Novartis

Pharmaceutical

AnalyticalQC&AS&TExpert

€65–95k ~AI est. Saluggia, Italy FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Analytical QC & AS&T Expert at Novartis. Skills: Analytical QC, AS&T laboratory, Method lifecycle, GMP compliance. Lead AS&T laboratory activities. Develop analytical methods”

Industry & Context.

Pharmaceutical
Problems you'll solve

Troubleshooting; Investigations; Risk management

What They're Looking For.

Must Have

Master degree in pharmacy or chemistry, 5 years in Quality Control department, Fluent in Italian

Nice to Have

Broad experience in QC environment, Good knowledge of English

What You'll Do.

Lead AS&T laboratory activities

Develop analytical methods

Validate analytical methods

Transfer analytical methods

Maintain analytical methods

Monitor analytical methods

Oversee method transfers

Support troubleshooting

Support investigations

Support CAPA implementation

Ensure GMP compliance

Ensure GLP compliance

Ensure QMS compliance

Ensure pharmacopoeia compliance

Ensure regulatory dossier compliance

Plan analytical activities

Coordinate analytical activities

Coordinate stability studies

Monitor method performance

Manage risk initiatives

Evaluate new technologies

Implement new technologies

Qualify new technologies

Evaluate laboratory equipment

Implement laboratory equipment

Qualify laboratory equipment

Provide technical support

Provide analytical support

Support investigations for QC

Support continuous improvement projects

Ensure proper documentation

Ensure training practices

Ensure safety practices

Ensure stakeholder collaboration

Ensure effective communication

How You'll Work.

Team & Collaboration

External partners; Internal and external teams

Full Job Description

**Job Description Summary** -Highly skilled and experienced laboratory professional who contributes by performing analytical release testing, investigational support, research support, and stability testing **Job Description** **Major Accountabilities:** * Lead and ensure execution of AS&T laboratory activities, aligning with plans, priorities, and production needs. * Develop, validate, transfer, maintain, and monitor analytical methods throughout their lifecycle, in collaboration with TRD and external partners. * Oversee analytical method transfers (TRD, sites, third parties) and support troubleshooting, investigations (OOS, deviations), and CAPA implementation. * Ensure compliance with GMP, GLP, QMS, pharmacopoeia standards, and regulatory dossier requirements. * Plan and coordinate QC & AS&T analytical activities, including stability studies, method performance monitoring, and risk management initiatives. * Evaluate, implement, and qualify new technologies and laboratory equipment according to regulatory and company standards. * Provide technical and analytical support to QC, including investigations and continuous improvement projects for quality, safety, and efficiency. * Ensure proper documentation, SOP management, training, safety practices, stakeholder collaboration, and effective communication across internal and external teams. **Essential Requirements:** * Master degree in pharmacy or chemistry, or broad experience in QC environment. * Fluent in Italian. Good knowledge of English. * At least 5 years in Quality Control department within the pharmaceutical industry. **Why Novartis?** Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: **Benefits and rewards:** Read our handbook to learn

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