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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: Animal Health Clinical Research Associate
Operationally manage the logistics of ongoing animal clinical trials performed at the Fort Dodge, IA site including, but not limited to: animal socialization, the collection of clinical samples and/or observations, clinical operations, and the execution of other study events.
Your Responsibilities:
* Animal Care and Procedures: Independently performs and completes animal procedures in compliance with regulations, working instructions, and SOPs, including administering test articles, collecting samples, and conducting health observations.
* Study Execution and Management: Leads and manages multiple assignments related to R&D animal product development, executes in-life study events, coordinates scheduling and resource management, and supports business-facing functions like study scheduling and sourcing.
* Protocol Development and Review: Reviews and provides recommendations for study protocols and SOPs, collaborating with stakeholders to identify potential impacts on study execution, animal welfare, and regulatory compliance.
* Data Management and Quality Assurance: Performs concurrent documentation of study activities, reviews raw data for accuracy, and ensures high-quality results.
* Collaboration and Communication: Establishes and maintains relationships with key stakeholders (Study Directors, Laboratory Staff, Animal Care Staff) and communicates effectively within the team and across functions.
Troubleshoots problems and implements corrective actions as needed.
What You Need to Succeed (Minimum Qualifications):
* Veterinarian Technician Certificate or Associate Degree in relevant field (examples: biology, animal science, etc.) with relevant animal experience.
* Required to achieve AALAS (American Association of Laboratory Animal Science) described LAT (Laboratory Animal Technician) within one year of employment.
What Will Give You the Competitive Edge (Preferred Qualifications):
* Bachelor of Science in relevant field (examples: biology, animal scienc...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 77000
Posted: 2025-07-02 09:16:15
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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: Sr.
Specialist - Downstream Operations Technician
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights incl...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2025-07-02 09:16:05
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Senior Software Engineer (Billing and Accounting)
Systems & Software - Remote
Join Harris' Systems & Software, a pioneering force in the Utility CIS arena, as a Senior Software Engineer.
Our focus is on developing business applications that push technological boundaries.
In this role, you will engineer backend solutions primarily for billing systems, designing new features and maintaining our industry-leading software package.
Your contributions will propel our customers and the entire utility sector forward.
We are particularly interested in engineers who have robust experience in backend billing and accounting applications, specifically within the utility industry.
You will collaborate with some of the brightest minds in the field, equipped with cutting-edge tools and technology.
Apply Instructions: A cover letter (including a description of finance / billing / accounting experience) must be submitted for consideration for this role.
Please upload your cover letter and resume by following this guide: (https://youtu.be/1wsIR7JjhOo).
This position is remote and open to candidates across Canada and the US.
Salary range: $80,000 to $110,000 USD.
What will be your impact?
* Provide backend technical leadership and mentorship to team members.
* Lead design reviews and support Professional Services, R&D, and Support Departments with escalated technical issues.
* Work alongside QA to promote best practices, ensuring high quality across the team.
* Manage and participate in code reviews, providing critical feedback on backend designs and code.
* Identify and address potential risks that could affect project timelines.
* Implement accounting best practices in the design of backend billing and reporting applications.
* Support utilities in financial auditing processes.
What are we looking for?
* B.S.
in Computer Science, Computer Information Systems, Math, Accounting, or equivalent work experience.
* 5+ years of professional software development experience with a strong focus on backend development.
* A strong grasp of mathematical concepts and a passion for problem-solving.
* Proficient in Unix/Linux environments.
* Experienced with Oracle and PL/SQL or MS SQL Server and Transact-SQL.
* Demonstrates excellent work ethic, initiative, and the ability to thrive in a fast-paced environment.
* Outstanding interpersonal skills, with a proven ability to communicate effectively with both internal and external stakeholders.
* Eager to learn and excel, both independently and as part of a team.
What will help you stand out:
* Experience programming in COBOL.
* Deep expertise in backend development for billing and/or accounting applications.
* Fundamental knowledge of double-entry accounting, especially including knowledge of how cash transactions can post to both sides of the ledger.
* Strong familiarity with the utility sector.
* Proven track re...
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Type: Permanent Location: Springfield, US-IL
Salary / Rate: 110000
Posted: 2025-07-02 09:15:57
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Manager, DnA Analyst Team, National Medical Care, Inc., a Fresenius Medical Care N.A.
company, Lexington, Massachusetts (Remote)
Will lead a team engaged in developing business, functional, data, systems integration requirements and conducting data analytics with data visualization for storytelling to executives and delivering data analytics solutions and products.
Critical to the success of using data to drive decisions, is the implementation of business analytics, dashboards, and interfaces to support Fresenius cross-functional business operations and DnA strategic vision.
The DnA Analyst team will serve as members of the Global Data and Analytics Community at FMC.
Specific duties include:
* Provide leadership, coaching and development plans for all direct reports to maintain an engaged and productive workforce, partnering with Human Resources on employee matters.
* Work as a primary liaison among stakeholders to elicit, analyze, communicate, and validate functional and technical requirements and business and data processes.
* Lead team members, as well as work individually at all levels of the organization to obtain knowledge that facilitates problem resolution.
* Work closely with project managers to ensure data analytics projects are collaboratively resourced and ensure requirements and data use cases are clearly documented, understood, and communicated.
* Mentor team members and serve as a resource:
+ Develop standards, models, use cases, and scenarios for learning and set expectations.
+ Evaluate information gathered from multiple sources, reconcile conflicts, decompose high-level information into details, and distinguish user requests from the underlying needs.
+ Contribute to functionality and process design for enhancing or creating analytical solutions.
+ Provide guidance to appropriate analytical methods and tools to conduct extensive data discovery, analysis, and data mapping to inform the requirements and design of solutions to meet business needs.
+ Ensure reliability of data for solutions using queries and analytical techniques during the design, development, and testing phases.
* Collaborates and communicates with various teams to provide data analysis to support overall goals.
Requirements:
Position requires either (i) a Bachelor’s degree (or an equivalent foreign degree) in Computer Science, IT or a closely related field and 6 years of experience as a Data Analyst or (ii) a Master’s degree (or an equivalent foreign degree) in Computer Science, IT or a closely related field and 4 years of experience as a Data Analyst. Must also have had 4 years of experience (which can have been gained concurrently with either primary experience requirement above) working with the following:
* Interpreting and designing the flow of data between applications to support a business process activity;
* Json, SQL, PBI, Python and Tableau devel...
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Type: Contract Location: Lexington, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-02 09:14:57
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
...
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Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2025-07-02 09:14:09
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Alternant(e) Assistant Manager Operations
Job Description
A propos du poste
En tant que personne, vous êtes un apprenant – quelqu’un qui prend toujours l’initiative d’améliorer les choses et d’entraîner les autres avec vous.
Vous vivez votre vie en accord avec les valeurs les plus élevées d’intégrité et de qualité, en veillant toujours à ce que vos responsabilités deviennent une réussite à long terme.
Dans le cadre de ce rôle d’Alternant Assistant Manager Opérations, vous nous aiderez à fournir de meilleurs soins à des milliards de personnes dans le monde.
Cela commence par VOUS.
Nous recherchons un(e) alternant(e) Assistant Manager Operations en contrat d’apprentissage de deux ans au sein de notre usine Kimberly-Clark de Villey Saint-Etienne (54).
Vous serez au cours de votre contrat d’apprentissage amené(e) à travailler sur les missions suivantes :
* Déploiement des Indicateurs de Performance :
Déployer des indicateurs de performance pour la sécurité, l'environnement, la qualité, l'adhérence au planning de production, la performance des machines et les ressources humaines.
Déployer des paretos sur les indicateurs de panne, déchets et perte de vitesse concernant la performance des machines.
Sensibiliser les équipes de production à l'importance de la performance et assurer le déploiement des indicateurs dans toutes les équipes.
* Accompagnement au Déploiement de l’outil SAP PM :
Aider l'équipe projet SAP PM à déployer notre nouvel outil de GMAO (Gestion de Maintenance Assistée par Ordinateur).
Constituer les nomenclatures de pièces.
Accompagner les équipes dans l'utilisation du nouvel outil SAP PM.
A propos de nous
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
Vous connaissez déjà nos marques légendaires, tout comme le reste du monde.
En fait, des millions de personnes utilisent les produits Kimberly-Clark tous les jours.
Nous savons que ces incroyables produits Kimberly-Clark n’existeraient pas sans des professionnels talentueux, comme vous.
Chez Kimberly-Clark, vous ferez partie de la meilleure équipe qui s’engage à stimuler l’innovation, la croissance et l’impact.
Nous sommes fondés sur plus de 150 ans de leadership sur le marché et nous sommes toujours à la recherche de nouvelles et meilleures façons de performer - c’est donc là que vous avez une porte ouverte sur les opportunités.
Tout est là pour vous chez Kimberly-Clark.
Guidé par un objectif.
Piloté par vous.
A propos de vous
Vous performez au plus haut niveau possible et vous appréciez une culture de la performance alimentée par une bienveillance authentique. Vous voulez faire partie d’une entreprise qui se consacre activement à la durabilité, à l’inclusion, au bien-être et au développement de carrière.
Vous aimez ce que vous faites, surtout lorsque le travail que vous faites fait un...
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Type: Permanent Location: Toul Cedex, FR-54
Salary / Rate: Not Specified
Posted: 2025-07-02 09:12:26
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Gerente Júnior de Business Intelligence
Job Description
Nosso objetivo é oferecer um Melhor Cuidado para um Mundo Melhor e isso requer pessoas e equipes que se preocupam em fazer a diferença todos os dias.
Aqui, você irá contribuir com a sua experiência profissional, talento e motivação para continuar a levar nossas marcas cônicas e inovadoras para a vida de milhões de pessoas.
Nessa função, você vai nos ajudar a impactar a vida de milhões de pessoas ao redor do mundo.
Tudo isso começa com VOCÊ!
O Gerente Júnior de Business Intelligence irá atuar na estruturação e evolução da estratégia de dados da empresa.
Esse profissional será responsável por liderar iniciativas de análise e visualização de informações, garantindo que os dados sejam utilizados para embasar decisões estratégicas e melhorar a performance do negócio.
Principais Responsabilidades:
* Gerenciar e estruturar processos de Business Intelligence, garantindo a integração entre tecnologia e estratégia de negócios.
* Supervisionar a criação de dashboards e relatórios analíticos, assegurando que os dados sejam apresentados de forma clara e acionável.
* Realizar análises aprofundadas de sell-out e outros KPI’s da indústria, traduzindo números em insights estratégicos.
* Participar e apoiar nas discussões de negócio, trazendo dados e insights
* Orientar e apoiar analistas na manipulação de dados, modelagem em SQL e aprimoramento de ferramentas como Power BI.
* Definir melhores práticas de governança e qualidade de dados, garantindo confiabilidade e consistência nas informações utilizadas pelo negócio.
* Identificar oportunidades para automação de processos e aprimoramento contínuo das análises de Business Intelligence.
* Fomentar a cultura de dados na empresa, garantindo que diferentes áreas utilizem informações estratégicas para embasar suas ações.
Sobre nós
Você já conhece nossas marcas Huggies®.
Intimus®.
Poise®.
Plenitud®.
e os produtos da Kimberly Clark não existiriam sem profissionais talentosos como você.
Aqui, você fará parte de uma equipe comprometida em impulsionar a inovação, o crescimento e o impacto de nossas atividades.
Temos mais de 150 anos de liderança de mercado e estamos sempre em busca de novas e melhores formas de desempenho – portanto, esse é o seu momento de aproveitar nossas oportunidades em aberto.
Esperamos por você na Kimberly Clark.
Somos inspirados por um propósito e guiados pelo desempenho.
Somos uma empresa comprometida com a inclusão, a equidade e a diversidade, para impulsionar nossos resultados de negócio e impactar positivamente a vida de pessoas colaboradoras, consumidoras, fornecedoras e comunidades.
Trabalhamos todas as nossas vagas visando promover uma cultura inclusiva, ou seja, respeitamos e abraçamos a diversidade de gênero, raça, orientação sexual, religião, nacionalidade, idade e deficiência.
Acreditamos n...
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Type: Permanent Location: Sao Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-07-02 09:12:21
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Your Job
Are you passionate about exploring new ideas and breaking through conventional norms? At Georgia-Pacific, we share your enthusiasm for pushing boundaries and embracing creative solutions.
We constantly challenge the status quo, take calculated risks, and strive to improve the products we make.
We are seeking a Product Developer - Retail Tissue to help us extend an ideal balance of softness & strength® in our Angel Soft® bath tissue products at our Technical Center in Neenah, Wisconsin.
Our product developers represent the needs and desires of our consumers to design, manufacture, and deliver advantaged products.
As a product developer, you will have the unique opportunity to deepen your technical expertise in product design, leverage your creativity to tackle challenging problems, and apply a consumer-centric lens to delivering innovation.
Our Team
The Georgia-Pacific Angel Soft® retail bath tissue product development team leads the technical development of our Angel Soft® bath tissue products.
We are entrepreneurs who innovate daily and collaborate cross-functionally to design products and execute projects that create value for our consumers, customers, communities, and company.
We value lifelong learners who want to contribute and grow with us.
This position is located at the Neenah Technical Center (NTC), the central site for research, development, and lab services for Georgia-Pacific's North American Consumer Products business.
What You Will Do
* Collaboration: Work with other product developers, business stakeholders, consumer research, quality, operations, and our technology platforms to drive year-over-year product, performance, and cost improvements.
* Consumer Focus: Connect consumer and market needs to product performance to develop and test alternatives and set technical specifications on product design.
* Design and Experimentation: Design, experiment, evaluate, and execute alternatives to test new product designs and hypotheses, including leading product trials on our pilot and production manufacturing equipment.
Analyze data sets using advanced statistical methods and data analysis tools to support strategic decision-making.
* Product Support: Provide technical support on product specifications, product claims, data substantiation, intellectual property, and overall product points of view to our business teams and other capability partners.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in paper science, engineering or physical science or at least 3 years of product development experience in paper products.
* Experience working in an R&D, product development, OR manufacturing environment independently leading technical projects or experiments, product development activities, and scaling up to commercial feasibility.
* Technical knowledge of papermaking and converting.
* Able and willing to travel an average of 25%.
What Will Put You Ahead
* Advanced...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-07-02 09:04:51
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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:
Responsible for the sorting of health care linen into categories and load sizes as designated by management.
Key Responsibilities:
· Move loaded carts to different areas of the facility.
· Operate machinery so that soiled linen is evenly distributed on the linen belt
· Sort soiled linen into classifications established by management
· Wear appropriate PPE and adhere to safety guidelines
Position Requirements:
· Requires repetitive motion.
· Ability to stand, walk, bend, stoop, twist and reach.
· Ability to lift up to 30 pounds.
· Ability to push or pull a cart that may weigh up to 300 pounds.
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 experience tremendous growth and related opportunities for advancement.
Complete an on-line application at www.novohealthservices.com!
All applicants will be considered for employment without attention to race, color, sex, sexual orientation, gender identity, national origin veteran, or disability status.
We are proud to be an equal opportunity workplace and an affirmative action employer.
Drug-Free Workplace.
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Type: Permanent Location: St Louis, US-MO
Salary / Rate: Not Specified
Posted: 2025-07-02 09:04:09
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The Workday Finance QA Analyst is responsible for testing and validating configuration completed by the Finance and IT configurators and completing the QA documentation for change management.
Key Accountabilities/Deliverables:
* Work with the Company’s Finance and IT teams to identify and understand business requirements.
* Coordinate and track the Finance support tickets to completion.
* Monitor and track shared email box to route incoming requests.
* Ensure all relevant processes and operational protocols are followed during Workday implementation.
* Coordinate and assist stakeholders to design and perform testing.
* Perform related duties, or as required or requested by supervisor.
Technical Knowledge and Understanding:
* Ability to use all Microsoft Office software, including Word, Excel, and PowerPoint.
* Strong communication skills both written and oral.
* Strong background in understanding, documenting, and analyzing complex business processes and related problems.
* Ability to communicate and coordinate with individuals at all levels inside and outside the organization.
Experience:
* 1+ years experience in QA or Testing role using Workday.
* Experience with Workday implementation preferred.
* Experience with configuration and support of business processes reporting.
* Experience in Finance or Operations.
* Strong background in driving efficiency of an organization of relevant size, complexity, and scale.
Applicants must be authorized to work for any employer in the U.S.
We are unable to sponsor or take over sponsorship of an employment Visa for this position.
#LI-Hybrid
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At Core Specialty, you will receive a competitive salary and opportunities for professional development and advancement. We offer medical, dental, vision, and life insurances; short and long-term disability; a Company-match of 100% of a 6% contribution 401(k) plan; an Employee Assistance Plan; Health Savings Account, Flexible Spending Account, Health Reimbursement Account, and a wellness program
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-07-02 08:44:50
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
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-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
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 Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in High Wycombe, United Kingdom.
The Manager, 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 provide 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.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling ...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:46
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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:
Beerse, 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-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
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 Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in Beerse, Belgium.
The Manager, 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 provide 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.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling and target labeling.
* Contri...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:45
-
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
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-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
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 Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in Allschwil, Switzerland.
The Manager, 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 provide 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.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling and target lab...
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Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:40
-
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:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson is currently seeking a Quality Control Analyst to join our CAR-T Hub 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/.
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 built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Biotech analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP
* regulations
* Maintain a safe work enviroment in compliance with all applicable environmental, health and
* safety regulations
* Perform peer review of laboratory data
* Author and update SOPs, Wis and Protocols to support daily operations of the lab using the
* document management system
* Support laboratory related invetigation records and CAPAs
* Assist in the execution of internal audits
* Provide input to functional laboratory meetings
* Provide input and tak actions as a QC representative at cross-laboratory meetings
SHE responsibilities:
* Always strictly apply all applicable prevention rules and procedures
* Make correct use of the personal and co...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:40
-
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:
Customer/Commercial Quality
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium
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/
J&J Innovative Medicine is recruiting for a Commercial Quality Specialist reporting to the Commercial Quality Cluster Head and to be based in Beerse (Belgium).
Position Overview
As a Commercial Quality Specialist, you will be at the forefront of ensuring compliance with Johnson & Johnson Innovative Medicine Quality Policies & Standards to drive our commitment to high quality products and services.
Your responsibilities will include:
* Inspection Readiness: Keep the organization prepared for audits and inspections.
* Internal Audits: Own the internal audit schedule and assist in completing both internal and external audits.
* Training Oversight: Provide in-depth knowledge and strategic oversight on training processes for the local organization.
* Nonconformances: Lead nonconformance investigations and implement Corrective and Preventive Actions (CAPA).
* Change Controls: Coordinate the management of change controls for new product launches.
* Quality System Management Review: Prepare and complete the review of the Quality System with the senior leadership teams.
* Metrics: Keep oversight on the key performance indicators and metrics.
Implement appropriate actions to address any negative trends.
You will execute the tasks to support our patients in Belgium, The Netherlands and Luxembourg.
Requirements
We are seeking a person who is passionate about quality and meets the following qualifications:
* Educational Background: A degree or equivalent in a science-related field is helpful.
* Pharmaceutical Knowledge: An understanding of relevant pharmaceutical legislation and good distribution practices will be important for success.
* Attention to Detail: Able to work accu...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:33
-
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:
Strategy & Corporate Development
Job Sub Function:
Digital Strategy & Deployment
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a R&D Data Science & Digital Health – Scientific Content Lead.
This position has a primary location of Titusville, NJ but is also open to Springhouse, PA; New Brunswick, NJ; Boston, MA; and San Diego, CA.
This position will require up to 25% in travel.
Johnson & Johnson Innovative Medicine develops treatments that improve the health of people worldwide.
Research and development areas encompass oncology, cardiovascular and metabolic disorders, immunology, pulmonary hypertension, retinal disorders, and neuroscience.
Our goal is to help people live longer, healthier lives.
We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market – from patients to practitioners and from clinics to hospitals.
To learn more about Janssen, one of the Pharmaceutical Companies of Johnson & Johnson, visit https://www.janssen.com/johnson-johnson-innovative-medicine.
About the Role:
We are seeking an experienced and motivated R&D Data Science & Digital Health – Scientific Content Lead.
This role will be responsible for creating high-quality scientific content based on published research, conference proceedings, competitive intelligence, press releases, and key healthcare-focused databases.
The focus will be on the domains of data science, real-world evidence, artificial intelligence (AI), machine learning, and digital health industry trends occurring across the pharmaceutical landscape.
Key Responsibilities:
• Curate and develop scientific content and regular reports from various sources, including research publications and databases, to identify and assess emerging trends, technology, and data with strategic impact for JJIM R&D DSDH and beyond Collaborate with internal JJIM stakeholders to translate complex scientific, technical, and business information into actionable insights.
• Inform strategic planning and decision-making processes across the organization through well-structured content.
• Present findings and insights to senior-level audiences, ensuring clarity and understanding
• Partner with internal communications teams to effective...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-07-02 08:40:06
-
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:
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-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
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 Manager, Global Labeling Product Leader.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; or Horsham, PA.
The Manager, 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 provide 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.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeut...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:53
-
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:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Purpose
Local Medical Safety (LMS) ensures pro-active Benefit Risk Management throughout product life cycle by translating global safety data to insights and actions, and tailoring to local specificities and needs.
We support activities related to the pharmacovigilance regulatory requirements of Marketing Authorization Holders (MAH) and/or study sponsors, as applicable.
Please note that this role is available with the same job title, but different levels of experience.
While you are welcome to apply to any or all of the postings, we recommend focusing on the experience that aligns with your profile.
2+ years of experience - R-020042
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
You will be responsible for:
Ensuring the local Pharmacovigilance (PV) system is managed in compliance with local regulations and company policies/procedures at local, regional, and global levels and in accordance with any PV agreements with third party business partners.
Conducting local benefit-risk activities to ensure pro-active benefit-risk management throughout the product life cycle.
ICSR MANAGEMENT AND OVERSIGHT
Ensuring local collection, review, reporting, reconciliation, and follow up of Individual Case Safety Reports (ICSR) and implementation of the local literature process.
Maintain active involvement in day-to-day ICSR management related activities as applicable, and Maintain oversight of corresponding vendor activities as required.
Aggregate reports
Leading Preparation, review, tracking and timely submission of aggregate reports to all relevant local authorities or other official bodies, where applicable.
Local Safety compliance
Providing insights into ICSR inbound and outbound compliance metrics, perform ICSR reconciliations and leading actions as needed.
Acting as a CAPA content owner and subject matter expert, owning actions as required.
Performing or overseeing procedural document review and improvement, conducting impact assessments as required on local level and support implementation of Global PV relevant documents as applicable.
Responsible for timely provision of high quality and accurate contributions to PSMF, as required.
...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:39
-
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:
Product Safety
Job Sub Function:
Product Safety Risk Management
Job Category:
Scientific/Technology
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
We are searching for the best talent for an Associate Director, Safety Analysis Scientist to be located in Horsham, PA; Raritan, NJ; or Titusville, NJ.
Purpose: The Associate Director (AD), Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products.
In partnership with the Medical Safety Officer (MSO), is responsible for the preparation of scientific safety analysis and evaluations, which are required for regulatory compliance and to aid in safety-related decisions for marketed products and products in development.
The AD, SAS will support product Safety Management Teams (SMTs) and work in close collaboration with other cross-functional safety partners to determine a product’s safety strategy, complete safety analyses and evaluations, proactively review safety data/lead safety data review meetings and interpret safety information to make a recommendation, supporting SMT deliverables as required.
The AD, SAS will assist the Medical Safety Officer (MSO) with activities related to the SMT and with contributions to key safety and clinical documents.
They will have in-depth product knowledge, will serve as product point of contact, and will provide training to, and oversight of deliverables prepared by, other team members as needed (for complex reports).
The AD, SAS will function with a high level of independence, with minimal guidance from the Director, Safety Analysis Scientist (SAS) Therapeutic Area Lead (TAL), be able to link discussions to content, and consistently deliver high quality results with minimal guidance.
The AD will quickly build alliances and be able to independently influence other safety partners t...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:36
-
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:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Purpose
Local Medical Safety (LMS) ensures pro-active Benefit Risk Management throughout product life cycle by translating global safety data to insights and actions, and tailoring to local specificities and needs.
We support activities related to the pharmacovigilance regulatory requirements of Marketing Authorization Holders (MAH) and/or study sponsors, as applicable.
Please note that this role is available with the same job title, but different levels of experience.
While you are welcome to apply to any or all of the postings, we recommend focusing on the experience that aligns with your profile.
4+ years of experience - R-020046
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
You will be responsible for:
Ensuring the local Pharmacovigilance (PV) system is managed in compliance with local regulations and company policies/procedures at local, regional, and global levels and in accordance with any PV agreements with third party business partners.
Conducting local benefit-risk activities to ensure pro-active benefit-risk management throughout the product life cycle.
ICSR MANAGEMENT AND OVERSIGHT
Ensuring local collection, review, reporting, reconciliation, and follow up of Individual Case Safety Reports (ICSR) and implementation of the local literature process.
Maintain active involvement in day-to-day ICSR management related activities as applicable, and Maintain oversight of corresponding vendor activities as required.
Aggregate reports
Assisting with the preparation, review, tracking and timely submission of aggregate reports to all relevant local authorities or other official bodies, where applicable.
Local Safety compliance
Providing insights into ICSR inbound and outbound compliance metrics, perform ICSR reconciliations and leading actions as needed.
Acting as a CAPA content owner and subject matter expert, owning actions as required.
Performing or overseeing procedural document review and improvement, conducting impact assessments as required on local level and support implementation of Global PV relevant documents as applicable.
Responsible for timely provision of high quality and accurate contributions to PSMF, as...
....Read more...
Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:35
-
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:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson Innovative Medicine develops treatments that improve the health and lifestyles of people worldwide.
Our development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease, diabetes, hematology, metabolic disorders, immunologic disorders, pulmonary hypertension and reproductive medicine.
The successful candidate will be employed in the department of Chemical Process Research & Development (CPRD).
The CPRD organization focuses on the development of synthetic methodologies and processes for small molecules, oligonucleotides, peptides, antibody-drug conjugates and other emerging modalities.
CPRD aims to provide world-class production processes of active pharmaceutical ingredients (APIs) by enhancing efficiency, safety, and cost-effectiveness.
Its key objectives include refining synthetic routes, scaling up processes from the laboratory to commercial levels, ensuring regulatory compliance and minimizing environmental impact.
Within this department, the Process Analytical Research (PAR) subdepartment plays a critical role in providing analytical data and expertise for all chemical process development activities.
PAR ensures quality and performance through the design and implementation of state-of-the-art analytical methods while also generating and documenting essential end-to-end knowledge.
We currently have an open position for a Principal Scientist, High-Throughput Analytical Chemistry within the PAR team, specializing in analytics for biocatalysis and chemocatalysis high-throughput experimentation.
Job Description
As a Principal Scientist, you will focus on providing innovative analytical solutions to support high-throughput experimentation (HTE) in biocatalysis and chemocatalysis.
Your role will involve developing methodologies and platforms that enable efficient analysis, reporting and characterization of synthetic routes for small molecule production and related modalities.
Key Responsibilities
* Develop and implement analytical methodologies to support HTE labs for biocatalysis and chemocatalysis.
* Build and oversee the analytical platform necessary for efficient HTE screenings.
* Demonstrate a strong knowledge of h...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:25
-
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:
Allschwil, Basel-Country, Switzerland
Job Description:
Target group
Doctoral student (4 months).
About the company
At Johnson & Johnson (J&J), we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
The Global Epidemiology team’s mission is to advance patient health by enabling informed decision-making through generating reliable real-world evidence (RWE) on the safety and benefits of J&J products.
The project
The scope of the project is a systematic literature review of the epidemiology estimates (i.e., incidence and prevalence) for a given cardiovascular/cerebrovascular condition(s).
The intern will lead this effort in a classical literature review step-by-step approach: will design the search strategy, perform screening and extraction, assess the quality of the included studies, and prepare the final report.
The intern will work with other epidemiologists within the department and will be involved in the discussions to help contextualize and interpret the findings.
The intern will also have an opportunity to participate in other department events (e.g., educational webinars, team meetings, networking, etc.).
Location: J&J Basel Office (Hegenheimermattweg 167A, 4123 Allschwil, Switzerland), with a possibility for partial remote work (2 days/week max).
Time period: expected start – Q3 2025 on a full-time basis.
The candidate
* Doctoral student in epidemiology, public health, or a related field.
* Good experience in systematic literature reviews.
* Has a good understanding of epidemiology study designs and analytical methods.
* Strong interest in cardiovascular/cerebrovascular research.
* Strong interest in pharmaceutical research.
* Has good communication, collaboration, and networking skills.
* Has good presentation skills; fluent oral and written English.
#JNJEMEAInternship #JNJEMEAStudentCareers
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Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-07-02 08:39:08
-
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:
Process Engineering
Job Category:
People Leader
All Job Posting Locations:
Raritan, 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
We are searching for the best talent for a Technical Fellow (Director), Advanced Therapies -MSAT to be in Raritan, NJ, Titusville, NJ, Horsham, PA, or Spring House, PA.
Purpose:
The Technical Fellow serves as a subject matter expert (SME) in CAR-T manufacturing and Quality Control analysis, playing a pivotal role in ensuring the quality and safety of cellular therapies.
This position is critical in addressing challenges that arise when non-conforming products or deviations are generated during the manufacturing process, which can impact patient treatment.
The Technical Fellow actively engages with healthcare providers to navigate these challenges, facilitating clear communication and collaborative problem-solving.
In addition to direct interaction with healthcare providers, the Technical Fellow curates and analyzes manufacturing case studies to expedite the release of drug products.
This role requires deep expertise in key areas, including apheresis collection, cryopreservation, cell processing, quality control testing, and quality release processes.
The Technical Fellow provides insights to both internal manufacturing teams and external partners, ensuring adherence to the highest standards of quality.
The Technical Fellow is also an integral member of various site/network operational teams, including planning, release, clinical/commercial rapid response teams, safety management, and site escalations.
In this capacity, they contribute to the development of robust strategies that maintain the validated state of cell therapy processes while supporting lifecycle management initiatives involving new technologies, automation, and technology transfer.
Finally, this role serves as a key thought leader and scientific expert driving manufacturing trend investigation teams towards root ca...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-07-02 08:38:56
-
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 Training
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Trainer Opleiding & Ontwikkeling – Strategy & Support
De functie in het kort
Deze functie draagt sterk bij aan de ontwikkeling de juiste attitudes binnen een cultuur waarbij leren een aangeboren onderdeel is van wat we doen en hoe we ons gedragen en waar mensen gemotiveerd zijn om te leren, te groeien en te presteren.
De specialist opleiding & ontwikkeling zorgt er voor dat alle mensen op alle niveaus binnen de organisatie de nodige kennis en vaardigheden bezitten en of ontwikkelen om te kunnen voldoen aan de korte- en lange-termijnambities van de organisatie, rekening houdend dat de juiste attitudes ten opzichte van de trainingsdoelstellingen gehandhaafd worden.
De juisten doelstellingen worden opgesteld in functie van de stakeholders.
Deze worden bekomen door het uitvoeren van adequate trainingsbehoeften analyses.
Daarna staat de specialist garant voor het ontwikkelen, uitwerken, implementeren en evalueren van de verschillende leerinitiatieven.
Dit zal gaan om een contract van onbepaalde duur.
Wat verwachten we van jou?
Onder hoofdtaken verstaan we:
* Je werkt samen met interne stakeholders en teams om de leerbehoeften te identificeren (analyse van trainingsbehoeften) en om leeractiviteiten in te plannen.
* Je gaat leeractiviteiten en materialen ontwerpen die de overdracht van het leren naar de werkplek ondersteunen.
* Leeractiviteiten uitvoeren en evalueren.
* Voortdurende focus op het vergroten van het leervermogen van de doelgroep.
* Het weten wanneer en hoe trainingen aan te bieden en te integreren in dagelijkse activiteiten op de werkvloer.
* Het beoordelen van de leervoortgang van de toegewezen focusgroepen.
* Ondersteuning en coachen van stakeholders bij het opleiden van hun collega’s.
* Faciliteren van bijeenkomsten waar medewerkers kunnen ontdekken met hoe en met wie ze kunnen samenwerken om hun leerdoelstellingen te bereiken
* De organisatie adviseren over L&D.
* Je onderzoekt en rapporteert over nieuwe ontwikkelingen en inzichten in L&D die kunnen leiden tot betere organisatieprestaties.
* Je onderzoekt en experimenteert met nieuwe en innovatieve didactische leermethodes.
* Ontwerpen en implementeren van processen om de kennisproductiviteit te verbeteren en de kennisover...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:38:39
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Spring House, Pennsylvania, United States of America, Toledo, Spain
Job Description:
AI/ML Senior Scientist in Drug Discovery Data Sciences
Next Generation Automation refers to the bidirectional coupling between automated lab equipment and Artificial Intelligence (AI). Through successive iterations, such closed-feedback loop systems facilitate the AI-driven design, execution and analysis of experiments and utilize a wealth of in silico methodologies including active learning, multi-parametric dynamic optimization, model predictive control, Model-based Design of Experiments, and others.
Within the Drug Discovery Data Sciences organization of Johnson & Johnson Innovative Medicine we have an open position for a senior scientist that will play a pivotal role in our strategic effort to transition automation into the next generation.
To do so, the new member will collaborate within interdisciplinary teams comprising biologists, medicinal chemists, data scientists, computational chemists and IT experts across all therapeutic areas.
They are expected to utilize their expertise and know-how to bridge the gap and close the loop between existing automation and in silico solutions and develop new modeling suites according to the needs of each project.
Role and responsibilities
* Co-develop system engineering plans for closed loop automation projects from PoC to production.
* Develop and productionize the in silico suites by using AI/ML and other appropriate modelling methodologies.
* Actively participate in evaluation of third-party solutions.
* Work closely with IT, engineering and Lab-tech to implement solutions.
* Communicate results in audiences with heterogeneous background.
Requirements
* A PhD with an AI/ML publication track record.
* Previous experience with Process or Lab Automation.
* Familiarity with Model Predictive Control and DOEs or similar mathematical capabilities.
* Knowledge of Python development and affinity with AWS (or similar cloud environments).
* Strong interpersonal, organizational and communication skills.
* Motivation to be part of a team that celebrates diversity and off...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-07-02 08:38:36
