Sr. Associate Quality Control, Biopharma (JP4361)

Location: Thousand Oaks, Ca
Date Posted: 06-14-2018
Job Title:  Sr. Associate Quality Control, Biopharma (JP8361)
Location: Thousand Oaks, Ca
Type: Contract
Duration: 24 months with possible extension
Business Unit:  Pre-Pivotal Rapid Analytics and LMRT - LC/CE Group
3Key Consulting Inc. is looking for Sr. Associate Quality Control for a global, CA-based, bio-pharmaceutical company.
  • Perform testing and data review for HPLC/UPLC (high and ultra-high liquid chromatography), titer, small scale protein purification using TECAN and plate reader, titer assay (UPLC), CE (capillary electrophoresis), CEX (cation exchange), AEX (anion exchange), Glycan Mapping and HILIC (hydrophilic interaction) testing.
  • Operate high-throughput, robotics sample handling and/or auto-sampler systems to manage samples, purify, and test
  • Obtain assignment and follow scientific direction of client staff, flag issues and seek guidance appropriately
  • Generate complete accurate and concise documentation and reports using electronic systems and laboratory notebook
  • Perform general laboratory housekeeping activities
  • Comply with safety guidelines and site-specific procedures which include but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books
  • Interact with multiple functional areas in a highly matrixed-team environment, which may include Manufacturing, Process Development, IS, Facilities, Engineering, and Quality Control
Day to day responsibilities include:
  • Perform analytical assays per company procedure.
  • Operate by following company's safety and regulatory requirements.
  • Document experimental data and write reports if needed
Top Must Have Skill Sets:
Basic Minimum Qualifications:
  • B.S. or M.S. degree in Analytical Chemistry, Physical, Life Sciences or related technical discipline.
  • 1-5 years’ experience performing analytical testing. Preferred Qualifications
  • Proficient executing analytical test methods in one or more of the following areas: HPLC/UPLC (high and ultra-high liquid chromatography), titer, ATOLL purification using TECAN robot and plate reader, CE (capillary electrophoresis), CEX (cation exchange), AEX (anion exchange) HILIC (hydrophilic interaction) testing and Glycan Mapping.
  • Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
  • Experience with operation, maintenance, and troubleshooting of laboratory equipment and instrumentation related to analytical testing.
  • Strong organizational, communication and time management skills
  • Ability to address client questions independently with sound scientific judgments on the work they reported to the clients
Employee Value Proposition: working in a leading pharmaceutical company, learning state of the art technologies
Red Flags: Past behavior issues, lack of qualification in education and related working experience
Interview Process:  phone and in-person interviews
3KC Talent Acquisition Team
this job portal is powered by CATS