Company
QASpecialistQMSSupport
Neural analysis suggests this role is
optimal for Mid+ candidates.
“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.
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
Applying for this QA Specialist QMS Support role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about this company?
Real rants from real employees. Read before you apply.