implementation process as well data integrity. They will be responsible for writing test scripts and documentation as well as reviewing test and design documentation.
The client has another Labware LIMS system so if this person has experience with both of these it can be very helpful.
- Computer Systems Validation
- Technical Writing
- Review test/design documentation
- Data integrity
- Labware LIMS
Job Type: Contract