QC Microbiologist II – Micro Ops & Compliance Specialist

AbbVie Inc.; Singapore; Remote; SGD 60,000 - 90,000; Full time

Job summary

AbbVie Inc. is seeking a QC professional to ensure smooth operational activities for routine and new product introductions in a cGMP/EHS compliant environment. The role emphasizes infrastructure support, instrumentation calibration, and cross-functional collaboration to sustain quality and efficiency.

Responsibilities include handling lab documentation, contributing to audits, and supporting continuous improvement initiatives while delivering timely outcomes in a fast-paced biopharma setting.

Qualifications

• Analytical thinking with problem-solving skills and technical writing skills.
• Independent and motivated.
• Good GMP knowledge/Experience in laboratory.
• Good Collaborator with cross functional teams.
• Able to work towards timeline.
• Minimum 4 years for Bachelor graduate with relevant work experience in Biotechnology / Pharmaceutical industry is preferred.

Responsibilities

• Support QC micro-operations with timely test/release of routine or new product introduction activities.
• Assist in financial planning and ensure spending aligns with latest estimates.
• Serve as SME for QC Micro, addressing infrastructure/instrumentation needs and compliance readiness to cGMP/EHS/Regulatory standards.
• Support lab infrastructure and calibration/maintenance initiatives.
• Contribute to New Product Introduction projects and continuous improvement efforts; participate in audits and issue resolution.

Skills

Analytical thinking

Problem solving

Technical writing

Independent

GMP knowledge

Cross-functional collaboration

Timeline management

Education

Bachelor's degree in Sciences / Pharmacy / Engineering

Job description

AbbVie Inc. is seeking a QC professional to ensure smooth operational activities for routine and new product introductions in a cGMP/EHS compliant environment. The role emphasizes infrastructure support, instrumentation calibration, and cross-functional collaboration to sustain quality and efficiency.

Responsibilities include handling lab documentation, contributing to audits, and supporting continuous improvement initiatives while delivering timely outcomes in a fast-paced biopharma setting.