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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, High Wycombe, Buckinghamshire, United Kingdom, Leiden, Netherlands
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
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-003029
* United Kingdom, Belgium, Netherlands - Requisition Number: R-006636
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Global Labeling Operations Specialist.
This position is a hybrid role and can be located in High Wycombe, United Kingdom; Beerse, Belgium; or Leiden, Netherlands.
The Global Labeling Operations Specialist will be responsible for the following:
* Act in role of Reference Safety Information (RSI) steward in support of Clinical Trial management, including monitoring changes to comparator labels. Communicate changes to Clinical, Safety, and Regulatory teams in accordance with documented timelines; and tracking completion of impact assessments.
* Track key labeling milestones and deliverables using tracking tools, document repositories, and other related systems and technologies.
* Support the development, preparation, monitoring, and communication of Key Performance Indicators (KPIs) and metrics related to comparator labels and other labeling outputs and processes.
* Manage/monitor process communications, department mailboxes, and collaboration portals.
* Provide input and support for audits and inspections.
* Support process improvements and successful commu...
....Read more...
Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-03-29 07:08:23
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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 Engineering
Job Sub Function:
Manufacturing Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Raynham, Massachusetts, United States of America
Job Description:
Johnson & Johnson is currently recruiting for an Engineering Internship (Summer 2025) for our site located in Raynham, MA.
Candidates will be required to be onsite.
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/.
Here, your career breakthroughs will change the future of health, in all the best ways.
And you’ll change, too.
You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love.
Amplify your impact.
Join us!
The J&J Engineering Summer Internship Program is an 8-week internship experience targeted to rising first-year college students who are pursuing a STEM course of study at the university level.
Internships are hosted in J&J sites across the US and will support either the Supply Chain or Research & Development functions.
This first-of-its kind internship program provides each selected student with real-life hands-on experience, coaching and mentoring, networking opportunities, as well as the opportunity to meet people from various schools throughout the country.
As this unique internship is targeted at students who have very likely never worked in a corporate environment, an intentionally designed, engaging educational experience has been planned throughout the internship to ensure you feel supported and have all the tools you need to be successful.
When you join our family, you will work on projects that improve your leadership, analytical, and project management skills.
Cross-functional teamwork provides an opportunity to partner with a variety of people in the organization across all our sectors; Innovative Medicine, MedTech, and Corporate/Enterprise.
We offer an interactive team environment, where your capabilities and skills will be developed t...
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Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:08:16
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Intégrer Johnson & Johnson Innovative Medecine, la division pharmaceutique du Groupe Johnson & Johnson, leader mondial dans le domaine de la santé (126500 collaborateurs dans le monde, 265 entreprises présentes dans 60 pays), c'est participer au développement de solutions thérapeutiques innovantes et partager notre volonté de changer la prise en charge médicale pour mieux répondre aux nouveaux enjeux de santé publique.
Rejoindre nos équipes, c'est s'épanouir dans une entreprise à taille humaine tout en bénéficiant des opportunités d'un grand groupe.
Nous travaillons pour que chacun puisse exprimer le meilleur de soi-même, afin de valoriser toutes les individualités.
Nous agissons en faveur de la diversité des talents qui nous rejoignent.
Ancrées dans notre Credo, la diversité et l’inclusion contribuent à valoriser le caractère unique de chacun de nos collaborateurs.
Johnson & Johnson est fier d'être un employeur qui prône l'égalité des chances.
Johnson & Johnson Innovative Medecine France recrute un analyste Business Intelligence en alternance
Contrat Alternance d’une durée de 12 mois - début en Septembre 2025
Localisation : Issy-Les-Moulineaux
Intégré au sein de l’équipe Business Intelligence, vous assisterez l’équipe Business Intelligence, dont les enjeux sont la compréhension fine de nos marchés et le pilotage de la performance de nos produits via des reportings clairs facilitant les prises de décision et la conduite d’études de marché.
Dans ce cadre, votre rôle sera :
* Accompagner les business analystes dans le suivi de la performance, et sur leurs besoins Ad Hoc : réalisation de brief études de marché, synthèse de veille concurrentielle, Cadrage et animations de workshop, …
* Être en support de l’équipe excellence opérationnelle dans la co-construction et la pérennisation de dashboard harmonisés sur les différentes aires thérapeutiques
* De former les équipes et jouer le rôle de modération sur notre plateforme de remontée d’insight.
Qualifications - External
Vous êtes actuellement étudiant en 3è cycle parcours scientifique, école de commerce, DESS, école d’ingénieurs, statisticien + 3e cycle marketing.
Vous possédez :
* u...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-03-29 07:08:15
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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:
Scientific/Technology
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
About Oncology
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.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
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 MSL to be in Shefayim.
Key Job Activities:
* Keeping abreast of medical and scientific knowledge
* Creating and fostering a network of partnerships with experts
* Working cross-functionally within the company to become a valuable team member
* Providing high level scientific engagement with experts, while utilizing multichannel platforms
* Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
* Scientific support and training to company sales representatives and other peers
* Supports and initiates evidence generation via research and publications
* Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
* Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
* Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
* Actively involved in strategy and action plans related to local reimbursement of products
The role is mainly field-based ( 85%) , requires agility with regards to travel & work hours
Requirements:
Education
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
* Previous experience working in the pharmaceutical industry or research company- an advantage
* High-competency in project & customer-affairs management
Knowledge:
* Deep scientific & clinical kn...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-03-29 07:08:07
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
People Leader
All Job Posting Locations:
Chicago, Illinois, United States, Santa Clara, California, 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/.
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
This position is fully remote but must be located in the Chicago area.
The Regional Sales Director will build and develop a regional sales team to deliver best in class performance for revenue and growth.
Responsible for building and managing the regional sales force and generating revenue and creating a successful strategy.
Work closely with Marketing, R&D and Area VP of Sales to identify market needs and execute on the sale/commercialization of new products.
Essential Job Functions
* · Build, oversee and help drive a team of regional field sales representatives that maximize sales revenues, attain corporate objectives and exceed sales goals
* · Forecast annual, quarterly, and monthly sales revenue streams accurately
* · Identify, develop, and implement effective sales plans and strategies
* · Develop specific revenue plans for sales teams as needed to ensure growth in all products/services targeted by the organization
* · Provide coaching, advice, support, motivation or information to help individua...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:59
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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 Planning
Job Sub Function:
Inventory Management
Job Category:
People Leader
All Job Posting Locations:
US014 MA Raynham - 325 Paramount Dr, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Senior Manager, Global Inventory Management.
This position is primarily located in West Chester, PA with consideration for other J&J Medtech locations within the US, Ireland, and Switzerland.
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):
Ireland - R-006580
Switzerland - R-006579
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The manager will be accountable for delivering inventory targets and optimization programs for DPS (globally); covering Joints Reconstruction, TECA (Trauma-Extremities-Craniomaxillofacial-Animal), Spine, Sports & Shoulders and Power Tools/ Robotics.
This program covers primary and secondary Hubs Entitlement, including some Regional/Market DCs (via MEIO), Lead Time improvement, Cycle Inventory optimization, among others.
Responsibilities:
* People: Leads and develops a team of planning analysts, who drive Inventory Management for all DePuy Synthes Platforms: Joints and TECA (Trauma / Extremities / Craniomaxillofacial / Animal), assessing and implementing improvement plans.
* Process: Drives adherence to Plan Transformation Blueprints
* Lead: Serves as planning primary point of contact for Global Inventory; collaborates with DPS Regional SC Planning teams, Finance and Commercial Business Partners to deliver targets and contingency plans.
* S&OP/IBP: Accountable for Global operational inventory monthly reporting process and budget cycles (BP, JU, NU and revisions).
* Parameter optimization: Drives detailed understanding of key inventory parameters, such as MOQ, EOQ, lead times, master data and supply variability trends.
* Multi-Echelon Inventory Optimization (MEIO): Drives maturity of MEIO process / tool and challenges inventory policies.
* LRFP: Coordinates annual Long Term / Strategic...
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Type: Permanent Location: West Chester, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:55
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, 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
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-003029
* United Kingdom, Belgium, Netherlands - Requisition Number: R-006636
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Global Labeling Operations Specialist.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; or Horsham, PA.
The Global Labeling Operations Specialist will be responsible for the following:
* Act in role of Reference Safety Information (RSI) steward in support of Clinical Trial management, including monitoring changes to comparator labels. Communicate changes to Clinical, Safety, and Regulatory teams in accordance with documented timelines; and tracking completion of impact assessments.
* Track key labeling milestones and deliverables using tracking tools, document repositories, and other related systems and technologies.
* Support the development, preparation, monitoring, and communication of Key Performance Indicators (KPIs) and metrics related to comparator labels and other labeling outputs and processes.
* Manage/monitor process communications, department mailboxes, and collaboration portals.
* Provide input and support for audits and inspections.
* Support process improve...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:47
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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:
Communications & Corporate/External Affairs
Job Sub Function:
Corporate Social Responsibility
Job Category:
Professional
All Job Posting Locations:
Mumbai, India
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/.
Position Summary
The Global Health Equity team advances equitable access to quality care through championing nurses and community health workers, enabling community-centered and culturally conscious care, and supporting access to our medicines and technologies.
The Senior Manager, Global Health Equity India, will cultivate existing and develop new partnerships to strengthen collaborative efforts across India, with responsibility to implementation and management of GHE programs.
This is an external facing role that requires positive relationship and partnership leadership skills, the ability to operationalize plans, and a proactive approach to bring partners to the table.
This role will also contribute to programmatic design and evolution that will translate into local/regional implementation strategies.
This individual is responsible to craft and deliver comprehensive plans, inclusive of, but not limited to:
* Existing Partnership Oversight and Management: Leverage and nurture significant external partner relationships and resources for scaled implementation to increase health impact goals.
* External Relationship Development: Evaluate and analyze current partnerships while recommending future collaborations that align with organizational strategy.
This role involves scanning and assessing the external public health ecosystem to identify organizations’ needs for partnerships and matching these with the capabilities that Johnson & Johnson can bring as an extensive cross-sector and cross-functional entity.
* Initiative Generation and Scaling: In collaboration with the global Program Delivery & Impact team, this person will work closely to support Strategy, Grants, Impact, and Deliv...
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Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:37
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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:
R&D Product Development
Job Sub Function:
R&D Digital
Job Category:
Scientific/Technology
All Job Posting Locations:
Bangalore, Karnataka, India, Hyderabad, Andhra Pradesh, India, Mumbai, Maharashtra, India
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.
Within J&J Innovative Medicine, the R&D Business Technology team is the strategic information technology partner providing innovative technology solutions that enables Global Development to expertly deliver on our portfolio and helps provide transformative medicines to patients around the world while proactively improving agility, embracing innovation and creating the organization we need to deliver in the future.
The Lead Engineer will own the vision and prioritization of new technical features and improvements for our products within Clinical Data Management and Analytics to meet business needs.
This position encompasses both execution and transformation roles behind technical solutions, ensuring that the product’s architecture aligns with the technology roadmap and adheres to our engineering standards.
The role will be responsible for designing and implementing secure, scalable, and efficient cloud solutions while also overseeing operational processes to ensure efficient performance and reliability.
This role will require building strong internal and external partnerships and will collaborate daily with other team members located in US, Europe and Asia.
It uniquely combines technical and programming skills with a broad exposure to clinical data processing as well as collaboration with multiple functions in clinical development.
Key Responsibilities
Technical Leadership and Expertise:
* Define and lead all aspects of the overall engineering and technology architecture, roadmap, and technical decisions, using modern design patterns and architectural principles for the product needs in coordination with the Technical Product Manager, Product Group Lead Engineer, and Business U...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:10
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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 Control
Job Category:
People Leader
All Job Posting Locations:
San Lorenzo, Puerto Rico, United States (inactive)
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Johnson & Johnson is currently seeking a Quality Microbiology Supervisor, Laboratory to join our outstanding team in San Lorenzo, Puerto Rico.
In this role under the direction of the Quality Laboratory Leader and with the objective of maintaining high quality standards for the product manufacturing process and the compliance with regulatory requirements, you will supervise day-to-day activities of the Quality Control Laboratory Technicians, in accordance with QSR and Ethicon written specifications and quality standards.
You will be responsible for establishing and overseeing the laboratory and/or equipment, providing a variety of testing services and technical support to customers and supporting Enterprise-wide initiatives that enhance the overall level of compliance!
Key Responsibilities:
* Supports Internal Compliance Function as required (QSR/ISO training, internal and external audits, trends analysis, etc.).
* Coordinate the most efficient use of laboratory resources for the analysis and disposition of raw materials, in-process, stability samples and final products.
* Ensures compliance of areas of responsibility with the department, company, OSHA, ISO and QSR concerning safety, good housekeeping practices and manufacturing practices.
* Monitor the performance of the CME (Controlled Manufacturing Environment), including but not limited to Product Bioburden monitoring.
* Coordinates and monitor the Plant’s Dose Audit Program.
* Provide expertise in the design, development, and implementation of suitable quality systems for new or existing products & processes.
Facilitate the design transfer process between corporate and plant environments.
* Directly supervises QA Laboratory Technicians and QA Coordinators as required and trains, develops and evaluates subordinates.
Qualifications
Education:
* A minimum of a Bachelor’s degree or University equivalent in Scientific discipline is required, a concent...
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Type: Permanent Location: San Lorenzo, US-PR
Salary / Rate: Not Specified
Posted: 2025-03-29 07:07:06
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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:
Project/Program Management Group
Job Sub Function:
Project/Program Management
Job Category:
Professional
All Job Posting Locations:
Wien, Austria
Job Description:
Aufgaben:
* Selbständige organisatorische Unterstützung von Projektverantwortlichen bei medizinisch-wissenschaftlichen Veranstaltungen (z.B.
Kongresse, Workshops, Advisory Boards).
* Primärer Ansprechpartner für interne und externe Stakeholder bei organisatorischen Anliegen.
* Planung und Durchführung von Events, inklusive Logistik, Budgeteinhaltung und Einhaltung interner Richtlinien.
* Koordination von Meetings und Kommunikation mit allen Beteiligten sowie Überwachung der Projektfristen.
* Verwaltung diverser Verträge und Abwicklung von Zahlungsprozessen an Lieferanten/Dienstleister.
* Einhaltung aller Compliance-Vorgaben und gesetzlicher Anforderungen, einschließlich der Sicherstellung der erforderlichen Dokumentation für HCBI.
Kompetenzen:
* Dienstleistungsorientierung und Teamfähigkeit.
* Gute IT-Kenntnisse für verschiedene Systeme.
* Erfahrung im Eventmanagement und Vertragswesen ist von Vorteil.
Wir freuen uns auf Ihre Bewerbung, wenn Sie eine strukturierte und serviceorientierte Arbeitsweise mitbringen!
Für diese Position bieten wir Ihnen ein Jahresbruttogehalt ab EUR 41.000 (exkl.
variablen Anteils, auf Vollzeitbasis) in Österreich.
Die Bereitschaft zur Überzahlung, abhängig von beruflicher Qualifikation und Erfahrung, ist gegeben.
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Type: Permanent Location: Wien, AT-9
Salary / Rate: Not Specified
Posted: 2025-03-29 07:06:54
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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:
Communications & Corporate/External Affairs
Job Sub Function:
External Communications
Job Category:
Professional
All Job Posting Locations:
US017 NJ New Brunswick - 1 J&J Plaza
Job Description:
Johnson & Johnson is recruiting for a Director, Global Finance Communications.
This position is in New Brunswick, New Jersey.
Position Summary
The Director, Global Finance Communications will lead communications strategies that amplify J&J’s narrative regarding its financial positioning, business focus and strategic direction to external, financial and investor community and business media audiences.
The Director will be responsible for partnering directly with Investor Relations, business segments, communications colleagues, media relations and key stakeholders to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements, and other key financial events.
The Director will serve as the direct partner to the VP, Investor Relations, and Media Relations team, triangulating key messages and communications approaches to critical investor engagements and financial media opportunities for the CFO and other Finance leaders.
Responsibilities
* Lead communications strategies that amplify J&J’s financial positioning, business focus and strategic direction to the external, financial and investor community and business media audiences.
* Partner with Investor Relations and across business segments, communications colleagues, media relations and key stakeholder groups to develop, manage, optimize and executive communications strategies for quarterly earnings, financial reporting, M&A Announcements and other key financial events such as the annual shareholders meeting and investor days.
* Serve as the direct partner to the VP, Investor Relations and Media Relations team, triangulating key messages and optimal communications approaches to critical financial engagements, business and industry media and media opportunities for the CFO and other Finance leaders.
* Develop and maintain relationships with key media, trade, influential stakeholders, and communication partners.
* Lead a matrixed team of indirect resources, peer groups and agency vendors.
Required
* A minimum of bachelor’s degree
* 10+ years of experience in Communications
* People management with a focus on engagement and development
* E...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-29 07:06:53
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ERM is seeking a Senior Consultant, Safety and Industrial Hygiene with industry experience, to play a key role in growing our business in the Health and Safety service line.
The ideal candidate will bring H&S technical capability and deep understanding of business processes to help our clients proactively address their EHS risks and challenges.
As a health and safety professional, you will be responsible for supporting on a range of health and safety management projects to build a sustainable business locally, while networking with ERM's global technical team to share best practices across the industry.
This is an excellent opportunity for a senior-level professional looking to advance their career with a global Sustainability leader, and work with a team of outstanding professionals in over 40 countries around the world.
RESPONSIBILITIES:
* Support development and implementation of Safety Management Systems and risk assessments to ensure effective risk control and regulatory compliance.
* Perform incident investigations, development of corrective actions, verification/validation of controls, and learning from incidents. Support root cause analyses in conjunction with client leadership.
* Support life safety programs such as control of hazardous energy, fall protection, electrical safety, machinery safety, powered industrial vehicle, materials lifting, hot work, and fire safety.
* Support client industrial hygiene programs, including leading the qualitative and quantitative assessment of exposure risk.
* Assist in the development of solutions to complex technical and regulatory issues and concerns.
* Contribute to expanding ERM’s Safety Services business.
Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients.
Develop and expand client relationships that generate repeat business.
* Develop and manage innovative, behavior and performance outcome-focused approaches and programs for a variety of clients with complex technical/regulatory issues.
Design and direct corporate H&S strategies and programs in areas such as industrial hygiene, behavior-based safety, safety culture and leadership, serious injury and fatality risk reduction, compliance auditing, EHS management systems, process safety and risk management, construction safety, high-impact training, and general compliance support.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Manage a variety of tasks to achieve scope, budget and schedule targets while ensuring we meet and exceed our clients' expectations on deliverables.
* Build client relationships and nurture repeat business by continuously striving to Build a network within and outside of ERM that will enable you to leverage your skills and solve challenging multi-disciplinary client challenges.
REQUIREMENTS:
* BS/MS degree preferred. Equ...
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Type: Permanent Location: Ewing, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-29 07:06:28
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ERM is hiring a Construction Safety Specialist for a key data center construction project in Frederick MD. In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs for several ongoing construction projects.
The Construction Safety Advisor will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a full-time (40 hours), fixed-term position for a duration of 9 months, renewable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments.
And pre-task plans
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
* Coordinate local business continuity, emergency response, and crisis management plans.
Develop and test the plans.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with data center construction or large projects.
CHST certification a plus.
* Knowledge of construction project management software tools (i.e.
ProCore, eBuilder, SmartTagIt, etc.) is a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, fall protection, material handling, and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* A background and knowledge working with specific trades such as electricians, ironworkers, pipefitters etc.
is a plus.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability ch...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2025-03-29 07:06:28
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-03-28 07:37:15
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Operator – Packaging
As an Operator - Packaging at Elanco, you will play a crucial role in the manufacturing process of our farm and companion animal products.
You will work in a dynamic, team-oriented environment, contributing to production goals while adhering to safety, quality, and compliance standards.
Your work will directly impact the production of high-quality animal health products, supporting Elanco’s mission to improve animal health and enhance animal production globally.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Operate various production equipment such as compactors, forklifts, and sampling tools to support the manufacturing process
* Ensure compliance with current Good Manufacturing Practices (cGMP) and environmental standards throughout all production tasks
* Accurately document and verify production data, including batch records and equipment logs, to ensure traceability and regulatory compliance
* Maintain a safe work environment by adhering to all safety guidelines, wearing required PPE, and performing daily housekeeping to ensure cleanliness and organization of the work area
* Collaborate with team members across departments to address operational issues, improve quality, and meet production targets
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED (or equivalent experience)
* Required Experience: Previous experience in a manufacturing or production environment is beneficial but not required; strong mechanical and troubleshooting abilities are preferred
* Top 2 skills: Basic computer skills for data entry and documentation, excellent attention to detail to ensure accuracy in production and compliance
What will give you a competitive edge (preferred qualifications):
* Certification in the use of forklifts, Skid Loaders, Ariel Lifts, and other industrial equipment (depending on departmental needs)
* Previous experience working in a regulated manufacturing environment (cGMP or similar)
...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-03-28 07:28:16
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Record-to-Report Accounting Manager (Global Business Services)
Job Description
Record-to-Report Accounting Manager
Your Job
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.
Role Overview & Primary Accountabilities:
Operations
* Oversee Financial Reporting & Analysis, General Accounting and RTR Operations functions, including timely and accurate recording of all related transactions in accordance with accounting policies and procedures
* Manage monthly close process for Financial Reporting & Analysis, General Accounting and RTR Operations including reviewing account reconciliations, journal entries, key performance indicators, and financial statements.
* Prepare and review financial reports and analysis related to Financial Reporting & Analysis, General Accounting to provide insights to senior management.
* Work closely with cross-functional teams such as procure to pay, order to cash, country finance teams, logistics, and operations to ensure proper accounting treatment of transactions related to Financial Reporting & Analysis, General Accounting and RTR Operations.
* Ensure compliance with all relevant accounting standards, policies, and procedures.
* Ensure that all financial information is timely and accurate, and that appropriate controls are in place to manage financial risk.
* Develop and implement process improvements to drive standardization, increase efficiency, and effectiveness of the Financial Reporting & Analysis, General Accounting and RTR Operations functions.
* Manage and develop a team of accounting professionals, providing coaching and feedback to promote growth and development.
Leadership & Transformation
* Build a stable and sustainable talent pool and driving expertise in the respective subject matter while ensuring succession plans are in place across all levels in the team.
* Develop leadership capabilities of team leaders to enhance collaboration, strategic thinking, and developing talent.
* Be a team player with strong networking and interpersonal skills to build trust among other peers, team members and stakeholders, whilst positively instilling a ‘transform to grow’ mindset across the Record to Report function.
* Be a change champion by demonstrating out of the box thinking and challenging the status quo to enhance business process efficiency and drive growth opportunities for GBS and helping create high performing teams.
K-C Internal Only
* Develop an insights and foresights driven team to manage transformation effectiv...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-03-28 07:24:26
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Quality Engineer - DX
Job Description
Your Job
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 your role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
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 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 at Kimberly-Clark; you just need to log on!
Led by Purpose.
Driven by You.
About You
You’re driven to perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and the business.
Main responsibilities:
* Develop and execute manual and automated test scripts using Selenium and other automation tools to ensure the quality of our web platforms.
* Perform thorough testing of web applications, identifying and documenting defects and issues.
* Ensure that all testing covers compliance scenarios, such as user consent, data handling, and privacy regulations (CPRA/CCPA, GDPR).
* Collaborate with developers and product owners to ensure quality standards are met throughout the development lifecycle.
* Continuously improve testing processes and methodologies to enhance product quality and efficiency.
* Monitor and report on test results, providing insights to improve product performance and compliance.
* Stay updated on the latest testing tools and technologies, applying them to enhance our QA processes.
* Work closely with legal and compliance teams to ensure that all testing aligns with regulatory requirements.
* Participate in code ...
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Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-03-28 07:24:02
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Get to know us: NOVO Health Services offers linen management solutions to the healthcare industry.
NOVO Health keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
NOVO's wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
NOVO's regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
POSITION SUMMARY:
The Soil Room Attendant is responsible for removing soil from bags, sort and prepare for washing.
ESSENTIAL FUNCTIONS:
• Open up bags at the breakout table and send linen up the belt.
• The primary cart mover (the attendant closest to the soil cart) brings the empty soil cart away from the belt, puts a new cart in area and takes the empty cart and pushes it to the cart area.
• The bag breaker attendant breaks open the bags.
• The attendants on the belt perform the following tasks:
o One attendant sorts of large pieces consisting of bath blankets, flat sheets, draw sheets and thermals.
o The second attendant sorts the second largest pieces – underpants, patient gowns, and fitted sheets.
o The third attendant will handle all the rest of the pieces such as bath towels, washcloths, hand towels, and scrubs.
• The last stage of the soil room process is hoist and weigh or staging.
The attendant pulls the full slings away as they fill up, puts an empty sling in, weighs the full one, records the information and hangs it.
• Adhere to quality standards in terms of soil sorting and cart cleaning.
• Understand, observe and adhere to all safety procedures and policies.
• Assist and perform other duties as assigned.
High School Education, GED and formal education / training preferred.
• Good analytical skills to be able to determine number of carts required for orders.
• 1 to 2 years of experience in manufacturing, production, or service industry
• Ability to work in a noisy fast paced environment.
• Ability to stand, walk, bend, stoop, twist, reach, and stack individual items from machine for long periods.
• Ability to lift up to 100 pounds.
• Ability to push or pull a cart that may weigh 100 pounds.
• Demonstrated customer service and organization skills.
• Strong interpersonal and communication skills.
What we can offer you as a full-time associate:
Competitive pay
Paid Holidays
Paid Time Off Program (PTO)
401(k) w/Employer Match
Flexible Spending Account (FSA)
Health Savings Account (HSA)
Medical, Dental, and Vision Programs
Basic Life/AD&D Insurance
Long-Term Disability (LTD)
Why work for Novo Health Services?
NOVO Health Services strives to be the employer of choice in the hospital sterile and hygienically clean linen industry.
To do that, we provide a safe, positive work environment where our associates ...
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Type: Permanent Location: Rockmart, US-GA
Salary / Rate: Not Specified
Posted: 2025-03-28 07:19:55
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SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains.
SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply.
SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH.
Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery.
SRI is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions.
Get to know us: SRI-Healthcare, with headquarters in Atlanta, GA, offers linen management solutions to the healthcare industry.
SRI keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
SRI’s wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
SRI’s regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
SRI-Healthcare is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with both Healthcare Laundry Services as well as Sterilized Reusable Surgical Solutions.
Job Summary:
We are currently looking for a Soil Sorter, at our Mebane, NC Healthcare Laundry facility.
We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills.
If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
The successful candidate will:
* Able to understand and follow Standard Operating Procedures (SOP’s).
* Open laundry carts and empty hamper bags onto sorting table.
* Sort linen by fabric type.
* Accurately weigh sorted loads and send linen to washers via negative air system as well as operate laundry equipment in either automatic or manual mode.
* Identify instruments, sharp items, hospital-owned linen, and other foreign objects and place them in appropriate receptacles.
* Place empty laundry carts in cart wash and operate washing machinery.
* Deposit all instruments and other washable, returnable objects in wash rack and process through dishwasher or commercial washer, as well as wash all stainless basins.
* Completely clean and disinfect soil sort area at end of shift.
* Mentor / train fellow associates.
* Other duties as assig...
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Type: Contract Location: Mebane, US-NC
Salary / Rate: Not Specified
Posted: 2025-03-28 07:19:23
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland, High Wycombe, Buckinghamshire, United Kingdom, Turnhout, Antwerp, Belgium
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
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-000701
* Canada - Requisition Number: R-002921
* United Kingdom, Belgium, Switzerland - Requisition Number: R-002952
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and can be located in Beerse, Belgium; High Wycombe, United Kingdom; or Allschwil, Switzerland.
The Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provides advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
This role may collaborate with external partners.
* Contribute to and implement the global labeling strategy, including demonstrating an understan...
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Type: Permanent Location: Turnhout, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-28 07:11:50
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Provides statistical support to specific segments of a study/development program, including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and/or marketed product needs in Janssen.
Demonstrates data analytics expertise based on a foundation of statistical principles and uses relevant computational tools for study, experiment, or trial research objectives.
Ensures application of appropriate statistical methods and generation of accurate and reproducible results working independently or by providing specifications to statistical programming colleagues.
Produces clear, concise, well-organized, and error-free computer programs and statistical reporting content.
Collaborates and communicates effectively with cross-department team members and senior colleagues to deliver on goals and objectives.
Proactively recognizes need for additional help for complexities or integration beyond on own expertise.
Coaches more junior colleagues in techniques, processes and responsibilities.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-03-28 07:11:47
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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:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Professional
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
MISSIONS
Assurer l’assistance administrative et organisationnelle du Directeur et de ses équipes afin de contribuer à l’efficacité des actions menées par la Direction.
ACTIVITES PRINCIPALES
Par la maîtrise des logiciels spécifiques (Concur, eMarket Place, ICD, CRM, iMR, Docsouring…) et la connaissance des procédures opératoires internes et le respect du code de conduite de l’entreprise :
Assister et assurer le secrétariat du Directeur et de ses équipes
- Gérer l'agenda du Directeur et organiser ses déplacements.
- Coordonner les rendez-vous en interne et en externe.
- Traiter les notes de frais.
- Gérer les commandes auprès des fournisseurs, les contrats et suivre le règlement des factures ainsi que le classement des documents correspondants, selon les règles de l’entreprise.
- Coordonner et piloter le suivi du budget dans le respect du budget alloué en début d'année.
(Collaboration avec le P2P, clôture annuelle)
- Assister l’onboarding des nouveaux collaborateurs de la Direction
Supporter l’activité des équipes en fonction des demandes spécifiques de la Direction marketing-ventes
- Accompagner l’équipe marketing dans la gestion du matériel promotionnel
- Gérer les indemnités RP mensuelles pour l‘équipe ventes
Coordination et organisation des reunions et des séminaires
- Organiser l’ensemble des réunions interne et externe de la Direction et des évènements spécifiques en relation avec des prestataires externes.
en particulier, participer à l’organisation des séminaires et des réunions de mi-cycle
- Collecter, organiser l’information pour les réunions de service.
- Assister aux réunions, rédiger et diffuser les comptes rendus
Faciliter la diffusion de l ’information
- Assurer l’interface et la coordination entre les différents services
- Etablir un relationnel de qualité avec des interlocuteurs internes et externes variés
- Favoriser une collaboration efficace au sein la Direction
Être l'interlocutrice privilégiée des équipes concernant les outils d'entreprise (sensibilisation et accompagnement sur les nouveaux outils)
Formation générale :
Formation supérieure 1er cycle de type BTS, DUT
Expérience professionnelle :
E...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-03-28 07:11:39
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Wilson, North Carolina, United States of America
Job Description:
Johnson & Johnson Family of Companies is currently recruiting for a Senior EHS Engineer Occupational Safety in Wilson, NC.
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 Summary:
The Senior EHS Engineer Occupational Safety is responsible for supporting and delivering the BioNC all Occupational Safety requirements incl.
for instance EHS by Design, Machine Safety, Electrical Safety, Construction Safety, Contractor Mgmt.
and linked Risk Assessment processes in compliance with Johnson & Johnson (J&J) requirements and US Code requirements, project design and delivery process in support of J&J's North Carolina Biologics expansion program etc.
Key Responsibilities:
* Provide technical support and guidance on EHS standards and best practices to various project stakeholders.
* Participate and support project Risk Assessments/ RA, HazOp process and ensure identified action are incorporated into design delivery process.
* Document all EHS reviews at various stage-gates in the project and manage measures to achieve action closure in a timely manner.
* Ensure EHS compliance and Occupational Safety considerations are integrated into design processes from the earliest stages to prevent rework and ensure compliance.
* Collaborate with project teams to ensure U.S.
Occupational Safety requirements incl.
J&J machine safety requirements etc.
are fully incorporated into the vendor bid stage technical review process and EHS compliance considerations are fully integrated into design processes at the earliest stages possible to prevent rework and ensure compliance delivery.
* Conduct risk assessments/RA and develop compliance strategies in line with regulatory and J&J...
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Type: Permanent Location: Wilson, US-NC
Salary / Rate: Not Specified
Posted: 2025-03-28 07:11:35
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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 Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Latina, Italy
Job Description:
- As Project Leader ensure planning and coordination of the activities in collaboration with the various departments involved in the implementation of the projects
- Proactively identifying risks to define mitigation strategies
- Assess the business impact, quality, compliance and safety involving stakeholders from other departments
- Ensure compliance with the time of introduction, balancing the base business production needs
- Ensure timely communication to MSAT Sr Mgr and Global Functions to align with the production plans themselves
- Ensure the timely availability of quality documentation for the project execution
- Performs and/or support investigations for non-conformances in case of occurrence during project activities
- Process Analytical Technologies, Multivariate Analysis & chemometrics application
Requirements
· Master’s degree in Engineering, Farmacy, CTF or Chemistry
· At least 6th month experience in the pharmaceutical industry (Oral Solid production is preferred)
· Academic knowledge of lines, processes, materials and equipment for pharmaceutical process (oral solid pharma production competence is preferred).
· Good knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products
· Basic experience in Project Management
· Able to work in a multidepartment and dynamic environment and to deal urgencies on the shop floor
· Ability to coordinate a cross functional team to ensure the correct execution of the project activities according to the agreed timing
· Skills of ownership and accountability
· Skilled in problem-solving and decision making
· Knowledge and basic experience in PAT, MVA and Chemometrics applications.
· Fluent in English (B2 level and above)
· Capacity to lead calls with costumers
· Capability to easily connect with people and prepare smart proposals for project approaches
· Excellent oral and written communication skills
· Ability to present scientific data and concepts effectively to international standards
....Read more...
Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-03-28 07:11:21
