Kashiv Biosciences LLC specializes in biosimilar manufacturing and process equipment support, offering HVAC and BMS maintenance, equipment validation, and intellectual property services for downstream cell culture processes. The company operates in a GMP-compliant environment, providing technical expertise in bioreactor, fermenter, and downstream process equipment maintenance and IP strategy development.
Open Positions
Validation Engineer
B.Tech/B.E in Engineering, 5+ years of experience, GDP/GMP knowledge. Solid communication skills required
Upstream Manufacturing Manager
Bachelor's in Sci or Biochem, 10+ years biopharma experience. Expertise in upstream cell processes & GMP knowledge are required. Strong communication & computer skills needed
Process Equipment Engineer
Bachelor's degree in mechanical, electrical, or related field. 8-12 years of process equipment maintenance experience in drug substance facilities. Knowledge of GMP/GDP processes and equipment qualification
Downstream Manufacturing Scientist
Bachelor's degree in related science. 4-5 years of biopharmaceutical experience. GMP & aseptic manufacturing experience
Upstream Manufacturing Scientist
Bachelor's in Sci. + 3 yrs biopharma exp. GMP/ aseptic manufacturing experience required. Strong computer/communication skills a must
Upstream Production Specialist
Bachelor's degree. 10+ years experience in Upstream Mammalian Cell culture production. Exposure to Perfusion and bioreactors
QC Analyst III
Bachelor's in a related field or master's with 8+ yrs exp. GMP lab experience. Strong background in protein chemistry, and cGMP. SOP & regulatory guide knowledge is essential
QC Analyst II
Bachelor's degree in bio/chem/chemistry or related field with 8-10 years experience. Master's degree with 6 years experience. Strong background in analytical chemistry & regulatory guidelines
Validation Engineer
BS or MS in engineering/med/pharma. 4+ years of experience. Biology experience highly desirable. Proficiency in MS Office suite
AGM-GRA (Regulatory Affairs)
Masters degree in Regulatory Affairs/Pharmaceutical Biotechnology, 12-15 years of experience, and exposure in regulated markets. Biosimilars and NCE/ANDAs experience is required
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