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Transcend GTO-QM, Clinical Quality

Job in Toronto, Ontario, C6A, Canada
Listing for: 7710-Janssen-Ortho Inc. (formerly Ortho-McNe Legal Entity
Full Time position
Listed on 2026-08-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 196526 - 266839 CAD Yearly CAD 196526.00 266839.00 YEAR
Job Description & How to Apply Below

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

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:
Toronto, Ontario, Canada

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 curses, 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.

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…
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