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Reference # : 17-77338 Title : Excellent job opportunity of Quality Control Analyst III, Canton, MA, 7444154
Location : Canton, MA
Experience Level : Start Date / End Date : 08/25/2017 / 08/25/2019  
Description
Job Title:             Quality Control Analyst III(7444154)
Duration:             2 Years
Location:             Canton, MA
Client:    A Big Pharmaceutical Company


 Duties:
  • Performs operations necessary for quality testing and plays a role in implementing new technology within quality control.
  • At more senior levels, provides an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.
  • Completes routine testing of raw materials, in-process and final products in accordance with SOPs for product release and validation.
  • Aids in the development of test methods.
  • Conducts data review and preliminary evaluation of results.
  • Solves problems using limited predetermined options such as repeating the assay when parameters are not met to determine the cause, etc.
  • Provides input to the technical composition of operating documentation.
  • Work is closely supervised.
  • Follows standard practices to obtain solutions.
  • Contributes to the completion of routine technical tasks.
  • Failure to achieve results can normally be overcome without serious effect on schedules and programs.
  • Contacts are primarily with immediate supervisor and other personnel in the section or group.
 Experience:
  • 6 to 9 years.
  • 2-4 years related experience in a cGMP environment in a pharmaceutical or Medical Device required.
Skills:
  • Conduct routine testing for product release and stability functions as per written procedures in a compliant manner.
  • Hands on experiance in Cell Based assays, Plaque Assays, ELISA , HPLC and spectrometric methods
  • Experience in GMP envirnoment with ability to follow procedures in all aspects of lab activity and in good documentation practices
  • Instrument and Assay troubleshooting
  • Investigations of routine laboratory events such as OOS , OOT's  ,deviations and CAPA's.
Required:
  • Documentation, Medical Device , Quality Control , Analytical Chemistry,  Biochemistry
Additional
  • CGMP, Chemistry , ELISA,  GMP,  HPLC,  Laboratory , Operations Solutions , SOPS, Testing
Education:
BS in Analytical Chemistry/Biochemistry or Biology. Prior experience in Cell Based assays is highly desired.

Interested candidates can share their most updated resume at ridhi.thapa@artechinfo.com or reach out to me at 973-295-4583