Regulatory Document Writer

£19000 - £21000/annum
15 Jun 2017
15 Jul 2017
Contract Type
Full Time
Exciting opportunity to join an internationally renowned research laboratory in a unique new role!

Are you a budding scientist looking for a new challenge outside of the lab?
Do you want to take a step in the direction of project management? Are you an organised and analytical thinking individual?

In this pivotal role you will work closely alongside Study Directors/Project Managers to:
• Establish and amend laboratory study plans in collaboration with external sponsors
• Keep study schedules updated throughout the study process
• Ensure study documents are compliant with regulatory requirements (GLP, GMP) and SOP’s and respond to QA audit findings
• Assist in the preparation of study reports
• Manage and archive study documentation

Successful applicants must have:
• Minimum 12 months experience within a regulated analytical laboratory
• Document editing experience
• Great attention to detail
• Experience within GMP, GLP, or GCP accreditation is helpful
• Excellent time keeping
• Superb communication skills

Applications are invited from enthusiastic and motivated individuals who are looking for a progression away from the lab!

Apply to VRS now for this exciting opportunity!

Key Words: Analytical Chemist, Pharmaceutical, Biopharmaceutical, Analyst, GC, Study Support, Administrative, Project Management, GMP, GLP, GCP, HPLC, Chromatography, Mass Spectrometry, Mass Spec, Manchester, Greater Manchester, North West, VRS5526LW