Quality Operations (Bio) Trainee Attach and Train Program

The Attach & Train Programme is a structured talent development programme designed to build skilled talent for Singapores advanced biomedical manufacturing sector through practical industry-based training that develops the technical skills and capabilities needed to support the industrys current and future workforce needs. 

As a Training & Document Control Trainee you will work alongside experienced professionals during a 15-month structured training programme. You will support Quality Operations activities to help ensure that manufacturing and production processes meet AbbVie quality operational and compliance requirements. 

Due to the nature of the programme and its eligibility requirements applicants must be Singapore Citizens or Permanent Residents. 

 
What Youll Do 

• Support Quality Operations activities across manufacturing warehouse engineering and QC areas to help ensure compliance with approved company policies procedures and GxP requirements. 
• Assist with the review of incoming material inspection packages batch records manufacturing logs line-clearance activities and Quality Logs including QA Hold and QA tag-out activities. 
• Support the release of incoming materials in-process materials and finished product batches under the guidance of experienced Quality professionals. 
• Participate in investigations related to non-conformances in materials QC testing manufacturing processes warehousing or products including root-cause analysis and corrective and preventive action (CAPA) implementation. 
• Assist with quality data trending identify potential quality or compliance risks and contribute to continuous-improvement and Kaizen initiatives. 
• Develop knowledge of change management by supporting cross-functional risk assessments change-control activities and coordination with global Quality teams. 
• Participate in Annual Product Quality Reviews Product Quality Assurance activities quality-system implementation new product introduction and operational-excellence projects. 
   

What Youll Learn 

• Practical manufacturing Quality experience through exposure to material controls batch documentation production-floor oversight and product release activities in a regulated pharmaceutical environment. 
• Core investigation and compliance skills by supporting deviation investigations root-cause analysis CAPAs quality risk management and change-control processes. 
• Cross-functional collaboration and continuous-improvement skills by partnering with Manufacturing QC Engineering Warehouse and Quality teams to identify opportunities to strengthen site processes. 

Qualifications :

• Bachelors degree in Science (e.g. Biology or Chemistry) Pharmacy Engineering or a related discipline. Fresh graduates are welcome to apply. 
• Internship project or work experience in pharmaceutical or biopharmaceutical Quality Compliance or GxP environments is a plus. 
• Familiarity with GxP requirements quality systems quality risk management and standards applicable to APIs and biologics. 
• Exposure to SAP and TrackWise is a plus. 
• Strong analytical planning and organisational skills with attention to detail. 
• Good verbal and written communication skills with the ability to collaborate effectively across cross-functional teams. 
• Highly motivated adaptable and committed to maintaining high standards of quality integrity and compliance. 

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

Work :

No

Employment Type :

Full-time