Microbiologist II

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

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

Purpose: The primary role is to ensure smooth QC operational activities support to routine or new product introduction per cGMP/EHS/Regulatory expectations with global/site standards. Enables QC functional operational readiness, infrastructure/instrumentation support and compliance readiness.

Major Responsibilities:

Team Support

• Responsible for supporting QC micro-operations by timely conduct of test/release of routine or new product introduction activities.
• Develops technical competency and jointly creates a great place to work in.

Financial Support

• Supports financial spending are within the latest best estimates.

Compliance (Quality and Safety)

• SME for QC Micro - Operational readiness (Eg: Environment, Utilities and Product test), infrastructure/instrumentation needs and compliance readiness (Eg: Track & Trend) against cGMP/EHS/Regulatory compliance expectations to global/site procedures.

• Authors/Reviews lab documentation per cGMP or EHS expectations of the global/local site procedural needs.

• Support in resolution of manufacturing/laboratories investigation or exceptions for timely closure or issue resolution.

• Support in internal/external audits and enables audit response for a successful outcome in sustaining licenses to operate.

Infrastructure & Instrumentation

• Supports QC function infrastructure/instrumentation needs through supporting PM/CAL or Technological refresh needs.

New Product Introduction, Projects & Continuous Improvement

• Support in New Product Introduction (Small molecule or Biologic product) are conducted (TMT, Eqmt qualification) and delivered to enable a successful / timely program launch.

• Any other task/projects assigned by line manager.

Qualifications

• Bachelors in Sciences (i.e. Biologicals, Biomedical, Chemistry, Life Sciences, Pharmaceutical), Pharmacy, or Engineering (i.e. Biomedical, Chemical, Pharmaceutical), or equivalent.

Essential Skills, Experience, and Competencies (includes Licenses, Credentials)

• 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.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html