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Johnson & Johnson Health Care Systems Inc.
(JJHCS), a member of Johnson & Johnson's Family of Companies, is recruiting for Enterprise Operations (EO), Contract Operations (CO) Intern to support our U.S.
Region Enterprise Contract Management (ECM) team located in Raritan, NJ.
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.
ECM is an organization under JJHCS which serves as the Center of Excellence that delivers outstanding solutions for Commercial Healthcare, Government & Regulatory, Systems, Processes and Training, and Risk Mitigation & Governance.
The Contract Operations (CO) team is responsible for supporting agreements with Distributors, Consolidated Service Centers (CSCs), Certified Kit Assemblers (CKAs), Group Purchasing Organizations (GPOs) and various other commercial agreements for MedTech and Innovative Medicine sectors in partnership with Strategic Customer Groups (SCGs) and Supply Chain Customer Solutions.
The Intern will ensure contracting systems are up-to-date and aligned with MedTech and Innovative Medicine agreements.
They will work closely with internal business partners to review, validate, and analyze product, pricing, and rebate strategies, ensuring system accuracy reflects the intended strategy.
Additional duties include supporting ad hoc projects, conducting account analyses, maintaining systems, and other related tasks.
Key Responsibilities:
* Interpret and implement contracting strategies; develop and analyze reports.
* Ensure compliance with SOX guidelines and departmental policies.
* Perform data analysis, trend analysis, and problem-solving across various business areas.
* Communicate effectively with internal and external stakeholders.
* Troubleshoot and resolve pricing or rebate discrepancies.
* Adapt to evolving department needs in a fast-paced environment.
* Identify and implement process improvements and automation opportunities.
* Act decisively while considering cross-departmental impacts.
* Share knowledge with peers and business partners.
Education:
* Enrollment in a Bachelor's degree program is required.
* Minimum cumulative GPA of 3.0 is strongly preferred.
Experience and Skills:
Required:
* Advanced proficiency with MS Excel, including Pivot Tables and VLOOKUPS.
* Strong verbal and written communication skills.
* Strong time management and organizational skills.
* Self-motivated with the ability to work independently, think critically, solve problems, and challenge the status quo.
* ...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:30
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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/
Für unser Team in Deutschland suchen wir eine(n)
Associate Local Trial Manager (m/w/d)
Location: Neuss, 2 Tage Home Office pro Woche möglich
Ihre Aufgaben und Verantwortlichkeiten:
Der Associate Local Trial Manager (LTM) (m/w/d) unterstützt die lokale Durchführung einer globalen klinischen Studie in einem oder mehreren Ländern.
Der Associate LTM ist innerhalb unserer Abteilung der primäre Ansprechpartner für Aktivitäten rund um die initiale Studieneinreichung auf Länderebene für die ihm/ihr zugewiesenen klinischen Prüfungen unter Einhaltung der internen Vorgaben sowie der gesetzlichen Bestimmungen.
Im Einzelnen sind dies die folgenden Tätigkeiten:
• Projektleitung für die initiale Einreichung von klinischen Prüfungen
• Verantwortung für die erfolgreiche initiale Einreichung der klinischen Prüfung in Deutschland und ggf.
Österreich und der Schweiz gemäß den aktuellen gesetzlichen Bestimmungen (u.a.
EU-CTR) und zeitlichen Fristen
• Koordination der Aktivitäten mit dem MitarbeiterInnen des lokalen Studienteams, bestehend aus Local Trial Manager (LTM), Site Managern (SM) und Clinical Trial Assistenz (CTA)
• Primärer Ansprechpartner in Deutschland sowohl für interne als auch für externe Partner (z.B.
CROs, lokale/internationale J&J-MitarbeiterInnen) für JnJ Systeme und/ oder Prozesse
• Vertretung der Interessen des Unternehmens in allen prüfungsbezogenen Belangen nach innen und außen (z.B.
gegenüber Ethikkommissionen)
• Entwicklung und Ausarbeitung der benötigten lokalen Unterlagen, u.a.
mit den teilnehmenden Prüfzentren
• Sicherstellung der Vollständigkeit aller relevanten Dokumente gemäß gesetzlichen Bestimmungen und internen Richtlinien für den Start der klinischen Prüfungen
• Übersicht über die Einhaltung der Qualitätsvorgaben Ihr Qualifikationsprofil:
• Mindestens 2 Jahre Erfahrung in der Pharmazeutik und/oder klinischen Studien (gerne mit Monitorerfahrung) sind erforderlich, mit entsprechenden Kenntnissen aller relevanten Gesetze und Verordnungen, insbesondere mit Hinblick auf alle Aktivitäten rund um die fristgerechte und gesetzeskonforme initiale Einreichung der klinischen Prüfung.
Andere relevante Erfahrungen und Fähigkeiten können jedoch vom einstellenden Manager bei der Bewertung der Eignung d...
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Type: Permanent Location: Rhein-Kreis Neuss, DE-NW
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:30
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Johnson & Johnson Innovative Medicine is recruiting for a Field Excellence Training Lead, Oncology located in Toronto, Ontario.
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.
The Field Excellence Training Lead, Oncology role is an exciting opportunity to strategically partner and serve as a learning performance consultant with Therapeutic Area business stakeholders across the enterprise to proactively identify, consult, and capture learning needs for therapeutic area (TA)/ business-specific capabilities.
Key Responsibilities:
* Proactively identify, consult, and capture TA specific product and technology learning needs and shape solutions
* Partner closely with business unit (BU) leads to discuss and engage in annual training requirements and prioritization
* Oversee TA / business-specific capability offering / learning portfolio strategy and ongoing improvements for TA curriculums.
Adult Learning consultant support for subject matter expert content and training
* Oversee the execution of across enterprise field compliance training requirements
* Monitor impact of TA / business-specific learning programs on performance and discuss learning evaluation and measurement feedback with respective L&D stakeholders
* Understand suite of J&J IM Learning Excellence capabilities and remain current on related tools, techniques, strategies, etc.
to inform business on optimal solution.
Manage learning platform content and dashboarding (J&J Learn)
* Conduct facilitation of TA / business-specific capability programs as required
Education:
* A minimum of a Bachelor's Degree is required.
A Master's in Learning is preferred.
Experience and Skills:
Required:
* 5 or more years ...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:29
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Pharm Transcend CoOp - Plan/Source | June - Dec 2025
At Johnson & Johnson Innovative Medicine, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We are Janssen.
We collaborate with the world for the health of everyone in it.
Pharm Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one "clean" ERP as a standardized platform for growth and efficiency gains.
The program will simplify the Pharm ERP landscape from 7 to 1, standardizing processes in order to have a cost effective, fit for purpose digital backbone that will enable us to support the Pharm business with agility.
Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.
The Transcend Pharm Supply Chain Plan/Source team is offering the chance to:
• Support the analysis of current business processes and identify areas for improvement
• Conduct data analyses and development of data models to support process development
• Update process flows & financial flows
• Assist in gathering and documenting business requirements and user stories
• Collaborate with cross-functional teams, including Logistics, Finance, Customer Excellence and Make and to ensure alignment on project goals.
• Prepare regular reports on project performance, including team status updates and key performance indicators (KPIs).
• Assist in the preparation of project documentation
* Being legally authorized to work in the United States and not requiring sponsorship for employment visa status (e.g.
H1-B status) now or in the future is required.
* Be enrolled in an accredited college/university during the co-op session
* Pursuing a Bachelor's degree in Business or relevant fields with concentrations in Supply Chain, Finance or Operations.
* A minimum GPA of 3.0 is required.
* You have strong problem-solving skills for developing innovative solutions and meeting project objectives.
* You have demonstrated critical thinking skills and are able to prioritize objectives.
* You are detail-oriented, highly organized, and able to manage multiple tasks with a strong sense of urgency.
* You possess good interpersonal skills and can work effectively in a collaborative team environment.
* You are proficient with Microsoft Office, Word, Excel, PowerPoint and other commonly used software.
* Availability to work full-time (40 hours/week) during the co-op session.
* Demonstrating strong oral and outstanding written communication skills is a plus.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientatio...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:29
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R&D Data Science & Digital Health DSAI Intern Summer 2025
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years.
We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
With $81.6 billion in 2018 sales, Johnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets.
There are more than 250 Johnson & Johnson operating companies employing approximately 130,000 people in 60 countries throughout the world.
Calling all big thinkers and world-changers who want to drive their careers forward across more than 250 leading businesses in consumer, pharmaceutical and medical technology.
If you have the talent and desire to touch the world, Johnson & Johnson has the career opportunities to help make it happen.
Position Components
In this role, you will work with colleagues in the JNJ Innovative Medicine R&D Data Science & Digital Health organization and partner with key businesses across JNJ Innovative Medicine (formerly Janssen) to apply advanced data science and analytics to answer key research questions.
As an intern, you will get the opportunity to work on cutting-edge problems at the intersection of artificial intelligence and drug discovery.
You will be a member of a dynamic team comprising data scientists and subject matter experts to create and iterate on data science solutions.
Projects include, but are not limited to, developing, and applying predictive and generative artificial intelligence methods for molecular property prediction and generation with the ultimate goal of drug discovery.
Interns could be located out of our US locations in San Diego, San Francisco, Titusville, Raritan, Spring House, Boston as well as remote.Minimum qualifications:
* Currently pursuing a PhD degree in Data Science, Computer Science, Electrical Engineering, Statistics, or related quantitative discipline.
* Strong working knowledge of machine learning with demonstrated research experience, as evidenced by publications, public code contributions, etc.
* Proficiency in Python and hands-on experience with Deep Learning frameworks such as PyTorch or TensorFlow to tackle scientific problems.
* Strong technical communication and presentation skills.
* Ability to understand and write academic research papers.
Preferred qualifications:
Experience in one or more of the following:
* Extensive research experience working with sequence models (e.g.- with Large Language Models (LLMs)).
* Familiarity with Hyperbolic Deep Learning, Hierarchical Learning, Differential geometr...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:28
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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 implementation, improvement and harmonization of laboratory quality systems.
* Responsible for ensuring all laboratory systems comply with GMP/GCTP and J&J guidelines and quality standards, including support to regulatory filings and sub-system owner for laboratory systems.
* Perform the activities, encompassing activities in support of laboratory systems, e.g.
equipment qualification, compendia and quality standard review, stability program administration, analytical change control, LIMS, Empower, training, etc.
* Leads and supports projects within laboratories aimed at improving on financial targets, efficiencies and productivities achieving increasing agility and flow throughput, reducing cost, cycle time, inventory reduction, performance improvement and error reduction.
* Ensures required GMP/GCTP, EHS and role-related training required to work safely and in compliance with regulatory requirements and as defined by their training matrix.
* Proactively supports GMP/GCTP compliance, permanent audit readiness, identification of compliance risks and breaches.
* Any other duties as assigned by the Quality Control Manager or Lab Lead.
* ラボの品質システムの実装,改善,調和に責任を持つ。
* すべてのラボ システムが GMP/GCTP および J&J ガイドラインおよび品質基準に準拠していることを確認する責任がある。これには,ラボ システムの規制当局への提出やサブシステム オ-ナ-へのサポ-トも含まれる。
* 試験室システムを支援する活動を実施する。機器の適格性評価,公定書および品質基準のレビュ-,安定性試験プログラム管理,変更管理,LIMS,Empower,トレ-ニングなど。
* ファイナンス目標,効率性,生産性を向上させ,アジリティとフロ-スル-プットの向上,コストの削減,サイクルタイム,在庫の削減,パフォ-マンスの改善,エラ-の削減を目的としたラボ内のプロジェクトをリ-ドおよびサポ-トする。
* 安全かつ規制要件に準拠し,トレ-ニング マトリックスで定義されているとおりに作業するために必要な,必要な GMP/GCTP,EHS,および役割関連のトレ-ニングを受ける。
* GMP/GCTPコンプライアンス,恒久的な監査準備,コンプライアンス リスクと違反の特定...
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Type: Permanent Location: Sunto-Gun, JP-22
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:27
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
In this role, you will perform sophisticated technical work including the design, manufacture and operation of structures, machines and systems.
DUTIES & RESPONSIBILITIES:
o Responsible for communicating business related issues or opportunities to next management level
o Follow all Company guidelines related to Health, Safety and Environmental practices
o Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
o Provides technical support for project planning, development, implementation, and modification; gives extensively to engineering standards development balancing corporate and customer needs.
o Exercises independent judgment on some details of work.
o Performs assignments that have sophisticated objectives and require the investigation of multiple variables.
o Performs work which involves sophisticated conventional types of plans, investigations, surveys, structures, or equipment with sophisticated features for which there may be no precedents.
o Assignments usually include several of the following: equipment design and development, test of materials, preparation of specifications, process study, research investigations, and report preparation.
o Performs duties assigned as neededQualifications and Skills Required:
* • Lean/Six Sigma knowledge preferred.
* • Demonstrates some understanding of common engineering analysis tools such as statistical process control (which are applied in conjunction with continuous improvement principles).
* • Demonstrates some awareness of other engineering specialties and upstream partners, including Quality Engineering and New Product Introduction teams.
* • Demonstrates understanding of health and safety requirements.
* • Demonstrates basic knowledge of equipment efficiency and manufacturing & maintenance excellence concepts (OEE, SOL, etc.).
* • Demonstrates understanding of the need for cost management and its importance for customers and consumers.
* • Demonstrates basic knowledge of product costs (i.e.
COGS), Design to Value concepts, and key levers that impact improvement or degradation in cost performance
* • Is able to deliver oral and written communications around process improvement projects.
* • Demonstrates organized, analytical approach to problem solving.
* • Demonstrates developed verbal and written communication skills
...
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Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:26
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In partnership with the US Region, the Contract Solutions Intern is accountable for supporting and designing the contract platform(s) needed to enable the ongoing execution of evolving regional contracting strategies.
This is done by:
* Managing and supporting system strategy and platform growth.
* Supporting the management of the portfolio of contract strategies and solutions.
* Supporting to ensure a competent and trained contracting workforce.
* Supporting, measuring, monitoring and reporting through governance on the success of the US Region in maintaining a harmonized environment.
* Monitoring commercial and regulatory trends and sharing channel expertise and best practices.
Role Objective
The Intern, Contract Solutions is responsible for providing business process and technical application support by addressing System Development Life Cycle (SDLC) documentation changes, coordinating or performing bug fix testing, any other business related error handling and change controls with key contracting applications such as Model N (branded Integrated Contracting Solution (ICS) & Contract Optimization Revenue Excellence (CORE)) and others.
The Intern monitors applications, issue resolution and communication across the U.S.
Region and partners with IT on proactive analysis and trending of issues.
Major Responsibilities
* Monitor application and issue resolution, partner with IT on analysis and trending of issues, and handle communication across the U.S.
Region.
* Responsible for supplemental data requests within key contracting applications.
* Serve as point of contact for key contract applications including ICS & CORE, and legacy systems; receive and triage problems identified with business users, collaborate with IT team to conduct a root cause analysis and communicate outcomes and next steps to partners, coordinate notifications with US region on identified issues, challenges, and direction.
* Coordinate the successful signature of any SDLC requirements following the remediation of known issues including leading the change control process, coordinate or perform bug fix testing because of identified issues.
* Analyze and trend logged issues, recommend improvements to the US region management to reduce future anticipated issues, serve as a user-level advocate to ensure system performance expectations are met or maintained, craft metrics to summarize performance of system and environment.
* Recommend actions for improvement, develop and deliver presentations to the US region during future state operational channel governance meetings on trending, performance, and recommend and contribute to the management of the project pipeline or other system support issues.
Key Competencies/Skills/Requirements
Analyses:
* Analyses
* System Knowledge
* Data Knowledge and Reporting
Business Knowledge:
* Contracting Process and Knowledge
* Industry Knowledge
* O...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:26
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R&D Data Science & Digital Health DSAI Intern Summer 2025
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years.
We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.
Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
With $81.6 billion in 2018 sales, Johnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets.
There are more than 250 Johnson & Johnson operating companies employing approximately 130,000 people in 60 countries throughout the world.
Calling all big thinkers and world-changers who want to drive their careers forward across more than 250 leading businesses in consumer, pharmaceutical and medical technology.
If you have the talent and desire to touch the world, Johnson & Johnson has the career opportunities to help make it happen.
Position Components
In this role, you will work with colleagues in the JNJ Innovative Medicine R&D Data Science & Digital Health organization and partner with key businesses across JNJ Innovative Medicine (formerly Janssen) to apply advanced data science and analytics to answer key research questions.
As an intern, you will get the opportunity to work on cutting-edge problems at the intersection of artificial intelligence and drug discovery.
You will be a member of a dynamic team comprising data scientists and subject matter experts to create and iterate on data science solutions.
Projects include, but are not limited to, developing, and applying predictive and generative artificial intelligence methods for molecular property prediction and generation with the ultimate goal of drug discovery.
Interns could be located out of our US locations in San Diego, San Francisco, Titusville, Raritan, Spring House, Boston as well as remote.Minimum qualifications:
* Currently pursuing a PhD degree in Data Science, Computer Science, Electrical Engineering, Statistics, or related quantitative discipline.
* Strong working knowledge of machine learning with demonstrated research experience, as evidenced by publications, public code contributions, etc.
* Proficiency in Python and hands-on experience with Deep Learning frameworks such as PyTorch or TensorFlow to tackle scientific problems.
* Strong technical communication and presentation skills.
* Ability to understand and write academic research papers.
Preferred qualifications:
Experience in one or more of the following:
* Extensive research experience in Causal Discovery/Inference/Causal Representation Learning.
* Familiarity with Bayesian experimental design and Bayesian Optimization is a plus.
* Experien...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:26
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Synthetic Organic Chemistry Summer Intern, Johnson & Johnson Spring House (Undergraduate Student)
Job Description
Johnson & Johnson is currently seeking an undergraduate student for a synthetic organic chemistry intern position, located in Spring House, PA.
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 www.jnj.com.
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.
We are currently seeking an outstanding and motivated individual to work in the Discovery Chemistry group located in Spring House, PA, as a summer intern.
The internship program is focused on providing an undergraduate college student the opportunity to learn about the role of organic chemistry in drug discovery research.
The position offers real-life training in the skills and tools relevant to perform as a drug discovery chemist.
The synthetic organic chemistry intern will:
* Work collaboratively with a Johnson & Johnson scientist
* Synthesize, purify, and characterize novel drug-like compounds
* Enable reaction discovery to address key synthetic challenges
* Participate and present at project team meetings
* Be exposed to various other functions within the drug discovery teams at Johnson & Johnson
* Participate in campus-wide activities across the Spring House summer intern community
* Be based in Spring House, PA (suburban Philadelphia area)
* Permanent US work authorization without the need for sponsorship now, or in the future (F1 or H1B requires sponsorship in the future).
* Candidates must be sophomore, junior, or senior students enrolled in an accredited college/university pursuing a B.S.
degree or equivalent in chemistry.
* Completion of introductory organic chemistry laboratory and coursework is required.
* A minimum G.P.A.
of 3.2 is strongly preferred.
* Prior undergraduate research experience (outside of standard curriculum) is preferred.
* Familiarity with modern analytical techniques (NMR, MS, HPLC), various reaction techniques, and safe laboratory practices is preferred.
* Candidates must be legally authorized to work in the United States and not require sponsorship for employment visa status (e.g.
H1-B status) no...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:25
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Johnson & Johnson is currently seeking a medical advisor to join our team in Shefayim.
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/ .
Key Job Activities:
⢠Keeping abreast of medical and scientific knowledge
⢠Creating and fostering a network of partnerships with experts
⢠Working cross-functionally within the company to become a valuable team member exhibiting lateral leadership
⢠Providing high level scientific engagement with experts, while utilizing multichannel platforms
⢠Initiator and coordinator of medical education activities and advisory boards, in alignment with Medical Manager
⢠Scientific support and training to company sales representatives and other peers
⢠Supports and initiates evidence generation via research and publications
⢠Gains valuable scientific insights contributing to the short & long-term strategic plans of the therapeutic area
⢠Skillful in implementing innovative solutions and ideas for multichannel engagement and data-collection
⢠Champions medical benefits of products and contributes to the fostering of innovative therapeutic approaches for patient's benefits
⢠Actively involved in strategy and action plans related to local reimbursement of productsEducation
MD, D.M.D, D.V.M, Ph.D.
(Pharmacy or Science)
Experience:
With preference for:
⢠At least 2 years working experience in the pharmaceutical industry or research company
⢠High-competency in project & customer-affairs management
⢠Experience working in a hybrid environment
Knowledge:
⢠Deep scientific & clinical knowledge
⢠In-depth understanding of medical data, research & its interpretation
⢠High level communication & presentation skills
JOB SPECIFIC COMPETENCIES/SKILLS REQUIRED:
1.
Demonstrates ability to keep up-to-date with medical and scientific knowledge
2.
Excellence in interpersonal and communication skills
3.
Excellent presentation skills and business acumen
4.
Able to effectively utilize new systems & digital platforms
5.
Able to operate in a highly complex and ever-changing business environment
6.
A team-player
7.
High ethical standards, working aligned with Johnson & Johnson Credo values and relevant references for business integrity
8.
The role is mainly field-based, requires agility with regards to travel & work hours
Personal Attributes:
⢠Excellent people skills & service orientation
⢠High capability to multi-task and function in a hybrid environment
⢠High capacity to learn and manage new processes and innovative solutions
â...
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Type: Permanent Location: Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:24
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Immunology Medical Affairs Program Management Internship -Summer 2025
At J&J Innovative Medicine, we aspire to develop breakthrough treatments to transform the future of health, discovering new pathways and modalities to be in front of diseases and find cures.
Inspired by patients, we apply rigorous science with compassion to confidently address the serious health problems of today and develop the potential medicines of tomorrow.
The Medical Affairs Division of J&J Innovative Medicine provides practical, industry-specific scientific and analytical experience.
Johnson & Johnson Innovative Medicine is recruiting for an Immunology Medical Affairs Program Management intern located in Horsham, PA.
This position will be part of the Program and Alliance Management and Clinical Operations Teams with Immunology Medical Affairs.
The Program Management intern will coordinate across workgroups, assist with clinical project management of ongoing and new research activities (company sponsored trials and interval safety reports) and support specific projects within the immunology group.
The Program Management intern will also assist with short and long-term strategic planning including integrated evidence generation planning and business planning activities.
Responsibilities
* Work collaboratively with US Immunology Medical Affairs Staff under the direction of a Program Manager supporting ongoing projects
* Assist with activities and projects within Medical Affairs including but not limited to the creation and maintenance of metrics, creation of dashboards and PowerPoint presentations
* Participate in ongoing team meetings
* Be exposed to various functions within the larger Immunology Medical Affairs/Research & Development/Commercial organizations
Eligibility Criteria
* Enrolled in an accredited college/university pursuing a Bachelor's degree in a science-related field (e.g., Biochemistry/Biology/Chemistry) or graduate study in PharmD, PhD, MPH or other master's program in a science-related field
* Completed two or three years of college coursework
* Must be permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future.
Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long-term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.
Required Qualifications
* A minimum GPA of 3.0
* Detail-oriented, analytical, highly organized, and able to manage multiple tasks
* Ability to work individually (independently) as well as on a team
* Strong oral and written communication skills
* Proficient with Microsoft Office including Word, Excel (with a high proficiency with generating tables and graphs), and PowerPoint
Preferred Qualifications
* Technical competencies in...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:24
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Do you want to make a difference and be part of a highly motivated team? Thanks to our groundbreaking medicines, we can significantly improve the lives of patients.
To ensure the greatest and fastest possible patient benefit, we need reinforcement.
If you are a confirmed networker and the healthcare sector is your home, love direct customer contact and want to use your strong negotiating skills for the benefit of patients, we need you!
As a Key Account Specialist Gastroenterology, you will be responsible for looking after our most relevant key customers, in particular hospitals, clinics and large office-based customers in your region.
Thanks to close collaboration with all key customers and your negotiating skills, you will ensure success of our large portfolio and that our innovative medicines in the field of gastroenterology are available to patients.
Your in-depth customer and market analyses and observations as well as your creativity and innovative strength enable you to identify potential and opportunities at an early stage, with which you can provide targeted support to our customers in optimising patient and therapy management.
Your responsibilities:
* As a commercial expert in the pharmaceutical industry, you will be supporting our key customers, as well as doctors' networks, purchasing groups and other partners, to ensure the prescription and optimal use of our products as well as the negotiation of corresponding contracts
* Market analyses to identify potential, trends and opportunities in good time
* Use of all means of communication and channels (omnichannel), organisation of customer events to promote scientific exchange, efficient use of your activities and resources to achieve the best possible increase in patient outcomes.
* In collaboration with the x-functional team, especially Sales, Marketing and Medical, you will actively support the implementation of our national brand strategy.
With your extensive knowledge and network, you will assure a successful partnership with all partners
* In all your activities, you will ensure adherence to all Johnson & Johnson compliance guidelines.
* Scientific or paramedical training/ or a SHQA diploma
* Business education a plus
* Several years of experience in the pharmaceutical industry and in customer care
* Existing network in and broad knowledge of the Swiss healthcare sector
* Strong strategic and analytical thinking as well as customer and service orientation
* Confirmed sales, negotiation and communication skills
* Strong standout colleague and enjoy working in a dynamic market as well as in a "dedication" team
* Very good knowledge of French and English (German a plus), as well as an interest in new digital communication formats
Promoting and developing talent are core values of the Johnson & Johnson workplace culture.
People who want to realise their potential in an international company will find the best cond...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:23
-
Do you want to make a difference and be part of a highly motivated team? Thanks to our groundbreaking medicines, we can significantly improve the lives of patients.
To ensure the greatest and fastest possible patient benefit, we need reinforcement.
If you are a confirmed networker and the healthcare sector is your home, love direct customer contact and want to use your strong negotiating skills for the benefit of patients, we need you!
As a Key Account Specialist Gastroenterology, you will be responsible for looking after our most relevant key customers, in particular hospitals, clinics and large office-based customers in your region.
Thanks to close collaboration with all key customers and your negotiating skills, you will ensure success of our large portfolio and that our innovative medicines in the field of gastroenterology are available to patients.
Your in-depth customer and market analyses and observations as well as your creativity and innovative strength enable you to identify potential and opportunities at an early stage, with which you can provide targeted support to our customers in optimising patient and therapy management.
Your responsibilities:
* As a commercial expert in the pharmaceutical industry, you will be supporting our key customers, as well as doctors' networks, purchasing groups and other partners, to ensure the prescription and optimal use of our products as well as the negotiation of corresponding contracts
* Market analyses to identify potential, trends and opportunities in good time
* Use of all means of communication and channels (omnichannel), organisation of customer events to promote scientific exchange, efficient use of your activities and resources to achieve the best possible increase in patient outcomes.
* In collaboration with the x-functional team, especially Sales, Marketing and Medical, you will actively support the implementation of our national brand strategy.
With your extensive knowledge and network, you will assure a successful partnership with all partners
* In all your activities, you will ensure adherence to all Johnson & Johnson compliance guidelines.
* Scientific or paramedical training/ or a SHQA diploma
* Business education a plus
* Several years of experience in the pharmaceutical industry and in customer care
* Existing network in and broad knowledge of the Swiss healthcare sector
* Strong strategic and analytical thinking as well as customer and service orientation
* Confirmed sales, negotiation and communication skills
* Strong standout colleague and enjoy working in a dynamic market as well as in a "dedication" team
* Very good knowledge of German and English, as well as an interest in new digital communication formats
Promoting and developing talent are core values of the Johnson & Johnson workplace culture.
People who want to realise their potential in an international company will find the best conditions with us.
...
....Read more...
Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:23
-
Johnson and Johnson is recruiting for an Associate Clinical Account Specialist (ACAS), to be located in the San Jose, CA area.
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/.
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.
Job Summary
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of BWI's systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding businessgoals.
The anticipated base salary for this position is $70,000- $85,000 depending on location.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus.Theannual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year.
Bonuses are awarded at the Company's discretion on an individual basis.
Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance.
Employees may be eligible to participate in the Company's consolidated retirement pl...
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Type: Permanent Location: San Jose, US-CA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:22
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Johnson & Johnson Innovative Medicine is recruiting for a Senior RA Professional Global, Oncology.
The position will focus on a range of novel product solutions to deliver solutions to treat cancers directly into the tumor.
This position can be located in Spring House, PA; Horsham, PA; Titusville, NJ; and Raritan, NJ.
Any other Johnson & Johnson campus locations/remote options, could be considered for the right candidate.
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.
This position will support the Regional Regulatory Leaders and/or Global Regulatory Leader (GRL) for regulatory activities for compounds in development and/or marketed products in the assigned portfolio within the Oncology therapeutic area.
Key Responsibilities:
* Participate in global regulatory team meetings and provide advice the applicable regulatory requirements, project-specific regulatory issues.
* Build an understanding of the regional regulatory environment (relevant laws, regulations, guidance and competitive landscape) for assigned products.
* Assist in strategy development by researching regulatory and medical information in preparing submissions to North American Health Authorities (HAs).
* Assist in the preparation of HA meetings and act as back-up for contact with HA as needed.
* Ensure responses to HA queries are made in a timely manner, and that content is consistent with the regulatory strategy.
* Provide regulatory support throughout registration process and life-cycle management.
* Work cross-functionally and lead team meetings as appropriate.
* Review development plans, protocols and submission plans, ensuring alignment with regulatory requirements.
* Support the development...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:22
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Job Title: Quality Engineer
Location: DePuy Synthes, Blackpool
Are you passionate about quality engineering and keen to work in the dynamic medical device sector? DePuy Synthes, a leader in the development of innovative medical technologies, is looking for an experienced Quality Engineer to join our team in Blackpool.
If you thrive in a fast-paced, high-impact environment and are dedicated to ensuring the highest quality standards, this role is for you!
What You'll Do:
As an Engineer in Quality Engineering, you will be part of a committed Quality team, collaborating with the Quality Engineering Team Leader.
In this crucial role, you will ensure the ongoing quality and compliance of our manufacturing processes in Base Business.
Your work will focus on maintaining and improving the Quality System to meet key regulatory standards including ISO 9000, ISO 13485, FDA QSRs, and the Medical Devices Directive.
Your key responsibilities will include:
* Monthly Trending & Dashboard Reviews: Track and analyze Non-Conformance (NC) data for production processes and generate insights for dashboard reviews.
* Root Cause Analysis & Action Plans: Investigate issues in products or processes, identify root causes, and develop corrective actions to ensure product quality.
* Collaborate with Engineering: Partner with the Engineering team to define, introduce, and optimize new or improved manufacturing processes.
* Validation Master Plan Ownership: Take ownership of the Validation Master Plan and coordinate quality validation reviews.
* Preventive & Corrective Maintenance: Support operations to ensure that maintenance activities are completed to schedule.
* Process Improvement & Lean Manufacturing: Work with teams to ensure compliance in continuous improvement activities, driving Lean Manufacturing initiatives.
* Regulatory Compliance: Ensure consistency to all relevant regulations governing business and quality operations.
What We're Looking For:
To excel in this role, you will need strong technical expertise and a proven understanding of quality systems and regulatory requirements in a medical device environment.Key qualifications include:
* Education: A minimum of a degree in a scientific field.
* Experience: At least 3 years in a quality, technical, or manufacturing role within a regulated industry.
* Knowledge:
* In-depth knowledge of Good Manufacturing Practices (GMP).
* Familiarity with ISO 13485, FDA QSRs, and validation processes.
* Proficient with Quality Toolbox techniques such as FMEA, root cause investigations, Lean, and Six Sigma.
* Strong analytical and problem-solving skills.
* Excellent interpersonal skills, with the ability to engage optimally across all levels of the organization.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, se...
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Type: Permanent Location: Blackpool, GB-BPL
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:21
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Johnson & Johnson is seeking a highly motivated Manufacturing Technician to join our team in Gurabo, Puerto Rico.
As a Manufacturing Technician at Janssen Pharmaceutical Companies, you will have the opportunity to make a significant impact on the lives of people by helping to produce life-changing medications.
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/.
Responsibilities:
* Operate machinery across various functional areas of manufacturing.
* Assemble and disassemble equipment, components, and product packaging.
* Adjust, inspect, and approve the assigned packaging line and components before starting production.
* Operate and perform light mechanical maintenance on assigned packaging equipment.
* Follow work instructions and document packaging activities using ePES and SAP systems.
* Document and verify equipment calibrations before use.
* Conduct inventory counts and document material usage and rejected material.
* Check product appearance, components, expiration dates, and batch numbers during the packaging process.
* Segregate, pack, identify, and document rejected products and waste materials.
* Clean machinery, equipment, and packaging areas before and after tasks.
* Minimum of a Technical Degree in Mechanical, Electrical, Instrumentation, or related field, and two (2) years of experience in the pharmaceutical and/or medical devices industry; or High School Diploma and five (5) years of experience in the pharmaceutical and/or medical devices industry required.
* Proficiency in using computerized inventory control and document management systems is required.
* Knowledge and application of Good Manufacturing Practices (GMP), Documentation Regulations, Occupational and Environmental Safety is required.
* Must be available to work 1st, 2nd, and 3rd shifts, as well as overtime, weekends, and irregular schedules is required.
* Certification in Yellow Belt (Lean/Six-Sigma) is preferred.
* Basic knowledge of manufacturing processes from raw materials to finished products is preferred.
* Basic troubleshooting skills preferred.
* Proficiency in SAP, e-PES, and Our Source computer programs.
Preferred.
* Verbal and written communication skills in English and Spanish preferred.
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 fue...
....Read more...
Type: Permanent Location: Gurabo, US-PR
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:20
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[ Innovative Medicine ] TA Specialist /Manager , Lung Cancer , Oncology , Medical Affairs
The TA Specialist or Manager of Medical Affairs, Lung Cancer will be responsible for conducting Medical Affairs activities for the J &J solid tumors products primarily focused on proper usage and value maximization, reporting to the Associate Director, Lung Cancer, Oncology, Medical Affairs Japan.
A strong insight into oncology and knowledge of the Japan market is required.
The TA Specialist or manager will be an expert in medical strategy development (Medical Affairs Plan, Business Plan, Integrated Evidence Generation Plan) and will lead disease area (DA) Leads to develop overall strategy for lung cancer under his/her supervision with a goal to address medical and scientific issues and to ensure the appropriate use of all relevant J&J Medical Affairs supported products.
Identify and devise strategies to address crucial gaps using critical relationships across Medical Affairs, Regional & Global Medical Affairs, R&D, Business Units, Market Access, and others.
Responsible and accountable for Medical Affairs strategy of lung cancer including compounds/product development/business plans.
Ensure the smooth execution of all the medical and scientific activities including evidence generation.
Lead and c ollaborate with internal and external stakeholders including key opinion leaders and patient associations to develop and implement the overall Medical Affairs strategy for new and developing products aligned with company brand strategy.
Ensure development of publications arising from Medical Affairs studies and lead and works with relevant teams on broader communication strategy.
Responsible for ensuring that all Medical Affairs activities are compliant with Japan Legislation and HCC rules.
The position is based in Tokyo, Japan.
Key Responsibilities:
• Lead or support to develop and execute Medical Affairs strategy for lung cancer
• Plan and execute Advisory Board Meeting
• Lead Competitive Intelligence and analyze the external environment
• Collaborate with Regional/Global M edical A ffairs counterparts
• Lead Integrated Evidence Generation Plan.
• Partner with key internal and external experts on shaping Medical Affairs strategy.
• Lead to plan and execute Company Sponsored Study and Collaborative Study.
Education:
• Bachelor of Science degree required.
• PhD in life sciences and/or MD preferred.
Experience and Skills:
Required:
* 5 years of experience with Medical Affairs, R&D, Marketing in the pharmaceutical industry, or equivalent skills are required.
* Strong track record in developing and implementing clinical research and medical strategies including evaluation of value-oriented research and communication strategies.
* Deep understanding of local regulatory policy and industry's code of practice related to drug registration, pharmaceutical promotion and clinical study is preferred.
* Interpersonal flexibi...
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Type: Permanent Location: To-Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:17
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Position: Director of Manufacturing Engineering
Location: Limerick
Contract: Full Time/Permanent
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/.
Job Position Summary
This role is reporting directly to the Sr.
Director, Vision Care Manufacturing Engineering who leads the global Engineering function.
You will provide strategic and technical leadership and tactical direction to the diverse and hardworking team of Engineers, Technicians and Project Managers focused on driving and delivering a sustainable competitive advantage and operational excellence in safety, quality, delivery and cost at the Contact Lens for the Ireland site.
Holding a critical leadership position at the Limerick site and within the overall Vision Care business, this role will be to advise and control the activities of the Automation & Controls, Manufacturing Engineering, Injection Molding and Capital Project Management Office (PMO) functions in developing and deploying technical solutions on highly automated production equipment and processes demonstrating innovative, state of the art technologies such as 3-D printing, robotics and vision systems!
In addition to crafting the strategic direction and conceptual roadmap for the Limerick launch and production site and Manufacturing Engineering network, you will lead and supervise innovative change across all manufacturing assets through both equipment upgrades as well as automation, robotics, IIOT, and other innovative Industry 4.0 technologies!
You will use Lean, Six Sigma, manufacturing asset management and reliability engineering tools and techniques to optimise throughput, cycle-time, yield as well as reliability, availability, longevity, operational safety and overall total cost of ownership for all manufacturing equipment and production systems.
You will have primary responsibility for leading and supervising the Limerick site Capital Investment portfolio with responsibilities ranging from long-term planning, forecasting and budgeting to Capital Appropriation Request approval and reporting of Supply Chain funded projects.
Beyond steering the capital portfolio, you will build the capabilities of a project management office (PMO) tasked with direct management of capital projects as well as prioritisation and governance over the portfolio of site and platform projects.
Develops and continually improves business process over the entire project lifecycle ensuring optimal Total Cost of Ownership, efficiency, compliance and successful execution of the ...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:17
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Job Title: Specialist EQ - Supplier Quality
Location: Beerse, Belgium
Company: Johnson & Johnson Innovative Medicines (IM)
Overview:
Johnson & Johnson Innovative Medicines (IM) is seeking a dynamic Specialist EQ - Supplier Quality to join our team.
Based in Beerse, Belgium, this role offers an exciting opportunity to give to the global pharma sector by coordinating the quality and compliance of suppliers, while serving as a trusted partner to the Advanced Therapies IM Supply Chain manufacturing sites.
Key Responsibilities:
As a Specialist EQ - Supplier Quality, you will play a meaningful role in ensuring our suppliers meet J&J's high-quality standards, regulatory requirements, and business objectives.
You will collaborate closely with internal teams and suppliers, ensuring compliance with J&J policies and improving our reputation for excellence in the industry.
Key areas of responsibility include:
* Account Ownership (20-30%):
* Lead quality oversight for low criticality suppliers within the IM Portfolio.
* Supervise the quality and compliance status of suppliers, ensuring smooth management of activities such as change control, deviation management, complaints handling, and quality agreement updates.
* QA Specialist Support (70-80%):
* Support SQ operations and act as the point of contact for the Supplier Quality-Advanced Therapies (SQ-AT) SPOC team.
* Lead non-conformances, supplier investigations, change controls, documentation, and various QMS-related processes.
* Assist with audit/inspection support to ensure compliance and continuous improvement.
* Project Management (5-10%):
* Lead or contribute to low/medium impact projects within EQ and the IM sites, focusing on process optimization and central initiatives to improve EQ-SQ management.
Example of Responsibilities:
* Planning and driving supplier qualification and monitoring for critical materials sourced for drug manufacturing.
* Conducting audits, technical visits, and proactive supplier engagement to ensure alignment with quality standards.
* Assessing nonconformances, CAPAs, and supplier complaints, taking corrective actions as vital.
* Handling change control processes and reviewing quality agreements.
* Providing support during inspections from customers and health authorities.
* Owning the establishment of quality requirements and ensuring supplier specifications are met.
* Building positive relationships with external partners to ensure the reliability of external manufacturing processes.
Qualifications:
* A graduate degree (or equivalent experience) in Science, Bioengineering, Pharmacy, or a related field.
* Proven understanding of the pharmaceutical industry, cGMP, and regulatory requirements.
* Familiarity with quality systems, quality processes, investigations, and risk analysis.
* Fluent in both Dutch and English, with outstanding communication skills to engage with intern...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:17
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Johnson and Johnson is recruiting for an Associate Clinical Account Specialist (ACAS) , to be located in the Dallas, TX area.
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/.
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.
Job Summary
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of BWI's systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding businessgoals.
The anticipated base salary for this position is $75,000- $85,000 depending on location.
The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus.Theannual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation's performance over a calendar/performance year.
Bonuses are awarded at the Company's discretion on an individual basis.
Thispositionis eligible fora companycarthrough the Company's FLEET program.
Employeesmay beeligible to participate inCompanyemployee benefit programssuch ashealthinsurance, savings plan,pensionplan,disability plan, vacationpay,sicktime,holidaypay,and work, personal and family time offin accordance with the terms of the applicable plans.
Addit...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:16
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En Johnson & Johnson creemos que la salud lo es todo.
Nuestra fortaleza en innovación en atención médica nos permite construir un mundo donde se previenen, tratan y curan enfermedades complejas, donde los tratamientos son más inteligentes y menos invasivos y las soluciones son personales.
A través de nuestra experiencia en Medicina Innovadora y MedTech, estamos en una posición única para innovar en todo el espectro de soluciones de atención médica y ofrecer los avances del mañana para impactar profundamente la salud de la humanidad.
Obtenga más información en https://www.jnj.com/
Declaración DE&I
Durante más de 130 años, la diversidad, la equidad y la inclusión (DEI) han sido parte de nuestro tejido cultural en Johnson & Johnson y están integradas en la forma en que hacemos negocios todos los días.
Arraigados en Nuestro Credo, los valores de DEI impulsan nuestra búsqueda de crear un mundo más saludable y equitativo.
Nuestra fuerza laboral diversa y nuestra cultura de pertenencia aceleran la innovación para resolver los desafíos de atención médica más apremiantes del mundo.
Sabemos que el éxito de nuestro negocio (y nuestra capacidad para ofrecer soluciones significativas) depende de qué tan bien comprendamos y satisfagamos las diversas necesidades de las comunidades a las que servimos.
Es por eso por lo que fomentamos una cultura de inclusión y pertenencia donde se valoran todas las perspectivas, habilidades y experiencias y nuestra gente puede alcanzar su potencial.
En Johnson & Johnson, todos pertenecemos.
Estamos buscando al mejor talento para la posición que estará localizado en Monterrey .
Propósito: El propósito de este cargo es asistir de manera oportuna en los procedimientos quirúrgicos dentro de los hospitales asignados, asegurando el manejo adecuado de los equipos, instrumental y consumibles necesarios para las cirugías, así como colaborar en el proceso de facturación y cobro de los servicios prestados.
Además, se espera garantizar el cumplimiento de los procesos de calidad y la atención integral al paciente durante las intervenciones quirúrgicas.
Funciones:
• Asistir a médicos, enfermeras y demás profesionales de la salud en los procedimientos quirúrgicos dentro del ámbito del hospital asignado.
• Gestionar el manejo adecuado y oportuno del equipo e instrumental quirúrgico, asegurando su correcto funcionamiento y disponibilidad.
• Realizar el proceso de lavado, desinfección y esterilización de todo el instrumental y equipo quirúrgico, garantizando su conformidad con los estándares de higiene y calidad.
• Controlar y resguardar el inventario de equipo, instrumental y material desechable, asegurando su disponibilidad durante las cirugías.
• Elaborar y entregar los reportes e inventarios requeridos, manteniendo la trazabilidad y el cumplimiento con las normas establecidas.
• Apoyar en la capacitación básica del personal de nuevo ingreso en cuanto a la operació...
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Type: Permanent Location: Monterrey, MX-NLE
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:16
-
Johnson & Johnson is hiring for a Sr.
Regulatory Operations Specialist - Shockwave Medical to join our team.
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.
Shockwave Medical, Inc., recently acquired by Johnson & Johnson, is a pioneer in the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Shockwave Medical aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Senior Regulatory Operations Specialist is an individual contributor who will help secure and retain global regulatory approvals for medical devices by archiving, creating, and maintaining specific categories of regulatory documentation and data.
Works closely and partners with Regulatory colleagues and other internal departments to meet assigned deliverables and identify areas of improvement within Regulatory Operations efficiently and effectively.
The function of the Senior Regulatory Affairs Specialist, Operations, includes providing submission publishing/verification support and Regulatory compliance support.
Under direction of responsible Regulatory Affairs Management, works independently with minimal oversight.
Essential Job Functions
* Publisher for worldwide regulatory submissions in compliance with geography-specific regulatory requirements
* Verify and qualify review of submissions and other responses to regulatory agencies
* Archive correspondence sent to and received from Regulatory Agencies and Notified Body
* Track original and renewals of ann...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:15
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Johnson & Johnson is hiring for a Sr.
R&D Engineer, Systems - Shockwave Medical to join our team located in Santa Clara, CA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
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.
Shockwave Medical, Inc., recently acquired by Johnson & Johnson, is a pioneer in the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Shockwave Medical aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Sr.
R&D Engineer, Systems will work with cross-functional teams to develop and sustain products at Shockwave Medical that satisfy customer needs and drive business strategies.
The Sr.
R&D Engineer, Systems will engage in specification writing and development; test and report writing and development; execute testing; DHF maintenance; and provide support to other departments as required.
Essential Job Functions
• Design and develop product(s) and documentation in full compliance with the company's Design Control requirements and consistent with FDA, ISO, and MDD criteria
• Participate on cross-functional development teams that manage projects from concept through commercialization
• Evaluate existing document architecture and assess gaps and dependencies
• Work with stakeholders to establish project needs and functional group interfaces.
• Work with on-market groups and data sets to assess device performance.
• Support sustaining activities for on-market products
• Support quality audits and follow-up activities.
• Ensure lab notebooks are doc...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-02-07 07:10:15
