-
Responsible for actual practice (implementation and accountability) of safety control procedures.
Responsibilities include collection, evaluation and planning/implementing safety assurance measures in responsible therapeutic area (mainly Joint), following company standard operating procedures (SOPs), internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations and corporate policies, and to contribute to identifying potential safety issues.
Key Responsibilities:
Case processing:
• Make a final safety assessment of collected information for decisions in Seriousness,
expectedness and causality of safety information with due date for reporting to PMDA.
Monitor and manage the adverse event occurrence.
Make report to PMDA.
• Develop and maintain safety process with stakeholders such as spontaneous report,
literature cases (Japanese article, foreign article) and foreign cases.
Safety assurance measures and acceleration of proper use:
• Plan necessity of safety measure
• Participate in product risk management including NPI and change control.
• Generate and revise package insert and user manual for the responsible product.
• Negotiation between JJKK and operating company and/or PMDA about package insert.
• Planning and implementation of measures to promote proper use.
Compliance & continuous improvement:
• Complete Training of Local and global SOPs and guidelines, Relevant Japanese
regulations and compliance with the requirements.
• Provide GVP-related training.
• Participate in inspections and audits including provision of requested data.
• Continuous improvement of GVP process including usage of digital tools.Education:
• Bachelor's degree or educational equivalent (Health science or other directly related field
or equivalent combination of education is preferred.)
Experience and Skills:
Required:
• Manages own work: ability to prioritize, plan and organize work assignments, and able
to work under strict timelines.
• Ability to work both independently and in collaboration with others.
• Proactive approach/uses own initiative appropriately.
• Logical thinking, Decision-making and problem-solving skills
• Strong commitment to achieving goals and flexible execution capability.
• Positive attitude
Preferred:
• Knowledge of Joint reconstruction products.
Medical device or pharmaceutical industry
experience
• Experience in Vigilance, Marketing, Regulatory Affairs, Quality Assurance or experience
as a sales representative.
• Knowledge or experience of Digital technology and service
Other:
• Work style based on J&J flex
• Good verbal and written communication skills in Japanese
• English in business level
• Good IT literacy
....Read more...
Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:43
-
§ Start up and run CNC machine in a safe and effective manner that ensures maximum performance and longevity of equipment; / 以安全和有效的方式启动和运行 CNC 车床,确保机器高效持久运行;
§ Follow manufacturing specifications to consistently produce products to the required quality standard; / 遵循生产技术规范,始终生产符合质量标准的产品;
§ With the assist of setter /engineer to modify the machine settings to compensate for tool adjustments and renewal, or for material variations; /, 在刀具调节和更新或物料变化时 , 在换型人员或者工程师的指导下修改机器设置;
§ Operate ancillary equipment such as bar feeders or internal probes in line with specifications ; / 按照技术规范操作辅助设备例如棒料送料器或内部探针;
§ Down load CNC programs from / to an external PC or control system; / 自 / 至外部 PC 或控制系统下载 CNC 程序;
§ Change over jigs and fixtures and ensure they are stored and controlled to prevent damage or incorrect use ; / 转换治具和夹具,放置和控制好确保防止损坏或不当使用;
§ Follow quality specifications to consistently produce products to the required tolerances and specifications, report to cell leader for quality issue as required; / 遵循质量规范始终按照要求的公差和规范生产产品,按要求将质量问题报告给生产线主管;
§ Comply with all aspects of good manufacturing practice to maintain full material and product traceability; / 遵守生产管理规范的所有方面,维护全部物料和产品可追溯性;
§ Accurately record job transactions and WIP monitoring; / 精确记录工作处理和工作中监控;
§ Other job assign by cell leader.
/ 生产线主管分配的其它工作。l Knowledge of machining, understand the movement and control of the axial of the machine tool.
Experience of tool management and tool change, understand offset of the tools, can operate the machine tool and do some necessary maintenance of machine tool, such as PM check list and cleaning.
了解操作的机床,掌握机床轴的控制及运动,熟悉刀具的使用与控制,熟悉刀具补偿的设定,掌握机床的操作以及机床的必要维护,如点检,清洁;
l Can use and protect fixture properly.
能正确使用与保护夹具;
l Can use and protect gage properly.
能正确使用与保护量具;
l Basic mathematics skills tolerance knowledge;
基本的数学技能及公差知识;
l Understand quality procedure, meet the quality requirement, can deal with the nonconformance and scrap according to the procedure.
Complete the work consistence with the GMP requirement;
了解质量流程, 满足质量要求: 包括不合格品,报废品的控制以及返工的流程,掌握要求的 DHR 与 GMP 知识;
l Good working habit (5S), quality sense;
良好的工作习惯 (5S) 与质量意识;
l Understand production process, and execute according to the requirement;
理解相应生产流程, 能按标准要求操作;
l Understand EHS requirement of relative position, wear the PPE accordint to the requirement;
理解相应岗位的安全要求,明白 PPE 佩戴要求;
l Team work spirit;
团队精神;
....Read more...
Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:42
-
Johnson & Johnson is recruiting for a Global Access Management (GAM) Compliance Analyst, located in Paranaque City, Manila.
The GAM Compliance Analyst will be responsible for Global Access Management (GAM) governance over applicable information technology controls and compliance activities related to relevant policies and procedures across supported J&J organizations.
The GAM Compliance Analyst will also be responsible for performing reviews of system access for users of ERP and non-ERP systems.
The analyst ensures there are appropriate mitigating controls for identified segregation of duties (SOD) conflicts and acts as Subject Matter Expert (SME) for GAM governance and related projects/ due diligence activities.
Key Responsibilities:
Access Management
* Review completeness and appropriateness of access/change/removal requests from business users.
* Review access requests against the role matrix/library and ensure approvers are correct based on the approval matrix.
* Perform Segregation of Duties (SOD) review to ensure the access requested does not conflict with existing access and manual job responsibilities.
* Assigning/documenting appropriate mitigating controls on new/existing valid/accepted SOD conflicts.
* Prepare weekly movement reports to ensure that the system access of transferred employees is up-to-date, and the system access of terminated users is revoked on time.
* Perform access and SOD recertifications periodically and ensure remediations are completed on time.
* Perform accurate and on-time segregation of duties (SOD) assessments by establishing tools and guidelines to ensure that mitigating control libraries and SOD rulesets are up-to-date and complete.
* Prepare and update SOPs and Work Instructions documentation.
* Prepare documentation for internal and external audits related to access management controls (e.g., walkthroughs and documentation).
* Conduct IT access management controls and GAM refresher training and provide continuous support to business reviewers/approvers and related process owners.
Due Diligence and Projects
* Perform due diligence reviews (e.g., role mapping and SOD assessment) and manage access deployment to stakeholders in projects involving process migrations/transitions
* Support the business by monitoring risks related to organization, technology, and process changes to ensure that the system roles remain appropriate.
* Provide access management compliance support for new/existing systems.
* Identify opportunities for continuous process improvements.
Other tasks that may be assigned Experience and Qualifications
• University Degree in Finance, Business Management, IT or a related field
• Professional Certification/s (e.g., CISA, CPA) is an advantage
Mandatory Technical Qualifications:
• Basic skills in MS Office applications (Excel, Outlook, Powerpoint, Word)
• Planning, time management skills.
• Strong Analyt...
....Read more...
Type: Permanent Location: Manila, PH-00
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:38
-
Business Improvements 业务改进
§ Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
支持质量改进活动,对产品 / 过程进行持续改进和成本改善。
§ Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
评估和分析质量工具及项目的有效性,比如 PDCA ,六西格玛,改善,精益技术和 / 或其他改进工具。
§ Conduct benchmarking to develop more effective methods for improving quality .
通过标杆管理开发更有效的质量管理方法提升质量。
§ Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management.
开发合适的质量管理方法应用于质量工程和质量合规的发展,运用在新产品导入和产品生命周期管理。
Compliance/Regulatory 合规管理
§ Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc.
评估和分析现有产品和制程是否合规,比如 QSRs , ISO13485 等法规要求
§ Champions compliance to applicable Global Regulations and standards (e.g.
QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
支持工厂的内外部审核,遵守适用的法规和标准 ( 例如 QSRs, ISO, EN 和 MDD) 要求。
§ Conduct periodic line audits to assess for production controls such as lot segregation.
Review results of area audits to ensure that corrective and preventive actions are adequate.
执行周期审核评估生产现场是否合规。审阅区域审核的结果确保纠正和预防措施有效。
New Product/Process Introduction 新产品 / 制程导入
§ Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.
协调研发和其他的跨部门合作确保相关领域质量管理可控。比如设计管理,风险管理,研发失效的调查 / 纠正等方面。 /
§ Supports new product introduction as part of design transfer.
支持新产品导入业务活动,作为研发项目转移的-部分。
Product Quality, Control & Disposition and Performance Standards 产品质量控制处理和执行
§ Supports activities related to the Material Review Board.
支持材料审核相关业务活动
§ Conduct investigation, bounding, documentation, review and approval of non-conformances, CAPAs and customer complaints.
Escalation of quality issues as appropriate.
执行 NC , CAPA 和客户投诉的调查分析,审阅和批准。
§ Accountability and ownership for material identification, material segregation, classification of defect types including the successful application of...
....Read more...
Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:38
-
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahren Sie mehr unter https://www.jnj.com/
Abiomed ist ein innovatives Medizintechnik-Unternehmen mit einer inspirierenden Mission "Patients First." und einem einzigartigen Firmenmotto "Herzen regenerieren.
Leben retten".
Mit mehr als 3.000 Mitarbeitern ist Abiomed eines der am schnellsten wachsenden Medizintechnik-Unternehmen weltweit mit dem Firmenhauptsitz in Danvers, USA sowie Standorte in Aachen und Berlin, Deutschland, Tokio, Japan und Singapur.
Abiomed ist Teil von Johnson & Johnson MedTech.
Abiomed ist ein Arbeitgeber mit attraktiven Arbeitsbedingungen und einer wertschätzenden Unternehmenskultur, bei dem die Bedürfnisse der Mitarbeiter im Fokus stehen.
Abiomed begeistert und bindet außerordentliche Talente durch Zusammenarbeit, Leidenschaft und kontinuierliche Weiterentwicklung.
Wir suchen aktuell einen Regional Clinical Educator / Clinical Consultant (m/w/d), für den Raum München .
Spannende Aufgaben warten auf Sie:
* Patientenbetreuung: Verbesserung der Patientenergebnisse durch eine fachgerechte Ausbildung und Beratung des medizinischen Personals.
* Betreuung aller Kliniken, in denen Patienten mit Impella® Produkten behandelt werden.
* Reportings von klinisch relevanten Daten, Dokumentation von Ergebnissen und eine enge Zusammenarbeit mit unseren Teammitgliedern und Vertriebskollegen.
* Klinische Beratung: Durchführung von Trainings zur Steigerung der klinischen Auslastung und Leistung unserer Kunden.
Verwaltung von Schulungen für unsere neuen und bestehenden Kunden.
* Training/klinische Demos: Unterstützung bei der Koordination von klinischen Demos vor Ort.
Ihr Profil
* Erfolgreich abgeschlossene klinische oder klinisch-technische Ausbildung, idealerweise als Gesundheits- bzw.
Krankenpfleger(in) oder Kardiotechniker(in) / Klinischer Perfusionist(in).
* Mehrjährige Berufserfahrung in der direkten Patientenbetreuung auf Intensiv- oder Pflegestation, im OP oder im HKL.
* Überzeugendes Auftreten und die Fähigkeit, langfristige Kundenbeziehungen weiterzuentwickeln und zu fördern.
* Gute Kommunikations- und Präsentationsfähigkeiten sowie Teamfähigkeit.
* Hohe Flexibilität und 80% Reisebereitschaft innerhalb der vorgegebenen Regionen sowie Einsatzbereitschaft für Notfallsituationen.
Wir bieten:
* Angenehme, offene Unternehmens...
....Read more...
Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:38
-
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 pharmaceutical, medical devices and diagnostics markets, 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/ .
1.
포지션 : Associate Territory Manager
2.
계열사 : 존슨앤드존슨 서지컬비전 (Surgical Vision)
3.
근무지 : 서울시 용산구
4.
근무 형태 : Regular
[Responsibilities]
1.
Actively promote J&J products and services aligned with core mission, corporate strategies, policies, procedures (Foundation list) and Code of Conduct.
2.
Assist in the development and implementation of strategic sales plans.
3.
Perform sales calls (HCP / Distributors) to promote, sell, demonstrate and service J&J's products and services to existing, and potential customers in its operating room or relevant hospitals and provide brief training and education for both existing and potential customers to gain market share if needed
4.
Manage current distributors throughout effective communication to develop assigned territories and ensure maximum coverage of all accounts within territory geographic areas to maintain optimum level of exposure and effective time management.
5.
Maintain a high level of product knowledge after internal product and relevant training
6.
Provide on-going field intelligence reports on competitive activity, changes in market, distribution, pricing as well as input on customer preferences and product features.
7.
Develop business plans which identify opportunities within current customer base and help formulate sales strategies in conjunction with team sales manager or national sales manager
8.
Support and Provide necessary supports including trainings to customers within the assigned territory to achieve individual and company goals
9.
Participate in product and skills development programs, managing own self development.
10.
Evaluate and improve job skills continually
11.
Develop and maintain professional selling skills
[Requirements]
- Bachelor's degrees or above.
- 3-6 years of experience in health care business are preferred
- Understanding of sales & business planning & relevant account
- Good inter-personal relationship
- Proactive, positive & innovative mind
- Strong analytical, problem solving and project management skills
- Good communication & negotiation skills
- Excellent English communication (Writing & Oral) ability
- MS Office skills (Word, PPT, Excel) proficiency
[ 지원 방법 ]
www.careers.jnj.com 접속 -> Position Number 2506231881W 검색 -> 해당 모집 공고의 "Apply Now" 클릭 후 온라인 지원 프로세스 진행
[ ...
....Read more...
Type: Permanent Location: Yongsan-gu, KR-41
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:37
-
Key Responsibilities Include:
• Responsible and accountable for Medical Affairs strategy of therapeutic/disease area (TA/DA) including compounds/product development/business plan.
• Collaborates with internal and external stakeholders including key opinion leaders to develop and implement the overall Medical Affairs strategy for product lifecycle aligned with company brand strategy.
• Responsible for people development and operational budget management of TA/DA group.
• Responsible for ensuring that all Medical Affairs activities are compliant with Japan Legislation and HCC rules.
• Manage the high-performing organization and to provide the healthier working environment.
• Evaluating, developing and implementing training programs designed for further improvement of strategic capability by assessing needs, skills and scientific knowledge
• Providing advanced scientific information on Janssen products (incl.
reactive off-label information) to HCPs in compliance with internal and external regulations
• Supervise all activities of each member in the group; Supervise to manage and utilize medical information for business; Supervise to handle inquiries from internal as well as external customers; Oversee the maintenance of product FAQ portfolio on Janssen products; Supervise providing appropriate information to relevant dept; Overseeing of Handling call center operation; Supervise reviewing materials to be distributed to external customers
• Driving functional excellence and alignment
• Managing operational TA budget and allocating human resources based on brand strategy and product life cycle
• Developing & managing TA strategy aligned with other critical functions/regions (R&D/BU/AP/GL); Supervision of Medical Affairs Plan (MAP)
Provides input into early development through core membership of TASTe; Assigning members for TA activities & product teams (JCoT, CVWG, IEGP etc ); Provides input into brand strategy
• Leading entire TA activities by providing clinical direction and strong leadership
• Accountability and supervision of MAP and monthly report by products
• Accountable for execution of all TA activities
• Collaborates with functional directors to improve the functional excellence and alignment
• Leading members in TA/DA departments
• Accomplishing TA objectives by establishing plans and KPI measurements with functional directors.
• Establishing good relationship with internal stakeholders (BU/R&D/AP; group level, individual issue or task oriented)
• Developing professional capabilities for TA departments including TA knowledge, data generation capability, and leadership.
• Managing TA/DA budget and human resources
• Managing operational budget and allocating human resources upon Medical Affairs plan
• In collaboration with finance controller and alignment with AP/GL MAF
• Managing MAF initiated clinical/non-clinical study
• Evaluating new IIS proposals
• Develop clo...
....Read more...
Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:37
-
Position Summary:
(Briefly state the objectives of this position)
A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site.
A Site Manager II 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, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols.
A Site Manager II may contribute to process improvement, training and mentoring of other Site Managers.
Principal Responsibilities:
(List Major Responsibilities and duties of the position.
Describe scope of responsibilities.)
1.
Acts as primary local company contact for assigned sites for specific trials.
2.
May participate in site feasibility and/or pre-trial site assessment visits
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.
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 and activate the site in shortest possible timeframe.
6.
Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
7.
Ensures site study supplies(such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trial conduct.
8.
Ensures that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented.
9.
Arranges for the appropriate destruction of clinical supplies.
10.
Ensures site staff complete data entry and resolve queries within expected timelines.
11.
Ensures accuracy, validity and completeness of data collected at trial sites
12.
Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropria...
....Read more...
Type: Permanent Location: Chengdu, CN-51
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:36
-
* Documents business critical issues in Customer/Commercial Quality and tracks regulatory changes.
* Applies in-depth knowledge of Customer/Commercial Quality and surfaces policies that may impact organizational objectives.
* Conducts routine collection and dissemination of feedback to ensure continuous improvement of the quality management system.
* Completes processes to ensure internal organization's alignment with overall quality priorities.
* Implements formal escalation processes to surface issues of product quality, regulatory compliance, and quality systems.
* Analyzes complex research and data related to regulatory changes, external trends, and strategy.
* Contributes to customer handling complaint process, and establishes and maintains Quality System Elements.
* Coaches more junior colleagues in techniques, processes, and responsibilities.
* Understands and applies Johnson & Johnson's Credo and Leadership Imperatives in day-to-day interactions with team.
The main responsibilities are as following in accordance with execution of the Quality Management Systems and compliance, which involve change control, repack/relabel tracking, complaint handling, and reporting serious adverse events.
1.
Support the implementation and maintenance of the Quality System to ensure awareness and continuous education across the local organization.
2.
Coordinate with stakeholders, establish and drive the execution of corrective and preventive actions, ensuring the timely closure of CAPA actions, including those involving 3PL DC.
3.
Consolidate and track quality compliance metrics, identify and analyze gaps with targets, recommend initiatives for continuous improvement of quality performance, and enforce compliance.
4.
Serve as a subject matter expert and provide training to the country on the quality system, auditing behaviors, complaint vigilance, and process improvement methodologies, techniques, tools, and language to enhance processes and improve business results.
5.
Drive the execution of complaint vigilance and pharmacovigilance in the country, ensuring the timely closure of product-related complaint cases and Adverse Event reporting.
6.
Ensure the material & product control within DC, including stop shipmen, return goods, inbound discrepancy and stop shipmen
7.
Partner with Commercial business partners and key stakeholders to deliver on-time NPI, A&D, and/or POLO to enable high quality and innovative products / disruptive solution into the market that drive growth.
8.
Supplier Audit program and ensure inspection readiness and provide strategic focus for quality and compliance by working with appropriate functional areas to identify continuous improvement opportunities
9.
Undertake project assignments from the line manager.
* Knowledge of Standards:
* Good understanding and application of MD/Pharm GDP, ISO 13485, ISO 14971 and other international standards.
In...
....Read more...
Type: Permanent Location: Taipei, TW-TPQ
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:35
-
Word jij onze enthousiaste Maintenance Technician Meet & Regeltechniek?
Bij Johnson & Johnson Innovative Medicine, Biologics in Leiden gebruiken we onze biotechnologische kennis en ervaring om complexe biologische medicijnen en vernieuwende therapieën te produceren.
We werken met levende cellen aan de behandeling van ziekten zoals ontstekingsziekten en bloedkanker.
Wat ons drijft, is het geloof dat patiënten wachten en dat er geen tijd te verliezen is.
Dit ga je doen als Maintenance Technician Meet & Regeltechniek
Als Maintenance Technician ben jij verantwoordelijk voor het uitvoeren van gepland onderhoud en het snel en efficiënt oplossen van storingen.
Met jouw expertise in meet- en regeltechniek, aangevuld met mechanische en elektrische vaardigheden, maak je een cruciaal verschil in ons team.
Je draagt bij aan de productie van innovatieve, 'custom-made' geneesmiddelen en hebt een significante impact op de gezondheidszorg.
Samen met je team waarborg je de continuïteit van de operationele site, waarbij je de gestelde deadlines en onze interne procedures respecteert.
Jouw verantwoordelijkheden
* Repareren en onderhouden van technische installaties, systemen en apparatuur.
* Testen van technische installaties, systemen en apparatuur.
* Analyseren en verhelpen van storingen.
* Toepassen van je meet- en regeltechnische kennis
* Advies geven vanuit jouw specifieke deskundigheid met betrekking tot storingen en onderhoud.
Het team
De maintenance-afdeling van Johnson&Johnson is een dynamische mix van collega's uit verschillende landen, die samen nieuwe perspectieven en innovatieve oplossingen verkennen.
We werken met zowel gebouwgebonden- als productie-installaties, en jouw ontwikkeling staat centraal.
Bij ons krijg je de vrijheid om je werk zelf in te richten en we moedigen initiatief aan, met een sterke focus op het behalen van persoonlijke en bedrijfsdoelen.Hier herken jij jezelf in
Je bent een teamspeler die zowel preventief als correctief onderhoud uitvoert.
Je communiceert effectief met collega's en andere afdelingen, wat essentieel is voor het snel oplossen van (complexe) problemen.
* Teamplayer met een sterke can-do houding en een servicegerichte instelling.
* Sterke probleemoplossende vaardigheden.
* Resultaatgerichte, initiatiefrijke en gedreven persoonlijkheid.
Jouw profiel:
* MBO-HBO werk- en denkniveau in elektrotechniek en instrumentatie.
* Technische ervaring in een industriële omgeving, met sterke vaardigheden in storingsoplossing en preventie.
* Uitgebreid begrip van elektrotechnische veiligheidsnormen, waaronder NEN3140.
* Proactieve houding voor een veilige en efficiënte werkomgeving.
* Pré: Ervaring in de GMP-gereguleerde farmaceutische industrie.
Wat je van ons kunt verwachten
Werken bij Johnson&Johnson betekent bijdragen aan innovaties die levens verbeteren.
Je wordt onderdeel van een gemotiveerd team dat zich richt op innovatieve medicijnen met dir...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:34
-
The Group Manager of Medical Affairs, Lung Cancer MSL Group will lead a multifaceted critical function for the operating company by supporting multiple products, reporting to the Associate Director, Lung Cancer, Medical Affairs Japan.
A strong insight into the Lung Cancer disease area (DA) and knowledge of the Japan market is required.
The Group Manager will take full responsibility for the MSL group in charge.
Responsible for organizational operation and people management of the MSL group.
Collaborate with Capability and & Digital Excellence Groups to develop the capabilities of group members.
Responsible for building strong relationships with HCPs (including KOLs) in line with brand strategy and for conducting medical and scientific communication with HCPs to improve access and clinical utility of J&J products based on the trends of the pharmaceutical industry (medical policy, administrative guidelines, etc.), discuss with related parties in the company, propose ideas, and play a role in leading to the development of medical care.
Collaborate with Medical Leads during Integrated Medical Affairs Plan (IMAP), and Integrated Evidence Generation Plan (IEGP), and lead MSLs to provide scientific information/insights from customers.
Responsible for developing the MSL activity plan, clarifying goals, and supporting and guiding the activities of each member to achieve maximum results.
Evaluate the risks of each activity of the group and implement risk management at an appropriate level.
Utilize the cross-departmental stakeholder network within the company to organize and coordinate team roles and issues.
Responsible for ensuring that all MSL activities comply with Japanese legislation and HCC rules.
The position is based in multiple places in Japan.
Key Responsibilities:
• Lead Lung Cancer MSL group members
• D evelop the MSL activity plan aligned with IMAP and execute the plan
• B uild strong relationships with HCPs (including KOLs)
• Supervise and mentor team as well as hiring.
Education:
• Bachelor of Science degree required.
• PhD in life sciences and/or MD preferred.
Experience and Skills:
Required:
* Experience of Oncology in pharmaceutical industry or medical institute
* People management ability and organizational management ability is essential.
* High communication skills are essential to be able to discuss on an equal footing with internal/external stakeholders and build a strong relationship of trust.
* E xperienced in leading and completing numerous complex projects
* Business level of Japanese and English communication
* Presentation skills and business acumen as a necessity.
Preferred:
* Work experience of 5 years in pharmaceutical industry or medical institute is desirable.
* Work experience as MSL is desirable.
* Experience with Lung Cancer is preferred.
* People management experience preferred.
* Deep understanding of local regulatory policy and industryʼs...
....Read more...
Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:33
-
Ready to make a real impact in groundbreaking medicine?
Join us at the Johnson & Johnson CAR-T Job Event for QC Analysts and Lab Technicians in Beerse !
We're revolutionizing cancer treatment! Cell therapy represents a new approach to fighting cancer, harnessing the incredible power of a patient's own immune system.
Our Chimeric Antigen Receptor T-cell (CAR-T) therapy enables engineered cells to target and destroy cancer cells with precision-and we need passionate professionals like YOU!
Whether you're into quality control, cryopreservation, or biotech, this is your chance to explore exciting career opportunities within our CAR-T department!
️ Mark your calendars for March 10th and April 7th and get ready for a half day filled with insights and opportunities! Meet our amazing team, tour our state-of-the-art labs, and participate in panel interviews.
Discover how you can contribute to the future of medicine!
Our dedicated team in our Beerse site are excited to meet you, answer your questions, and share more about our inspiring work and projects!
✨ Don't miss out-register now and start your journey with us!
Please note: Registration does not guarantee an invite, as there are limited spots available.
An official invite will follow once you have spoken with a member of our team.
Meet our departments in the testimonials below on LinkedIn!
Cryo: https://www.linkedin.com/posts/jnjinnovativemedicinebelgium_car-t-cryopreservation-activity-7155539930587230208-WcNb?utm_source=share&utm_medium=member_desktop
Biotech: https://www.linkedin.com/posts/jnjinnovativemedicinebelgium_werkenbijjanssen-biotech-qualitycontrol-activity-7130137260179496960-qA8b?utm_source=share&utm_medium=member_desktopQualifications & Experience: Join the Fight Against Cancer!
We're seeking passionate individuals ready to make a difference as QC Analysts or Lab Technicians! If you hold a background or a degree in Biomedical Laboratory Technology, Pharmaceutical, Biotechnological, Biochemical, or Biological Sciences-or have equivalent lab experience-we want to hear from YOU!
Do you have experience in a microbiological lab within the pharmaceutical industry? That's a plus! Familiar with cGMP regulations? Even better! Here are the qualities we look for in candidates:
* Quality-conscious and detail-oriented - because precision saves lives.
* Results-driven and proactive - we're pushing the boundaries of what's possible!
* Fluent in English - to collaborate effectively on a global scale.
* Flexible and positive - adaptability fuels innovation, as our CAR-T departments will be running in shifts (Early-late).
⏰
* Team players and independent thinkers - both qualities are key to our success!
This is your chance to contribute to a company that's changing the world! If you're ready to bring your skills, passion, and drive to Johnson & Johnson, register now and take the first step towards an exciting and rewarding career! ⚡️✨
For over 130 years...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:33
-
Job Position Summary
Sales Rep は,売上目標達成に責任を持ち,担当エリアの営業活動の計画立案と実行を行う。販売代理店とのコミュニケ-ション•販売戦略の企画立案 / 実行を行う。
エリア担当者として, LT メンバ-やリ-ジョナルセ-ルスマネジャ-,エリアマネジャ-に対して客観的かつ建設的に必要な意見具申を行う。
Duties/ Responsibilities
担当エリアの売上目標達成および社内ガイドラインに基づくプライシングコントロ-ルを行う
重要顧客とネットワ-クを構築し良好な関係を維持する
市場,顧客,競合に関する情報を常時収集し,エリア内外に共有するとともに必要に応じて関係部門にもフィ-ドバックする
新製品上市に向けた営業戦略を担当エリアにおいて積極的に実行する
製品の安全•適正使用に関する社内および顧客向け教育プログラムの立案を必要に応じてサポ-トする
エリア内外の市場動向を把握し,製品戦略に基づくエリア戦略を積極的に実行する
各関連法規,コンプライアンスを遵守し,社内規定に沿った活動を行う
製品苦情に対して社内ル-ルに沿って,関係部門と協業しながら迅速かつ適切に対応する
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/.Experience:
•医療業界の営業職経験 ( 3 年以上が望ましい)
医療業界での営業職経験無しでも営業職経験があれば OK
•眼科領域における経験( 1 年以上が望ましい)
眼科領域での営業職経験無しでも営業職経験があれば OK
• PC スキル( Microsoft Excel, Word, Power Point, Outlook など)
•戦略的•論理的思考 •プレゼンテ-ションスキル,優れた対人コミュニケ-ションスキル
•営業職における過去の実績(目標を上回る実績,表彰歴など)
•業界知識(眼科領域,法令, HCC ガイドライン,競合,その他)
•前向きに事業の成長に取り組むマインド
•普通自動車免許必須
....Read more...
Type: Permanent Location: Ken-Nagoya, JP-23
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:31
-
Johnson & Johnson is currently seeking a Production Student to join our team located in Nes-Ziona, Israel.
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 local company develop and manufacture innovative surgical solutions by delivering healing, stop bleeding, bone fusion, and leakage prevention products for surgeries, as well as treatment of auto-immune diseases.
Job Description:
* Support the production management team in improving production processes and procedures, with an emphasis on operations, safety, and quality.
* Enhancing processes through quality systems or innovations via digitalization.
* Work with quality systems (e.g., Windchill, CW, ETQ)
* Collaborate with control systems (e.g., LIMs, Priority)
* Update procedures as part of corrective actions (e.g., deviations, GC, etc.)
* Work as part of a team
* The position requires working three shifts per week, with each shift lasting 9 hours, according to the work plan.
* Registered student in Industrial and Management, Biotechnology Engineering, Chemical Engineering or with an equivalent engineering degree, with at least one year till graduation - must
* Proficiency in computer applications is a must
* Reading and comprehension in Hebrew and English is required
* Availability for three full days working days (9 hours each)
* Familiarity with Priority - an advantage
* Technical understanding and aptitude
* Ability to work independently and learn autonomously
#LI-AB6
#LI-Hybrid
....Read more...
Type: Permanent Location: Ness Ziona, IL-M
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:30
-
Health Economics, Market Access and Reimbursement Manager
Role Purpose
Johnson and Johnson Innovative Medicine Poland is currently recruiting a Health Economics, Market Access and Reimbursement Manager located in Warsaw to lead accelerated, broad market and patient access and funding for J&J IM key innovative brands.
The successful candidate will play a key role as part of the HEMAR team and will lead Pricing and Reimbursement processes in hemato-oncology and immunology areas.
The role reports into the HEMAR Lead.
This role is vital for shaping our overall strategy and is a key responsibility within our team.
Over the past few years, our company has changed a lot, especially with the fresh ideas from our new General Director.
This leadership has helped us redefine our values and focus, leading us to earn awards like "Best Employer" and "Best Place to Work."
Our HEMAR team is made up of young and ambitious people, and we have a new HEMAR Director with extensive international experience in the pharmaceutical industry (Aneta Skwarlinska).
The pipeline of JnJ in Hematology and Immunology is really broad, and we are growing as a Company - currently top 3 in Poland.
As HEMAR department we are responsible for providing broad and timely access for the patients, optimize the value of both the Company and its products, through the development of a positive external image perceived by payers.
We do this by effectively communicating the innovative value the Company and its medicines provided to patients and to the community.
Key Responsibilities:
You will ensure access for patients to our innovations by combining scientific, economic and communication aspects:
* You define the optimal strategy for local pricing and reimbursement dossiers and evidence generation, including health economic modelling and budget impact analyses, and ensure timely submission to local health authorities;
* You ensure market access excellence by capturing events in the healthcare environment that impact market access and establishing relationships with internal and external partners and key pricing and reimbursement decision makers;
* You actively cooperate with national and international cross-functional teams to integrate market access strategies into product plans;
* You support the European pricing and reimbursement teams with information on local pricing and reimbursement requirements and contribute to the European strategies;
* You represent the company externally with regard to market access and ensure leading presence at meeting with authorities, clients, industry associations and other partners regarding the pharma business.
Education:
University degree - economics/statistics/health economics/pharmacology;
Experience and skills expected:
* Experience in a multinational pharmaceutical company with proven at least 4 years' experience in Market Access role;
* Minimum 2 years' experience in full reimbursement process coordination ...
....Read more...
Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:28
-
Über Johnson & Johnson MedTech
Bei Johnson & Johnson glauben wir, dass Gesundheit alles ist.
Unsere Stärke im Bereich der Gesundheitsinnovation befähigt uns, eine Welt zu schaffen, in der komplexe Krankheiten verhindert, behandelt und geheilt werden und Behandlungen intelligenter, weniger invasiv und Lösungen persönlich sind.
Durch unsere Expertise in innovativer Medizin und MedTech sind wir in der einzigartigen Position, innovative Lösungen in das gesamte Spektrum der Gesundheit zu injizieren, um die Durchbrüche von morgen zu erzielen.
Wir verbinden Wissenschaft, Technologie und Entschlossenheit, um die Gesundheit der Menschheit tiefgreifend zu verbessern.
Erfahre mehr unter https://www.jnj.com/
Biosense Webster
Mit dem Geschäftsbereich Biosense Webster ist Johnson & Johnson führend im Bereich der kardiologischen Elektrophysiologie.
Die "Elektrophysiologie" ist ein Spezialgebiet zur Untersuchung und Behandlung von Herzrhythmusstörungen in der Kardiologie.
Die Aufgabe der Elektrophysiologie besteht darin, Herzrhythmusstörungen (insbesondere Herzrasen) bei einer Herzkatheteruntersuchung mit Hilfe von Elektrodenkathetern zu diagnostizieren und kurativ zu therapieren.
Was unser Team ausmacht
Biosense Webster ist geprägt durch einen starken Innovationscharakter sowie eine moderne und schnell, aber gesund wachsende Organisation.
Teamgeist, das richtige Mindset und eine offene Kultur machen den Erfolg und die Zufriedenheit unseres Teams aus.
Wir leben das "WIR": wir feiern nicht nur unsere Erfolge gemeinsam, sondern es herrscht eine positive Fehlerkultur, in der bemüht sind, Herausforderungen schnell und unkompliziert, gemeinsam zu lösen.
Wir kultivieren das Lachen und haben Freude an unserer Arbeit.
Wir schätzen Charakterköpfe mit Teamgeist, die Verantwortung übernehmen, sowie innovativ und lösungsorientiert voranschreiten.
Möchtest Du auch mit Deinem Engagement mitgestalten sowie mit Leidenschaft große Ideen voranbringen? Dann werde Teil unseres Teams!
Zur Verstärkung unserer Teams in Deutschland suchen wir ab dem 01.04.2025 mehrere
Associate Clinical Consultant (d/m/w) Biosense Webster im Außendienst
Region: OST
Die Position Associate Clinical Consultant (ACC) ist eine 8-monatige Einstiegsposition für Personen mit wenig bis gar keiner Erfahrung in der Elektrophysiologie (EP).
Nach 12 Monaten wird der ACC zum Clinical Consultant (CC) befördert.
Das sind Deine Aufgaben & Verantwortlichkeiten:
• Du übernimmst die Beratung und Unterstützung des medizinischen Fachpersonals bei der Bedienung des CARTO® 3 Navigationssystems bei elektrophysiologischen Eingriffen.
Das CARTO® 3 Navigationssystem wird angewendet, um Herzrhythmusstörungen zu lokalisieren und anschließend effektiv zu beseitigen.
• Als Vertriebsrepräsentant und erster Ansprechpartner für das gesamte Produktportfolio im Bereich der minimalinvasiven Elektrophysiologie zeigst Du die unterschiedlichen klinischen Einsatzmöglichkeiten des CARTO® 3 Sys...
....Read more...
Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:28
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where sophisticated diseases are prevented, treated, and cured, where treatments are 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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver significant solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we cultivate a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
We are seeking a dedicated individual with a strong passion for quality who thrives in a dynamic, multifaceted pharmaceutical production environment.
The ideal candidate will enjoy collaborating with diverse teams and business partners, while also finding fulfillment in mentoring and developing our emerging talent.
If you are someone who energizes others and takes pride in fostering growth within a team, we would love to hear from you.
At the J&J IM SC Beerse site, we produce and release a variety of product types, including Steriles, Liquids & Creams, and Transdermals.
The Janssen Beerse Site Quality Department ensures that all GMP activities-spanning manufacturing, packaging, labeling, testing, release, and distribution of commercial products from the Campus Belgium-are conducted in full compliance with GMP legislation.
Within this department, the QA Lab team plays a meaningful role in ensuring compliance with daily quality control testing activities.
Additionally, the team is responsible for the release of excipients and packaging materials for further processing.
As the Manager of the QA Lab, you will lead and run the QA Lab team, supporting the physico/chemical, microbiology, and packaging labs.
Your focus will be to ensure the safety, efficacy, and timely delivery of products to patients, achieved through the deployment of appropriately qualified and validated testing and material release processes.
You will also ensure compliance with all internal and external regulatory requirements and expectations.
Together with your team you support the daily quality operations within the quality control area:
* Support and approval of investigat...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:28
-
About Johnson & Johnson
At Johnson & Johnson,we believe health is everything.
Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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/ .
Responsible for promoting our pharmaceutical products to the healthcare professionals with the aim to bring our innovative treatment solution to our patients and for mentoring TA/TS.
Essential duties and responsibilities:
• Develop long-term strategic plan to achieve sales objectives and other qualitative objectives
• Manage the call plan for both existing and new customers and manage the assigned territories
• Make regular visits to identify customers' needs and provide treatment solution to HCP
• Analyze ordering pattern & product sales and prepare all the related reports and presentation as required.
• Provide customer services to our HCP
• Collaborates with other departments to achieve company objectives
• Provide accurate sales forecast
• Mentor junior sales representative or new comers
• Demonstrate as a role model in sales function
• Relay market insight to management.
• Comply with Integrity and compliance standards Essential knowledge and skills:
• Science background is preferred but not a must
• Bachelor Degree or above
• Minimum 4 year solid experience in selling & customer management in the healthcare industry for KAE
• Demonstrate effective communication skills
This Is What Awaits YOU At J&J
• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Many opportunities to work on challenging pro jects and assignments.
• Possibilities for further personal as well as professional development.
• Many employees benefits:
* Supportive team culture, flexible working hours, employee development and wellness support,
* Refreshment in the workplace, company gym, JJ Club, corporate events
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
....Read more...
Type: Permanent Location: Mongkok, CN-91
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:27
-
About Johnson & Johnson:
Johnson & Johnson is the world's leading manufacturer of healthcare products and related services.
With a strong culture of caring, the company aims to make a positive impact on the world, one person at a time.
Operating in over 250 countries, Johnson & Johnson is involved in pharmaceuticals and medical devices.
Position Overview:
The Franchise Controller (FC) will be a key member of the BUF (Business Unit Finance) team and responsible for all finance-related matters of the Electrophysiology and Neurovascular Franchise within MedTech.
This role requires a strong background in finance and controlling, preferably with international experience in the medical device industry.
The FC will work closely with the Franchise leadership team and serve as a finance business partner.
Responsibilities:
Financial Support:
l Provide financial analysis and support for various initiatives within the Franchise.
l Lead the Business Planning process for the responsible Franchise, including the annual Business Plan, Forecasts/Updates, Long Range Financial Plan and Strategic Planning.
l Collaborate with other team members within MedTech BUF and FP&A CoE in Singapore to ensure timely and accurate financial reporting.
l Conduct variance analysis and prepare management reports for the responsible Franchise's period closing activities.
l Provide proactive feedback on financial implications to key stakeholders and drive recovery plans, control investments and expenses to achieve business objectives.
Management Support:
l Support and challenge the Franchise Head and other members of the Franchise leadership team as a core business partner.
l Prepare presentations and present in global and/or regional business reviews.
l Make recommendations and take actions to achieve the Business Plan.
Requirements:
l Minimum of 10 years of accounting/controlling experience, preferably with international exposure.
l University degree in Accounting or Business Economics (Master's level preferred) or equivalent certifications (J-CPA, US-CPA, CMA).
l Strong analytical and problem-solving skills.
l Experience as a business partner with a deep understanding of complex business dynamics.
l Fluent in English, both written and spoken.
Proficiency in Japanese is highly preferred.
l Strong interpersonal skills with the ability to influence stakeholders across functions and levels.
l Knowledge of the medical device industry is desirable, with a strong interest in the field.
l Proficiency in Excel/Word/PowerPoint and the ability to drive continuous improvement.
l Positive attitude, accuracy, and timeliness in all deliverables.
l Balanced and decisive decision-making skills.
l Proactive mindset and a continuous improvement mindset.
l Strong communication and presentation skills.
....Read more...
Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:27
-
Johnson & Johnson is currently recruiting for an Advanced Surgical Consultant in Ausrin, Texas, United States area to join our Abiomed team.
Possible relocation assistance provided.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
Coverage Areas: St.
Louis
Role & Responsibilities:
* Train, educate, and support combined CT/Heart Failure programs on the proper use of the Impella 5.5 with SmartAssist
* Full customer immersion (ie.
input on patient selection and subsequent surgical support) within 5.5 sites to ensure optimal patient outcomes.
* Train, educate and, provide support in conjunction with the Medical Office and Engineering team to support EFS/PMA efforts and full commercialization of the BTR pump and future Surgical and Heart Failure focused technologies.
* Device expertise and support on Impella 5.0/ LD in order to assist with the adoption of the full portfolio beyond 5.5 commercial launch responsibilities.
* Clinical and technical expertise and support of Breethe Oxy-1 to assist with device integration and support of system adaptation into applications beyond the initial commercial launch.
* Participate when able with launch, training, and education of combined Surgical/ Heart Failure programs on the proper use of the Breethe Oxy-1 system with the Breethe Clinical Team.
* Internal collaboration with the Commercial Team, Training Team, Engineering Team, Marketing, Professional Education, Clinical, as well as with R&D.
* Maintain contact with all customers to evaluate clinical and educational needs.
* Performs device training on full Impella Surgical Device line-up.
* Be a functional expert and provide advanced acumen on the durable, acute, and, hemo...
....Read more...
Type: Permanent Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:26
-
Johnson & Johnson MedTech is currently seeking a Field Service Engineer to join our national team supporting VRAS (VELYS Robotic-Assisted Solution).
Region: Midlands area - Leicestershire, Nottinghamshire, Warwickshire, West & East Midlands.
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/
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued, and our people can reach their potential.
At Johnson & Johnson, we all belong.
Role Purpose:
As a Field Service Engineer at Johnson & Johnson MedTech, you will join a new team focused on supporting Orthopaedic robotic and endoscopic equipment.
After completing your training, your responsibilities will include commissioning, performing planned and corrective maintenance, and participating in projects for integrating new robotic equipment.
You will leverage your expertise to foster long-term customer relationships and promptly address customer needs and concerns.
Joining us means being at the forefront of the evolving healthcare landscape.
What you will be doing:
* Commission new robotic equipment at hospitals.
* Perform corrective maintenance, address breakdowns, and identify root causes to maximize equipment uptime.
* Service robotic and arthroscopic equipment in the field.
* Conduct preventative maintenance on fluid management systems and ablation tools at the Leeds service center as needed.
* Communicate with customers and service coordinators to schedule and execute preventive and corrective maintenance and service bulletins.
* Act as the liaison between the company and customers on administrative and technical matters, fostering trust and relationships.
* Enhance troubleshooting skills and utilize diagnostic software to minimize breakdowns and provide customer feedback.
* Participate in regional and international forums to discuss issues related to J&...
....Read more...
Type: Permanent Location: Birmingham, GB-BIR
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:25
-
Johnson and Johnson Innovative Medicine R&D is recruiting for a Director, DSDH, Discovery and Portfolio Strategy, Immunology.
This outstanding leader and data science expert will work to optimize our discovery and development portfolios with a focus on translation of genomics, transcriptomics, proteomics, and metabolomics data to inform target identification and validation, as well as biomarker discovery.
This role requires knowledge of sophisticated analytics of multivariate data domains, and utilizing artificial intelligence and machine learning techniques to optimize programs across discovery and development.
This includes novel uses of multi-omic and clinical data from multiple sources, including, but not limited to: large biobanks; preclinical and clinical studies; and real-world data.
Analyses will drive precision medicine strategy for target discovery and patient stratification.
This role will also support integrating data science and digital health throughout development programs across the portfolio.
This role will report to the Vice President, DSDH, Immunology, Cardiopulmonary, and Communicable Diseases.
Key Responsibilities:
The ideal candidate will have a strong understanding of disease biology and AI/ML techniques and their application in biomarker and drug discovery, as well as experience with inflammatory diseases.
The candidate should have strong stakeholder management skills, and will be responsible for ideating and executing the strategy of AI and ML-based target and biomarker discovery for the Data Science and Digital Health team that is aligned to immunology, all in close partnership with internal stakeholders and partners.
The candidate's work will be tightly coupled with our Immunology Discovery and Translational Science & Medicine, Population Genetics, and R&D Data Science teams.
* Create the strategy and process for evaluating target opportunities from the perspective of multi-omics biology, drawing upon a combination of internal and external resources.
* Develop tools and platforms to enable AI/ML-driven discovery and translational science initiatives.
* Collaborate with scientists and clinicians to develop data-driven strategies for precision medicine in immunology by being forward-looking and foreseeing the path to launch.
* Chart the path for the use of real-world data integrated within clinical programs to accelerate development, and strengthen understanding of unmet need and opportunities to benefit patient subtypes within and across immunology indications.
* Manage a robust portfolio of Data Science projects spanning RWE to Computer Vision to Digital Health from a milestone perspective
Remain current on the constantly evolving landscape of Immunology, genomics, bioinformatics and AI/ML research and the use of RWD in search of new strategies for strengthening the portfolio.
* PhD or MD with 5 years of progressive experience or MS with 7 years of progressive experience
* Biolo...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:25
-
Johnson & Johnson is recruiting for a Director Project Management, located in EMEA
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
As the world's largest and most broadly-based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, build healthier communities, and put a healthy mind, body, and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science, and ingenuity to profoundly change the trajectory of health for humanity.
At Engineering & Property Services (E&PS) we take care of all J&J buildings around the world providing end to end services from Real Estate, Engineering & Strategic Project Delivery to Facilities Management.
We have a profound influence on the entire J&J Enterprise, providing innovative workplaces where our employees can collaborate and grow, and delivering flexible site solutions which enable our business to best serve our important customers and patients.
The Director Project Management Netherlands is part of the E&PS EMEA Project Delivery team being accountable of the performance of a portfolio of capital projects to be implemented within the country, leading a team of internal and external resources.
Main responsibility of this role is to deliver large capital construction and infrastructural projects, acting as E&PS Project Director ensuring a smooth project execution by leading and coordinating multiple functions, managing, and mitigating risks, communicating project progress, issues, and solutions to management.
The candidate for this role will have excellent leadership experience in large Capital Project Management, sound experience and knowledge of process engineering, pharmaceutical and medical technologies and proven experience of people leadership, multicultural and diverse teams' management.
This position will require to establish positive relationships with other E&PS functions (Real Estate, Facility Management and Service Partners), Procurement, EHS, IT, Finance and Affiliate's Engineering Groups, establishing highly collaborative partnerships.
Key Responsibilities:
* Lead large capital construction projects (> $50-100M) in partnership with the business, taking direct responsibility for facility design, procurement, construction, commissioning and qualification ensuring that cost, schedule, and cash-flow targets are met.
* Lead/coordinate a group of Project Managers and Subject Master Experts assigned to deliver the capital projects portfolio in The Netherlands.
* Lead the alignment with Business partners defining business needs, business solutions and projects prioritization, acting as first point of contact in case of critical issues.
* Lead portfolio planning and projects resourcing, using internal and external partners capabilities to adequately and timely reso...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:24
-
Job Description:
At Sparklight/Cableone and our Cable One family of brands, we keep our customers and associates connected to what matters most.
For our associates, that means: a thriving and rewarding career, respect for the communities where they live and work, a focus on health and wellness, an excellent work/life balance, and an open and inclusive workplace.
We are open to hiring remote if we find the right talent in any of the following states: AL, AR, AZ, FL, GA, IA, ID, IL, IN, KS, LA, MD, MN, MO, MS, NC, ND, NE, NM, NV, OR, OK, PA, SC, SD, TN, TX, UT.
What you will do to contribute to the company's success
* Lead the efforts for CableOne and its Subsidiary compannies to comply with PCI level 1 requirements.
* Manage all aspects of CableOnes PCI DSS Compliance Program including CableOnes Subsidiary companies.
* Review Security Standards to ensure that they comply to industry standards
* Design & Modify Cable One Security Standards in accordance with Cable One culture and risk tolerance.
* Process requests for the Cable One information security risk management process.
* Assist in the governance of the Cable One Security Program.
* Gather evidence of compliance standards and identified security risks.
* Other duties and/or responsibilities not specifically set forth above may, however, be assigned as needed.
Whenever practicable and, in accordance with legal guidelines, reasonable accommodation[s] will be made to enable an otherwise qualified individual with a disability to perform the essential functions of the position.
Qualifications
* Bachelor's degree or eight years of IT security experience; or an equivalent combination of education and/or experience in a related field.
* At least 5 years of PCI experience.
* Experience as a PCI ISA or the ability and willingness to achieve PCI ISA.
* Excellent communication skills with the ability to explain requirements of PCI standards.
* Ability to effectively interact, communicate, and collaborate with other departments/agencies to advance security goals on time and within constraints.
* Ability to work with a team and independently
* Experience in the areas of policy and planning, security operations.
* Certifications highly desired (Security+, CISA, PCIP, PCI ISA)
* Knowledge of SOX, NIST, Risk Management.
Core Competencies
* Committed: Values each customer, while working hard to keep their business and support our communities.
* Helpful: Delivers support in the ways that are most useful to our customers and addresses their needs with expertise, respect, and empathy.
* Proactive: Understand what our customers need, and actively works to make their relationship with use seamless, easy, and rewarding.
* Personal: Knows our customers well, and tailors our communications and interactions to address their needs and expectations.
Benefits
Cable One and our family of brands appreciates th...
....Read more...
Type: Permanent Location: Phoenix, US-AZ
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:23
-
[ä¼ç¤¾æ¦è¦]
ã¸ã§ã³ã½ã³â¢ã¨ã³ãâ¢ã¸ã§ã³ã½ã³ã¯,å¥åº·ãããã¹ã¦ã ã¨èãã¦ãã¾ãããã«ã¹ã±ã¢ã¤ãã-ã·ã§ã³ã«ãããç§ãã¡ã®å¼·ã¿ã,è¤éãªç
ãäºé²â¢æ²»çâ¢æ²»çã,æ²»çãããã¹ã-ãåãã,ä½ä¾µè¥²ãªãã®ã«é²åãã,-人ã²ã¨ãã®æ£è
ããã«åã£ãã½ãªã¥-ã·ã§ã³ãæä¾ãããã¨ãã§ããä¸çãç¯ãåã«ãªãã¾ãã Innovative Medicineã¨MedTechã«ãããå°éæ§ãçãã,å°æ¥ã®é£èºçãªé²åã«åãã¦ãã«ã¹ã±ã¢ã½ãªã¥-ã·ã§ã³ã®å¹
åºãé åã§ã¤ãã-ã·ã§ã³ãæ¨ãé²ã,人ã
ã®å¥åº·ã«å¤§ããªã¤ã³ãã¯ããä¸ãã¦ããã¾ããhttps://www.jnj.com/
ããã¥-ã·ã³ã»ã¹äºæ¥æ¬é¨ã§ã¯,æ´å½¢å¤ç§å»ã«å¯¾ãã¦,å¤ç§çæè¡ã«ä½¿ç¨ããçä½å
åºå®ã¤ã³ãã©ã³ã(å¤å·è£½åâ¢äººå·¥é¢ç¯è£½å)ãåãæ±ã,ãã®å®å
¨æ§åã³æå¹æ§ã®åèæ´»åãªãã³ã«æ£è
æ§ãæ±ãã課é¡ã¸ã®ã½ãªã¥-ã·ã§ã³å¶æ¥ãæ
å½ãã¦ããã ãã¾ããç
æ°ãæªæã«ããçã¿ãææ
¢ãã,æ£è
ãã-人ã²ã¨ããæãæã"èªåãããçæ´»"ãåãæ»ããµã-ãããã¦ãã¾ãã
ä»åã¯ãã©ã¦ããã¸ãã¹/Mitek ãã¸ãã¹ã®å¶æ¥è·ãåéãã¦ãã¾ãã
ãã©ã¦ããã¸ãã¹ã¯,åè¢ã®å¤å·è£½åãåãæ±ã,æ´å²çã«ã-ã±ãããª-ã-ãç¶æã,ããã¦ä»å¾ãæ°è£½åã®å°å
¥ãç¶ç¶çã«è¨ç»ãã¦ãã¾ãã
å§åçãªè£½åã-ããã©ãªãªã¨ã»-ã«ã¹ã«ãã¬ãã¸ã«ãã,æ´ãªãã·ã§ã¢ã¢ããã¨å
±ã«ä»ç¤¾ã®è¿½éã許ããªããã¸ã·ã§ã³ãç®æãã¦ãã¾ãã
Mitekãã¸ãã¹(ã¹ã-ãæ´å½¢é å)ã¯, å復æ§è©é¢ç¯è±è¼,è
±æ¿æè£ä¿®å¾©è¡ãªã¨ãã«ç¨ããã¹-ãã£-ã¢ã³ã«-ãä¸çã¦ãåãã¦çºå£²ãå½å
ã«ããã¦ãæåã«çä½å
å¸åæ§ã®è£½åãå°å
¥ã,éå±è£½,PEEK製ãå«ã,ææâ¢èâ¢è¡â¢èâ¢è¶³é¢ç¯ã®é±å¸¯ç修復è¡ã«å¯¾å¿ããå¤æ§ãªã©ã¤ã³ã¢ãããããããã¦ãã¾ãã
ã©ã®é¨éãå»å¸«ã¸ã®è£½åããã¢-ã·ã§ã³,å½ç¤¾è£½åã®å®å
¨ä½¿ç¨ãç®çã¨ããæè¡ç«ä¼ã,代çåºã¨ååããç©æµç®¡çã主活åã¨ããªããæ£è
æ§ã®QOLåä¸ã追åãã¦ããã¾ãã
å»çæ¥çã¸ã®è²¢ç®ããããæ¹,èªèº«ã®å¶æ¥åãæé·ããããæ¹,æ¯é-度æ
å½è
ã¨ã話ããããæéãããã ããã°ã¨æãã¾ãã
[æ¥åå
容]
â¢å»å¸«ã¸ã®è£½åç´¹ä»,æ
å ±æä¾,æè¡ã®æã¡åãã
â¢æè¡ã®ç«ä¼ã
â¢æè¡ã®æºåç©,å¨æ¢°ã¨ã¤ã³ãã©ã³ãã®æé
,ããã«ä»éããå»çæ©å¨ã®èª¬æ
â¢å»å¸«,代çåº,çè·å¸«åãã®åå¥åå¼·ä¼ã®éå¬
â¢äºåå¦ç(è³æãè¦ç©æ¸ã®ä½æ)
â¢å»å¸«ã¨ã®ã³ãã¥ãã±-ã·ã§ã³
â¢æ°è£½åãªã©ã®PR,æ
å ±æä¾
â¢æé
å
容ã®ç¢ºèªãã©ã®ããã«è£½åã使ç¨ãããããææ¡
â¢OPå¾,æ£è
æ§ã®ãªãããªã®é²æç¶æ³ãªã©ãã伺ããã¦ãã©ã-ãè¡ã
â¢OPç«ä¼ã
â¢çè·å¸«ããã¸å¨æ¢°ã®çµã¿ç«ã¦ããæ¡å
â¢å»å¸«ã«ãå¨æ¢°ã®æ£ãã使ãæ¹ãªã©OPã®ãµã-ããè¡ã
â¢å¹³å2~3å/æ¥ãããã®ç«ä¼ãã«å
¥ã(Traumaã®ã¿)
â¢è²©å£²ä»£çåºã¨ã®ã³ãã¥ãã±-ã·ã§ã³ â¢è²©å£²æ¦ç¥ã®ä¼ç»ç«æ¡ / å®è¡[å¿åè¦ä»¶]
â¢æ³äººå¶æ¥çµé¨2年以ä¸ã®æ¹
â¢å
¨å½è»¢å¤ãå¯è½ãªæ¹
â¢æ®éèªåè»é転å
許ããæã¡ã®æ¹
[æè¿è¦ä»¶]
â¢å»çæ©å¨å¶æ¥ã®çµé¨ããæã¡ã®æ¹
[è³æ ¼/å
許]
â¢æ®éèªåè»å
許
DE&I 声æ
130 年以ä¸ã«ããã,ãã¤ã-ã·ãã£,ã¨ã¯ã¤ãã£,ã¤ã³ã¯ã«-ã¸ã§ã³ (DE&I) ã¯ã¸ã§ã³ã½ã³â¢ã¨ã³ãâ¢ã¸ã§ã³ã½ã³ã®ä¼æ¥æåã®-é¨ã§ãã,æ¥ã
ã®ãã¸ãã¹ã«æ·±ãé¢ãã£ã¦ãã¾ããä¼æ¥ç念ã§ããæãä¿¡æ¡(Our Credo)ã«æ ¹ããã DE&I ã®ä¾¡å¤è¦³ã®ä¸,ç§ãã¡ã¯ããå¥åº·ã§ããå
¬å¹³ãªä¸çã®åµé ã追åãã¦ãã¾ããããã¦,å½ç¤¾ã®å¤æ§ãªç¤¾å¡ã¨å¸°å±æèã®æåã¯,ä¸çã«ãããå«ç·ã®ãã«ã¹ã±ã¢èª²é¡ã解決ããããã®ã¤ãã-ã·ã§ã³ãå éããã¾ãã
å½ç¤¾ã®ãã¸ãã¹ã®æå,ããã¦ææ義ãªã½ãªã¥-ã·ã§ã³ãæä¾ã§ãããã©ããã¯,ç§ãã¡ããµ-ãã¹ãæä¾ããã³ãã¥ããã£ã®å¤æ§ãªã-ãºãã©ãã ãç解ã,å¿ãããã«ããã£ã¦ãã¾ããã ãããã,ç§ãã¡ã¯ããããèãæ¹,è½åã,çµé¨ãè©ä¾¡ãã,社å¡-人ã²ã¨ããèªãã®æ½å¨è½åãçºæ®ã§ãããã,ã¤ã³ã¯ã«-ã¸ã§ã³ã¨å¸°å±æèã®æåãè²ãã§ãã¾ãã
ã¸ã§ã³ã½ã³â¢ã¨ã³ãâ¢ã¸ã§ã³ã½ã³ã§ã¯,ç§ãã¡å
¨å¡ã«å±
å ´æãããã¾ãã
(確èªé
ç®)
â¢éå»5年以å
ã«ããã¦,ç
æ°(ç
æ°ã®æ²»çã«ä¼´ãçç¶ãå«ã¿ã¾ãã)ãåå ã¨ãã¦,åã¯åå ã¯æããã§ãªãã,æèã失ã£ããã¨ãããã
â¢éå»5年以å
ã«ããã¦,ç
æ°ãåå ã¨ãã¦,身ä½ã®å
¨é¨åã¯-é¨ ã,-æçã«æãéãã«åãããªããªã£ããã¨ãããã
â¢éå»5年以å
ã«ããã¦,ååãªç¡ç æéãåã£ã¦ããã«ãããããã,æ¥ä¸,æ´»åãã¦ããæä¸ã«ç ãè¾¼ããã§ãã¾ã£ãåæ°ãé±3å 以ä¸ã¨ãªã£ããã¨ãããã
â¢éå»1年以å
ã«ããã¦,次ã®ããããã«è©²å½ãããã¨ãããã
*飲é
ãç¹°ãè¿ã,絶ããä½ã«ã¢ã«ã³-ã«ãå
¥ã£ã¦ããç¶æ
ã3æ¥ ä»¥ä¸ç¶ãããã¨ã3å以ä¸ããã
*ç
æ°ã®æ²»çã®ãã,å»å¸«ãã飲é
ããããããå©è¨ãåãã¦ãã ã«ãããããã,飲é
ãããã¨ã3å以ä¸ããã
*ç
æ°ãçç±ã¨ãã¦,å»å¸«ãã,é転å
許ã®åå¾åã¯é転ãæ§ããããå©è¨ãåãã¦ããã
....Read more...
Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-18 07:05:23
