Transcend GTO-QM, Clinical Quality

360Pharma; Beerse; Presencial; EUR 90.000 - 140.000; Jornada completa

Descripción de la vacante

360Pharma is seeking a Global Template Owner – Quality Management for Clinical/R&D to drive standardization across our SAP S/4 HANA program. The role leads the Global Template design, governance, and implementation, ensuring alignment with the Transcend blueprint and delivering consistent processes across markets.

The candidate will act as a Change Champion, support testing and validation activities, and collaborate with regional teams to optimize the end-to-end Clinical/R&D Quality landscape

Formación

• Minimum 10 years of relevant work experience.
• Experience in complex, multi-ERP environments.
• Experience with ERP processes post-transformation/implementation.

Responsabilidades

• Serve as subject matter expert for Clinical/R&D Quality activities.
• Develop, document and steward the Global Template aligned with the Transcend roadmap.
• Support global standardization and process harmonization across markets.

Conocimientos

Interpersonal skills

Negotiation

Communication

Leadership

Educación

Bachelor’s degree

Project management certs

Descripción del empleo

We are searching for the best talent for an IM Transcend: Global Template Owner – Quality Management – Clinical/R&D Quality! T

Are you ready to be part of a multi-year global business transformation initiative that will transform and standardize our core business processes and products across Plan, Source, Make, Quality, Deliver, and Data, and enable our integrated data strategy through a single SAP S/4 HANA instance?

As a member of the Quality Management team, this role will lead the consolidation of Clinical/R&D Quality business processes and support the creation of the Global Template aligned with the Transcend Global roadmap rollout.

Key Responsibilities:

• Serve as the Innovative Medicine subject matter expert for all Clinical/R&D Quality activities to drive global S/4 HANA capability standardization, alignment, and adoption.
• Ensure all Clinical/R&D Quality processes and designs align with the Transcend future‑state blueprint.
• Act as a Change Champion across Clinical/R&D Quality to support global standardization and process harmonization.
• Develop, document, and steward the Global Template, ensuring integrity, consistency, and alignment across all markets.
• Apply strong global and business-focused reasoning in handling critical issues, business risks, and the development of mitigation strategies.
• Build and optimize business processes aligned with the future-state Clinical/R&D Quality ecosystem architecture and support adoption across regional organizations.
• Support the execution of Business Simulation and User Acceptance Testing, as needed, ensuring deployment team understanding of intended template designs.
• Document and map all end‑to‑end Clinical/R&D Quality processes, ensuring high-quality and up‑to‑date knowledge center content.
• Provide insights and support for training design, compliance documentation, and ongoing process updates.
• Develop and implement standard testing approaches and tools to ensure consistent process validation.Support quality compliance, system validation, and change control processes to maintain an ongoing compliant state and ensure operational excellence.

Qualifications:

EDUCATION:

• Minimum of High School or equivalent diploma/degree is required; Bachelor’s / University or equivalent degree strongly preferred
• Certifications are helpful in one or more of the following: PMP, FPX, or equivalent project management; APICS; and/or Lean/Six Sigma /Process Excellence

Experience and skills:

Required:

• Minimum 10 years of relevant work experience
• Business functional experience (i.e., Operations, Supply Chain, and/or Finance) working in a complex, multi-ERP / system environment
• Experience in operating or supporting large-scale ERP processes following transformation/implementation programs
• Experience in supporting, improving, developing, implementing, and leading operational technological processes within a global organization
• Strong interpersonal, relationship building, and negotiating/influencing skills, with demonstrated ability to collaborate and communicate at various levels including program teams / execution and senior leadership / strategic levels
• People management and development experience (direct or indirect reports and internal/external partners)

Preferred:

• Pharmaceuticals, Life Sciences, or other regulated industry experience
• Experience with business process design, engineering, or optimization
• Proven experience with large-scale SAP ERP replacement project(s)
• Experience effectively leading and governing multi-functional decision-making bodies
• Experience in deploying and/or improving standardized work processes, tools, and templates

Other:

• Requires proficiency in English (written and verbal) to communicate effectively and professionally; proficiency in German, Dutch, or Italian is helpful
• May require up to 30% domestic and international travel depending on work location and business needs
• Requires the ability, through our flexible work policy, to work on-site a minimum of three days each week, with the option for two remote workdays each week

Preferred Skills:

• Compliance Management, Controls Compliance, Developing Others, Digital Assurance, Digital Governance, Human-Computer Relationships, Inclusive Leadership, Leadership, Performance Measurement, Process Optimization, Program Management, Quality Control (QC), Quality Standards, Quality Validation, Regulatory Compliance, Stakeholder Engagement, Standard Operating Procedure (SOP), Strategic Change, Team Management