Overview
Reference Number: JO-2304-514617
Document Controller- Quality Management Systems
Rate: Negotiable
Job Type: Permanent
Location: Oxfordshire
Looking for Document Controllers local to Oxford who want to work within the LifeSciences/Biotechnology/Pharmaceutical industry
For more information reach out to Kellie.Saul@cpl.com
Job Title: Document Controller
Location: Oxfordshire, UK
Salary: Attractive salary + Benefits which includes private healthcare and 2 days working from home
** Please read **
The following requirements are essential for this position:
• Full right to work in the UK
Cpl Life Sciences is collaborating with an emerging biotechnology company who are looking to add a Document Controller to their Quality team. The successful candidate will be responsible for the company’s global eQMS system that controls all documentation management and training. You will also help with the administration of the quality system modules including CAPAs and other quality events.
This role would be great for any university graduate that would like to step into the life sciences industry and work within a growing quality team. Here you will report directly into the US Director of Quality Assurance, and work very closely with the UK Director of Quality Assurance. This global exposure so early on in your career creates a wealth of opportunity for you moving forward, given you will have exposure to both the UK and US markets.
You do not need to have any prior experience within quality or the biotechnology industry. This role presents a rare opportunity to step in to a first-to-industry role and we’re very excited to see what the incumbent achieves working at such a sought after business!
Contact/How to Learn More: To find out more information or apply, contact Kellie Saul by emailing your CV and Cover Letter to kellie.saul@cpl.com and quote JO number: JO-2304-514617
The Technical Operations team at Cpl Life Sciences (previously Clinical Professionals) is a specialist division that focuses exclusively on the recruitment of Quality Assurance, Scientific and Engineering for pharmaceutical companies, medical device companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities.