AbbVie Manufacturing Specialist in Singapore, Singapore

Manufacturing Specialist

Singapore, Central Singapore, Singapore


Requisition #1803564

  • Perform technical writing and investigation of non-conformances in collaboration with Operations

  • Identify and put in place appropriate corrective and preventative actions in conjunction with Operations team

  • Structure common Operations Training modules and Train new hires on such modules

  • Trends Key Performance Indicators and implement measures to streamline work processes and procedures

  • GMP Document Authoring and Revision

  • Electronic Batch Record Co-Authoring, Revision and improvement

  • Participates / leads operations improvements and new product introduction projects

  • Work with Quality systems (e.g. CAPA and change plans) and Operations Related System (LIMS, SAP, PI, Maximo, MS Office)

  • Assist in regulatory inspections, detailing investigations and change plans.

  • Work on continuous improvement projects


  • Degree in Engineering, Science or equivalent

  • Minimum 2 to 5 years of relevant experience in the Bio manufacturing plant

  • Strong working knowledge of GMP systems such as Trackwise, SAP, LIMS, MES systems are preferred

  • Experience with cGMP documentation and record maintenance

  • Experience with Regulatory inspections is required

  • Strong ability to lead and drive cross functional teams

  • Excellent attitude towards work, with strong drive to drive tasks to closure

  • Agility, able to work under stress and cater to different priorities

  • Good presentation and strong technical writing skills

  • Good interpersonal and communication skills

Posting Grade:

ยท Grade: 12

Job Grades are determined by the country in which the payroll is based.