Microbiologist (Micro) I, II, & III

Kashiv BiosciencesPiscataway, NJ
Hybrid

About The Position

Kashiv BioSciences, LLC is a fully integrated biopharmaceutical company. Kashiv BioSciences, LLC, in the United States, and its subsidiary, Kashiv BioSciences Private Limited, in India (together “Kashiv BioSciences”) operate together with robust infrastructure and highly skilled teams that provide global R&D, clinical, manufacturing, regulatory, and IP capabilities. We believe our people, partners, and shared purpose fuel our work to advance patient care and access to important medicines. Microbiologist reports to and takes direction from Microbiology Management. This individual works closely with Management on department strategy and work projects.

Requirements

  • A 4-year Bachelor's degree, preferably in a science or engineering discipline
  • Previous experience for Micro I (0 to 2 years or more), Micro II (2 to 5 years or more), and Micro III (5 plus years) in a cGMP biologics/biosimilars manufacturing laboratory environment is required.
  • Working knowledge of cGMP regulations (21 CFR210/211/820) is desired.
  • Working knowledge of Deviation, CAPA, Change Control, and Validation/Qualification (IQ/OQ/PQ) is desired.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and/or correspondence.
  • Ability to speak effectively before groups or employees of the organization.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Must be able to read, write, and understand English.
  • Ability to work flexible hours as needed.
  • Ability to work under pressure and meet deadlines.

Nice To Haves

  • Certification from professional organizations such as ASQ and ISPE is desired but not required.

Responsibilities

  • Coordinates microbiological testing, release of product, and testing for validation protocols.
  • Performs organism identification.
  • Performs technical review of batch filling records to ensure quality of aseptic processes.
  • Reads and interprets microbiological cultures and other related tests, including but not limited to environmental monitoring, sterility tests, growth promotion, and microbial limits tests.
  • May perform validation, technology transfer, and troubleshooting, and write policy procedures for quality initiatives.
  • Reviews and approves environmental monitoring data, laboratory equipment, and records.
  • Prepares process and status reports, assigns and monitors document numbers, and reviews documents for accuracy and completeness.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards
  • Trains other Microbiologists on Department methods, processes, and procedures.
  • Works with other departments to accomplish Company goals or projects.

Benefits

  • Yearly Bonus (0–2 years or more of manufacturing biologics/biosimilars Quality Assurance experience) - up to a 8% yearly (discretionary) cash bonus
  • Yearly Bonus (2-5 years or more of manufacturing biologics/biosimilars Quality Assurance experience) - up to a 8% yearly (discretionary) cash bonus
  • Yearly Bonus (5 plus years or more of manufacturing biologics/biosimilars Quality Assurance experience) - up to a 8% yearly (discretionary) cash bonus
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