GMP Bioconjugation Manufacturing Associate II

Abzena; Bristol Township (Bucks County); On-site; USD 55,000 - 75,000; Full time

Job summary

Abzena in the United States is seeking an Associate I/II to support large-scale bioconjugation manufacturing under cGMP. This role covers manufacturing, development, and processing of drug substances to ensure quality and on-time delivery to customers.

You will communicate production status, work with process development, QC and QA, and contribute to continuous improvement while following safety and regulatory requirements. This is a hands-on, on-site role in a dynamic biopharma setting.

Qualifications

• Bachelor’s degree in chemistry, biology or engineering.
• A minimum of 2 years’ experience in a GMP pharmaceutical environment preferred.
• Experience with cGMP manufacturing operations and GxP principles.
• Understanding and application of cGMP requirements.

Responsibilities

• Works in GMP environment and ensures regulatory compliance.
• Batch Documentation/Record Generation and materials handling.
• Equipment setup, operation, cleaning and calibration.
• Participate in continuous improvement activities and CAPA proposals.
• Interfaces with process development, Quality Control and Quality Assurance.
• Ensure proper execution of Master Batch Records and SOPs.

Skills

GMP experience

cGMP

GxP principles

Education

Bachelor’s degree in chemistry, biology or engineering

Job description

Abzena in the United States is seeking an Associate I/II to support large-scale bioconjugation manufacturing under cGMP. This role covers manufacturing, development, and processing of drug substances to ensure quality and on-time delivery to customers.

You will communicate production status, work with process development, QC and QA, and contribute to continuous improvement while following safety and regulatory requirements. This is a hands-on, on-site role in a dynamic biopharma setting.