Bioprocess Manufacturing Associate II — GMP

WuXi Biologics; Cranbury Township (NJ); On-site; USD 30,000 - 47,000; Full time

Job summary

WuXi Biologics in Cranbury, NJ is seeking a Bioprocessing Associate II to support the production of Drug Substance at our MFG18 facility. This role reports to the Manufacturing Supervisor, Downstream, and emphasizes cGMP compliance and safe operations.

The position requires a science/engineering background and 0–2 years in biopharma manufacturing, with familiarity in GMP processes, batch records, and SOPs. Training and career development are emphasized within a collaborative team.

Qualifications

• Certificate, Diploma, Degree in Science or Engineering is essential.
• 0–2 years' experience in biopharmaceutical cGMP manufacturing.
• Direct experience in biopharmaceutical manufacturing is an advantage.
• Thorough knowledge of current Good Manufacturing Practices (GMP).
• Knowledge of biotech manufacturing processes and related batch records/SOPs.
• Basic understanding of bioprocessing/biotechnology.
• Ability to work with SAP and TrackWise systems.

Responsibilities

• Assist in maintaining a safety orientated cGMP culture.
• Support production to meet output targets and quality standards.
• Prepare work for shifts, including buffers and material requirements.
• Execute production operations per SOPs and batch records.
• Support continuous improvement using Lean/Six Sigma tools.
• Report deviations to Supervisor or Senior Team Member.
• Maintain housekeeping and training compliance.
• Adhere to safety policies, procedures and regulatory standards.

Skills

GMP knowledge

Biopharma manufacturing

cGMP compliance

Bioprocessing basics

SAP

TrackWise

Communication

Education

Science/Engineering degree

Tools

SAP

TrackWise

Process automation systems

Job description

WuXi Biologics in Cranbury, NJ is seeking a Bioprocessing Associate II to support the production of Drug Substance at our MFG18 facility. This role reports to the Manufacturing Supervisor, Downstream, and emphasizes cGMP compliance and safe operations.

The position requires a science/engineering background and 0–2 years in biopharma manufacturing, with familiarity in GMP processes, batch records, and SOPs. Training and career development are emphasized within a collaborative team.