Global Applications Leader - IT Strategy & Compliance

Corden Pharma - A Full-Service CDMO

Lisboa

Hybride

EUR 90 000 - 130 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Cafeteria
Dynamic and exciting work environment
Hybrid working opportunities

Résumé du poste

CordenPharma is seeking a Global Application Senior Manager to own a portfolio of business-critical applications, ensuring performance, compliance, security, and continuous improvement across global sites.

You will define roadmaps, lead evaluations and upgrades, coordinate validation activities, and partner with stakeholders, IT teams, and vendors to enable scalable, compliant digital operations in a GMP environment.

Qualifications

  • Experience managing enterprise laboratory and manufacturing applications in GMP environments.
  • Proven IT project leadership with cross-functional teams.
  • Strong stakeholder and vendor management skills.
  • Fluent in English.

Responsabilités

  • Act as Global System Owner for multiple business-critical applications.
  • Define roadmaps aligned with business and IT strategies.
  • Lead evaluations, upgrades, and global implementations.
  • Ensure governance, compliance, security, and regulatory alignment.
  • Coordinate system upgrades, testing, validation, and deployment.
  • Deliver user training and support key-user communities.
  • Serve as main contact for suppliers, auditors, business users, and local IT teams.
  • Ensure qualification and audit readiness of assigned systems.

Connaissances

IT project management
Stakeholder management
Vendor management
Analytical skills
Communication skills
English fluency

Formation

Bachelor's degree in IT/CS/Engineering

Outils

ELN
Signals ELN
ChemDraw
MODDE
SOLO
Chromeleon

Description du poste

CordenPharma is seeking a Global Application Senior Manager to own a portfolio of business-critical applications, ensuring performance, compliance, security, and continuous improvement across global sites.

You will define roadmaps, lead evaluations and upgrades, coordinate validation activities, and partner with stakeholders, IT teams, and vendors to enable scalable, compliant digital operations in a GMP environment.

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