Talent.com
Johnson and Johnson
Transcend GTO-QM, Clinical QualityJohnson and Johnson • Toronto, CA
No longer accepting applications
Transcend GTO-QM, Clinical Quality

Transcend GTO-QM, Clinical Quality

Johnson and Johnson • Toronto, CA
13 days ago
Job type
  • Full-time
Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, 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 jnj.com 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 cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine . 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, 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 Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource. Required Skills: 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 The anticipated base pay range for this position is : $139,750-$189,750 Additional Description for Pay Transparency: As applicable for the role - Under current guidelines, this position is eligible for a discretionary performance bonus. The Company uses Artificial Intelligence in its assessment of applicants. This job posting is for an existing position.
Create a job alert for this search

Transcend GTO-QM, Clinical Quality • Toronto, CA

Similar jobs

Pharma QA Specialist – GMP & Health Canada Compliance

iHealth Solution LtdToronto
Full-time

An established industry player is seeking a dedicated Quality Assurance Specialist to ensure compliance with Good Manufacturing Practices and Health Canada regulations.In this pivotal role, you wil... Show more

 • Promoted

Remote CQ Documentation & IV Lead

Project Delivery Partners Pte LtdToronto
Remote
Full-time

A specialized project delivery consulting company in Toronto is seeking a Documentation and IV Execution Lead to support ongoing client projects.The successful candidate will have at least 10 years... Show more

 • Promoted

Expert Clinical Leader in Healthcare Innovation

SE HealthMarkham, ON, CA
Full-time

Join SE Health as an Expert Clinical Leader to innovate patient care.This advanced practice position thrives on developing model care solutions and advancing clinical excellence through collaborati... Show more

 • Promoted

Clinical Research Associate Ensuring Quality Monitoring and Compliance

Syneos HealthToronto, ON, CA
Full-time

Enhance clinical research integrity as a proactive Clinical Research Associate.Drive compliance and data accuracy while fostering strong relationships with site teams in a flexible environment.In t... Show more

 • Promoted

Associate Director, Quality Assurance, Gmp - C$143,700 - C$181,800 A Year

Xenon PharmaceuticalsNorth York, Canada
Full-time

The Associate Director, Quality Assurance, GMP will ensure adherence to GMP regulations and regulatory requirements in support of Xenon’s clinical development programs and NDA preparation. Show more

 • Promoted

QA Leader: Food Manufacturing & ISO/HACCP

Eco Guardian Inc.Aurora, York Region, CA
Full-time

A leading manufacturing company in Canada seeks a Quality Assurance Manager to establish and lead their Quality Department.The ideal candidate will have at least 7 years of experience in food manuf... Show more

 • Promoted

Data Quality Specialist

Michael Garron HospitalToronto
Full-time

The Data Quality Specialist is responsible for leading initiatives that enhance coding quality, clinical documentation integrity, and performance under QBP–HBAM–HIG methodologies.This role ensures ... Show more

 • Promoted

Director Quality & Pharmacovigilance

E.A. AssociatesToronto, Ontario, Canada
Full-time

Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Exciting Leadership Opportunity in Quality & Patient Safety!.Are you ready to lead with purpose ... Show more

 • Promoted

Remote Quality & Regulatory Operations Lead

RadformationToronto, ON, CA
Remote
Full-time

A leading healthcare technology firm is seeking a QARA Operations Lead to oversee quality and regulatory deliverables.This role involves ensuring alignment with product development timelines while ... Show more

 • Promoted

Clinical Regulatory Specialist: Start-up & Compliance

Centricity ResearchToronto, ON, CA
Full-time

A leading clinical research network is hiring a Regulatory Specialist in Toronto, Ontario.This full-time role involves preparing and submitting regulatory documents essential for clinical trials, e... Show more

 • Promoted

GMP Cell Therapy Manufacturing Specialist

Apex SystemsToronto, ON, CA
Full-time

A leading biotechnology firm in Toronto is seeking a GMP Manufacturing Specialist to develop and execute cGMP manufacturing processes for cell therapeutics in clinical trials.The role involves hand... Show more

 • Promoted

Everest Biostatistics Director Role

Everest Clinical ResearchMarkham
Full-time

Join Everest Clinical Research as the Associate Director of Biostatistics, where your expertise will shape clinical trial strategies and project management.This role offers a blend of operational l... Show more

 • Promoted

Quality & Risk Specialist — Healthcare Process Improvement

Circle of Care, Sinai HealthToronto, ON, CA
Full-time

A healthcare organization in Toronto is seeking a full-time Quality and Risk Specialist.This role requires expertise in quality improvement and risk management, collaborating with stakeholders for ... Show more

 • Promoted

Scientist III – Vaccine Quality Assurance

EurofinsToronto, ON, CA
Full-time

Join Eurofins Scientific as a Scientist III, focusing on the vital quality assurance processes of vaccine development.If you excel in mass spectrometry, this is your opportunity.As a Scientist III,... Show more

 • Promoted

Quality Control Associate I in Cutting-Edge Medical Innovations

CCRMToronto, ON, CA
Full-time

Launch your career as a Quality Control Associate I in the revolutionary field of cell and gene therapy.Utilize your skills to support crucial quality control initiatives that bring innovative trea... Show more

 • Promoted

Quality & Regulatory Operations Lead

RadformationToronto, ON, CA
Full-time

Get AI-powered advice on this job and more exclusive features.Radformation creates solutions that detect medical errors and save clinical time for clinicians with a focus in radiation therapy.Using... Show more

 • Promoted

Director Health System Transformation & Strategy Realization

Innovative Medicines Canada - Médicaments novateurs CanadaToronto, Ontario, Canada
Full-time

Director Health System Transformation & Strategy Realization.Direct message the job poster from Innovative Medicines Canada - Médicaments novateurs Canada.Innovative Medicines Canada has an excitin... Show more

 • Promoted

Director Quality & Pharmacovigilance - C$175,000 - C$200,000 A Year

E.A. AssociatesNorth York, Canada
Full-time

The Director will lead quality assurance and pharmacovigilance, ensuring compliance with regulations and driving improvements within the pharmaceutical industry. Show more

 • Promoted

Quality Engineer

LuxoftToronto, ON, CA
Full-time

As a Senior Quality Engineer in the Real Asset Technology team, you will develop quality standards and strategies across the team by defining and implementing automated test strategies and leading ... Show more

 • Promoted

Senior Manager – Validation & Technology Transfer (VTT)

Deciem Beauty Group Inc.Toronto, ON, CA
Full-time +1

Senior Manager – Validation & Technology Transfer (VTT).We are a collective of disrupters and doers, of creatives and scientists, with a mission to reimagine the world of beauty.Since inception, ou... Show more