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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:
Human Resources
Job Sub Function:
Talent Management
Job Category:
Professional
All Job Posting Locations:
New Brunswick, New Jersey, United States of America
Job Description:
We are searching for the best talent for Manager, Succession Planning, to be based in New Brunswick, NJ.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
Johnson & Johnson is seeking a collaborative and detail-oriented Manager, Succession Planning to support the enterprise-wide succession planning process and annual Executive talent rhythm.
This role will work closely with talent leaders, global services, and HR partners to ensure the effective intake, tracking, and presentation of succession planning data.
The ideal candidate will demonstrate strong organizational skills, a keen eye for design, and the ability to create professional presentations for senior audiences.
Key Responsibilities
Succession Planning Support & Stakeholder Partnership
* Assist in the execution of the end-to-end succession planning process, partnering with talent leaders, global services, and HR to update and track succession planning data.
* Support the annual EC talent rhythm by coordinating timelines, collecting inputs, and preparing materials for senior leadership reviews.
* Collaborate with stakeholders to update Workday reports and contribute ideas for developing dashboards that provide actionable succession insights for talent leaders.
Presentation & Content Development
* Create polished, professional presentations for senior audiences, synthesizing content and ideas from multiple contributors.
* Understand the flow and structure of presentations to effectively communicate key messages and recommendations.
* Partner with colleagues to update training materials and playbooks, ensuring content is visually engaging and accessible for executive talent management leaders.
Talent Development Program Coordination
* Help manage the process of soliciting nominations for VP+ external development programs and CEO-sponsored initiatives, ensuring high-potential talent is identified and supported.
* Coordinate with HR and talent leaders to maintain accurate records of program nominations and participant outcomes.
Data & Process Improvement
* Contribute to the ongoing improvement of succession planning processes, including intake forms, tracking tools, and reporti...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-11-14 07:25:32
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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: 2025-11-12 07:17:27
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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:
Non-Standard
Job Sub Function:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Geel, Antwerp, Belgium
Job Description:
Over Innovatieve Geneeskunde
Onze expertise op het gebied van innovatieve geneeskunde wordt geïnformeerd en geïnspireerd door patiënten, wier inzichten onze wetenschappelijke vooruitgang voeden.
Mensen met een visie zoals jij werken in teams die levens redden door de medicijnen van morgen te ontwikkelen.
Sluit je bij ons aan om behandelingen te ontwikkelen, genezingen te vinden en de weg te banen van het laboratorium naar het dagelijks leven, terwijl we patiënten bij elke stap van het proces ondersteunen.
Ga voor meer informatie naar https://www.jnj.com/innovative-medicine
We zijn op zoek naar het beste talent voor Chemisch Magazijn Operator Volcontinue in Geel, Belgie
Heb jij ervaring in een geautomatiseerde magazijn en een passie voor innovatie? Als je ja zegt, dan zijn wij op zoek naar jou!
Dit betreft een tijdelijk contract met kans op verlenging.
U bent verantwoordelijk voor:
* Verwerking van binnenkomende en uitgaande leveringen.
* Voorbereiding van orders voor productie.
* Nauwkeurig afwegen van grondstoffen en producten, inclusief gevaarlijke stoffen.
* Controle van productieorders voor distributie.
* Logging van werkzaamheden volgens procedures.
* Zorg dragen voor orde en netheid in het magazijn, zowel als verbeteringen aandragen.
* Naleven van veiligheidsinstructies bij het werken met chemische stoffen.
* Transport van goederen met reach- en heftruck.
Kwalificaties/Vereisten:
* Hoger Middelbaar Onderwijs of gelijkwaardig door ervaring.
* Minimaal 3 jaar ervaring in een commerciële, distributie of industriële omgeving.
* Vereiste taal: Nederlands
* Technische scholing en kennis van SAP, Excel en Word zijn een plus.
* Bereidheid om in een volcontinu ploegen systeem te werken.
* Bereidheid om te werken met complexe procedures.
* Ervaring met besturingssystemen en digitalisatie.
* Senior profiel die gaat voor verbetering en zelfstandig zorg dragen.
* Affiniteit met digitale veranderingen.
Bij Johnson & Johnson willen we dat elke kandidaat zich ondersteund voelt tijdens het sollicitatieproces.
Ons doel is om de ervaring duidelijk, eerlijk en respectvol te maken voor jouw tijd.
Dit kun je verwachten:
* Beoordeling van d...
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Type: Permanent Location: Geel, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-11-11 07:16:08
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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: 2025-11-10 07:17:44
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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:
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 ...
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Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-11-10 07:17:27
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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:
Beerse, Antwerp, Belgium
Job Description:
Job Description
Position Title: Senior QA Associate Cryo Lab Beerse, CAR-T EMEA
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
We are searching for the best talent for a Senior QA Associate Cryo Lab to be located in Beerse.
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/.
Within J&J Innovative Medicine Supply Chain, a member of Johnson & Johnson's Family of Companies, we are recruiting a QA Associate Cryo Lab (M/F/X).
The position will be based in Beerse, 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, Janssen has constructed two CAR-T manufacturing centers in the Ghent area (Belgium), where CAR-T investigational medicinal and commercial CAR-T products are manufactured.
The newly build Cryo Lab will be operated from the existing Janssen Beerse site to provide the manufacturing facilities of their patients starting material.
The QA Associate Cryo Lab works together with the QA Cryopreservation Manager and is accountable for the implementation of the overall EMEA CAR-T quality system in the Cryo Lab including compliance oversight, release of the cryopreserved apheresis material...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-11-10 07:16:26
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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...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-11-10 07:14:58
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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: 2025-11-08 07:21:14
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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:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Process Improvement
Job Category:
Professional
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Technical Writer II.
Purpose: The Technical Writer will support manufacturing with engineering change orders (ECO), work instructions (WI), job instruction breakdowns (JIBs), training documentation, and creating and editing of short videos to support technical procedures.
This position will also support the engineering team on validation protocols and reports.
You will be responsible for:
* Develop and update process documentation including assembly procedures, test procedures, routers, travelers, BOMs, process flows, and process FMEAs.
* Work with the training team to develop short videos that can supplement hands on training.
* Ability to work in cross-functional teams that span global operations.
Proficient in English verbal and written communication.
The ability to translate WI and JIBs to and from German or work with a translator is necessary.
* Must enjoy team approach over individual contributions.
Ability to be a liaison with manufacturing assemblers and engineering teams to develop and edit work instructions and assembly documentation.
* Support and enforce company goals and objectives, policies and procedures, Good Manufacturing Practices, Good Documentation Practices, FDA QSR and ISO regulations.
Knowledge of FDA QSR and ISO regulations required.
* Regularly report on project status and key project metrics through scorecard presentations.
* Assist engineering team to qualify and optimize processes and tooling via documentation for IQ/OQ/PQ, ...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-11-05 07:22:13
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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:
Supply Chain Manufacturing
Job Sub Function:
Manufacturing Process Improvement
Job Category:
Professional
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose: The Technical Writer will support manufacturing with engineering change orders (ECO), work instructions (WI), job instruction breakdowns (JIBs), training documentation, and creating and editing of short videos to support technical procedures.
This position will also support the engineering team on validation protocols and reports.
You will be responsible for:
* Develop and update process documentation including assembly procedures, test procedures, routers, travelers, BOMs, process flows, and process FMEAs.
* Work with the training team to develop short videos that can supplement hands on training.
* Ability to work in cross-functional teams that span global operations.
Proficient in English verbal and written communication.
The ability to translate WI and JIBs to and from German or work with a translator is necessary.
* Must enjoy team approach over individual contributions.
Ability to be a liaison with manufacturing assemblers and engineering teams to develop and edit work instructions and assembly documentation.
* Support and enforce company goals and objectives, policies and procedures, Good Manufacturing Practices, Good Documentation Practices, FDA QSR and ISO regulations.
Knowledge of FDA QSR and ISO regulations required.
* Regularly report on project status and key project metrics through scorecard presentations.
* Assist engineering team to qualify and optimize processes and tooling via documentation for IQ/OQ/PQ, preventive maintenance, Gage R&R Studies, Process Capability St...
....Read more...
Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-11-05 07:22:04
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Procurement Specialist
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 join our North America Procurement Warehouse, Indirect Services team.
You’ll make a difference by developing and executing category strategies in support of the North America business segment to achieve variable cost productivity, working capital, and business financial goals.
In this role, you’ll lead the supplier selection, development, and overall supplier management processes, including managing the entire contract life cycle from request for proposal (RFP) to supplier exit. In addition, you will work closely with the global procurement lead, business units, and cross-functional teams to achieve strategic sourcing objectives for the commodity.
In this role, you will:
* Develop, maintain, and execute assigned category strategies, category knowledge, and processes, ensuring the category strategies are informed, relevant and up to date
* Provide input on market dynamics (e.g., identify potential suppliers, assess market trends, etc.), supplier landscape, and business needs.
* Monitor supplier performance indicators and initiate supplier reviews as required or in accordance with agreed programs to drive improvement and reduce risk across the regional enterprise
* Build relationships with suppliers based on the foundation of trust and credibility by demonstrating integrity, commitment, and results orientation to drive and deliver results
* Maintain an effective business relationship with all suppliers and stakeholders based on clear, concise group and personal communication
* Support execution of NA category cost / sourcing events and initiatives
* Manage day-to-day inquiries from stakeholders related to the procure-to-pay process
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
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 we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you ...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-31 07:23:40
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
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/.
Johnson & Johnson has entered into an agreement to acquire Intra-Cellular Therapies, Inc, a biopharmaceutical company focused on the development and commercialization of therapeutics for central nervous system (CNS) disorders. With a differentiated commercialized therapy and promising clinical-stage pipeline that complements our current areas of focus, this acquisition brings us one step closer to achieving our ambition of becoming the #1 neuroscience company worldwide.
Intra-Cellular Therapies, a Johnson & Johnson company, is on the path to be the #1 leader in neuroscience.
With an exceptional suite of products and a commitment to transforming patient lives, we are expanding our CAPLYTA® medical team to support our growing impact in psychiatry.
The Director, Medical Communications & Scientific Exchange (MCSE) role will provide strategic leadership, direction and oversight for neuroscience MSL communications, medical communications, and Scientific/Congress communications strategies across the ITCI portfolio.
This position is responsible for developing and executing strategies for providing quality and compliant data dissemination, medical information services, medical education and medical review of externally facing resources.
This position also includes responsibilities in recruiting, hiring, training and providing stretch opportunities for the organization.
Creates a work environment that promotes continuous learning, open exchange and sharing, and fostering a team environment amongst associates.
This is a home office (Titusville, NJ) based position with up to 20% travel.
This role will report to the VP, US Medical Affairs ITCI.
Key Responsibilities:
* Lead the development of...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-31 07:08:39
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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: 2025-10-31 07:07:16
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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:
Sales Enablement
Job Sub Function:
Customer Success Management
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Customer Success Associate – Shockwave Medical to join our team located in Santa Clara, CA.
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Customer Success Associate will provide professional, day-to-day support and communications with our field sales representatives and clinical specialists, as well as customers, by utilizing a broad knowledge of Shockwave Medical products, services, and policies.
In addition to processing trunk stock, consignment, and direct orders, the CSA will play an essential role in order management analytics and value-added initiatives.
Essential Job Functions
* Be the point-person for a US sales region, owning all the case requests and order needs.
* Actively manage Customer Service cases in Salesforce to ensure response times to customers meets and exceeds service level agreement levels.
* Significant knowledge of account deta...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-18 08:21:55
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Global Operations Communications is a team of global communication business partners, responsible for strategic communications around Global Operations topics.
With our communications expertise, we drive conversations and share our strong story with employees, customers, patients, thought leaders and other key audiences.
We work with our colleagues to shape and protect the company's reputation through strategic, proactive communications that engage, inform and inspire our external audiences, colleagues and collaborative partners.
And we are looking for a new team member.
Your responsibilities
Your development and training are our priority: Therefore, we attach great importance to you being able to work on diverse tasks and always learning something new.
Within the scope of your traineeship, you will gain insights into the various instruments of corporate communication for Global Operations and actively shape them.
Your tasks include in particular:
* You manage your own projects from the initial idea and target group analysis, through the communication concept to the final implementation
* You are involved in editorial strategy and planning for Global Operations Communications, identifying topics of interest for the respective stakeholders and create and maintain editorial plans
* You independently write articles for internal & external media (e.g., intranet, newsletters, social media, info screens, events)
* You help the team develop and implement new measures with your creative ideas and impulses, so that together we can take communication to a new level
Your profile:
* You have successfully completed a degree (Bachelor or Master) in media studies, communication studies, journalism, corporate communications, communication management or a similar course of study
* You have already gained editorial experience in corporate communications or journalism
* You are enthusiastic about writing and preparing various topics for different communication channels and enjoy working conceptually
* You are good at and enjoy organizing e.g.
meetings or town halls and setting-up structured comms planning
* You are creative and contribute innovative ideas for employee and leadership communication
* You are a team player and enjoy interacting with people
* You have good knowledge of Google applications and Office applications
* You are proficient in English and not afraid of talking to internationals in person, via phone or emai...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-15 08:19:09
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Job Category:
Manufacturing/Operations
Job Family:
Plant Production
Work Shift:
GN (United States of America)
Job Description:
The Alternate Chunk Utility positions are responsible for filling in for Vacations, Floating Holidays, Sick days and any other reason for a vacancy for all Chunk Positions (Chunk Heavy Utilities, Chunk Cutters, Chunk Knockdown, Chunk Operators, and CSPs).
The Alternate Chunk Utility will be cross-trained on all Chunk positions and Chunk production lines.
As the partner learns all of these positions, future cross training in Material Handling and/or Shred will be required as needed.
Work with Leaders and fellow partners to ensure Food Safety and Partner Safety.
Understand and execute standard operating procedures relative to position.
Perform all PCP and CCP checks required for position.
Follow reaction plan for Food Safety, Food Quality and customer requirement outages.
Be able to identify and understand customer requirements and assist in assuring proper operation of equipment.
Record accurate data on production reports.
Other duties may be assigned.
Follow reaction plan for Food Safety, Food Quality and customer requirement outages and by contacting TA/TL.
Complete sanitation of production lines for both midweek sanitations and full cleanups.
Position will also assist in preventative maintenance on equipment.
* English speaking / reading is required in this position as well as the comprehension of the English Language
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, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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Type: Permanent Location: Clinton, US-MO
Salary / Rate: Not Specified
Posted: 2025-10-03 09:00:09
