Quality Assurance Specialist
Novartis is hiring a Quality Assurance Specialist. Level rates it ; you can apply on Level.
AI in this role
Ensure quality compliance, data integrity, and regulatory adherence for pharmaceutical products and medical devices at Novartis.
Job Description Summary
#LI-OnsiteLocation: Selangor, Malaysia
Relocation Support: This role is based in Selangor, Malaysia. Novartis is unable to offer relocation support: please only apply if accessible.
Make quality count where it matters most: protecting patients and ensuring trusted medicines reach them safely. As a Quality Assurance Specialist, you will strengthen quality and compliance across pharmaceutical products and medical devices, collaborating with internal teams, external partners, and regulatory authorities. You will help maintain robust quality systems, support inspection readiness, oversee product-release activities, and promote a strong culture of data integrity and continuous improvement across the organization.
Job Description
Deadline for applications: 28th October 2026.
Major Accountabilities:
- Maintain quality systems and procedures supporting Good Manufacturing Practice and Good Distribution Practice compliance.
- Oversee product release against registered specifications and applicable regulatory requirements.
- Monitor key quality indicators, identify gaps, and coordinate timely risk-mitigation actions.
- Manage inspections, complaints, deviations, recalls, product tampering, and corrective and preventive actions.
- Provide quality oversight for third-party manufacturing, packaging, labelling, storage, and distribution activities.
- Support medical-device compliance, licensing, safety actions, complaint handling, and regulatory reporting.
- Promote data-integrity awareness and coordinate plans that strengthen a culture of responsible data management.
- Partner with supply chain, regulatory affairs, external suppliers, and regulatory authorities on quality matters.
Essential Requirements:
- Degree in life sciences or a related field.
- Experience in quality assurance or quality control within the pharmaceutical or healthcare industry.
- Knowledge of Good Manufacturing Practice and Good Distribution Practice requirements.
- Understanding of local pharmaceutical regulations, quality standards, and applicable medical-device requirements.
- Fluency in written and spoken English and the local language.
- Strong communication, collaboration, and stakeholder-management skills across cross-functional and external partnerships.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Skills Desired
How we rate this
Quality Assurance Specialist at Novartis rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.
Prepare for this job
A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where quality assurance was part of your work. What did you do?
- Tell me about a project where gmp was part of your work. What did you do?
- Tell me about a project where gdp was part of your work. What did you do?
- Tell me about a project where regulatory compliance was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Quality Assurance, Gmp, Gdp, and Regulatory Compliance. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
Want an expert to read your CV for this job?
Free. Send your CV and the role you want next. We reply by email within 2 to 4 business days.
Get new software engineering jobs by email
One email a week with the new software engineering jobs, each rated for how much AI is in the work. No recruiter spam, unsubscribe in one click.
Free. One email a week. Unsubscribe in one click.
Similar roles
Software Engineering roles that involve little AI, at other companies.
What kind of AI work fits you?
Answer 12 practical questions in about three minutes. Get a simple profile, the work it points to, and live roles to explore next.
Find my next step