QC Associate – Global QC Technology Innovation Team job vacancy in Kite Pharma – Jobs in Wyoming

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Job Details
Company Name : Kite Pharma
Company Location : Frederick, MD
Job Position : QC Associate – Global QC Technology Innovation Team
Job Category : Jobs in Wyoming

Job Description :

Job Description

Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in our mission!

Kite is seeking a highly motivated individual and experienced leader to join Kite as QC Associate, Global QC Technology Innovation group, to work on new technologies and take cell therapy QC assays to next level.

Responsibilities (include but are not limited to):

  • Perform critical reagent testing by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
  • Work with internal and external resources to maintain lab in an optimal state.
  • Maintains laboratory instruments for calibration and routine maintenance
  • Monitor the GMP systems currently in place to ensure compliance with documented policies.
    Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.
  • Gather metric information for use in continuous improvement of areas of responsibility.
  • Perform other duties as required.

Basic Qualifications:

  • Bachelor’s Degree OR
  • AA Degree and 2+ years of experience in biotechnology or related field and Quality Control experience OR
  • High School Degree and 3+ years of experience in biotechnology or related field and Quality Control experience

Preferred Qualifications:

  • Strong knowledge of GMP, SOPs and quality control processes.
  • Identifying, writing, evaluating, and closing OOS’s and investigations.
  • Proficient in MS Word, Excel, Power Point and other applications.
  • Strong written and verbal communication skills.
  • Ability to communicate and work independently with scientific/technical personnel.
  • Familiarity with few of analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
  • Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).
  • Preferred: Experience in the biotech and/or pharmaceutical industry.
  • Potential shifts are Sunday – Wednesday or Wednesday – Saturday. Business need may require alternate work schedule, such as swing shift hours.



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