GMP Biochemist: Protein Purification & QC Expert

Revvity; San Diego (CA); On-site; USD 28,000 - 41,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

Life and Disability Insurance

Paid Time-Off

Parental Benefits

Compassionate Care Leave

401k with Company Match

Employee Stock Purchase Plan

Job summary

Revvity in San Diego, CA is seeking a GMP recombinant protein Biochemist responsible for purification, conjugation, formulation and quality control for GMP product release. This role supports manufacturing, manages batch records, materials, and collaborates with QA/QC teams to ensure ISO/GMP compliance.

Responsibilities include purification using IMAC and Protein A Sepharose, conjugation, in-process testing, and contributing to CAPA, training and validation efforts in a collaborative multitask

Qualifications

• BS in Life Science or related field as minimum.
• Extensive experience in protein or antibody purification.
• Experience in ISO/GMP manufacturing environments.
• Detail-oriented and able to work in small teams.

Responsibilities

• Purify recombinant proteins using affinity matrices (IMAC, Protein A Sepharose).
• Purify proteins and perform conjugation and polishing via chromatography/AKTA FPLC.
• Conduct in-process quality testing such as purity and endotoxin.
• Support internal safety and regulatory audits.
• Assist with data entry, batch records, and equipment validation.

Skills

Protein purification

GMP ISO compliance

Quality control

Documentation & SOPs

Team collaboration

Education

Bachelor of Science in Life Science

Tools

AKTA FPLC

Protein A Sepharose

Job description

Revvity in San Diego, CA is seeking a GMP recombinant protein Biochemist responsible for purification, conjugation, formulation and quality control for GMP product release. This role supports manufacturing, manages batch records, materials, and collaborates with QA/QC teams to ensure ISO/GMP compliance.

Responsibilities include purification using IMAC and Protein A Sepharose, conjugation, in-process testing, and contributing to CAPA, training and validation efforts in a collaborative multitask