Company

QASpecialistQMSSupport

Hong Kong FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“QA Specialist QMS Support. Skills: Quality Management Systems, GxP, Quality Compliance, Quality Assurance, Risk Management, Project Management. Manages Quality aspects and projects within area of responsibility.. Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems”

Industry & Context.

Problems you'll solve

Problem Solving Skills

What They're Looking For.

Must Have

Quality Management Systems, GxP Experience, Quality Compliance, Quality Assurance, Technological Expertise

Nice to Have

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

What You'll Do.

Manages Quality aspects and projects within area of responsibility.

Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems

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

Ensures the timely collection

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

Escalation 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

Review quality deliverables to ensure compliance

with health authority requirements and SOPs

including procedural documents

clinical trial material

Prepare and review GxP 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

How You'll Work.

Team & Collaboration

Collaboration

Communication Scope

Communication skills

Process & Methodology

Project Management

Full 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 qualit

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