Abbott Posted October 9, 2026

APAC Compliance, Commercial & Distribution QA Associate Director

Singapore, Central Singapore, Singapore FULL_TIME
Quality Associate Director
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Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

We are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to

Career development with an international company where you can grow the career you dream of.

A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

As the APAC Compliance, Commercial & Distribution QA Associate Director, you will work with the APAC Region Commercial affiliates and sites to provide support and guidance regarding quality systems, compliance, commercial quality, distribution quality, audits, and regulatory requirements to ensure compliant, authentic, safe and efficacious products are supplied across the region.

What You’ll Do

Provide Quality Systems leadership, tactical and strategic direction, and technical support to commercial affiliates in the APAC region.

Maintain quality systems supporting regional supply chain and distribution activities, including GDP training, internal audit programs, document control, quality manuals, returns management, complaints and discrepancy investigations, and CAPA processes.

Provide GDP support to affiliates, including audits, compliance support, event management, and exception handling.

Select and approve Logistics/Transport Service Providers and Third-Party Warehouses for APAC Supply Chain operations.

Collaborate closely with Supply Chain, Distribution, Master Data, QA Supplier Management, and Global Product Protection teams on projects including counterfeit prevention, regional warehouses, temperature monitoring, transport optimization, serialization, supply chain validation, and material listing approvals.

Develop and manage the APAC Commercial Affiliate Quality Plan and provide training to ensure compliance with quality goals and standards.

Support local market outsourcing activities and product launches through management of the First Lot Quality Review program.

• Implement and manage quality systems and training programs supporting CAPA, validation, complaint registration, physician sample handling, inspection reporting and tracking, and policy implementation.

Drive Management Review processes for commercial affiliates and advise senior management on compliance status and risk.

Oversee Quality and Compliance activities across the APAC region to ensure products are supplied in accordance with regulatory and business requirements.

Manage APAC regional Quality Systems and support global and strategic initiatives through implementation across the region.

Lead regional GMP training management and represent APAC in corporate initiatives related to training, metrics, management reviews, document management systems, and quality management systems.

Support GxP audits for APAC suppliers and affiliates and conduct due diligence audits for new business opportunities.

Requirements

University degree for Life Sciences required.

At least 15 years of combined experience in QA, Operations, or Technical Functions within a pharmaceutical environment.

Working experience with commercial and distribution quality will be advantageous.

2 to 3 years’ experience managing complex projects or programs.

Ability to use quality tools such as quality risk management, root cause analysis, benchmarking, gap analysis, pareto analysis, fish-bone diagrams, and process mapping for fact-based decision making.

Project management and troubleshooting skills.

Ability to communicate both written and orally to all levels of management and across different cultural backgrounds.

Knowledge of international regulations and industry best practices for quality systems and compliance.

Ability to identify problems and initiate corrective and preventative actions.

Sound decision-making skills contributing to high levels of competence, confidence and credibility.

Well-developed interpersonal, communication and negotiation skills.

Continuous improvement methods and application (for example: Lean, Six Sigma, Class A, etc.)

Change management experience.

Experience in or working with regulatory organizations

Apply Now

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

Job details

Seniority
Associate Director
Function
Quality
Therapeutic area
Not listed
Location
Singapore, Central Singapore, Singapore
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 383 comparable Associate Director Quality roles across 94 biopharma companies.

383Comparable roles tracked
359Currently active
94Companies hiring similar roles
35Countries represented

Salary context

76 of 383 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) Mid Shift · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $208,845 (median $159,000)

Where these roles are based

Top locations among the 383 comparable roles

United States167
China29
Ireland26
India20
Japan13
United Kingdom13

+ 29 more countries

Seniority mix

383 of 383 peers have a known seniority level

Manager183
Senior166
Associate Director34

Therapeutic area mix

0 of 383 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
Sanofi-Aventis Singapore Pte Ltd City of Singapore, Singapore Manager
Same function Adjacent seniority Same country
50%similar
Amgen Singapore Manufacturing Pte. Ltd Singapore Manufacturing, Singapore Senior
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Singapore Pte Ltd City of Singapore, Singapore Manager
Same function Adjacent seniority Same country
50%similar
Boehringer Ingelheim Singapore, Singapore Manager
Same function Adjacent seniority Same country
50%similar
Glaxo Wellcome Manufacturing Pte Ltd Tuas, Singapore Senior
Same function Adjacent seniority Same country
50%similar
AbbVie Singapore, sg Senior
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
QC Manager, Microbiology
Sanofi-Aventis Singapore Pte Ltd · City of Singapore, Singapore · Manager
Function Therapeutic area Adjacent seniority Country
50%
Commercial Quality Manager, ROPU ASKAN (Singapore, Singapore, Central Singapore)
Boehringer Ingelheim · Singapore, Singapore · Manager
Function Therapeutic area Adjacent seniority Country
50%
Senior QA Specialist
Pfizer Asia Mfg Pte Ltd · Tuas, Singapore · Senior
Function Therapeutic area Adjacent seniority Country
50%
Sr. Project Leader - Design Assurance
Abbott · Singapore, Central Singapore, Singapore · Senior
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.