Our client is searching for an experienced Quality Control Validation Lead to join their QC computer systems validation team.
\xc2\xb7 Ensures data integrity by following regulatory requirements and policies pertaining to analytical instruments and computer software applications. Completes QC analytical instrument and software validation deliverables, writes GMP procedures, validation documents and executes test scripts. Approves final project documents and writes final validation summary reports.
\xc2\xb7 Min Bachelor or Master\'s Degree. Preferred area of study in Microbiology, Biochemistry, , Chemistry or Related Science Fields (Computer Sciences)
\xc2\xb7 Working experience within a regulated cGMP industry is a must
\xc2\xb7 Experience working in Quality Control Laboratory or enterprise computer systems. and GMP Quality Systems such as TrackWise, LIMS, iLAB, MODA, C3ME, and Empower would be at an advantage
\xc2\xb7 Significant experience in Analytical Laboratory testing (ie: protein purification and characterization, protein chromatography, SDS-PAGE, Western blotting, and amino acid analysis, TOC, Bioburden, Endotoxin, Elisa, Flow cytometry, Microbiology).
\xc2\xb7 Project management experience is preferred to independently drive projects to on-time completion.
If you are interested in the position, do kindly drop your most updated resume to (Attn: QC Systems Specialist)