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Reference # : 17-66158 Title : Excellent job opportunity of Quality Control Analyst II, Allston, MA, 7310082
Location : Allston, MA
Experience Level : Start Date / End Date : 08/01/2017 / 09/30/2017  
Description
Job Title: Quality Control Analyst II
Location: Allston, MA
Duration:  3 Months
Shift: Fri-Mon 6am to 4:30pm (weekend shift)
 
Duties:
Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and the qualification of new instrumentation utilized in the Quality Control laboratory.
 
This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs for product release and validation. Responsibilities include:
  • Performing UV-Vis spectrophotometry assays for in-process and final product samples
  • Performing HPLC methods for final bulk material/finished goods
  • Performing maintenance on complex laboratory equipment including HPLC and GC systems
  • Review of QC Data for compliance to procedures and specifications
  • Calculation and evaluation of results
  • Participation in training of less experienced staff
  • Transferring methods from support groups to the QC laboratory
  • Authors protocols and technical reports related to the implementation of QC equipment
 Effectively demonstrates an understanding of CGMP's and how it applies to specific responsibilities:
  • Following accurate oral and written procedures for testing of in-process and final product samples
  • Communicates inter-departmentally and with outside contacts to solve technical issues
  • Exercises sound judgment and decision making when problem solving
  • Revises standard operating procedures as needed
  • Works independently under general supervision and direction
  • Work in compliance with CGMP's
 Skills:
  • Proficient in Outlook and Microsoft Word and Excel and lab based data management systems
  • Ability to lift 40 lbs
  • Exp with UV Vis Spectroscopy and wet Chemistry
  • Scientific technical writing ability
 Education:
  • Bachelor's Degree in Life Sciences discipline
  • 2 years experience in CGMP lab environment
  • Or Master's Degree in Life Sciences discipline and 1 year experience in CGMP lab Environment
Interested candidates can share their most updated resume at ridhi.thapa@artechinfo.com or reach out to me at 973-295-4583