About this role
The Attach & Train Programme is a structured talent development programme designed to build skilled talent for Singapore’s advanced biomedical manufacturing sector through practical, industry-based training that develops the technical skills and capabilities needed to support the industry’s current and future workforce needs.
As a Pharmaceutical Technologist, your development will take place through a 15-month structured on-the-job training programme within our API Manufacturing team. You will work alongside experienced professionals to support the production of high-quality active pharmaceutical ingredients (API) under rigorous quality and compliance standards, helping to ensure a safe and reliable supply of medicines to patients.
Due to the nature of the programme and its eligibility requirements, applicants must be Singapore Citizens or Permanent Residents.
What You’ll Do
- Operational and Technical
- Execute batch manufacturing instructions with flawless adherence to established procedures and process-critical steps.
- Independently perform key API processing unit operations (e.g., charging, vessel transfer, filtration, drying, pack-off) with minimal supervision.
- Verify batch recipes and manufacturing documentation, provide input on DCS recipe design, and support digitalization and continuous improvement initiatives to drive manufacturing excellence.
- Safety
- Maintain a safe working environment in line with EHS policies, participate in the site Emergency Response Team, and contribute to safety risk assessments and process hazard analyses.
- Quality
- Ensure timely resolution of batch documentation errors and complete all records per GMP/GDP standards, keeping the plant audit-ready at all times.
- Communicate issues promptly to stakeholders and fulfill ongoing training requirements.
- Schedule
- Deliver assigned tasks on time, proactively managing complexities to prevent delays, and escalate scheduling risks promptly to the Manufacturing Supervisor.
What You’ll Learn
- The opportunity to grow with AbbVie's only manufacturing site in Asia, located in Singapore, gaining exposure to cGMP manufacturing within Active Pharmaceutical Ingredients (API) operations.
- Hands-on technical proficiency in key API unit operations — including solid and liquid charging, vessel transfer, filtration, drying and pack-off — while operating DeltaV and POMS/MES systems.
- Develop a strong foundation in batch documentation, quality/safety compliance (GMP/GDP, PHA) and continuous improvement.
- Diploma or Bachelor’s Degree in Chemical Engineering, Pharmaceutical Science, or an equivalent technical-related discipline. Fresh graduates are welcome to apply.
- Exposure to DeltaV distributed control systems and MES through internships, projects or prior experience would be an advantage.
- Excellent interpersonal skills and communication skills.
- Able to work comfortably in 12-hour rotating shift (Day/Night).
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