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.

Upload your CV/resume or any other relevant file. Max. file size: 128 MB.
I would like to be contacted via SMS
I have read and agree to the Clinical Professionals Group Privacy Policy

Find our privacy policy here