Recombinant Protein Biochemist: Manufacturing & Purification

Revvity

San Diego (CA)

On-site

USD 28,000 - 37,000

Full time

12 days ago

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Benefits offered by this job

Medical, Dental, and Vision Insurance
Life and Disability Insurance
Paid Time-Off
Parental Benefits
401k with Company Match
Employee Stock Purchase Plan

Job summary

BioLegend, Inc. in San Diego, CA seeks a recombinant protein manufacturing biochemist to join the Molecular Cellular Biology group. You will participate in expression and purification of recombinant proteins, prepare buffers and media, and perform bacterial culture and purification steps.

The role emphasizes maintaining batch records, supporting audits, inventory, and cross-functional project work, with hands-on lab work and documentation in an ISO/GMP environment.

Qualifications

  • Bachelor's degree in Life Science or related area is required.
  • 6 months of hands-on bacterial or mammalian cell culture experience.
  • Preferred: 1 year of biotech protein or antibody manufacturing experience in ISO/GMP.

Responsibilities

  • Prepare buffers, including cell culture media, for experiments.
  • Transform and culture bacterial cells (1–50 L).
  • Purify recombinant protein via affinity methods and perform quality checks.
  • Maintain batch records and quality documentation per ISO13485:2016.
  • Support inventory management and cross-department transfers for QC.
  • Assist in audit readiness, CAPA, and NC investigations.

Skills

Bacterial culture
Mammalian cell culture
Protein purification
ISO/GMP experience
Documentation
MS Office

Education

Bachelor's degree in Life Science or related area

Tools

MS Office

Job description

BioLegend, Inc. in San Diego, CA seeks a recombinant protein manufacturing biochemist to join the Molecular Cellular Biology group. You will participate in expression and purification of recombinant proteins, prepare buffers and media, and perform bacterial culture and purification steps.

The role emphasizes maintaining batch records, supporting audits, inventory, and cross-functional project work, with hands-on lab work and documentation in an ISO/GMP environment.

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