Transcend GTO-QM, Clinical Quality
Job in
6300, Zug, Kanton Zug, Switzerland
Listed on 2026-08-10
Listing for:
Disability Solutions
Full Time
position Listed on 2026-08-10
Job specializations:
-
Manufacturing / Production
Regulatory Compliance Specialist, Change Management, Quality Engineering
Job Description & How to Apply Below
Learn more at
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Quality
Job Sub Function:
Digital Quality
Job Category:
People Leader
All Job Posting Locations:
Schaffhausen, Switzerland, Zug, Switzerland
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at
Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one "clean" ERP as a standardized platform for growth and efficiency gains.
This program will simplify the Pharmaceutical ERP landscape from 7 to 1, standardizing processes to have a cost-effective, fit-for-purpose digital backbone that will enable us to support the Pharmaceutical business with agility. Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
United States
- Requisition Number: R-089314
Switzerland
- Requisition Number: R-090763
Canada
- Requisition Number: R-090760
Belgium, Ireland, Netherlands, and Italy
- Requisition Number: R-090765
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for an IM Transcend:
Global Template Owner
- Quality Management
- Clinical/R&D Quality! This hybrid position will be located in Titusville, New Jersey. Alternate hybrid locations may be considered in Raritan, New Jersey;
Malvern, Pennsylvania;
Springhouse, Pennsylvania;
Toronto, Canada;
Latina, Italy;
Cork, Ireland;
Beerse, Belgium;
Leiden, Netherlands; or Zug or Shaffhausen, Switzerland.
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? Apply today for this exciting opportunity to shape and set the future direction for supporting and improving our new process across all areas.
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,…
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