GMP Biochemist I - Formulation, Vialing & QC

USLA BioLegend, Inc.; San Diego (CA); On-site; USD 28,000 - 37,000; Full time

Benefits offered by this job

Medical, Dental, and Vision Insurance

401k with Company Match

Paid Time-Off

Parental Benefits

Stock Purchase Plan

Job summary

Revvity is hiring a Biochemist I – GMP to join our US FDA-registered cGMP manufacturing facility in San Diego. You will formulate and vial regulated products, prepare buffers, and maintain batch records with GDP and ISO13485 compliance.

The role requires a Bachelor’s degree with 1 year of biotech experience and strong attention to detail in a fast-paced environment. You will collaborate with product development to ensure smooth transitions to manufacturing.

Qualifications

• Bachelor’s degree with 1-year biotechnology industry experience.
• 1 year of GDP experience and ability to document clearly.

Responsibilities

• Prepare buffers for manufacturing activities.
• Perform incoming inspection of raw materials.
• Formulate and vial regulated products (filling, capping, labeling).
• Maintain batch records and ISO13485/cGMP documentation.
• Assist in troubleshooting the manufacturing process.
• Data entry and processing of production orders.
• Work as part of a team on multiple projects.

Skills

GDP

Detail oriented

Communication

Education

Bachelor’s degree in biology/biochemistry/chemistry or related

Minimum 1 year biotechnology industry experience

Tools

GDP workflows

Job description

Revvity is hiring a Biochemist I – GMP to join our US FDA-registered cGMP manufacturing facility in San Diego. You will formulate and vial regulated products, prepare buffers, and maintain batch records with GDP and ISO13485 compliance.

The role requires a Bachelor’s degree with 1 year of biotech experience and strong attention to detail in a fast-paced environment. You will collaborate with product development to ensure smooth transitions to manufacturing.