4 publicaciones de empleo destacadas de shift leader en catalunya (¡Están contratando!)

Director, Internal Audit, TechOps
Novartis —Barcelona, Barcelona provincia
- Jornada completa
- Inglés
- Manufactura
MES Engineer
AG SOLUTION —Barcelona, Barcelona provincia
- Jornada completa
- Informática
- Sistemas ERP
- Inglés
21h
Compliance Excellence Director
AstraZeneca —Barcelona, Barcelona provincia
- Jornada completa
- Microsoft Excel
- Project management
- Grado
15h
MES Engineer
QUARIQ —Barcelona, Barcelona provincia
- Trabajo híbrido
- Informática
- Sistemas ERP
- Inglés
Solicitud rápida
7h

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MES Engineer
AG SOLUTION —Barcelona, Barcelona provincia
Experience: 2–5 years of experience in MES support, implementation, or administration in a manufacturing environment, preferably in the chemical, pharmaceutical…
21h
MES Engineer
QUARIQ —Barcelona, Barcelona provincia
Experience: 2–5 years of experience in MES support, implementation, or administration in a manufacturing environment, preferably in the chemical, pharmaceutical…
Solicitud rápida
7h

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Director, Internal Audit, TechOps

Novartis -
Barcelona, Barcelona provincia

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Detalles del empleo

Jornada completa

Cualificaciones

Gestión en la cadena de suministro
Logística
Inglés
Manufactura

Descripción completa del empleo

Summary

#LI-Hybrid
Location: Barcelona, Spain

You will play a pivotal role in safeguarding and strengthening Novartis’ Technical Operations by providing independent, strategic assurance across manufacturing and supply. As Director, Internal Audit, TechOps, you will lead complex, high‑impact audit and advisory engagements that shape how risks are identified, mitigated, and managed across end‑to‑end operations. Partnering closely with senior and executive stakeholders, you will bring deep operational insight, sound judgment, and a forward‑looking mindset to influence better outcomes, advance audit innovation, and help ensure we continue to deliver quality medicines to patients worldwide.

About the Role

Key responsibilities:

Oversee and provide overall direction for complex, risk‑based audit and advisory engagements across manufacturing and supply operations
Ensure audit scopes address end‑to‑end Technical Operations risks, including quality, compliance, technology, and third‑party models
Support audit planning and audit program development by identifying key Manufacturing & Supply risks and acting as a technical reference to ensure audit coverage remains risk‑based, relevant, and aligned to business priorities
Review audit findings and reports to ensure technical accuracy, clarity, and evidence‑based conclusions
Drive pragmatic, value‑adding recommendations that strengthen controls and enable measurable operational improvement
Act as a trusted advisor to senior leaders, maintaining independence while fostering constructive, credible partnerships
Provide direct line management to Senior Managers, setting clear strategic direction, overseeing performance and development, and ensuring consistent, high‑quality delivery of risk‑focused audit and advisory engagements across Technical Operations
Coach and develop auditors through hands‑on guidance, feedback, and knowledge‑sharing in Manufacturing and Supply
Advance digital, data‑driven, and artificial intelligence‑enabled audit practices in collaboration with enablement teams

Please be advised that this role has a global travel requirement circa 25%.

Essential Requirements:

Degree in technical or scientific discipline related to manufacturing, supply chain, logistics, or production planning
Substantial experience within internal audit functions in highly regulated industries, preferably pharmaceuticals, biotechnology, or medical devices
Strong practical knowledge of end-to-end processes in manufacturing operations, supply chain management, quality systems, and external manufacturing models
Proven experience leading audit and advisory engagements, managing senior stakeholders, and delivering high‑impact outcomes
Solid understanding of pharmaceutical regulations and standards, including Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and global health authority requirements such as FDA, EMA, and other international regulatory bodies
Demonstrated ability to operate in complex environments, influence senior leaders, and communicate audit conclusions with confidence and tact
Strong people management experience, with a track record of leading, developing, and motivating high‑performing teams.
Fluency in English (written and verbal) is required; additional languages are an advantage

Desirable Requirements:

Professional internal audit or supply chain certification, such as Certified Internal Auditor or Certified Supply Chain Professional
Experience applying data analytics or artificial intelligence‑enabled tools within internal audit or regulated operating environments

Commitment to Diversity and Inclusion

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

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Division

Corporate

Business Unit

Audit & Compliance

Location

Spain

Site

Barcelona Gran Vía

Company / Legal Entity

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.

Functional Area

Audit & Finance

Job Type

Full time

Employment Type

Regular

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