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 on LinkedIn, Facebook, Instagram, X and YouTube.
Job DescriptionPurpose: 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.
- 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.
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
AbbVie Singapore, Singapore, SGP Office
9 North Buona Vista Drive, Singapore, Singapore, Singapore, 138588


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