We have an exciting contract role for a Quality Manager for a rapidly expanding life science technology company in London Bridge.

You would be working with the Quality Director to lead or assist in the writing and implementing elements of the overall quality system. More of a quality systems experience is preferred over CSV.

They ideally need a Quality Manager who understands the regulations around clinical trials such as ICH GCP, CRF 21 part 11, ISO standards and CSV.

You would be working with the Quality Director to lead or assist in the writing and implementing elements of the overall quality system.  CSV experience is preferred . 

This is to start ASAP.  (Temp to Perm also considerd)

Helpful skills and attributes:

·       Experience working in an IT and/ or clinical trials environment

·       Experience of quality management strategy development including process and procedure development and documentation

·       Auditing experience is an advantage

·       Ability to determine good practice and identify opportunities for improvement

·       Risk Management knowledge and experience

·       Self-motivated, working independently, managing own workload

·       Working knowledge of techniques for planning, monitoring, data analysis and reporting

·       Ethical, with the ability to remain impartial and report all non-compliances

·       Organisational skills with attention to detail

·       Working in a start up environment 

Contact Bryan on 01273 729819 or E mail CV with availbility including  Current and expected salary to bryan@pop-science.co.uk