Associate Manufacturing Engineer - Drug Product

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical manufacturing firm in Singapore is looking for a qualified individual to manage production materials and ensure compliance with GMP requirements. The ideal candidate will have a Bachelor's degree in a related field and strong hands-on operational abilities. Responsibilities include overseeing production processes, drafting operating procedures, and optimizing workflows. The company offers comprehensive training programs and career development opportunities, making it an excellent choice for motivated professionals.

Benefits

Comprehensive in-house training program

Dual career development tracks

Opportunity for internal job rotation

Qualifications

• Bachelor’s degree in a relevant discipline such as Pharmacy or Biotechnology.
• Knowledge of GMP and expertise in aseptic production preferred.
• Solid foundational knowledge in pharmacy and biotechnology.
• Good English language skills and proactive problem-solving approach.

Responsibilities

• Manage production materials according to GMP requirements.
• Operate DP equipment and perform basic maintenance.
• Draft and revise operating procedures and batch records.
• Conduct deviation investigations and establish corrective actions.
• Optimize production processes for quality and efficiency.

Skills

Problem-solving

Communication

Team collaboration

Literature review

Hands-on operational ability

Education

Bachelor’s Degree in Pharmaceutical Manufacturing or related discipline

Tools

Microsoft Office

Job description

Responsibilities

• Responsible for the whole-process management of production materials, consumables, semi-finished products and finished products in strict accordance with GMP requirements
• Mastery of the principles of DP equipment, familiarity with the production process, you may be able to operate equipment independently and perform basic maintenance of related equipment
• In accordance with GMP requirements, draft and revise related operating procedures, batch production records and related files
• Strictly adhere to change control and deviation investigation process, organize the drafts and implementation of changes, conduct deviation investigations, and establish corrective and preventive actions
• Analyze and solve problems arising in the manufacturing process independently and understand how to contribute to solving problems and optimizing the process through literature review
• Continuously optimize production processes and workflows to ensure production quality and improve production efficiency
• Familiar with project production and transfer processes, capable of conducting gap analysis and project transfer
• As a project lead, communicate internally and externally with other departments and clients to ensure the effective implementation of the project and solve the problems arising in the project
• Participate in designing and recommending new plants
• Participate in audits related to DP manufacturing
• Adherence to company compliance requirements

Requirements

• Bachelor’s Degree with a major in any of the relevant disciplines: Pharmaceutical Manufacturing, Pharmaceutical Engineering, Pharmacy, Bioengineering, Biotechnology, Chemical Engineering, Microbiology, etc.
• Knowledge of GMP is preferred, and expertise in aseptic production is an advantage.
• Solid foundational knowledge in pharmacy and biotechnology, with proficiency in Microsoft Office.
• Good English language skills, literature review skills, and a proactive approach to problem-solving in the workplace.
• Strong hands‑on operational ability, with careful and conscientious equipment operation and timely record‑keeping.
• Good communication and presentation skills.
• Strong team collaboration, efficient execution, and a great sense of ownership.

Career Development

• Comprehensive in-house training program (E-learning / OJT / Mentorship)
• Dual career development tracks – Professional & Managerial Tracks
• Opportunity for internal job rotation / Cross‑BU transfer / Cross‑country assignment
• Cross cultural learning
• GMP greenfield start‑up experience