QC Microbiology Specialist - Micro Operations & Compliance

Allergan; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

AbbVie in Singapore seeks a QC Operations Analyst to ensure smooth QC activities for routine and new product introductions, aligned with cGMP and EHS standards. You will support instrumentation, track issues, and collaborate with cross-functional teams to maintain compliance readiness.

The role requires a Bachelor in Life Sciences or related field, 4+ years in biotech/pharma, and strong analytical and technical writing skills. On-site position with potential for growth and audits support.

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 by timely test/release of routine or new product introduction activities.
• Develop technical competency and contribute to a great workplace.
• Ensure financial spending aligns with latest estimates.
• Act as SME for QC Micro, readiness of infrastructure/instrumentation and compliance.
• Author/review lab documentation per cGMP/EHS/local procedures.
• Support audits and audit responses to sustain licenses to operate.
• Support PM/CAL and instrumentation refresh through QC infrastructure needs.
• Assist in New Product Introduction projects and timely program launches.
• Perform any other tasks/projects assigned by line manager.

Skills

GMP knowledge

Laboratory experience

Analytical thinking

Technical writing

Cross-functional teamwork

Independent

Biotech/pharma experience

Education

Bachelor's degree in Life Sciences

Job description

AbbVie in Singapore seeks a QC Operations Analyst to ensure smooth QC activities for routine and new product introductions, aligned with cGMP and EHS standards. You will support instrumentation, track issues, and collaborate with cross-functional teams to maintain compliance readiness.

The role requires a Bachelor in Life Sciences or related field, 4+ years in biotech/pharma, and strong analytical and technical writing skills. On-site position with potential for growth and audits support.