Biopharma Manufacturing Manager: Conjugation & GMP Ops

WuXi XDC; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

WuXi XDC in Singapore seeks an experienced leader for Manufacturing Operations & Process Execution in biopharmaceuticals. You will ensure SOP and MBR compliance, oversee conjugation and purification activities, and supervise equipment to ensure safe, efficient production.

This role leads FAT/SAT/IOPQ, facility maintenance, GMP compliance, and quality systems like TrackWise and MasterControl. You will drive SOP development, deviations handling, audits, training, and shift leadership to maintain

Qualifications

• Bachelor’s degree in a related discipline.
• Minimum 8 years of hands-on biopharmaceutical manufacturing experience.
• At least 3 years of team leadership and operational management.
• Familiar with GMP requirements and regulatory standards (HSA, FDA, NMPA, EU, ICH).
• Solid understanding of sterile manufacturing and pharmaceutical quality systems.
• Experience with ADC and/or CMO manufacturing is preferred.
• Familiar with Single-Use Technologies (SUT).
• Experience in downstream processing and/or bioconjugation manufacturing.

Responsibilities

• Oversee manufacturing operations in line with SOPs and MBR requirements; ensure documentation is accurate and timely.
• Perform and supervise biopharma conjugation, purification, weighing, sampling, and sample management activities.
• Operate and supervise equipment for conjugation and purification processes.

Skills

Team leadership

Operational management

GMP compliance

Quality systems

Education

Bachelor’s degree in Chemistry/Biochemistry/Biology/Pharmaceutical Sciences/Biological Engineering or related

Tools

TrackWise

MasterControl

GAIA

Job description

WuXi XDC in Singapore seeks an experienced leader for Manufacturing Operations & Process Execution in biopharmaceuticals. You will ensure SOP and MBR compliance, oversee conjugation and purification activities, and supervise equipment to ensure safe, efficient production.

This role leads FAT/SAT/IOPQ, facility maintenance, GMP compliance, and quality systems like TrackWise and MasterControl. You will drive SOP development, deviations handling, audits, training, and shift leadership to maintain