Reference Number: JO-2406-535820
QC Stability Coordinator
Rate: Negotiable
Job Type: Permanent
Location: Liverpool

QC Stability Coordinator

6 month contract

Up to £18.40PH


We have an opportunity for an experience QC Stability Coordinator to join a global pharmaceutical company that focusses on vaccines, this is an excellent opportunity contributing to helping protect the lives of millions of people across the world. The main purpose of the QC Support Specialist is to provide support to the QC Compliance and Improvement Manager across the sites QC activities.

This role will support the site stability program by effectively coordinating the process from start to finish with focus to the ICH guidelines. Responsible for the day-to-day requirements relating to the site stability program including protocol/report authoring and data analysis/trending.


• Science related degree

• Demonstrated GMP background in the pharmaceutical industry

• Experience of Quality Control testing techniques and industry practices

• Time management skills for planning and schedule of work

• Communication skills both written and verbal

• Strong Microsoft excel skills

• Analytical Mindset

• Science related degree

• Exp in data trending / software packages (JMP) desirable

For more information apply within or send your CV to mark.bathe@cpl.com

Upload your CV and any other relevant file.
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