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HomeBiotech JobsLonza QC Microbiology/Biochemistry Analyst Vacancy 2023 - Apply Online

Lonza QC Microbiology/Biochemistry Analyst Vacancy 2023 – Apply Online

Lonza QC Microbiology Analyst Vacancy 2023 – Apply Online

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Job Title: Quality Control Microbiology Analyst Nights

Eligbility Criteria: 

  • Bachelor or Associates Degree required in Microbiology, Biochemistry or Related Science field
  • Industry experience in a cGMP environment preferred
  • Use of Microsoft Suites (Word, Excel, Powerpoint)
  • Use of Laboratory computer systems (LIMS) and TrackWise preferred
  • Solid ability to interpret data
  • Prioritization and problem solving
  • Solid ability to communicate in both written and verbal format
  • Displays commitment to quality and performs job functions to the best of her/his ability

Job Description

The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. Also being able to participate in quality testing for ongoing customer stability studies. The QC Microbiology Analyst should be able to provide on-time, high quality results to meet Manufacturing demands.

*This position is a night shift role that reports to work Mon-Fri 10PM-6AM*

Training will be conducted during the day shift for a few weeks

While working 3rd shift, the employee will receive a 20% shift differential

While working on any Saturday or Sunday, this employee will receive an additional 5% shift differential

Key Responsibilities:

  • Running test samples for In-Process, Lot Release and Stability studies including bioburden, endotoxin, TOC
  • Reviewing assays
  • Training other members of the team as needed
  • Writing and/or updating Quality Records (Deviations, CAPA, Change Control) and Test Methods
  • Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required
  • Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors
  • Perform other duties as assigned
  • Level of this role is dependent on experience

Lonza QC

Apply Online

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