Analyst I/II/Senior, QC Analytical - Temporary

San Francisco, CA 94104

Posted: 09/10/2020 Employment Type: Contract Industry: Clinical & Scientific Job Number: 17902

Job Description


 

Primary Responsibilities
  • Author/revise technical reports and laboratory procedures (SOPs and methods)
  • Perform release, stability, and in-process testing in supporting production activities
  • Perform analytical testing in supporting technology transfers
  • Review data and performs analysis and interpretation of test results
  • Participate in method development, transfer and qualification/validation studies
  • Participate in equipment qualification/validation studies
  • Participate in deviation and OOS investigations
  • Perform QC lab support activities including but not limited to sample management, reagent preparation, and instrumentation maintenance and calibration

About you

Must Have/Required
  • B.S. degree in Biological Sciences with 0-2+ years of relevant experience or exposure to industry (QC Analyst I requirements) / B.S. degree in Biological Sciences plus 2-5+ years of relevant industry experience or M.S. degree in Biological Sciences plus 0-3+ years of relevant industry experience in quality control role (QC Analyst II requirements) / B.S. degree in Biological Sciences plus 5-8+ years of relevant industry experience or M.S. degree in Biological Sciences plus 3-5+ years of relevant industry experience in quality control role (QC Senior Analyst requirements)
  • Demonstrated experience in molecular/cell biology required (minimum 1 year)
  • Prior laboratory hands-on experience with a variety of analytical techniques including, but not limited to, ddPCR, gel electrophoresis, protein quantification, ELISA
  • Experience analyzing experimental data
  • Good to excellent technical writing skills
  • Must be capable of observing and adhering to lab safety standards and protocols
  • Successfully performs routine work independently with minimal instructions 
  • Excellent technical writing skills and verbal communication skills
  • Excels in a fast-paced team environment, handles multiple tasks concurrently, and in a timely fashion
  • Strong interpersonal skills, highly collaborative within a multi-discipline team and contributes to a supportive and positive work environment
  • Highly self-motivated and goal oriented
  • The hours and schedule for training period:
    • Monday – Friday, 12 pm - 8: 30 PM 
    • After training period will be a third-shift role 

May Have/Preferred
  • Prior experience in GMP QC environment (minimum 1 year) is strongly desired
  • Knowledge of cGMPs and regulatory requirements pertaining to biotechnology and pharmaceutical industries is strongly desired
  • Experience with HPLC techniques and/or experience with mammalian cell culture and cell-based assays

Meet Your Recruiter

Marissa Kochan

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