Description
We are currently working with a world leader in Biopharmaceuticals who are looking to bring on a QC Senior Associate asap. Some of the duties the successful candidate will be participating in are listed below:- Site ownership of stability program
- Manage all sample management activities throughout the site
- Create/own and approve protocols, sample plans, SOP and documentation
- Responsible for SAP and LIMS functions/ transactions within the sample management remit
- Site ownership of reference standards and reserves
- Out of hours responder for sample management equipment (fridges/freezers/incubators)
If you are someone with the following skills & experience please get in touch today!
- Bachelors degree in a science related field
- Biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry, with specific sample management/stability program management experience.
- Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
We are looking for someone with a passion for this role who has a strong knowledge of LIMS. For a confidential chat and the full Job Spec please call Jamie McLaren on .
To find out more about Real please visit www.realstaffing.com
Real Staffing, a trading division of SThree Partnership LLP | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales