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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.
L’alternant affaires pharmaceutiques participe à la conformité des activités opérationnelles des produits sous la responsabilité des Responsable Affaires Pharmaceutiques dans le respect de la réglementation en vigueur :
- S’assurer que l’ensemble de l’information promotionnelle et scientifique est en conformité avec la réglementation, les référentiels en vigueur et les procédures internes en lien avec la stratégie produit d’entreprise.
- Obtenir et maintenir les AMM, AAP, AAC, CPC ; assurer la conformité réglementaire et les activités de compliance associées.
ACTIVITES PRINCIPALES
* Participer à la bonne qualification des documents de communication transmis par les équipes internes et assurer leur conformité réglementaire.
* Veiller les changements de réglementation, de pratiques promotionnelles, les sanctions éventuelles, et évaluer leurs impacts sur les activités associées.
* Participer au dépôt des dossiers de publicité, leur suivi et leur archivage.
* Contribuer à la validation des documents de formation des délégués médicaux.
* Participer au dépôt et au suivi des dossiers d’AMM et leurs modifications, conformément aux exigences réglementaires locales ou européennes, en lien avec l’ANSM et/ou l’international.
* Prendre en charge les activités de compliance liées aux activités réglementaires : mise à jour les bases de données réglementaires et qualité, compléter les formulaires associés aux SOPs et assurer le suivi des modifications d’AMM pour garantir leur application dans les documents impactés.
* Participer au contrôle des BAT des articles de conditionnement (ACs), pa...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:15
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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:
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-007626
* Canada - Requisition Number: R-008148
* Belgium, Poland - Requisition Number: R-008149
* United Kingdom - Requisition Number: R-008152
* Switzerland - Requisition Number: R-008155
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 Senior Manager, Global Labeling Product Leader.
This position is a hybrid role and can be located in High Wycombe, United Kingdom.
The Associate Director, Global Labeling Product Leader is a leading expert individual contributor who is viewed as a valuable resource by peers and manages large projects or processes.
This individual will develop methods for planning, directing, coordinating and controlling the regulatory affairs activities related to new and modified products worldwide in compliance with corporate policies and strategies.
Ensure compliance with regulatory agency regulations and interpretations accounting for new and changing government regulations.
The Senior 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 (label...
....Read more...
Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:15
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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:
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-007626
* Canada - Requisition Number: R-008148
* Belgium, Poland - Requisition Number: R-008149
* United Kingdom - Requisition Number: R-008251
* Switzerland - Requisition Number: R-008155
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 Senior Manager, Global Labeling Product Leader.
This position is a hybrid role and can be located in Allschwil, Switzerland.
The Associate Director, Global Labeling Product Leader is a leading expert individual contributor who is viewed as a valuable resource by peers and manages large projects or processes.
This individual will develop methods for planning, directing, coordinating and controlling the regulatory affairs activities related to new and modified products worldwide in compliance with corporate policies and strategies.
Ensure compliance with regulatory agency regulations and interpretations accounting for new and changing government regulations.
The Senior 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 E...
....Read more...
Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:15
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Leiden, South Holland, Netherlands, Madrid, Spain, Prague, Czechia, Warsaw, Masovian, Poland
Job Description:
Position Summary:
The Senior CTISA is responsible for assisting with the operational components of all clinical trial applications submitted under the EU Clinical Trial Regulation (EU CTR) within the Clinical Trial Information System (CTIS).
This individual will collaborate with the Clinical Trial Submission Coordinator (CTSC), regulatory stakeholders, and Global Country Operations (GCO) teams to ensure that all clinical trial applications are submitted in CTIS, monitor the application's progress, and ensure the proper archiving of relevant documentation.
Principal Responsibilities:
Ensure complete and timely entry of application specific information into CTIS.
Upload the application package to CTIS, submit it within the system, and archive relevant documentation in internal source systems.
Perform document quality and completeness checks.
Support submission coordination efforts and track timelines and deliverables to ensure trials are delivered according to agreed schedules and milestones.
Perform relevant quality oversight and inspection readiness activities.
Assist CTSC, Regulatory and clinical stakeholders with applicable CTIS support.
Maintain expertise in CTIS operations to address inquiries from within the organization.
Demonstrate leadership at the trial level for complex or challenging trial applications.
Understand the responsibilities of the CTSC and collaborate effectively to ensure timely submissions.
Contribute to the development of processes or optimization of operational models.
Serve as a Subject Matter Expert (SME) in designated areas.
Mentor newly onboarded CTISAs Exhibit strong communication skills and engage in cross-functional discussions, both internally and externally.
Undertake additional activities as assigned by the Functional Manager.
Principal Relationships:
This position reports to the Manager of EU CTR and will collaborate closely with the Clinical Trial Submission Coordinator.
Education and Experience Requirements:
* Bachelor’s degree
* Minimum of 2 years of relevant EU CTR experience with associated skill sets.
* Deep understanding and demonstrated proficiency of the Clinical Tri...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:10
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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:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
San Lorenzo, Puerto Rico, United States of America
Job Description:
Johnson & Johnson is currently seeking a Senior Financial Analyst to join our team located in San Lorenzo, Puerto Rico.
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/.
The Senior Financial Analyst will support the San Lorenzo Biosurgery Manufacturing operation from a finance control standpoint providing accurate, timely, and meaningful financial analysis.
Participates in business planning, budgeting, and forecasting.
Utilize financial and general business expertise to provide analysis and leadership in Cost Accounting & Financial Reporting.
RESPONSIBILITIES:
Under limited supervision.
and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Support Production and all other Departments.
* Analyze the P&L and Cost of Production Accounts.
* Work with monthly closing and monthly schedules.
* Prepare Operational Measurements.
* Support Latest Estimate’s activities and analysis.
* Prepare month-end and quarterly reporting, including ERP system upload.
* Calculate Volume and Relief impact for new estimate and analyze actual results.
* Manage Annual Business Plan activities.
* Partner with Plant Leadership to drive efficiencies through data analysis and insights.
* Leverage Technology: Stabilize SAP Hana and adopt Signifi to drive efficiency and simplification.
* Present business-related issues or opportunities to the next management level.
* Supports financial reporting activities including the following:
+ Assists month-end expense & cost budgeting/tracking/reporting.
+ Performs analysis of capital appropriation requests and monthly spending of approved capital projec...
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Type: Permanent Location: San Lorenzo, US-PR
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:10
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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:
Marketing
Job Sub Function:
Events
Job Category:
Business Enablement/Support
All Job Posting Locations:
BR031 São Paulo
Job Description:
Nossa experiência em Medicina inovadora é informada e inspirada por pacientes, cujos insights impulsionam nossos avanços científicos.
Visionários como você trabalham em equipes que salvam vidas, desenvolvendo os medicamentos de amanhã.
Junte-se a nós no desenvolvimento de tratamentos, buscando curas e no pioneirismo desde o laboratório para a vida, enquanto apoia os pacientes ao longo de cada etapa do caminho.
Saiba mais em https://www.jnj.com/innovative-medicine
Descrição:
O Analista de Eventos Pleno responderá diretamente para o Supervisor de eventos e Operações, dando suporte às atividades desempenhadas.
Principais atividades:
* Suporte ao Supervisor de Eventos e Operações para operacionalização dos eventos médicos e promocionais solicitados pela Unidade de Negócio (BU) dentro das regras da cia.
* Planejamento, gestão de fornecedores, execução e controle/fechamento de todo o calendário de eventos da BU focal point
* Controle de documentos e acompanhamento dos eventos no sistema de Eventos vigente
* Comunicação com stakeholders internos (marketing, área médica, força de vendas, compliance, procurement, jurídico, entre outros) e externos (profissionais de saúde, fornecedores e sociedades médicas)
* Controle de budget dos eventos e Processo E2E dos pagamentos relacionados aos fornecedores de eventos
* Geração de relatórios e análises de execução para reports de desempenho para as BUs
* Apoio à Provisão financeira de eventos
* Solicitação de Eventos junto à agência global de viagens atuando no controle de RSVP (apoio aos profissionais de saúde) e andamento das demandas do evento
* Conhecimento das regras, processos e políticas da cia para suporte as unidades de negócios do time.
Qualificações:
* Organização
* Trabalho em equipe
* Comunicação assertiva
* Administração de conflitos
* Senso de urgência
* Colaboração
* Perfil agregador e inovador
* Ensino superior completo em Marketing, Turismo, Administração de Empresas, Comunicação , economia ou áreas afins
* Inglês intermediário.
* Bom nível do Pacote office, principalmente excel para geração de relatórios
Desejável:
* Conhecimento ...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:07
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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:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
Job Description:
Position Summary:
An Associate, Site Manager is an entry level site management role with typically 0-2 years of experience.
This role serves as the primary contact point between the Sponsor and the Investigational Site.
An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
Responsibilities may include assisting with site selection, site qualification assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
The Associate, Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to process improvement and training.
Some supervision from a more Senior, Site Manager (Senior SM or Lead SM) to help provide guidance to Associate, Site Manager.
Principal Responsibilities:
1.
Acts as primary local company contact for assigned sites for specific trials.
2.
May participate in site feasibility and/or Site Qualification Visit.
3.
Attends/participates in investigator meetings as needed.
4.
Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
Responsible for the implementation of analytical risk-based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
Occasionally may require assistance or oversight from Lead, Site Manager or LTM.
5.
Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process a...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:06
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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:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Manila, National Capital, Philippines, Paranaque, National Capital Region (Manila), Philippines
Job Description:
“Reimagine the possibilities” at Johnson and Johnson Global Finance! We live this motto every day by creating game‐changing business solutions for the world’s largest and most broadly‐based healthcare company.
As a member of our Global Finance team, you will have exclusive access to a network of financial professionals located in over 60 countries.
This new network will help you build on your current skills and explore opportunities to grow your career in J&J.
At J&J Global Finance, we value ideas for innovation and improvement and are committed to diversity and inclusion.
Together we will reimagine business processes to become more effective, more efficient, and improve customer experience.
We are proud to be an equal opportunity employer.
This role will be part of the Global Services Finance team in the Revenue Accounting process area.
The Global Services Finance organization provides best‐in‐class, cost‐effective financial Services and compliance—in a J&J way—to our Operating Companies around the world.
The Revenue Accounting team is responsible for complete and accurate accounting and reporting for all Sales, Returns & Billing adjustments.
This includes but is not limited to managing Revenue recognition, cut‐off & Rebate processes and reporting via the 'Bravo' system.
Key Responsibilities:
1.
Be compliant with applicable laws and regulations, and follow guidelines in the J&J Credo.
2.
Maintain Operational Excellence
* Responsible for executing accounting and daily operations for Revenue Accounting process area
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas
* Regular focus on Balance Sheet reconciliations to minimize open items
* On the job training for new team members / BPO partners
* Support auditors and legal authorities with the execution of required activities
* Understand, a...
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:06
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Senior Site Manager, Early Development (Senior Clinical Research Associate/ Senior CRA)
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Senior Site Manager, Early Development (ED), located United Kingdom to serve as the primary contact point between the Sponsor and the Investigational Site (both commercial and hospital) for the conduct of complex early development and/or clinical pharmacology (ED&CP) studies.
A Senior Site Manager Early Development is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), Healthcare compliance (HCC) requirements, applicable regulations, and guidelines from start-up through data-base lock.
Responsibilities include site assessments, pretrial assessments, site selection, site initiation, subject recruitment and retention, monitoring, and close-out.
Partners with the Clinical Trial Assistant (CTA), Trial Manager (TM), Site Strategy Lead (SSL) and Trial Delivery Leader (TDL) to ensure overall site management while performing trial related activities for assigned protocols.
The head office location is in High Wycombe, Buckinghamshire and this position is field-based with regular in-office requirement.
Preferably you will have experience in Haematology or Oncology but other therapeutic areas are considered.
As a Senior Site Manager, you will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure.
You should be flexible and be able to work independently.
We are seeking to hire a strong communicator, a quick learner, a problem solver...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-04-28 07:55:00
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
People Leader
All Job Posting Locations:
Grecia, Costa Rica
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
We are searching for the best talent for Senior Quality Engineering Leader to be in Grecia, Costa Rica.
Purpose:
The Senior Quality Engineering Leader will manage the quality engineering group to implement engineering solutions, conducts effective technical reviews and effectively implements and applies quality tools.
This organization will also support technical investigations, critical issues and corrective actions leading to product and process improvements which sustain the quality, safety, and efficacy of marketed devices within company portfolio.
You will be responsible for:
Under the direction of the Site Quality Lead and in alignment with all federal, state, and local laws and Johnson & Johnson corporate guidelines, your responsibilities will include:
* Apply Quality Engineering tools and methods for the effective and efficient sustaining and improvement of products/processes throughout the lifecycle.
* Defines and implements departmental strategies and services for disposable products development, manufacturing quality, and product quality assurance.
* Use Quality Engineering principles and problem-solving skills to develop and optimize products/processes that are aligned with the overall quality and business vision.
* Leading efforts with quality improvement opportunities as appropriate to products, continuous improvement, and customer satisfaction.
* Ensure effective risk management to prevent unanticipated failure modes and improve capability of processes.
* Responsible for communicating business-related issues or opportunities to next management level.
* Recommends, develops, and implements organizational strategies for optimizing Product Quality processes and activities.
* Lead a team of Quality Engineers including resource planning, hiring, training & development, assignment planning, supervision, mentoring and performance evaluations.
* Address quality and regulatory compliance issues.
* Act as a mentor to m...
....Read more...
Type: Permanent Location: Grecia, CR-A
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:59
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America, 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 Director, CMC Portfolio Management to be in Malvern, PA or Raritan, NJ.
Purpose:
The Director, CMC Portfolio Management will share oversight of the scientific projects within TDS as they relate to the internal portfolio.
The leader in this role will be responsible for maintaining this information and will be the single source of data for the rest of the organization.
You will be responsible for:
* the CMC Portfolio Strategy Leadership team, supporting that group with updated portfolio information on a regular basis.
* partnering with leaders across Discovery/Therapeutic Development & Supply/Innovative Medicine Supply Chain to maintain accurate information, to provide a regular report on development projects and capture changes to the portfolio as they happen in real time.
* sharing portfolio information to a large number of peers and leaders across DPDS and then further into J&J (TAs, PMO, Finance).
* challenging current paradigms with creative, out of the box thinking in a matrixed team, as well as to developing new more efficient processes, that enable TDS/DPDS to continue to drive scientific innovation and increased efficiency in execution and delivery of the portfolio will be critical.
Qualifications / Requirements:
Education:
* A minimum of a bachelor’s degree in life science or related field is required
* A Master’s degree or Ph.D.
in life science or related field is highly preferred
Required:
* A minimum of 10 years experience in pharmaceutical, biotechnology or a related industry is required
* CMC experience is required
* Excellent communication skills, both oral and written, as well as proven conflict...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:54
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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:
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-007626
* Canada - Requisition Number: R-008148
* Belgium, Poland - Requisition Number: R-008149
* United Kingdom - Requisition Number: R-008152
* Switzerland - Requisition Number: R-008155
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 Senior Manager, Global Labeling Product Leader.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; or Horsham, PA.
The Associate Director, Global Labeling Product Leader is a leading expert individual contributor who is viewed as a valuable resource by peers and manages large projects or processes.
This individual will develop methods for planning, directing, coordinating and controlling the regulatory affairs activities related to new and modified products worldwide in compliance with corporate policies and strategies.
Ensure compliance with regulatory agency regulations and interpretations accounting for new and changing government regulations.
The Senior 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 Inse...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:53
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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:
Chiyoda, Tokyo, Japan
Job Description:
RESPONSIBILITIES/PRINCIPAL DUTIES:
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
The Communications Manager will plan, develop and implement impactful and measurable communication programs with a priority to drive Johnson & Johnson MedTech Japan’s business growth, protect and enhance reputation, manage change and activate culture, and impact society.
By achieving the role’s responsibilities, the manager is expected to help position us as a leading medtech company in Japan.
Responsibilities include:
* Plan and execute innovative external communications strategies and initiatives to drive our business growth and enhance our reputation by leveraging new product and solution launches, developing disease awareness and public affairs programs, as well as identifying and developing stories to amplify our value.
The channels include earned media, paid media, and owned media (including website, social media, and video).
* Manage issues and crisis situation, including appropriate media handling, in partnership with and ensuring alignment with multiple stakeholders.
* Build and execute meaningful employee engagement strategies and initiatives to mobilize business strategies, manage change and activate our culture.
The channels include but not limited to all employee townhall meetings, other form of employee events, newsletters, intranet, internal social media as well as global and regional executives visit programs.
* Plan and execute our cross-sector employee engagement and external communications initiatives in partnership / alignment with other sectors’ C&PA teams.
* In achieving above-mentioned responsibilities, partner with and ensure alignment with local business partners and regional, global and other sectors’ C&PA t...
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Type: Permanent Location: Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:46
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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:
Strategy & Corporate Development
Job Sub Function:
Strategic Planning
Job Category:
Professional
All Job Posting Locations:
Shanghai, China
Job Description:
Applies highly-developed strategies for the implementation and milestones tracking of the departmental strategic planning goals and objectives.
Drives collaboration among the broader strategic planning function with relevant business and functional leaders to oversee global stakeholder communications and bridge the strategy to successful business execution.
Advises on cross-functional resources and engages key stakeholders to progress global and regional strategic planning projects and key end goals and deliverables.
Benchmarks commercial department activities to drive comprehensive strategic solutions that meet customer’s specific needs and requirements.
Develops and implements key performance measures, goals, and objectives along with project plans for team member action items and milestones.
Coaches team members to ensure all departmental procedures and protocols are in full compliance with state and federal regulatory, safety, and quality assurance requirements.
Leads frequent staff meetings to review current status of ongoing projects, as well as remaining deliverables to ensure all milestones will be successfully met to customer’s requirements.
Coaches and trains junior colleagues in techniques, processes, and responsibilities.
Integrates Johnson & Johnson’s Credo and Leadership Imperatives into team goals and decision making.
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:45
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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:
Post Doc – Drug Discovery & Pre-Clinical/Clinical Development
Job Category:
Career Program
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
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
Johnson and Johnson Innovative Medicine is seeking a dedicated Post-Doctoral, Oncology Research to join our Oncology Discovery team in Spring House, PA.
The focus of this position is on advancing our understanding of therapeutic mechanisms in oncology, particularly pertaining to novel payloads in antibody-drug conjugates (ADCs) and radioligand therapy (RLT).
This postdoctoral opportunity will last 24 months and offers a chance to contribute to novel therapeutic strategies in cancer treatment.
Key Responsibilities:
* Conduct lab-based research to elucidate the mechanisms of action (MOA) of novel next generation payloads in ADCs in the context of prostate cancer using CRISPR screens, confocal imaging and proteomics approaches.
* Perform conjugation processes to develop novel ADCs.
* Evaluate expression of prostate tumor associated antigens in pre- post standard of care therapy in pre-clinical models.
* Collaborate with cross-functional teams to assess the therapeutic index of ADCs in preclinical models.
* Design, execute, and interpret complex in vitro, ex vivo, and in vivo experiments relevant to cancer biology and treatment modalities.
* Participate in the development and implementation of biomarker strategies for oncology assets during preclinical and early clinical stages.
* Work alongside other oncologists, researchers, and translational scientists to facilitate data sharing and foster collaborative research efforts.
* Communicate results clearly to multidisciplinary teams, including computational bi...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:41
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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:
Santa Rosa, California, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Senior Quality Engineer! This position will be located in Santa Rosa, California.
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:
In this role, you will provide technical leadership on a daily basis by developing, establishing, and maintaining quality engineering methodologies, systems, and practices.
This position will also drive product/process improvements with the objective of product safety and high customer satisfaction.
Key Responsibilities:
* Must be able to interface well with Management, Manufacturing and R&D Engineering, and Supply Chain.
* Work with various departments to ensure timely closure of CAPAs, NCMRs, and Complaints.
Document deficiencies, including root cause, corrective and preventive action plans.
Ensure action plans are implemented in a timely manner.
* Lead and support test method validation plans/protocols and reports.
* Assist with risk analysis activities and maintaining up to date risk management documents.
* Establish Quality Inspection Plans for the release of components, assemblies, and finished devices.
Conduct quality inspections as needed.
* Support Manufacturing with equipment qualifications (IQ/OQ/PQ), process validations and process improvements.
Includes the use of various statistical techniques and quality tools.
* Experienced with statistical techniques, including design of experiments (DOE); able to analyze results.
* Evaluate significant product and/or process changes and enhancements which reduce defects, improve yields, and lower product cost.
* Support quality management programs such as supplier selection and certification.
Perform supplier evaluations as needed to assure sup...
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Type: Permanent Location: Santa Rosa, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
US010 PA Horsham - 800/850 Ridgeview Dr, US159 NJ Titusville - 1125 Trenton-Harbourton Rd
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 Manager, Clinical Supply Chain Data to be in Titusville, NJ or Horsham, PA.
Purpose: Our Digital Solutions team has responsibility for the digital transformation of Clinical Supply Chain, in support of planning, manufacturing, purchasing and delivering clinical supplies to thousands of clinics worldwide, in close collaboration with clinical supply functions, our commercial supply chain and IT partners.
As a key member of Digital Solutions, the candidate will drive the strategy and implementation of a robust Data infrastructure for digital clinical supply chain, partnering with JJT (J&J Technology) and Data Science teams.
Focusing on data integration, engineering, and governance, the successful candidate will play a pivotal role in ensuring that our data ecosystem is scalable, secure and promoting efficient data usage across the organization.
A critical requirement of this role is the right mix of technical expertise and business acumen, and a passion for leveraging data for solving business challenges.
The successful candidate will be a proactive and effective problem solver who is intellectually curious and has a proven track record of adopting best practices when dealing with data in the life sciences industry.
You will be responsible for:
Being a Product Owner for the following capabilities:
* Data Integration:
+ Integration between various technology platforms used in clinical supply chain, e.g., forecasting (4C), Randomization & Trial Supply Management systems (multiple RTSM vendors), SAP, E2E planning (OMP).
+ Data ingestion from various sources into our Data Lake.
+ Data exchange with external partners, i.e.
3PL’s and CRO/CMO’s....
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-28 07:54:36
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Your Job
Georgia-Pacific is now hiring Data Reconciliation Clerk for our facility in South Savannah, GA Recycling Plant.
Salary:
Starting at Pay Rate: $15-$17 per hour
Shift:
Monday- Friday 2:30pm- 11:30 pm
Physical Location:
2495 Tremont Rd.
Savannah, GA 31405
Our Team
Georgia-Pacific Harmon Recycling is one of the largest pure traders of recycled fiber in the world, trading in excess of 100 thousand tons per week.
We develop markets for our supplier's recovered materials and provide a reliable source of quality feed stock to our global customer base.
To learn more about our Harmon Recycling division, visit www.gapacrecycling.com
What You Will Do
* Record information from inbound/outbound loads.
Complete receiving and shipping documentation ensuring high level of accuracy.
* Standing/walking (continuously) up to 3 hours at a time.
* Pushing/pulling with force of up to 30lbs.
* Lifting material up to 50lbs.
* Push/pull (rarely) broom to collect loose debris on floor.
* Perform various housekeeping tasks, empty trash, clean breakroom, grounds, and dock cleaning as required.
Utilize broom and shovel as required to perform housekeeping functions.
* Pushing 5 to 10 lbs.
both push and pull with force of 10 lbs.
* (Self-selected height) horizontal over 20 ft.
on a concrete surface
Basic Qualifications:
* Prior experience in a manufacturing or warehouse environment.
What Will Put You Ahead
* Ability to obtain a fork truck certification within 1 year
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more than 30,000 employees in over 150 locations are empowered to innovate every day -to make everyday products even better.
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Our Benefits
Our goal is...
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Type: Permanent Location: Savannah, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-27 08:10:37
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INVISTA Camden is seeking a Water / Wastewater Treatment Shift Operator to join their team.
Our Team
The Water / Wastewater Treatment Shift Operator will work under the supervision of the utilities/power supervisor.
This position will work in the potable water and wastewater compliance areas.
The selected individual must be a minimum certified "C" level Water Treatment Operator.
The shift operator will perform a variety of tasks in the operation of INVISTA's water and wastewater treatment plants.
Technical guidance will come from the Water Treatment / Wastewater Treatment Lead operator.
This is a 12-hour rotating shift that includes days, nights, and weekends with alternating 48-hour and 36-hour work weeks.
Based on a 28-day cycle the average time off is 14 days per cycle.
What You Will Do
* Safe, compliant, and economic operation of systems in the Water / Wastewater / Utilities areas
* Take necessary corrective action steps during shifts to maintain processes within the specified operating parameters
* Read gauges and meters, start and stop equipment, operate valves to route and control flows, determine and set proper chemical dosages and flow rates
* Calibrate and perform predictive maintenance on laboratory and field equipment as required and perform minor preventive maintenance and inspections on mechanical equipment
* Collect samples and perform routine laboratory and field analysis as required
* Record data for all analyses performed and enter data into required computer applications as well as maintain daily logbooks and bench sheets
* Assist with belt press operations, unloading various bulk chemical tankers, job safety analysis and safe work permitting for maintenance and contractors
* Work effectively within a team environment to include internal, external, and regulatory personnel
* Troubleshoot water and wastewater treatment-related problems while having decisive and timely action in response to treatment, production, utility, and environmental upsets
Who You Are (Basic Qualifications)
* Previous experience using MS Office (Word and Excel) including creating and formatting spreadsheets, workbooks, and charts
* Minimum "C" Level Water Treatment Certification for the State of South Carolina
* Valid State of South Carolina driver's license or the ability to obtain
* Must have legal authorization to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship
What Will Put You Ahead
* "A" "B" C" or "D" level Biological Wastewater Treatment license
* "C" level Water Distribution license
* 30 hours of college credits in math or science
Physical Requirements and Working Conditions
* Must be able to work a 12-hour rotating shift to include weekends and holidays as well as overtime depending on business needs
* Must be willing and able to meet on physical requirements for the role (i.e.
climb ladd...
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Type: Permanent Location: Lugoff, US-SC
Salary / Rate: Not Specified
Posted: 2025-04-27 08:10:33
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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!
* Set and discuss with superiors about the target and Criteria for Evaluation in the beginning of the year and allocate resource to achieve them; monitors progress toward objectives and adjusts plans as necessary to reach them.
* Monthly discussion with superior about monthly target, sales plan, and routing plan.
* Increasing the abilities in term of technical and selling skills by attend the course and seminar.
* Maintains accurate records and documents actions, processes paperwork on a timely basis, documents important aspects of decisions and actions.
* Coordinates with others to achieve the optimal use of organization resources; maintains good working relationships with colleagues in other organizational units.
* Strive to achieve Sales BU, long-term growth, and profitability of Elanco.
* Develop self to conform to Elanco’s Values & Behaviors.
* Performs other miscellaneous duties as assigned by superiors.
* Contact and meeting with head of distributors.
* Co-working and meeting with sales team of distributors in each area.
* Support marketing and technical in each area.
* Create project in key customers and strategy push/pull sales.
* Communicate between Elanco, distributors, and customers.
* Training products and update information of products to distributors
* Ensuring of myself and my subordinates comply with the company rules and regulations including Ethics and Compliance and external laws and regulations
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
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Type: Permanent Location: Bangkok, TH-10
Salary / Rate: 845000
Posted: 2025-04-27 08:05:42
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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!
Pour notre site de production à Huningue (68) en France, nous recherchons notre Directeur Assurance Qualité H/F.
Résumé de la fonction :
* Assure la supervision Assurance qualité de site de production Elanco Huningue France.
* Garantir la mise en place et le maintien des activités qualité du site de Huningue en conformité avec les réglementations en vigueur (CSP, BPF et cGMP) et les directives globales Qualité.
* Anime son équipe.
* S’inscrit en partenaire du développement du chiffre d’affaires de l’entreprise.
* Supporte le responsable pharmaceutique du site en tant que responsable pharmaceutique intérimaire du site de Huningue en lien avec la fiche de fonction responsable pharmaceutique.
A ce titre remplace le Sr Directeur qualité pour toutes les activités AQCQ de Huningue en son absence en coopération avec le directeur CQ.
* Agit en tant que Qualified Person (au sens annexe 16 des EU GMP et règlement 2019-6) pour la libération des produits Huningue.
* Participe aux décisions stratégiques de l’usine en tant que membre du comité de direction.
Activités principales :
Management de l’équipe
* S’assurer de la bonne gestion de l’équipe
+ Recrutement des nouveaux collaborateurs
+ Motivation des collaborateurs du service,
* Application et respect au quotidien des valeurs de l’entreprise
* Définir les plans de formation du personnel et évaluer les besoins avec les Responsables concernés.
Organisation, coordination
* Recueillir et consolider les éléments de budget, le faire approuver et en contrôler le respect.
* Coordonner les activités au sein du service et veiller au suivi et à la réalisation des objectifs, tant pour les activités d'enregistrement, de la pharmacovigilance et du respect du système qualité.
* Identifier les nouveaux moyens (informatique, bureautique…) permettant d’améliorer l’efficacité du travail des collaborateurs.
* Gérer les affaires du service avec le souci permanent d’en accro...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 84000
Posted: 2025-04-27 08:05:40
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Dexco is a leading provider of innovative technology solutions tailored to the Canadian legal industry.
Our mission is to provide legal professionals with state-of-the-art tools that simplify their work and improve their productivity.
We are passionate about providing high-quality, customer-focused products and services, and we are looking for the next star for our dynamic sales team.
Responsibilities :
* Generate interest in Dexco’s products and services by executing outbound call campaigns and responding to inbound inquiries.
Understand the prospect’s business needs and present compelling solution concepts that address those needs.
* Deliver Dexco’s value proposition with conviction, instilling confidence in our ability to deliver results.
* Manage your pipeline and qualify sales opportunities.
* Build and maintain positive relationships with customers.
* Close sales by highlighting the benefits and features of the products.
* Follow market trends and stay informed competitors.
* Target and approach potential new clients.
* Visit clients and potential new clients
* Attend market related tradeshows across the country.
* Handle transactions accurately and ensure quality after-sales service.
* Collaborate with the team to meet sales quotas.
Required Skills :
* Proven track record in attainting and exceeding quotas
* Experience in SaaS software sales
* Exceptional verbal and written communication skills in both French and English
* Demonstrated curiosity and interest in technology, sales, and customer service.
* Strong organizational skills with the ability to multitask and work independently.
* Ability to build, maintain and forecast sales pipeline
* Fluent in French and English (Bilingual)
* Familiar with Office 365 and HubSpot (CRM) tools
What’s in it for you :
* Competitive salary with attractive commissions.
* Full benefits package (3 weeks' vacation, Health & Dental insurance, Retirement Savings Plans & more).
* Opportunities for career advancement within the company.
* Remote work.
*English and French as we have customers in the rest of Canada and the United States
*.
*Only successful candidates will be contacted
*.
Harris is an Equal Opportunity Employer and members of the following targeted groups are encouraged to apply: women, persons with disabilities, aboriginal peoples and visible minorities.
If you are a person with a disability, assistance with the screening and selection process is available on request.
The Harris Talent Acquisition team does not use text messages to contact candidates or solicit confidential information.
We encourage all candidates to apply for advertised positions.
They will be contacted either by a Harris manager or by a member of the Talent Acquisition team for an interview, once the required criteria have been met.
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 60000
Posted: 2025-04-27 08:05:35
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Harris School Solutions is seeking a talented and organized Documentation Specialist to manage our documentation strategy across multiple product lines.
This position is crucial for ensuring all product documentation is clear, comprehensive, and accessible to both internal teams and end-users.
You will partner closely with Product, Development, and Support teams to ensure documentation aligns with product goals and customer needs.
What's Your Impact:
* Strategy Development: Define and execute a comprehensive documentation strategy across multiple product lines, ensuring consistency, accuracy, and clarity.
* Cross-Functional Partnership: Work with product managers, developers, customer support, and other key stakeholders to gather requirements and comprehend product features to create effective documentation.
* Documentation Creation & Review: Oversee the creation, editing, and ongoing updates of product manuals, help guides, release notes, and knowledge base articles.
* Standardization & Best Practices: Establish and maintain documentation standards and processes, ensuring consistency and scalability across all product lines.
* Content Management: Develop and maintain content management systems to organize and store documentation.
* Continuous Improvement: Evaluate feedback from users and teams to improve documentation quality and ensure it meets evolving customer needs.
* Quality Assurance: Ensure documentation is error-free, adheres to company guidelines, and aligns with the brand’s voice and style.
* Reporting: Track and report on the progress of documentation projects and initiatives to leadership, providing regular updates and identifying any issues or resource needs.
What We're Looking For:
* Proven experience as a Documentation Specialist, Technical Writer, or similar role in a software/product environment.
* Solid knowledge of documentation processes, content management systems, and version control.
* Excellent written and verbal communication skills with a keen eye for detail.
* Ability to comprehend complex technical concepts and present them clearly to a non-technical audience.
* Solid project management skills, with the ability to handle multiple tasks and deadlines.
* Familiarity with software development and agile methodologies is a plus.
* Bachelor’s degree in English, Technical Writing, Computer Science, or a related field (preferred).
Why Join Us:
* Be part of an innovative company shaping the future of education technology.
* Collaborative and supportive team environment.
* Opportunities for professional growth and development.
* Competitive salary and benefits.
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Type: Permanent Location: Columbia, US-SC
Salary / Rate: 70000
Posted: 2025-04-27 08:05:35
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J oin PACS: Elevate Healthcare with Us!
PACS is elevating healthcare by r evolutionizing our approach to leadership and quality care.
Guided by our core values of love, excellence, trust, accountability, mutual respect, and fun , we strive to foster a culture of compassionate care within our teams and the communities we serve.
As we grow rapidly, exciting opportunities await you to engage in impactful projects and contribute valuable insights to stakeholders nationwide.
If you're ready to make a difference and embrace our mission of creating real change, we invite you to join us at PACS.
Together, let's shape the future of healthcare!
Join Our Team and Thrive!
At PACS , we believe our employees are our greatest asset.
That's why we offer an exceptional benefits package designed to enhance your well-being and support your lifestyle.
Our comprehensive benefits include:
* Health Coverage : Enjoy medical, dental, and vision plans to keep you and your family healthy.
* PTO and Vacation : Benefit from generous paid time off and holidays to relax and recharge.
* Financial Wellness : Take advantage of Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA) to manage your healthcare expenses effectively.
* Retirement Planning : Secure your future with our 401(k) plan, complete with company contributions to help you build your retirement savings.
* Support When You Need It : Our Employee Assistance Plan (EAP) provides confidential support for personal and professional challenges.
Join us at PACS and take advantage of a workplace that truly values you!
General Purpose
Identify the roles and responsibilities of the AIT in a Long-Term Facility.
This is a training position with direct oversite by a
licensed Precepting Administrator.
*
*
* All Essential Duties and Responsibilities of this position are under the direct supervisor of the Preceptor
*
*
*
Essential Duties
* Assists in analyzing the various operations within a nursing facility
* Acts as a liaison between the nursing facility, residents, families and outside community
* Compiles and develops reporting on budget projections, revenue and expenses
* Is a role model for our Mission, Vision and Values.
Ensures all employees, residents and families are treated with the utmost respect
* Actively involved in community groups and developing/maintaining relationships with local hospital leadership and physicians
* Monitors industry regulations, laws, compliance updates and makes changes as appropriate
* Uses time effectively to study for both Federal and State regulations and comes to a sound understanding of industry best practices
* Understands staffing level requirements and adheres to industry and company standards
* Assists in monitoring and directing execution of policy and procedural changes
* Actively involved in resolving HR issues and Risk Management situations within the facility
* Assists in capi...
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Type: Permanent Location: Farmington, US-UT
Salary / Rate: Not Specified
Posted: 2025-04-27 08:05:33
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Senior Formulations Scientist
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
In this role, you will:
Provide formulation expertise and leadership for commercializing and maintaining formulations for North America and global wet wipes.
This role resides within the KCNA Innovation Capabilities organization and will primarily be focused on supporting North American wet wipe product development and manufacturing.
The role will partner closely and work cross-functionally with KCNA R&E, Global Quality, Procurement, Maumelle and Beech Island. Leads moderate to large projects and carries out accountabilities with a collaborative mindset ensuring visibility of progress/results to all key stakeholders.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You 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.
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
To succeed in this role, you will need the following qualifications:
* Leads the scale-up, commercialization and maintenance of formulations used to produce wet wipe products that meet consumer, quality, regulatory and compliance needs.
* Closely partners with Personal Care and Family Ca...
....Read more...
Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-27 08:05:22
