Our Client is a pharmaceutical company with a global footprint. We are hiring for a Quality Control Analyst to join the QC Projects Team.
What you’ll do
This role will be working in the QC department on none-routine projects.
The role will involve:
- method transfer
- process validation
- data migration
- transferring new products from R&D including setting up all necessary QC requirements (protocols, methods, equipment etc).
- You will also be managing/analysing stability studies.
Mainly this will be carried out using the laboratory techniques HPLC/UPLC with Waters instruments and Empower Chromatography software.
You’ll work closely with your colleagues across the QC department
We are keen to receive applications from individuals qualified to degree level in chemistry, who can demonstrate achievements working in a pharmaceutical or fine chemicals laboratory. You will be a good team player and able to support the team, sometimes working to deadlines, with efficient and accurate analysis.
We are seeking good communication and time management skills. Ideally you will have worked for some time in industry (at least 2+ years) and have experienced a similar role. You will have experience of validation, instrument qualification, protocol writing and knowledge of/experience with CSV (Computer System Validation) would be an advantage. Knowledge and/or experience of using Trackwise for Deviations, Change Controls and Root Cause Analysis would also be advantageous.
Please register onto LiCa Scientific using the apply button and follow the process to submit your CV.
As this role calling for a high level of documentation compliance, applications with an out of date CV or spelling errors will be rejected. If you are applying from a mobile device, we strongly advise you review the CV first before application.
Cover notes supporting your application are welcomed. On this occasion LiCa Scientific is acting as an employment agency.