Manufacturing Engineer

7 days ago

Tuas, Singapore NUSANTARA PRIME CONSULTING PTE LTD Full time

**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 troubleshoot 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
Contract length: 12 months

**Salary**: $3,000.00 - $5,000.00 per month

**Benefits**:

- Health insurance

**Experience**:

- Change Control: 2 years (preferred)
- Batch Record: 2 years (preferred)
- Pharmaceutical Company: 3 years (preferred)

Work Location: In person

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