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Portrait of Nanna Haddad

Nanna Haddad

Associate Partner

Copenhagen

Operations
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Competencies

Where Nanna is strongest.

  • Compliance & GovernanceExpert
  • Contract ManagementExpert
  • Leadership & ManagementExpert
  • Risk & Impact AssessmentExpert
  • Operational & Quality AuditExpert
  • Training and EducationExpert
  • Project ManagementSubstantial experience
  • ESG, NIS1/NIS2, AI ComplianceSubstantial experience

Clients

Novo NordiskKvik

Relevant project highlights

  1. 01Global pharmaceutical company: Audit and inspection readiness based on legal and compliance requirements
  2. 02Global pharmaceutical company: Led cross-site manufacturing compliance process groups to strengthen GMP discipline and FDA inspection readiness across all production sites
  3. 03Global pharmaceutical company: Structured deviation investigations in manufacturing using FDA-aligned root cause methods (5-Why, Ishikawa, FTA) to prevent recurrence
  4. 04Global pharmaceutical company: Coordinated manufacturing, QA, engineering and validation specialists to design and implement audit-proof CAPAs. Improved process robustness and fewer compliance gaps
  5. 05Global pharmaceutical company: Pilot testing of solutions on the shop floor and standardisation of successful practices across all sites. More consistent inspections and stronger FDA audit resilience
  6. 06Global pharmaceutical company: Embedded best-practice deviation management, data integrity and inspection-ready documentation standards across manufacturing teams
  7. 07Global pharmaceutical company: Updating of SOPs, policies, procedures and risk assessments
  8. 08Danish energy, engineering and interior companies: Assignments for several Danish companies
  9. 09Multi-site organisation: Led cross-functional compliance initiatives, driving audit readiness, regulatory alignment and consistent governance across sites and business units
  10. 10Multi-site organisation: Root cause investigations and corrective actions to resolve compliance deviations, reduce operational risk and strengthen process integrity
  11. 11Multi-site organisation: Enterprise-wide compliance frameworks, training and best practices, strengthening accountability and compliance culture

Career

  1. 2024 –ZILLION Consulting Group (Ørsted, Novo Nordisk)
  2. 2023 – 2024Compliance Lead & Specialist, Novo Nordisk
  3. 2020 – 2023Compliance Business Partner, Kvik /Ballingsløv
  4. 2017 – 2020COO, Legal Counsel, Rambøll
  5. 2013 – 2017Legal Counsel, LAW FIRM MAAC & Partner
  6. 2000 – 2013Lecturer - Trainer, Elementary School & College

Education

  • University of Copenhagen | Master of Law
  • TTE Frederiksberg | Bachelor of Teacher Education
  • Aalborg University | Languages & International Studies
  • Graduate Diploma | DPO & GDPR 2024
  • Graduate Diploma | Asset Management & Governance
  • Graduate Diploma | Risk Assessment & DPIA, GDPR
  • Graduate Diploma | AML/FATF Anno 2023
  • Bech-Bruun Academy | NIS1/NIS2 Rules & Framework
  • Bech-Bruun Academy | AI Act Rules & Framework

Skills

Languages
Danish, Scandinavian, English, France, Arabic
Systems
MS Office, PowerBI, Jira, Tableau
International
Germany, UK, France, Emirates, Brazil and US
Portrait of Nanna Haddad

Nanna Haddad

Associate Partner

Email
nanna@zcg.dk
Phone
+45 26 77 53 35
LinkedIn
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Nanna Haddad

Associate Partner

Copenhagen · nanna@zcg.dk · +45 26 77 53 35

www.linkedin.com/in/nanna-haddad-68b18b76/

Compliance specialist in GMP, FDA inspection readiness, root cause analysis and CAPA across multi-site manufacturing

Expertise

  • Compliance & GovernanceExpert
  • Contract ManagementExpert
  • Leadership & ManagementExpert
  • Risk & Impact AssessmentExpert
  • Operational & Quality AuditExpert
  • Training and EducationExpert
  • Project ManagementSubstantial experience
  • ESG, NIS1/NIS2, AI ComplianceSubstantial experience

Selected projects

  • Global pharmaceutical company: Audit and inspection readiness based on legal and compliance requirements
  • Global pharmaceutical company: Led cross-site manufacturing compliance process groups to strengthen GMP discipline and FDA inspection readiness across all production sites
  • Global pharmaceutical company: Structured deviation investigations in manufacturing using FDA-aligned root cause methods (5-Why, Ishikawa, FTA) to prevent recurrence
  • Global pharmaceutical company: Coordinated manufacturing, QA, engineering and validation specialists to design and implement audit-proof CAPAs. Improved process robustness and fewer compliance gaps
  • Global pharmaceutical company: Pilot testing of solutions on the shop floor and standardisation of successful practices across all sites. More consistent inspections and stronger FDA audit resilience
  • Global pharmaceutical company: Embedded best-practice deviation management, data integrity and inspection-ready documentation standards across manufacturing teams
  • Global pharmaceutical company: Updating of SOPs, policies, procedures and risk assessments
  • Danish energy, engineering and interior companies: Assignments for several Danish companies
  • Multi-site organisation: Led cross-functional compliance initiatives, driving audit readiness, regulatory alignment and consistent governance across sites and business units
  • Multi-site organisation: Root cause investigations and corrective actions to resolve compliance deviations, reduce operational risk and strengthen process integrity
  • Multi-site organisation: Enterprise-wide compliance frameworks, training and best practices, strengthening accountability and compliance culture

Career

  • 2024 –ZILLION Consulting Group (Ørsted, Novo Nordisk)
  • 2023 – 2024Compliance Lead & Specialist, Novo Nordisk
  • 2020 – 2023Compliance Business Partner, Kvik /Ballingsløv
  • 2017 – 2020COO, Legal Counsel, Rambøll
  • 2013 – 2017Legal Counsel, LAW FIRM MAAC & Partner
  • 2000 – 2013Lecturer - Trainer, Elementary School & College

Education

  • University of Copenhagen | Master of Law
  • TTE Frederiksberg | Bachelor of Teacher Education
  • Aalborg University | Languages & International Studies
  • Graduate Diploma | DPO & GDPR 2024
  • Graduate Diploma | Asset Management & Governance
  • Graduate Diploma | Risk Assessment & DPIA, GDPR
  • Graduate Diploma | AML/FATF Anno 2023
  • Bech-Bruun Academy | NIS1/NIS2 Rules & Framework
  • Bech-Bruun Academy | AI Act Rules & Framework

Skills

  • LanguagesDanish, Scandinavian, English, France, Arabic
  • SystemsMS Office, PowerBI, Jira, Tableau
  • InternationalGermany, UK, France, Emirates, Brazil and US

ZILLION Consulting Group · zcg.dk · contact@zcg.dk

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Contact

ZILLION Consulting Group ApS

Åhusene 9

8000 Aarhus C, Denmark

contact@zcg.dk

CVR 38204327

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