Quality Control Analyst I

at  Teva Canada Innovation

Cincinnati, Ohio, USA - 45213

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate12 Feb, 2020Not Specified12 Nov, 20192 year(s) or aboveMicrobiology,BiologyNoNo
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  • BS or higher in science related discipline, biology or microbiology is preferred
  • 0-2 years of experience in pharmaceutical or other FDA industry or related field
    Sub Function
    Manufacturing Quality Control
    Reports To
    Manager, Quality Control
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  • Perform Microbiological Examination of Raw materials, finished product, and media growth promotion per USP or applicable internal methods.
  • Perform Environmental monitoring of manufacturing environment and critical Utilities (water and gas systems),
  • Participate in microbial method validation and special projects related to improvement and validation projects.
  • Perform general laboratory duties, in house media preparation, and housekeeping
  • Documentation of data/reports per local procedures and GMP/regulatory requirements and experience with a technical writing is a plus. Knowledge of Aseptic Techniques, GLP, and GMP environment.
  • Able to operate basic software like Microsoft Office, LIMS, and EDMS.
  • Works independently and with the team effectively to achieve individual, team and organizational goals
  • Ability to wear respiratory equipment (PAPR), as needed, Ability to work occasional overtime and weekends to support business needs


Min:2.0Max:7.0 year(s)


Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy





Cincinnati, OH, USA