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Biotechnician - Clarification​/Tissue Culture

Job in San Diego, San Diego County, California, 92189, USA
Listing for: USLA BioLegend, Inc.
Full Time position
Listed on 2026-09-14
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production Associate / Production Line, Manufacturing & Industrial Operations
Salary/Wage Range or Industry Benchmark: 17.75 - 23.75 USD Hourly USD 17.75 23.75 HOUR
Job Description & How to Apply Below

Job Title Biotechnician
- Clarification/Tissue Culture Location(s)
San Diego
- Bio Legend

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.

Find your future at Revvity

Job Summary

The Biotechnician
- Clarification/TC at Bio Legend will be responsible for clarification and concentration of cell culture harvests;
In addition to, other production support related functions such as harvesting TC supernatants, preparing media, processing serum, and processing samples for the TC group. Additional duties will include washing dirty containers that are used throughout the process, lab cleanliness, monitoring supply stocks and completing batch records. The candidate will be a key member of our Manufacturing team and work closely with tissue culture and purification.

The successful candidate will be primarily responsible for performing large and small scale cell culture clarification and concentration, as well as various other support tasks for the tissue culture group. The desired candidate must be a team-player who is organized and has strong verbal and written communication skills and is able to work in a very fast paced environment. Great attention to detail is also a skill that will allow the candidate to be successful.

The candidate must also be able to multitask, work independently and meet deadlines.

Essential Functions

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

  • Large and small scale cell culture clarification and concentration
  • Perform analytical assays such as operating a nephelometer, and others as needed
  • Follow SOP’s, batch records and other compliance related documentation
  • Support clarification processes, including sample preparation, operation of relevant equipment, and basic troubleshooting.
  • Prepare buffers and media, label materials clearly, and maintain accurate batch and production records.
  • Maintain a clean, organized workspace and follow laboratory safety and quality procedures.
  • Collaborate with team members to report issues, update work logs, and support continuous improvement.
  • Carry out work in a dark room environment occasionally.
  • Other projects or responsibilities may be required.
Minimum Qualifications

Education and Experience
  • High School Diploma 1 year or more of biotech-related manufacturing experience
  • Associate’s degree in a life science 2 years relevant industry experience
  • Experience with TFF, filtration, buffer and media preparation, hybridoma production, bioreactors
  • Experience working in a regulated environment such as ISO 9001, ISO 13485, QSR or GMP is preferred
  • Familiarity with inventory control and/or ERP systems is a plus
  • Computer proficiency with the ability to use Microsoft Office products
  • Ability to communicate effectively (oral and written) and to multi-task in a fast-paced environment
Preferred Qualifications

Education and Experience
  • Associate’s degree in a life science 2 years relevant industry experience
  • Experience with TFF, filtration, buffer and media preparation, hybridoma production, bioreactors
  • Experience working in a regulated environment such as ISO 9001, ISO 13485, QSR or GMP is preferred
  • Familiarity with inventory control and/or ERP systems is a plus
  • Computer proficiency with the ability to use Microsoft Office products
  • Ability…
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