Senior Biotech Manufacturing Specialist (cGMP)

AbbVie Pte Ltd; Singapore; On-site; SGD 50,000 - 75,000; Full time

Job summary

AbbVie Pte Ltd in Singapore seeks a Biologics Production professional to operate within cGMP manufacturing environments. The role focuses on executing manufacturing operations, maintaining product quality, and supporting documentation and continuous improvement initiatives.

You will work across QA, QC and maintenance functions, participate in training, and be involved in transfer activities while adhering to safety and regulatory requirements. Shift work is required.

Qualifications

• Bachelor's degree in Science, Engineering or equivalent.
• 2+ years of relevant Biologics Production facility experience.
• Proven problem-solving skills and adaptability to new requirements.
• Strong working knowledge of Microsoft and SAP, LIMS, Atlas systems preferred.
• Experience with cGMP documentation and record maintenance preferred.
• Excellent teamwork and willingness to hands-on work.
• Willingness and ability to perform shift work.

Responsibilities

• Adhere to cGMP and safety requirements.
• Maintain good housekeeping of production facilities to ensure operational order.
• Identify areas for improvement and participate in continuous improvement projects.
• Participate in commissioning and qualification activities as required.
• Provide guidance and leadership in assigned area to ensure reliable processes.
• Ensure SOP/compliant documentation and GDP-aligned records.

Skills

Biologics production

cGMP

Problem-solving

Shift work

SAP

LIMS

Atlas systems

Team player

Education

Bachelor's Degree in Science or Engineering

Tools

SAP

LIMS

Atlas

Job description

AbbVie Pte Ltd in Singapore seeks a Biologics Production professional to operate within cGMP manufacturing environments. The role focuses on executing manufacturing operations, maintaining product quality, and supporting documentation and continuous improvement initiatives.

You will work across QA, QC and maintenance functions, participate in training, and be involved in transfer activities while adhering to safety and regulatory requirements. Shift work is required.