QA Intern – CMC & Bioanalysis (6-Month Training)

Prestige BioPharma limitedprestigebio.com; Singapore; On-site; SGD 13,000 - 20,000; Part time

Job summary

Prestige BioPharma in Singapore is seeking an Intern (CMC & Bioanalysis Quality) to support quality activities within the CMCB operations. No prior experience is required as on-the-job training will be provided, and you will assist with documentation control, CAPA follow-ups, SOP updates, and QA support.

You will help create trackers, archive historical QMS documents, and format laboratory protocols and reports to ensure consistency with documentation standards.

Qualifications

• GCE A Level or Diploma is required.
• No working experience required; on-the-job training provided.
• Proficiency in Microsoft Office programs.
• Good computer skills and willingness to adapt to technology.
• Able to start within short notice.
• Able to commit for minimum 6 months.

Responsibilities

• Provide support in quality-related activities within the CMCB operations.
• Assist in managing and maintaining documentation control within the QMS.
• Support CAPA follow-ups for laboratory operations and other quality events.
• Assist in creating and updating trackers for quality events.
• Assist with archival and organization of historical QMS documents.
• Assist in formatting laboratory protocols and reports for consistency and compliance.
• Support maintenance and updating of SOPs, training records, and backups in electronic systems.
• Perform ad-hoc tasks to support the quality team.

Skills

MS Office

Computer skills

Available on short notice

6-month commitment

Education

GCE A Level / Diploma

Job description

Prestige BioPharma in Singapore is seeking an Intern (CMC & Bioanalysis Quality) to support quality activities within the CMCB operations. No prior experience is required as on-the-job training will be provided, and you will assist with documentation control, CAPA follow-ups, SOP updates, and QA support.

You will help create trackers, archive historical QMS documents, and format laboratory protocols and reports to ensure consistency with documentation standards.