Technical Author Location: Cambridge Rate: ??400 p/d Contract: 6 months
Your new company
Our client are a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines. Operating in over 100 countries and their innovative medicines are used by millions of patients worldwide. Working on our clients' largest project Our Future Reimagined, a Technical Author is required to join their growing team in Cambridge.
Your new job in Cambridge
Based on a prestigious client site in Cambridge, you will be responsible for working with key stakeholders to understand their technical requirements. Once these are fully understood, you will then complete the validation plan, the work product log with all associated documentation as well as the privacy impact assessment and security assessment.
This is effectively creating IT technical documentation for compliance in a commercial/clinical environment.
What you'll need to succeed
The Technical Author based in Cambridge will have:
Strong experience writing technical documentation in a GXP environment
Experience of working in reasonably demanding timelines.
Experience working with global stakeholders
Experience working within a clinical/pharmaceuticals environment is highly desirable
Microsoft office - Word, Visio, Powerpoint
What you'll get in return
So what's in it for you? Well, you get the opportunity to work on a high-profile Workday project for a globally recognised Biopharmaceutical company, on a competitive day rate. Furthermore, you can enhance your skills and be directly involved in a high-profile project.
What you need to do now
If you feel this is something that you would be interested in, please apply and get in touch with our specialist recruiter Jack Butler.