QA Specialist QMS Support

Novartis.wd3.novartis Careers

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Hong Kong Until 8/22/2026 H-1B sponsor history First posted May 29, 2026 Last posted May 29, 2026
Job description

Job Description Summary

-Manages Quality aspects and projects within area of responsibility.
-Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems


 

Job Description

Major Accountabilities:

  • Support product release to the market and ensure compliant to registered version

  • Ensures the timely collection, monitoring, and reporting of Quality Key Performance Indicators (KPIs) for management reporting

  • Assists in Health Authority inspections and internal audits by supplying information and documentation in a timely manner

  • Support and track the implementation and maintenance of the local Quality system in in accordance with the Novartis Quality Manual

  • Manages processes and systems for all GxP Quality Assurance e.g. Change control, Training Management, Escalation Management, Risk Management. Ensures that processes are conducted in full compliance with the GxP and the Novartis Quality.

  • Contributes to an improvement of current processes and/or to an implementation of modified processes.

  • Ensures adequate tracking and on time completion of corrective and preventive actions (CAPA), inc escalation of issue related to the closure of CAPA, as appropriate.

  • Review quality deliverables to ensure compliance, with health authority requirements and SOPs, including procedural documents, records, third party work, contractors, clinical trial material, components, and gap assessments

  • Prepare and review GxP documentation; assists in the release of GxP documentation, filing and archiving of GxP documentation

  • Supports Compliance review of projects and inspection readiness and management

  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt


Key Performance Indicators:

  • Quality standards are understood, designed into work activity, and achieved.

  • In accordance with departmental objectives such as support of projects with agreed quality and delivery date, passing of internal and external inspections


Work Experience:

  • Quality Management Systems

  • GxP Experience

  • Quality Compliance

  • Quality Assurance

  • Technological Expertise


Skills:

  • Dealing With Ambiguity

  • Decision Making

  • Project Management

  • Risk Management

  • Collaboration

  • Regulatory requirements knowledge

  • Problem Solving Skills

  • Leadership

  • Communication skills

  • Data Integrity

  • Digital saviness

Languages:

  • English.


 

Skills Desired

Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Problem Solving Skills, Project Management, Regulatory Requirements knowledge, Risk Management
About this role

Summary

Supports GxP compliance, manages quality systems, assists audits, reviews documentation, and reports adverse events.

Job title

QA Specialist QMS Support

Experience level

Industry

pharmaceuticals

Location requirements

Hong Kong, on-site, no remote work allowed

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

GxPQuality Management SystemsRegulatory requirementsRisk ManagementData IntegrityCommunicationProblem Solving SkillsProject Management

Preferred skills

collaborationdigital savinessleadershipdealing with ambiguitydecision making

Specializations

GxPQuality Management SystemsRegulatory requirementsRisk ManagementQuality Assurance
Locations

Structured locations inferred from the posting.

Hong Kong

On-site City