Manufacturing Support Engineer

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

WUXI XDC Singapore Private Limited is seeking a capable manufacturing specialist to ensure GMP compliance, oversee equipment qualification and lifecycle, and support daily manufacturing activities in a regulated biopharmaceutical environment.

You will draft and maintain SOPs, participate in deviations, change controls, and collaborate with cross-functional teams to uphold quality and regulatory standards while contributing to continuous improvement.

Qualifications

• Bachelor degree or above in Chemistry, Biochemistry, Biology, Pharmaceutical, Biological Engineering, or related field.
• Minimum of 3 years of hands-on experience in biopharmaceutical manufacturing.
• Strong understanding of cGMP and GDP in regulated manufacturing.
• Quality mindset with attention to documentation.
• Good technical and operational skills to support manufacturing activities.
• Strong communication and coordination skills for teamwork.
• Proficient in Word, PowerPoint, and Excel for reporting.
• Basic leadership qualities and ability to support team activities.

Responsibilities

• Ensure compliance to GMP regulation and SOPs.
• Qualification and requalification of process equipment.
• Daily management of equipment including acceptance, asset registration, and equipment release.
• Equipment life cycle management from commissioning to qualification and decommissioning.
• Participate in investigation of deviation and variation.
• Draft/maintain SOPs and process documents.
• Support change control and audit.
• Any other work assigned by Supervisor.

Skills

GMP knowledge

Equipment qualification

Documentation

Regulatory compliance

Communication

MS Word/Excel/PowerPoint

Teamwork

Leadership basics

Education

Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical, Biological Engineering or related field

Job description

Job Responsibilities

• Ensure compliance to GMP regulation and SOPs.
• Be responsible in the qualification and requalification of the process equipment.
• Be responsible for the daily management of equipment, including equipment acceptance, asset registration form and equipment release.
• Responsible for equipment life cycle management (from commissioning to qualification and decommissioning).
• Participate in the investigation of deviation and variation.
• Drafting/maintaining SOPs and relevant process documents.
• Support change control and audit.
• Any other work assigned by Supervisor.

Qualification

• Bachelor degree or above in Chemistry, Biochemistry, Biology, Pharmaceutical. Biological Engineering, or related field.
• Minimum of 3 years of hands-on experience in biopharmaceutical manufacturing
• Demonstrates a good understanding of cGMP and GDP requirements in a regulated manufacturing environment.
• Exhibits a good quality mindset, with awareness of compliance and documentation requirements.
• Possesses good technical and operational skills to support routine manufacturing activities.
• Demonstrates good communication and coordination skills, enabling effective teamwork and collaboration.
• Proficient in basic use of Microsoft Word, PowerPoint, and Excel for documentation and reporting.
• Demonstrates basic leadership qualities, with the ability to support team activities when required.
• Possesses basic management skills, including task coordination and adherence to operational plans.