Manufacturing Engineer - Singapore - NUSANTARA PRIME CONSULTING PTE LTD

Wei Jie

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Wei Jie

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Description

Responsibilities:


  • Responsible for handling the development of operation protocols for upstream or downstream operations starting from the dispensary of raw materials up to end of manufacturing process.
  • Execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production
  • Support Change Records Assessment and GMP documentation Review.
  • Responsible for providing support to the assigned manufacturing operations by developing, coordinating, and facilitating small to medium projects to ensure planned, predictable production operations in compliance with GMP regulations.
  • Execute Continuous Process Improvements, CAPAs and Change Records in assigned area.
  • Provide routine and ad hoc support for planning, coordinating, execution, and performance improvement of key manufacturing processes such as product change over.
  • Manage project teams to trouble shoot medium to complex problems and support continuous process improvement. Facilitate root cause analysis (RCA) with input from SMEs, develop and implement change to improve performance.
  • Collaborate with multidisciplinary teams to achieve project objectives.
  • Assist in experimental design and troubleshooting as needed.

About You:


  • Bachelor's degree in a relevant life science or Engineering field (e.g., biology, biotechnology, biochemistry).
  • At least 1 year of experience in Manufacturing / GMP environment is preferred. Fresh graduate is welcome to apply.
  • Strong attention to detail, organizational skills, and the ability to work independently or in a team.
  • Excellent communication skills, both written and verbal, in English.
  • Adherence to safety protocols and regulatory compliance.
  • Adherence to safety protocols and regulatory compliance.

Job Type:
Contract


Salary:
$3, $5,000.00 per month


Schedule:

  • Monday to Friday

Experience:


  • Pharma/Biotech: 1 year (preferred)
  • Manufacturing / GMP environment: 1 year (preferred)
- operation protocols for upstream or downstream operations: 1 year (preferred)


Work Location:
In person

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