Bioprocessing Associate II - GMP Biotech Manufacturing

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 downstream manufacturing and drug substance production at the MFG18 site. You will work with a team to ensure GMP, quality, and safety across operations.

Reporting to the Manufacturing Supervisor, you will assist with training, equipment start-up, and batch record documentation while contributing to continuous improvement and lean initiatives in a fast-paced biopharma environment.

Qualifications

• Certificate, Diploma, Degree or equivalent in Science/Engineering or related field.
• 0-2 years' experience in biopharmaceutical cGMP manufacturing.
• Experience in biopharmaceutical manufacturing is an advantage.
• GMP knowledge and experience with batch records and SOPs.
• Ability to work with SAP and TrackWise systems.
• Basic understanding of bioprocessing/biotechnology.
• Knowledge of biotech manufacturing processes and related documentation.

Responsibilities

• Support production of biological products at MFG18 Cranbury facility.
• Assist with safety culture and cGMP compliance.
• Support start-up activities for facilities and equipment.
• Participate in production tasks to meet output targets and quality.
• Prepare for shifts: check buffers and material requirements.
• Perform operations per SOPs and batch records.
• Support continuous improvement with Lean/Six Sigma tools.
• Escalate deviations to supervisor and maintain safety standards.
• Maintain housekeeping and training compliance.

Skills

Communication

Interpersonal skills

Problem solving

Team collaboration

Initiative

Ethics/compliance

Education

Science/Engineering degree

Tools

SAP

TrackWise

Job description

WuXi Biologics in Cranbury, NJ, is seeking a Bioprocessing Associate II to support downstream manufacturing and drug substance production at the MFG18 site. You will work with a team to ensure GMP, quality, and safety across operations.

Reporting to the Manufacturing Supervisor, you will assist with training, equipment start-up, and batch record documentation while contributing to continuous improvement and lean initiatives in a fast-paced biopharma environment.