Tech WriterApply Now
Location: Cambridge, Massachusetts 02139
Employment Type: Contract
2 months + (there is a lot of work coming up, so could be much longer)
- LabVantage 8.3 or higher experience in pharma setting
- LES experience preferred
- Complex test method configuration including calculations across multiple data sets and/or foreign tables.
- Software Validation experience in GMP pharma environment
- Experience writing IQ, OQ, PQ test scripts
- Facilitating the execution of scripts
- Working with QA to resolve protocol execution discrepancies
- Demonstrated ability to understand and document system requirements
- Experience with Windows services and/or java
- Experience with Risk assessments and system upgrade validation
- Experience creating/maintaining the following document types
- User Requirements
- Functional Requirements
- Configuration Specification
- Design Specification
- User Acceptance Test
- Validation Summary Report
- Installation Qualification
- Operational Qualification
- Performance/Process Qualification
Trevor recruits for JVT's Life Sciences and Technology Practices where he specializes in finding, screening, and placing top-tier industry innovators at companies across multiple markets and verticals.
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