IVD Bioprocess Manufacturing Associate

VELA OPERATIONS SINGAPORE PTE. LTD.; Singapore; On-site; SGD 39,000 - 61,000; Full time

Job summary

VELA OPERATIONS SINGAPORE PTE. LTD. recruits for an IVD manufacturing role based in Singapore.

You will contribute to production through bulk formulation, dispensing, packaging, and kit assembly while upholding SOPs and ISO standards. The position supports manufacturing schedules and collaborates with Quality, R&D, and Supply Chain teams. The candidate will handle batch records, participate in CAPAs, and ensure safety, waste management, and document control in a fast-paced environment with a

Qualifications

• Bachelor's or Diploma in Life Sciences or Related Field required.
• ISO13485 and cGMP familiarity is advantageous.
• ERP systems (SAP) and document control experience preferred.
• Ability to follow safety and quality SOPs and maintain records.

Responsibilities

• Manufacture products to support scheduling, following SOPs.
• Conduct bulk formulation at micro to milli levels in lab setting.
• Operate dispensing for tubes, bottles, and plates (auto and manual).
• Print, label, assemble, and pack kits for shipment.
• Meet daily/monthly production targets with quality yield targets.
• Maintain batch records per ISO standards and perform waste disposal.
• Assist QA with root cause analysis and CAPA implementation.
• Support GMP biosafety, audits, and safety risk assessments.
• Inventory control of reagents via ERP systems and non-ERP tools.
• Participate in method transfer and process validation activities.

Education

Bachelor’s Degree or Diploma in Life Sciences or related field

Higher NITEC with at least 2 years relevant experience considered

Strong organizational skills

Effective communication skills

Problem solving

Teamwork

Adaptability

Integrity and urgency

Tools

SAP

Job description

VELA OPERATIONS SINGAPORE PTE. LTD. recruits for an IVD manufacturing role based in Singapore.

You will contribute to production through bulk formulation, dispensing, packaging, and kit assembly while upholding SOPs and ISO standards. The position supports manufacturing schedules and collaborates with Quality, R&D, and Supply Chain teams. The candidate will handle batch records, participate in CAPAs, and ensure safety, waste management, and document control in a fast-paced environment with a