Quality Control - Research Officer

Employer
Location
Switzerland
Salary
Highly Competitive Salary
Posted
Oct 06, 2016
Closes
Nov 03, 2016
Ref
SC.NP.9427
Contact
Nisha Patel
Result Type
Jobs
Position Type
Permanent
Hours
Full Time

Exciting new opportunity with a research-led, global pharmaceutical company!

My client, who focusses on the discovery and development of novel biological entities (mAbs) and Biosimilars, is based in Switzerland and is looking for a Quality Control - Research Officer specialising in Biologics.

You will be responsible for executing tests for GMP and PD projects in the bio-chemical laboratory and participating in general QC activities.

Key responsibilities for the individual with involve:

  • Execute testing for cGMP projects, development, validation and stability programs.
  • Contributing towards the maintenance and continuous improvement of procedures, techniques and equipment used in the QC department.
  • Provide support in validation, development and stability testing (generic tests).
  • Provide support in method trouble shooting.
  • Independent organization of operational activities in the QC laboratories according to the local HSE and quality guidelines.
  • Write documentation for work performed: generic analysis, data logging, generic/method validations studies, change requests, deviations and out of specifications.

You must have strong experience in HPLC techniques, Capillary Electrophoresis, SDS-PAGE, UV-VIS, cIEF, etc. and relevant QC experience, as well as, knowledge of current analytical techniques is a requirement.

Hands on experience in product (immunology) and development of therapeutic biologics are a plus.

If you would like more information about this great opportunity to work with a leading biopharma, please get in touch with Nisha Patel on 0203 861 8210 or via email on n.patel@proclinical.com.