Senior Quality Assurance Executive - IVD Product Development

AITBIOTECH PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

AITbiotech Pte Ltd in Singapore is seeking a Senior Quality Assurance Executive to own the design control system for our IVD product development program. You will work across R&D, bioinformatics and production to ensure quality from concept to release under ISO 13485 and regulatory frameworks.

This hands-on role covers risk management, validation, PMS, CAPA and documentation. You will manage design history files, change control, and liaise with external auditors as we prepare for HSA/EU IVDR

Qualifications

• 3+ years in QA/QA-RA at a medical device or IVD manufacturer within an ISO 13485 quality system.
• Direct experience with design control documentation, validation protocols and reports, or CAPA and change control.
• Working knowledge of ISO 13485 and ISO 14971.
• Experience documenting and authoring controlled documents: SOPs, protocols, validation reports, risk assessments.

Responsibilities

• Build the quality system for design and development, including SOPs and forms for design control, change control and risk management.
• Run design control on live projects; manage Design History File, design reviews, and revalidation decisions.
• Draft and close validation protocols and reports with R&D and bioinformatics teams; maintain risk management files per ISO 14971.
• Maintain Device Master Record elements and PMS processes; support regulatory submissions (HSA/EU IVDR).
• Coordinate internal audits, CAPA, nonconformity and supplier quality activities.

Skills

QA experience

ISO 13485 knowledge

Design control

CAPA & change control

Documentation writing

External audits

English writing

Molecular biology terminology

Education

Degree in life sciences or related field

Job description

Senior Quality Assurance Executive — IVD Product Development

AITbiotech Pte Ltd · Singapore · Full-time, permanent

About the role

At AITbiotech, we develop innovative molecular diagnostics and genomics solutions spanning qPCR, targeted sequencing, and integrated automation workflows.

We're looking for a QA professional to take ownership of quality for this new product development programme: design control across the development pipeline, and manufacturing quality for the kits we produce and release under our own name.

It's a broad, hands-on role in a small team. You'll work directly with R&D, bioinformatics and production, and you'll own the quality documentation that carries our products through HSA and EU IVDR registration.

If you're three to five years into a QA career and want scope beyond one product and one process step, this is the jump — the kind of breadth that takes considerably longer to reach in a large organization.

Key Responsibilities

Build the quality system for design and development

• Work with our external consultant on the gap analysis and procedure architecture, then own the system it produces
• Write and control the SOPs, templates and forms for design control, change control and risk management
• Manage the ISO 13485 scope extension: application, certification body liaison, audit preparation, findings closure

Run design control on live projects

• Own and control the Design History File for each product line — design plans, inputs, outputs, reviews, traceability matrices to ensure completeness and compliance with ISO 13485.
• Coordinate and minute design review gates with R&D and bioinformatics
• Manage design change control, including impact assessment and revalidation decisions
• Draft and close validation protocols and reports with R&D team

Risk and validation documentation

• Build and maintain risk management files in accordance to ISO 14971
• Draft, issue and close out validation protocols and reports with the scientists who generate the data
• Maintain the software documentation file for our bioinformatics pipeline (IEC 62304 — we'll train you if this is new)

Keep the system running

• Create, maintain and control the Device Master Record not limiting to specifications, drawings, production and assembly instructions, labeling, and packaging and QA procedures together with R&D team.
• Design and operate the Post-Market Surveillance (PMS) together with Regulatory Assurance, not limiting to complaint handling, vigilance reporting, CAPA, trend analysis and periodic safety update reports (PSUR).
• Document controls for documentation not limiting to the Device Master Record, CAPA, nonconformity, complaint handling,
• Maintain Supplier quality: qualification records, quality agreements, incoming acceptance criteria
• Control Manufacturing SOPs, work instructions and ensure updates are reviewed and approved.
• Internal audit programme, management review, training records
• Support HSA and EU IVDR submissions — technical documentation structure, GSPR checklists, ASEAN CSDT dossiers

What we're looking for

Essential

• Degree in life sciences, biomedical engineering, biotechnology or a related field
• 3+ years in QA or QA/RA at a medical device or IVD manufacturer, working hands-on inside an ISO 13485 quality system
• Direct experience with at least one of: design control documentation, validation protocol and report writing, or CAPA and change control
• Working knowledge of ISO 13485 and ISO 14971
• Practical experience building and maintaining risk management file, integrating risk controls into design, manufacturing, and post-market surveillance activities.
• You have personally authored controlled documents — SOPs, protocols, validation reports, risk assessments — not only filed and distributed them
• Involvement in at least one external audit or regulatory inspection, in any supporting capacity
• Clear, precise written English. This role is judged on documents that auditors read; it matters more here than in most QA jobs
• Comfortable with molecular biology terminology (PCR, NGS) — enough to talk to scientists about what they're validating

Advantageous, not required

• IVD specifically, rather than general medical devices
• HSA medical device registration experience, or exposure to EU IVDR / MDR
• IEC 62304 or software-as-a-medical-device documentation (genuinely rare — we'll train the right person)
• ISO 13485 internal auditor or lead auditor certification
• Experience with NGS or qPCR assay validation, or with clinical performance studies (ISO 20916 / ISO 15189)

What you get

• Ownership. You will be the person who builds AITbiotech's design control system, and your name will be on it.
• Breadth. Four product lines — NGS, qPCR, extraction, software — instead of one narrow corner of one product.
• Support where it counts. External consultant time is budgeted for the system architecture and certification body strategy, so you're not doing this from a standing start alone. Direct working relationship with the R&D Director.
• A defined growth path, including toward Person Responsible for Regulatory Compliance under EU IVDR as our EU route matures.
• Small company, real decisions, short distance between your work and whether the product ships.