GMP Biochemist I – Manufacturing & Formulation

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

Benefits offered by this job

Medical, Dental, and Vision Insurance

Life and Disability Insurance

Paid Time-Off

Parental Benefits

Comprehensive Care Leave

401k with Company Match

Employee Stock Purchase Plan

Job summary

BioLegend, Inc. is seeking a Biochemist I – GMP to support manufacturing of regulated products in our US FDA registered cGMP facility in San Diego.

You will formulate and vial products, maintain batch records, inspect buffers, and prepare materials for lyophilization, ensuring compliance with GDP and ISO13485. The role requires a bachelor’s degree and 1 year biotech experience, strong attention to detail, and teamwork in a fast-paced environment.

Qualifications

• Bachelor’s degree with 1-year biotechnology industry experience.
• 1 year of working experience with Good Documentation Practices (GDP)

Responsibilities

• Prepare various buffers for manufacturing activities.
• Perform incoming inspection of raw materials.
• Perform formulation and vialing of regulated products, which includes filling, capping, and labeling.
• Assist in troubleshooting the manufacturing process.
• Maintain batch records and other documentations in compliance with ISO13485:2016 and cGMP.
• Maintain/troubleshoot laboratory equipment and manage supplies.
• Perform data entry tasks, including processing production orders.
• Work as a team to advance multiple projects simultaneously
• Other projects or responsibilities may be required.

Skills

Attention to detail

Communication skills

Teamwork

Documentation practices

Education

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

1 year biotechnology industry experience

GDP knowledge/experience

Job description

BioLegend, Inc. is seeking a Biochemist I – GMP to support manufacturing of regulated products in our US FDA registered cGMP facility in San Diego.

You will formulate and vial products, maintain batch records, inspect buffers, and prepare materials for lyophilization, ensuring compliance with GDP and ISO13485. The role requires a bachelor’s degree and 1 year biotech experience, strong attention to detail, and teamwork in a fast-paced environment.