Senior Quality Assurance Manager

kingfisher hr solutions group

Singapore

On-site

SGD 180,000 - 240,000

Full time

6 days ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Kingfisher HR Solutions Group in Singapore seeks an experienced Senior Manager, Quality Assurance to establish and lead the regional QA function across Southeast Asia, building a scalable QMS and ensuring compliance across the end-to-end supply chain.

The role includes standing up pharmacovigilance foundations, safety reporting processes, and oversight of licensors, contract manufacturers, distributors, and logistics partners in a high-growth biopharma startup environment.

Qualifications

  • Minimum 8 years of Quality Assurance experience within pharmaceutical/biotech/life sciences.
  • Deep expertise in GMP and GDP, QMS, CAPA, change control and recall management.
  • Regional SE Asia/APAC distribution and regulatory environment knowledge.

Responsibilities

  • Develop and manage regional QMS and QA operations.
  • Ensure regulatory inspections readiness and compliance across supply chain.
  • Oversee Pharmacovigilance foundations, safety reporting and PV vendor oversight.
  • Partner with licensors, manufacturers, distributors, warehouses, and logistics providers.

Skills

Leadership
Stakeholder Mgmt
QA Oversight
GMP/GDP
PV Exposure

Job description

Seeking an experienced and entrepreneurial Senior Manager, Quality Assurance to establish and lead the company's regional Quality function across Southeast Asia. This is a unique opportunity to join a high-growth biopharmaceutical organization and play a pivotal role in building the quality and patient safety infrastructure that will support the successful commercialization of innovative therapies across the region.

About the Role

You will be responsible for developing and managing the regional Quality Management System (QMS), ensuring compliance across the end-to-end supply chain, and overseeing quality operations involving licensors, manufacturing partners, distributors, warehouses, and logistics providers. In addition, this role will assume responsibility for establishing foundational Pharmacovigilance (PV) framework, including safety reporting processes, adverse event management pathways, partner oversight, and compliance governance until a dedicated PV function is established. This is a highly visible and strategic position that combines operational excellence with the opportunity to build new capabilities within a dynamic biotech startup environment.

Responsibilities
  • Quality Management & Compliance
  • Regulatory & Inspection Readiness
  • Product Quality & Pharmacovigilance Oversight
  • Cross-Functional Partnership
Qualifications
  • Minimum 8 years of Quality Assurance experience within the pharmaceutical, biotechnology, or life sciences industry.
  • Strong experience supporting biologics, specialty medicines, or innovative therapies.

Deep expertise in:

  • GMP and GDP compliance
  • Quality Management Systems
  • Quality Agreements
  • CAPA and deviation management
  • Change control
  • Recall management
  • Quality risk management
  • Proven experience operating within regional Southeast Asia or APAC distribution and regulatory environments.
  • Knowledge of local GDP licensing requirements and Health Authority expectations, particularly within Southeast Asia.
  • Practical exposure to Pharmacovigilance, safety reporting, PV vendors, distributor oversight, or local safety compliance requirements.
  • Experience supporting pre-launch activities, Early Access Programs, or Named Patient Programs is advantageous.
Required Skills
  • Strong leadership and stakeholder management capabilities with the ability to influence both internal and external partners.
  • Proven success managing third-party quality providers, contract manufacturers, logistics partners, distributors, and service vendors.
  • Comfortable operating in a fast-paced startup environment with the ability to create structure, processes, and governance frameworks from the ground up.
  • Highly autonomous with strong problem-solving skills, sound judgement, and a hands-on approach.
  • Resilient, adaptable, and capable of balancing strategic priorities with operational execution.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Regional QA & PV Leader, Biotech (Southeast Asia)
Regional QA & PV Leader, Biotech (Southeast Asia)

kingfisher hr solutions group • Singapore

On-site
SGD 180,000 - 240,000
Senior Medical Affairs Manager (SEA | BioPharma)
Senior Medical Affairs Manager (SEA | BioPharma)

Atomic Recruitment SEA • Singapore

On-site
SGD 180,000 - 240,000
Director of Regulatory Affairs and Quality
Director of Regulatory Affairs and Quality

Barrington James • Singapore

On-site
SGD 180,000 - 340,000
Senior QA Executive
Senior QA Executive

p-con management pte. ltd. • Singapore

On-site
SGD 60,000 - 90,000
Quality Assurance Specialist
Quality Assurance Specialist

PHAIDON INTERNATIONAL (SINGAPORE) PTE. LTD. • Singapore

On-site
SGD 70,000 - 110,000
Regulatory Affairs Manager
Regulatory Affairs Manager

HAROLD CONSULTANCY • Singapore

On-site
SGD 120,000 - 180,000
Senior / Regulatory Affairs Executive – Asia Regional Access & Registration
Senior / Regulatory Affairs Executive – Asia Regional Access & Registration

OASIS BIO PTE. LTD. • Singapore

On-site
SGD 70,000 - 100,000
Senior Manager, Quality
Senior Manager, Quality

H&H Group | B Corp™ • Singapore

On-site
SGD 90,000 - 120,000
Senior Quality Specialist (QA/QC)
Senior Quality Specialist (QA/QC)

moleac pte. ltd. • Singapore

On-site
SGD 90,000 - 130,000
Senior/QA Executive (Materials)
Senior/QA Executive (Materials)

GLAXO WELLCOME MANUFACTURING PTE LTD • Singapore

On-site
SGD 90,000 - 120,000