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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 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 https://www.jnj.com
Job Function:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Gent, East Flanders, Belgium
Job Description:
Manager, Technology Product Owner, QCL E2E Quality – APR
The Quality, Compliance, & Sustainability organization within Johnson & Johnson Corporate Business Technology (SCT) is recruiting for a full-time Technical Product Owner to join the End-to-End Quality Product team to provide support to Quality & Compliance’s Automated Product Release (APR) capabilities being deployed across J&J manufacturing sites.
The QCL Technology team in partnership with the J&J Technology Global Supply Chain organization has responsibility for delivery of the technology product portfolio that supports a variety of key QCL products and provides outstanding customer experience across multiple channels within J&J.
This position can be based in Belgium or any other EMEA/Europe-based site that allows for travel to nearby Johnson & Johnson locations.
The E2E Quality Technical Product Owner for Automated Product Release will be a leader with a quality and patient-centric mindset that will drive digital transformation and innovation in the Quality/Manufacturing APR space.
This will require influencing technology strategic direction to shape the landscape of APR technology solutions while delivering on the vision and framework of the APR product group.
This includes SAP Batch Release Hub, Supplier/CMO data/digital solutions, and scaling of APR capabilities across IM manufacturing sites.
Key to success in this role is the ability to identify opportunities to transform the product release experience through the use of technology while improving the end-to-end product release lifecycle.
Key Responsibilities:
Product Ownership
* Shape the squad vision and product roadmap and lead the squad in delivering products / platforms features / work oriented around business impact.
* Shape and prioritize backlog, applying business expertise and understanding of customer needs, translate requirements into user stories & acceptance criteria.
* Lead a High-Performing Team (HPT) squad using Agile principles, fostering collaboration, innovation, and continuous improvement.
* Partner closely with Scrum Master, Solution Architects, Business Analysts, and Quality partners to ensure sprint...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-12-04 07:22:02
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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 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 https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Gent, East Flanders, Belgium
Job Description:
QA Associate, CAR-T (weekend)
Johnson & Johnson (J&J) is recruiting a QA Associate for the CAR-T hub in Europe.
The position will be based in Ghent Belgium.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, J&J has build two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are operating from the existing J&J Beerse site. CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.
In this role, you are reporting in the J&J QA CAR-T organization and work closely with your peers from Operations and Quality Control.
The QA Associate, CAR-T (weekend) is responsible to take part in, and oversee the release activities which take place during the weekend shift, i.e.
release of batches in line with all ATMP/GMP requirements whilst adhering to the established turn around timelines.
This position will involve working in a weekend shift (6AM - 6PM), on site.
Major Responsibilities:
* Batch Documentation Review/Release: Review and approve batch documentation to verify compliance with regulatory and company standards.
* Quality Assurance Oversight: Monitor and ensure adherence to Good Manufacturing Practices (GMP/ATMP) and other relevant quality standards during the manufacturing of CAR T-cell products.
Provide guidance during the weekend in relation to the QA oversight on manufacturing and logistics processes.
* Investigation Support and CAPA Management: Provide technical, quality, and compliance expertise to support in-depth investigations related to deviations, complaints, and other quality issues to ensure timely resolution.
* Inspection and Audit Support: Assist in the preparation, execution, and follow-up of internal and external inspections and audits to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements.
* Collaboration and Stakeholder Engagement: Foster and maintain effective working relationships with inte...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-12-03 08:22:34
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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 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 https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Gent, East Flanders, Belgium
Job Description:
Johnson & Johnson (J&J) is recruiting a QA Release Weekend Lead, with a Qualified Person accreditation, for the CAR-T hub in Europe.
The position will be based in Ghent, Belgium.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, J&J has build two CAR-T manufacturing centers in the Ghent area (Belgium). The QC laboratories are operating from the existing J&J Beerse site. CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.
In this role, you are reporting in the J&J QA CAR-T organization and work closely with your peers from Operations and Quality Control.
The QA Release Weekend Lead, CAR-T is responsible to take part in, and oversee the release activities which take place during the weekend shift, i.e.
release of batches in line with all ATMP/GMP requirements whilst adhering to the established turn around timelines.
Additionally, the function contributes to appropriate communication and hand-overs between the different work regimes (week and weekend shift).
This position will involve working in a weekend shift (6AM - 6PM) on site.
This lead position will rotate between the locations in the Ghent facilities.
You will be responsible for:
* Batch Documentation Review/Release: Review and approve batch documentation to verify compliance with regulatory and company standards.
* Quality Assurance Oversight: Monitor and ensure adherence to Good Manufacturing Practices (GMP/ATMP) and other relevant quality standards during the manufacturing of CAR- T products.
Provide QA oversight and guidance for manufacturing and logistics processes.
* Investigation Support and CAPA Management: Provide technical, quality, and compliance expertise to support in-depth investigations related to deviations, complaints, and other quality issues to ensure timely resolution.
* Inspection and Audit Support: Assist in the preparation, execution, and follow-up of internal and external inspections and audits ...
....Read more...
Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-12-02 07:29:25
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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 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 https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Risk Management
Job Category:
Professional
All Job Posting Locations:
Bangalore, Karnataka, India
Job Description:
J&J Innovative Medicine Principal Operations belongs to the Innovative Medicine Companies of Johnson & Johnson.
J&J IM Principal Operations is a global organization located in USA, Belgium, Ireland, The Netherlands, Singapore, and Switzerland.
Within J&J IM Principal Operations, our mission is to provide diligent stewardship of the Innovative Medicine business model, by protecting and optimizing the product intellectual property (IP) structures in close collaboration with J&J Innovative Medicine Commercial, R&D, Supply Chain, Tax and Treasury.
Currently we are looking for “IMPO UAM Authorization Analyst” to join the J&J Innovative Medicine Principal Operations organization in “Bengaluru, India
Role Purpose:
The purpose of the role is charged with fortifying user access security and compliance across global SAP S4 systems, while driving strategic UAM initiatives to support organizational growth and technological for business adaptation purposes.
J&J Innovative Medicine (IM) Transcend is a global, multi-year end-to-end business transformation program sought at modernizing foundational business processes through the implementation of SAP S/4 HANA.
This program focuses on core functionalities related to SAP Manufacturing, Order to Cash, Procure to Pay, and Finance processes.
The IMUAM team plays a crucial role in ensuring security requirements are crafted and implemented compliantly within this program.
Key Responsibilities:
* Drive security workshops to collect business and compliance requirements for role design, ensuring validation post-build for our S4 HANA Roles and Authorization requirement.
* Develop UAM strategies focusing on composite roles, Fiori tiles, business roles/user personas, and data security/UI masking concepts for S/4HANA.
* Perform data validation, conduct health checks, and provide compliance documentation.
* Design, test, and implement rule sets for SAP S/4HANA role design.
* Support role data and user account setup, offering advice on role design testing and coordinating business UAT activities.
* Manage authorization defects and support user cutover and Hypercare activities.
* Collaborate with the Business Adaptation team on training, communication, and ensuring site readiness.
* Faci...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:01
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Job Category:
Quality
Job Family:
Plant Quality Assurance
Work Shift:
Job Description:
Partners in this position will use knowledge of the production process to test and inspect product at various stages of completion and shelf life for compliance to the production schedule and customer specifications.
They will be required to understand customer requirements and assist in assuring proper operation.
Additionally, partners will be required to learn all duties of the lab grading process and line QA tasks for both departments.
Partners will be expected to follow and maintain all related CCP and PCP checks required by the position.
Partners will be expected to complete all checks in a timely and correct manner, serving as an example and resource to other partners.
Partners will need to understand and execute all relative standard operating procedures.
Partners must work with leaders and partners to ensure Food Safety and Partner Safety.
Partners will be responsible for following the reaction plan for Food Safety, Product Quality, and Customer Requirement outages, including contacting the proper leader(s).
Partners will need to be able to work with all partners and leaders in a respectful and effective manner, to allow completion of holds and resolution of issues in a timely manner.
Partners will need to accurately record data in various reports and spreadsheets.
Overtime based on Capacity and Non-Capacity needs.
Other duties may be assigned.
This position requires each bidder to test using computer tests produced by Wonderlic, Inc.
To be a successful bidder, partners will need to meet minimal testing requirements of these tests as part of the selection process.
Eligible partners will receive:
* A 401(k) plan that includes up to an 8 percent Schreiber match and has been recognized as Best-in-Class for companies with 5,000-plus employees.
* Competitive medical, prescription drug, dental and vision benefits without a waiting period, including second-opinion medical consultation with specialists
* Wellness resources, including a fitness reimbursement program and access to an interactive personalized online wellness program
* Paid vacation and holidays
* Professional growth and development opportunities through training and our Education Assistance Program
* Childcare costs.
Get up to $5,000 annually to help you with the cost of childcare. Monthly contributions toward childcare expenses, including independent babysitters.
Schreiber requires that an employee have authorization to work in the country in which the role is based.
In the event, an applicant does not have current work authorization, Schreiber will determine, in its sole discretion, whether to sponsor an individual for work authorization.
However, based on immigration requirements, not all roles are suitable for sponsorship.
An Equal Opportunity Employer, all qualified applicants will receive consideration for employment without regard to race, color,...
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Type: Permanent Location: Clinton, US-MO
Salary / Rate: Not Specified
Posted: 2025-11-27 07:47:17
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Job Category:
Manufacturing/Operations
Job Family:
Plant Production
Work Shift:
Wknd (United States of America)
Job Description:
Primary - Essential Functions
Perform all process CP, CCP, QP, and CQP checks required for the position.
Follow reaction plans for Food Safety, Food Quality and customer requirement deviations. Be able to identify and understand customer requirements and assist in assuring proper production operation.
* Must follow Good Manufacturing Practices and good housekeeping guidelines. Must follow safety guidelines, wear designated Personal Protective Equipment, and meet OSHA safety requirements.
* Must be able to identify and understand customer requirements.
* Perform manual labor tasks such as inspection, rework & sort operations as needed.
* Teamwork and compliance with plant policies and procedures.
* Utilize Process Excellence tools to improve plant performance and complete specific projects as directed by Department Team Leaders.
Must be engaged to learn P.E.
and SPS tools and support PE initiatives.
* Satisfactory attendance record.
Must be willing to work weekends, off-shifts, OT as needed.
Must be on-time to work.
* Must be able to work in other general labor positions in the Plant as needed.
* Other duties as assigned.
Demonstrated ability to properly identify product and record accurate data on production reports. Performs duties as required by plant leadership to ensure efficient & effective operation of the production processes. This list is not all inclusive but may involve assistance of the following processes and equipment:
* Peeling and opening product for rework
* Sorting of rework
* Manual or electric pallet jack
* Baader
* Palletizing
* Casing
* Plantwide sanitation
Secondary - Non-Essential Functions
* Willing to perform duties assigned, manage multiple priorities.
* Interpersonal Relations
* Deductive Logic
* Dependable (good attendance to work and meetings)
* Goal Oriented
* Adaptable
* Strong work ethic – willing to do what needs to be done in a timely manner even if it is outside of primary responsibilities
Interacting Relationship - Who you support and who supports you
* Interacts with team advisors, operators and other production workers.
Requires good communication and writing skills, must work well with others along with being a team player.
Expectations / Standards / Training Requirements
* Complete tasks as assigned by leader and others according to expectations. Must possess basic math, counting, calculator and basic computer skills. Forklift driving skills may be necessary. Training can generally be completed in a 2-week period or less.
* Perform all process CP, CCP, QP, and CQP checks required for the position.
Follow reaction plans for Food Safety, Food Quality and customer requirement deviations. Be able to identify and understand cust...
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Type: Contract Location: Clinton, US-MO
Salary / Rate: Not Specified
Posted: 2025-11-27 07:47:16
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Digital Procurement Innovation Consultant
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Kimberly-Clark is looking for an ambitious, self-driven and talented individual to be part of our Digital Strategy group under the Procurement COE team.
As part of the Digital Procurement team, the Digital Innovation Analyst will be responsible for identifying, testing and supporting the deployment of emerging digital solutions that create measurable impact across Procurement’s strategic priorities: cost & cash, resilience, innovation & growth, sustainability,
This role requires curiosity, structured experimentation and strong stakeholder engagement.
The analyts will play a key role in converting digital opportunities (AI, automation, supplier risk, intake tools, Supply technology, etc) into validated business pilots and actionable recommendations.
Responsibilities :
Digital scouting & innovation pipeline
* Identify and assess emerging technologies aligned with Procurement uses cases and priorities (for example : AI autonomous negotiation, Supply scoring, supplier onboarding, intake workflows, etc)
* Maintain a live pipeline of 5-10 active ideas, categorized by maturity (discovery, pilot, scale)
* Benchmark with market and peers and bring structured innovation proposals
Pilot execution & value validation
* Support the planning, execution and post-analysis of pilots in collaboration with IT, Global Business Center, category managers and suppliers
* Track KPIs for each pilot (adoption, ROI, scalability and feedback from users)
* Document learnings and contribute to go/no-go decision with the Digital Procurement lead
Stakeholder engagement & communication
* Build collaborative relationships with category managers, IT, Global Business Center, Legal, Supply and Finance to shape use cases
* Help translate technical capabilities into business value storytelling (slides, demos, reports, dashboards, etc)
* Participate in governance forums, show-and-tell session and Quarter Business Results to showcase results
About Us
Huggies®.
Intimus®.
Poise®.
Plenitud®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and ...
....Read more...
Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-11-27 07:45:35
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TEKsystems is seeking a talented and motivated Videographer to join our in-house creative team.
In this role, you’ll be responsible for producing engaging, high-quality video content that supports internal training programs and corporate communications across our operating companies.
This is a hands-on production role, where you’ll lead projects from concept through post-production, working both independently and collaboratively.
* content across digital platforms.
* Organize and maintain video assets and production equipment.
Responsibilities
* Plan, capture, and edit video content for internal training, communications, and marketing initiatives.
* Operate camera, lighting, and audio equipment in both studio and field environments
* Determine technical needs and ensure professional production quality across diverse settings
* Edit and finalize video content, ensuring brand consistency and high production standards
* Design and integrate motion graphics and simple animations to enhance viewer engagement
* Collaborate with eLearning designers and web developers to deliver video content across digital platforms
* Organize and maintain video assets and production equipment.
Qualifications
* Bachelor’s degree in Film, TV Production, Fine Arts, or a related field; or 4 years of professional video production experience.
* Proficiency with Adobe Creative Cloud, especially Premiere Pro.
* Strong understanding of video production techniques including lighting, audio, and green screen work.
* Experience with both studio setups and on-location shoots.
* Solid grasp of storytelling, pacing, and visual communication.
* Familiarity with interview setups and multi-camera environments.
Preferred Skills
* Basic color grading and audio post-production knowledge.
* Knowledge of video accessibility standards (closed captions, alt audio).
Soft Skills & Attributes
* Collaborative Mindset: You thrive in a team environment and work well with diverse departments and stakeholders.
* Strong Communication: You’re able to clearly explain production needs and creative ideas to technical and non-technical partners alike.
* Creative Problem Solving: You can adapt to changing needs, troubleshoot issues on the fly, and find smart solutions that keep projects on track.
* Attention to Detail.
* Time Management: You’re able to juggle multiple projects and deadlines while keeping a high standard of quality.
* Curiosity & Adaptability: You stay up-to-date on video trends and technologies, and are excited to learn new tools or techniques.
Requirements
* A demo reel and/or past work examples showcasing your production and editing capabilities.
* Travel: Up to 20%
Comprehensive Benefits Package:
Employees receive a competitive base salary or range of 65,000-75,000 (based on experience) + an annual bonus, and an exceptional benefits package i...
....Read more...
Type: Permanent Location: Hanover, US-MD
Salary / Rate: Not Specified
Posted: 2025-11-26 07:46:44
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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 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 https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Nonclinical Safety
Job Category:
Scientific/Technology
All Job Posting Locations:
San Diego, California, United States of America, Spring House, Pennsylvania, United States of America
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
Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Principal Scientist, Nonclinical Submissions Writer.
This position is a hybrid role and can be located in Spring House, PA or San Diego, CA.
The Senior Principal Scientist, Nonclinical Submissions Writer, within the Preclinical Sciences and Translational Safety (PSTS) organization, will prepare and review regulatory submission documents that summarize toxicology, safety pharmacology, drug metabolism, and pharmacokinetics studies. This role will collaborate closely with nonclinical safety, pharmacokinetic (PK) and discovery biology project leads, medical writers, global regulatory dossier leaders, and other subject matter experts (SMEs) to drive the integrated assessment of all nonclinical data in dossiers for submission to international health authorities.
This individual will represent PSTS as the main point of contact on cross-functional global dossier teams and ensure delivery of state-of-the-art submissions aligned with global requirements
Principal Responsibilities:
* Generate nonclinical submission documents to meet pipeline goals with timely, high-quality deliverables (e.g., Investigator’s Brochures, IND/CTA/NDA nonclinical modules, briefing books, health authority responses) across all programs and development phases.
* Partner with Nonclinical Safety, Drug Metabolism and Pharmacokinetics, Bioanalytical, and Pharmacology Leads and other SMEs to develop clear storytelling in submissions by positioning key messages, providing robust context, and clearly explained risk assessments.
* Plan, write, review, edit, and finalize nonclinical sections of regulatory documents for development compounds and markete...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-11-24 07:13:02
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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 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 https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Risk Management
Job Category:
Professional
All Job Posting Locations:
IN004 Bangalore
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are more inquisitive and less invasive, and solutions 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 https://www.jnj.com/.
J&J Innovative Medicine Principal Operations belongs to the Innovative Medicine Companies of Johnson & Johnson.
J&J IM Principal Operations is a global organization located in USA, Belgium, Ireland, The Netherlands, Singapore, and Switzerland.
Within J&J IM Principal Operations, our mission is to provide diligent stewardship of the Innovative Medicine business model, by protecting and optimizing the product intellectual property (IP) structures in close collaboration with J&J Innovative Medicine Commercial, R&D, Supply Chain, Tax and Treasury.
Currently we are looking for “IMPO UAM Authorization Analyst” to join the J&J Innovative Medicine Principal Operations organization in “Bengaluru, India
Role Purpose:
The purpose of the role is charged with fortifying user access security and compliance across global SAP S4 systems, while driving strategic UAM initiatives to support organizational growth and technological for business adaptation purposes.
J&J Innovative Medicine (IM) Transcend is a global, multi-year end-to-end business transformation program aimed at modernizing foundational business processes through the implementation of SAP S/4 HANA.
This program focuses on core functionalities related to SAP Manufacturing, Order to Cash, Procure to Pay, and Finance processes.
The IMUAM team plays a crucial role in ensuring security requirements are crafted and implemented compliantly within this program.
Key Responsibilities:
* Drive security workshops to collect business and compliance requirements for role design, ensuring validation post-build for our S4 HANA Roles and Authorization requirement.
* Develop UAM strategies focusing on composite roles, Fiori tiles, business roles/user personas, and data security/UI mas...
....Read more...
Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-11-10 07:14:58
