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The Test Technology Division of Applied Research Associates, Inc.
(ARA) has an exciting opportunity for an Environmental Health and Safety Manager to lead our safety initiatives at multiple test site locations.
As our Health and Safety Manager, you will be a pivotal leader responsible for developing, implementing, and overseeing comprehensive health and safety programs that align with our strategic objectives and ensure regulatory compliance across our operations.
You'll drive continuous improvement in our safety performance, cultivate a proactive safety culture, and potentially lead a team of safety professionals.
This is an exciting opportunity for a seasoned safety leader to champion best practices and make a significant, measurable impact.
Our multi-disciplined team is comprised of engineers, scientists, fielding and explosives technicians, and administrative professionals, supporting the government and commercial clients.
Our work is primarily performed in New Mexico on Kirtland Air Force Base, White Sands Missile Range and at our ARA test site in Moriarty, NM.
Due to the nature of work performed candidates must be U.S.
citizens eligible for a Department of Defense Secret, or higher, level security clearance.
Salary Range: $130,000 - $150,000 (Dependent on Qualifications and Experience)
Key Responsibilities:
* Strategic Leadership & Program Development
+ Develop, implement, and monitor comprehensive health and safety programs, policies, and procedures in accordance with OSHA and other National Consensus standards (ANSI, NFPA, DOT, and NIOSH) and site-specific regulations
+ Set strategic safety objectives, key performance indicators (KPIs), and annual safety plans
+ Ensure compliance with all federal, state and local health and safety regulations, proactively tracking and responding to legislative changes
* Risk Management & Incident Oversight
+ Lead comprehensive risk assessments and hazard analyses across all operations, developing and implementing effective control measures
+ Oversee the investigation of all incidents, accidents, and near-misses, ensuring thorough root cause analysis and the implementation of robust corrective and preventative actions
+ Manage and maintain accurate safety data, preparing reports for senior leadership on performance trends, compliance status, and improvement opportunities
* Safety Culture & Training
+ Champion a strong, proactive safety culture throughout the organization, engaging with all levels of employees from executive leadership to front-line staff
+ Design, deliver, and manage comprehensive health and safety training programs, ensuring all employees are adequately trained on relevant safety procedures and emergency protocols
+ Lead safety committees and foster active employee participation in safety initiatives
* Regulatory Liaison & External Relations
+ Serve as the primary ...
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Type: Permanent Location: Albuquerque, US-NM
Salary / Rate: Not Specified
Posted: 2025-10-10 08:24:55
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen.
Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM!
Das Team,
Die Pioneers for Excellence unterstützen gemäß der Lean Six Sigma Denkweise die produzierenden Betriebe sowie Support-Einheiten bei Prozessanalysen- und -verbesserungen, Visualisierung, Setzen von Standards und Capability Building.
Ein wichtiger Teil dessen ist das Durchführen von Root Cause Analysen, um durch gezielte Optimierungen Abweichungen im Bereich der Abfüllung und Verpackung von Medikamenten zu vermeiden.
Was dich erwartet
In der Funktion als Operational Excellence Partner (m/w/d) erwarten Dich folgende spannende Aufgabenbereiche:
Delivering Value Impact
* Du identifizierst die größten Wertverluste und findest die besten Möglichkeiten zur Verbesserung innerhalb der Organisation.
* Du bist der strategische Sparringspartner für Führungskräfte und begleitest sie dabei, ihre Performance zu steigern und Unternehmensziele zu erreichen.
* Du treibst, leitest und setzt wichtige Projekte zur Leistungssteigerung um, die direkt auf die Unternehmensziele und KPIs einzahlen.
Dabei führst du funktionsübergreifende Teams und stellst den Projekterfolg sicher.
* Gemeinsam mit den Business Ownern entwickelst du den Verbesserungsplan der Organisation und förderst so Zusammenarbeit und Verantwortungsbewusstsein.
* Du überzeugst Führungskräfte, als Sponsoren für Verbesserungsprojekte zu agieren und die nötigen Ressourcen bereitzustellen.
Lean Production System (LPS) und Standards implementieren und aufrechterhalten
* Du bist der Leader und Befürworter für LPS-Standards sowie Lean-Methodologien und -Tools.
* Du stellst sicher, dass das Lean Production System konsistent angewendet und kontinuierlich verbessert wird.
* Du coacht und trainierst deine Kollegen in Lean-Methodologien und -Techniken wie strukturierter Problemlösung, Root Cause Anal...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-10 08:22:56
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Dein Team
Unser Roche CustomBiotech Team ist verantwortlich für die Vermarktung von Biotech Produkten für die produzierende Diagnostik- und Pharmaindustrie (z. B.
Polymerasen, Nukleotide, Analysegeräte für Zellkulturen) in Europa, dem Mittleren Osten, Afrika und Lateinamerika.
Unser Sales- & Marketing-Team setzt sich aus Mitarbeitenden verschiedener Nationalitäten zusammen.
Als Teammitglied wirst du von Anfang an herzlich in unsere Gruppe aufgenommen und kannst deine eigenen Ideen einbringen.
Indem du uns in allen Tätigkeitsbereichen unterstützt, kannst du dein theoretisches Wissen mit praktischen Erfahrungen anreichern.
Während deiner Zeit bei uns steht dir nicht nur eine feste Ansprechperson, sondern auch das Know-how des gesamten Teams zur Verfügung.
Deine Aufgaben
Du willst endlich dein Wissen in einem anwendungsorientierten Umfeld einbringen? In diesem Praktikum erwartet dich ein ausgewogenes Verhältnis zwischen eigenen Projekten und der Unterstützung der Produkt- und Marketingmanager im Tagesgeschäft:
* Einbringen deiner naturwissenschaftlichen Expertise zur Präsentation, Beschreibung und Vermarktung unserer Biotech Produkte
* Vor- und Nachbereitung von internen Workshops, Marktanalysen, Erstellen und Zusammenführen von Präsentationen, Digitalisierung, etc.
* Gestalte als aktives Mitglied unseres Teams internationale Projekte mit und leite deine ersten eigenen Projekte
Dein Profil
* Du bist Masterstudent/in Fachrichtungen Biotechnologie, Biochemie, Biologie oder einer ähnlichen Fachrichtung.
Du bist vertraut mit Begriffen wie mRNA, Impfstoff, Zell- und Gentherapie oder PCR Technologien
* Du hast Interesse, dich zu den Themen Marketing und Produktmanagement im naturwissenschaftlichen Kontext weiterzubilden
* Du kannst souverän mit IT Anwendungen umgehen wie z. B.
Excel, Powerpoint, Google Docs
* Der enge Austausch mit dem Team macht dir Spaß, du bist motiviert, selbstständig und engagiert
* Du punktest mit deinem guten Deutsch und Englisch in Wort und Schrift
Deine Vorteile
* Wir ermöglichen flexible Zeiteinteilung mit einem ausgeglichenen Verhältnis zwischen dem Büro in Mannheim und Home-Office
* Modernes, neues Büro mit vielen digitalen Möglichkeiten der Zusammenarbeit
* 2092 € Vergütung pro Monat für ein Vollzeitpraktikum
* Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine
* Fitnesszentrum auf dem Roche-Campus
* Vernetzung mit anderen Studierend...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-10 08:22:05
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
People Leader
All Job Posting Locations:
Chiyoda, Tokyo, Japan
Job Description:
The Country Safety Head is responsible and accountable for ensuring all pharmacovigilance requirements for Johnson & Johnson Innovative Medicine is fulfilled.
Provides strategic leadership to the teams to ensure and enable the achievement of the overall strategic imperatives of Local Medical Safety (LMS) in Japan.
Essential Job Duties and Responsibilities
Ensure patient safety and product safety for entire Johnson & Johnson Innovative Medicine products.
- Accountable for the compliance of the Pharmacovigilance activities including safety information intake & reporting to GMS/PMDA, PV agreements with business partner/vendor, and Risk Management Plan.
- Accountable for all GVP-related activities, either directly or through deputization, including activities such as:
* Development and implementation of Japan Risk Management Plan (J-RMP), conducting Early Post-marketing Phase Vigilance (EPPV), analysis of safety information, and monitoring of benefit risk balance
* Launch readiness of the products from safety aspects before approval of (supplemental) J-NDA
* Maintaining favorable benefit-risk balance of the marketed products, with timely communication of relevant safety information available to Health Care Professionals
* Planning proper safety measures, decide to implement the plan or make proposals on the plan to the Marketing Supervisor-General depending on the definition of the measure in the procedural documents
* Implementation and monitoring of risk management plans and take the appropriate actions for the implementation if urgent safety restrictions, as required.
* Ensuring GVP requirements and all updates are reflected in the procedural documents and put in place.
- Oversight Japan Product Safety Committee (JPSC)
- Build the strong communication and work closely with relevant stakeholders such as Marketing Supervisor-General, Quality Assurance Manager, PMS Control Manager, Head of Medical Affairs, Safety Operational Organization like Business Unit and partner companies.
Leadership and strategic direction of all activities in Japan Local Safety Unit (J-LSU)
- Provide strategic leadership and vision for J-LSU
- Strengthen organizational development such as such as building a high-performance & engage...
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Type: Permanent Location: Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-10-10 08:20:21
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Business Enablement/Support
All Job Posting Locations:
Madrid, Spain
Job Description:
Within the Sales Organization, the Account Representative is responsible for promoting and communicating the benefits of the ETHICON Endomech & Energy portfolio in order to drive sales results.
The Sales representative serve as the principal point of contact between the business and its customers and have a range of responsibilities including identifying new potential customers while supporting existing clients with information and assistance related to the product portfolio.
The sales representative will be the responsible for the implementation and execution of the marketing strategies in a region and will be accountable for the achievement of the sales targets and business goals
This position is eligible for sales incentives/sales commissions
Responsibilities and Functions
* Responsible for sales target achievement in geography of responsibility
* Use consultative selling techniques to identify potential sales opportunities within the account.
* Support the surgical team during laparoscopic procedures
* Maintain a personal relationship with clients, negotiating prices, deadlines and other conditions with the client directly
* Educate customers on all Endomechanical and Energy products to optimize effective usage by providing technical and clinical information and in-service trainings.
* Prepare, plan, and implement training and product demonstrations in-house.
* Keep up with the latest clinical data supplied by the company and interpreting, presenting and discussing this data with health professionals during presentations
* Analyze data from company systems.
Responsible for analyzing the market in which you work: optimizing territory plans by consistently tracking market information, using data systems to run analysis on accounts/cost & impact decision making in accounts.
* Monitor competitor activity and competitors' products;
* Keep detailed records of all contacts and activity registries on a weekly basis
* Stay informed about the activities of health services
* Sector covered is Galicia Sur
Profile Requirements
* University degree in natural- or neuroscience (i.e., medical, psychology, chemistry, biology, pharmacy) or similar qualification or expe...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-10-10 08:20:13
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Global Commercial Strategy Organization, a group within Janssen Global Services and a member of Johnson & Johnson's family of companies, is recruiting for a Global Compound Market Access Leader for Oncology.
This position will be based in Raritan, NJ.
About Oncology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Lead the global market access strategy for the brand(s):
* Lead the Compound Market Access Team (CMAT), which includes the core functions within Global Market Access (i.e., Health Economics, Patient Reported Outcomes [PRO], Access Policy, Pricing, Real-World Evidence & Analytics) to deliver the global market access strategy & key value communication tools for the brand.
* Be responsible for the strategic planning and implementation of the payer value generation and access strategies for an Advanced Therapy Medicinal Products (ATMP) product aiming for an accelerated path to market.
* Serve as the leading resource on access strategies and is an active member of the global clinical and commercial product teams, as well as the disease area strategy groups.
* Be responsible for integrating pricing, payer research, health economic and epidemiology information to develop the optimal value strategy.
* Interact with Regional Market Access/Health Economics / Outcomes Research and Medical Affairs teams to coordinate and develop real world evidence generation in support of their access programs.
* Develop an integrated access strategy that reflects macro (health care reform, quality metrics, technology assessment) and disease specific (clinical profile, market segmentation, disease staging and clinical pa...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-10 08:20:08
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Chemical Research
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Join J&J Innovative Medicine as a Synthetic Chemist in Process R&D!
At J&J Innovative Medicine, we are committed to transforming lives through groundbreaking science and innovative therapies.
Our Department of Chemical Process Research & Development (CPRD) is dedicated to developing cutting-edge synthetic methodologies and processes for small molecules, oligonucleotides, peptides, and emerging modalities.
We are seeking a passionate Synthetic Chemist to join our Process R&D team and help accelerate the journey from discovery to life-changing medicines.
Your Role at J&J:
As a vital contributor to our Development Chemistry team, you will lead efforts to design and optimize innovative synthetic routes that meet the highest standards of safety, quality, and efficiency.
Working closely with engineers, analysts, crystallization, and safety experts, you will help translate laboratory discoveries into scalable, robust manufacturing processes.
Your work will directly support the rapid development and supply of active pharmaceutical ingredients (APIs) for clinical trials, registration, and commercialization.
Key Responsibilities:
Develop and implement creative, efficient synthetic processes for complex molecules.
Support process scale-up from laboratory to pilot plant, ensuring seamless technology transfer.
Collaborate across multidisciplinary teams to troubleshoot, optimize, and innovate manufacturing processes.
Contribute to our mission of delivering safe, effective, and accessible medicines to patients worldwide.
Drive continuous improvement and innovation in process chemistry, aligning with J&J’s commitment to excellence.
What You Bring:
Qualifications & Experience:
PhD in Organic Chemistry (Postdoctoral experience is a plus)
Demonstrated record of scientific excellence with peer-reviewed publications
Hands-on experience in state-of-the-art chemical laboratories
Creative problem-solver with a passion for innovation
Excellent communication skills in English (verbal and written)
Strong team collaborator with a proactive, constructive mindset
Willingness to challenge conventions and propose innovative solutions
Preferred Skills & Competencies:
Experience with automated synthesis, lab...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-10 08:20:00
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
Scientific/Technology
All Job Posting Locations:
San Diego, California, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson Innovative Medicine (JJIM) is recruiting for a Senior Scientist, Computer-Aided Drug Design (CADD) - In Silico Discovery to join our Therapeutics Discovery team located in either San Diego, CA (La Jolla area) or Spring House, PA (Philadelphia area).
The Therapeutics Discovery organization within JJIM is continuing to build scientific expertise in modeling, screening, pharmacology and chemistry to partner closely with therapeutic area scientists to develop groundbreaking new medicines in the areas of Immunology, Neuroscience and Oncology.
The In Silico Discovery (ISD) group in Therapeutics Discovery is seeking two excellent scientists to bring their expertise to exciting and novel areas of computational drug design.
Key Responsibilities Include:
* Design therapeutic molecules and calculate their properties using state-of-the-art methodologies integrating chemical, biological and structural data, cheminformatics, and artificial intelligence/machine learning techniques
* Serve as a scientific expert and to contribute in multi-disciplinary discovery project teams that include synthetic chemists, structural biologists, and other discovery scientists, by providing key computational expertise to advance drug discovery projects
* Collaborate within Janssen and with external academic and industrial partners to develop new computational technologies to address key questions in drug discovery
* Publish results in peer reviewed journals and present at scientific meetings
* Mentor junior scientists and/ or interns fostering their development as expert computational drug hunters
* Contribute to efforts to evaluate and assess novel protein targets of interest for their ligandability and tractabi...
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Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-10 08:19:42
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Aachen, North Rhine-Westphalia, Germany, Berlin, Germany, Frankfurt am Main, Hesse, Germany, Hamburg, Germany, Hamburg, Hamburg, Germany, Hannover, Lower Saxony, Germany, Munich, Bavaria, Germany, NEUSS, Germany, Neuss, North Rhine-Westphalia, Germany, Norderstedt, Schleswig-Holstein, Germany, Rhein-Kreis Neuss, North Rhine Westphalia, Germany
Job Description:
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/
Über MedTech
Wir arbeiten seit einem Jahrhundert an der Seite von Ärzten und Patienten, um das Gesundheitswesen immer wieder aufs Neue zu verbessern und zu optimieren sowie neu zu denken. Unser J&J-MedTech-Portfolio wird von Innovationen geprägt, die Barrieren an der Schnittstelle zwischen Biologie und Technologie aus dem Weg räumen.
Gemeinsam entwickeln wir die nächste Generation intelligenter, weniger invasiver und personalisierter Lösungen, um die größten und komplexesten gesundheitlichen Herausforderungen für Menschen auf der ganzen Welt zu bekämpfen.
Begleiten Sie uns auf unserem Weg, während wir Medizinprodukte weiterentwickeln und den Übergang von der Forschung ins echte Leben ermöglichen – immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/medtech
Interne Stellenausschreibung 09.10.2025 - 24.10.2025
Vollzeit oder 50-60% Teilzeit im Jobsharing Modell
Optionen für Remote-Arbeit können je nach Fall geprüft werden und müssen von der Firma genehmigt werden.
Wir suchen das beste Talent für die Position des
HEALTH ECONOMICS & MARKET ACCESS MANAGER - Surgery
STELLENPROFIL
Als Fachverantwortlicher für den Bereich Surgery ...
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Type: Permanent Location: Norderstedt, DE-SH
Salary / Rate: Not Specified
Posted: 2025-10-10 08:19:06
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ERM is hiring a Field Biologist to conduct post-construction mortality monitoring (PCMM) for avian species at a wind farm in Crockett County, TX.
Successful candidates must be flexible and responsive to a challenging and changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project.
The role of a field biologist requires both technical skills and strong organizational and communication skills.
This is a part-time (18 hours/ week), limited-term role with a duration of 1 year and the possibility of renewal.
Assignments will, on average, have a duration of 2 days per week.
RESPONSIBILITIES:
* Field biologist position to conduct post-construction mortality monitoring, which includes monitoring for bird mortality, search efficiency trials, and carcass persistence trials.
* Electronic data collection.
* Handheld and sub-meter accurate GPS data collection.
* Daily reporting and survey report compilation.
* Other duties as assigned or required.
* Compliance with ERM’s rigorous safety program.
REQUIREMENTS:
* Bachelor's degree in environmental science, Biology, or related field preferred.
* A minimum of 2+ years of Avian experience, ideally with PCMM experience.
* General bird identification skills required.
* Ability to work safely outdoors in variable weather conditions and on challenging terrain.
* Working knowledge of sub-meter accuracy GPS technologies and map interpretation skills (e.g., NWI, USGS, aerial photography).
* Must have a strong attention to detail in documentation of work.
* Must have strong organizational and communication skills.
* Desire to work in the field for an extended period and maintain a positive attitude.
* Willingness and ability to travel with overnight stays possible.
* Demonstrated independent and effective problem-solving and decision-making skills.
* Possess a valid driver’s license.
* Fluency in English and Spanish is highly preferred.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues.
We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strat...
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Type: Contract Location: Austin, US-TX
Salary / Rate: Not Specified
Posted: 2025-10-10 08:16:20
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Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the field of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
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Type: Permanent Location: Lisle, US-IL
Salary / Rate: Not Specified
Posted: 2025-10-09 09:05:11
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Your Job
The Principle Materials Engineer serves as one of Molex's key contributors in the field of polymer materials.
In a manner and direction consistent with the overall group vision and strategy, this individual is responsible for managing aspects of complex technical projects or programs related to materials or process technology innovation, selection, specification, evaluation, deployment, failure analysis, and / or testing.
The Principle Materials Engineer is also expected to support technology transfer and knowledge sharing with suppliers, external collaborators, and customers.
Our Team
Molex is a global leader in electronic components and solutions, with a strong focus on innovation, quality, and customer service.
The company has been in operation for over 80 years and has a strong presence in various industries, including automotive, telecommunications, consumer electronics, aerospace, defense, medical, and industrial automation.
Candidates can expect to work in a dynamic and fast-paced environment that values creativity, collaboration, and excellence.
Molex is committed to investing in its employees and providing opportunities for growth and development .
What You Will Do
* Deliver on various strategic project commitments configured to address the technical needs / opportunities identified through:
* direct engagement with internal stakeholders from product development and manufacturing
* group technology track roadmaps
* identified technical needs of the enterprise
Support the product development and manufacturing teams with materials application engineering support, support on design reviews and new product development challenges, materials and manufacturing process related problem solving and failure analysis, and technical engagement with the raw material supply base.
Monitor relevant research and development activities in universities and industry through literature searches, seminars, conferences, supplier visits, and external courses.
Create, identify, and help secure intellectual property through patents, publications, and / or trade secrets.
Conduct problem solving and failure analysis consultations, including sample management, coordination of work activities with internal and external analysis / testing facilities, and reporting of results, conclusions, and recommendations.
Review and update existing Molex Engineering Specifications related to raw materials.
Create new Engineering specifications and best practices as required to ensure strong and robust engineering practices related to raw materials and their processing enterprise-wide.
Operate and maintain the pertinent experimental, analytical, and testing equipment (not required to operate equipment on a regular basis.
Only occasionally).
Support management in the coordination and preparation of knowledge shares, technical seminars, and meetings.
Understand, support, and contribute to current Molex Total Quality Manage...
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Type: Permanent Location: Rochester Hills, US-MI
Salary / Rate: Not Specified
Posted: 2025-10-09 09:05:10
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General Purpose
Responsible for the regulatory oversight of multiple facility clinical programs located in different states.
This position provides support and education for nursing clinical programs.
The primary purpose is to assist with the design and implementation of clinical audits in vital areas requiring clinical improvement and then providing support and education that ensures regulatory compliance.
The position requires collaboration between Compliance Team members and Regional Teams (RDCS, ARDCS, RAI Specialists, IP Nurses).
This includes but is not limited to training of nurses in proper daily skilled documentation, wound documentation, and risk reduction.
Recommendations will strictly adhere to Medicare guidelines and PACS Best Practices.
Essential Duties
* Supports State and Federal Regulatory Compliance with monitoring, education, and implementation of
* clinical programs while collaborating with other members of the PACS Compliance Team and local PACS Regional Team members.
* Provides Facility Trainings as needed to support local facility clinical operations
* Educates and Mentors Registered and Licensed Nursing staff as necessary for proper daily skilled
* documentation and special focus areas including PDPM active diagnosis, fall management, wound treatment, and care planning in the EMR.
* Reviews EMR and Point Right to ensure strict compliance with Medicare guidelines
* Collaborates with Legal Team to monitor high risk liability areas and assist facilities to alleviate liability risk
* Tracks and trends clinical metrics for identified risk areas
* Participates in Facility CSR, Triple Check, and other meetings as directed
* Supports administrators in achieving clinical outcomes which adhere to industry standards of care and regulatory requirements.
* Intensive auditing responsibility of pertinent clinical topics.
* Monitors for trends affecting workflow, facility liability, and risk management
* Interface with other regional personnel to promote standardization across region
* Identifies opportunities within facilities for new programs (i.e.
Certified wound treatment)
* Supports facility with clinical reviews for probes, CERTs, ADR's, and ALJ's
* Reports to Vice President of Compliance Support any concerns with compliance or lack of adherence to company best practices
* Assists with Wound Module Training in the EMR
* Provides recommendations to supervisor for opportunities to improve company
* Must be able to travel by car and/or plane when necessary to reach assigned destination in a reasonable time frame
* Must maintain confidentiality of company and patient information
* Promotes positive attitude to coworkers and to company regarding the company, its mission statement, philosophies, and goals
* Inspire others to elevate their level of commitment
* Complete ongoing education with follow up in-service to appro...
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Type: Permanent Location: Farmington, US-UT
Salary / Rate: Not Specified
Posted: 2025-10-09 08:56:01
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Manufacturing Scientist/Quality Control Chemist Intern (Summer 2026)
As a Scientist Intern, you will be part of Animal Health Manufacturing (AHM) Lab team to deliver a practical solution to reducing analytical variability, a manufacturing technical project, or implementation of new lab methods.
Interns will have exposure to many career path and diverse subject matter experts as many projects have site-wide impact.
Your Responsibilities:
* Understand the Animal Health Manufacturing process, document using GMP guidelines, and understand the importance of the Quality Unit
* Work within cross-functional teams to implement process or Quality Control lab improvements
* Learn about quality control, fermentation, product recovery, product finishing, or companion animal packaging
* Study design improvement processes
What You Need to Succeed (minimum qualifications):
* Education: Currently enrolled in a Microbiology, Biochemistry, Chemistry, Chemical engineering, or related engineering fields
* Experience with Microsoft Suites
* Demonstrate laboratory/manufacturing experience
* A willingness to learn
What will give you a competitive edge (preferred qualifications):
* Have an interest in animal health manufacturing, problem solving, scientific method, or cross-functional skill development
* Strong communication and interpersonal skills
* Thrive in cross-functional team settings
* Strong organizational and time management skills
* Must be able to work exceptionally well independently and with minimal supervision
Additional Information:
* Travel: 0%
* Location: Elanco Clinton Laboratories – Clinton, IN
Our Internship Program
Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs.
All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career that counts.
* Internship Dates: May 18th – August 7th (12 Weeks)
* Competitive salary: $20-$40/hour (dependent upon major and year in s...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-10-09 08:42:27
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: US Farm Animal Beef Veterinarian Intern
Elanco Animal Health is seeking a highly motivated and enthusiastic Veterinarian Intern to join our Beef Unit for a unique and rewarding experience.
This internship offers the opportunity to gain practical experience in a dynamic industry, working alongside experienced professionals to provide technical expertise and support to our valued customers.
Responsibilities:
· Technical Advising: Provide technical support and guidance to customers on Elanco's package goods and feed additive portfolio such as antiinfectives, vaccine lines, parasiticides which is including product information, usage recommendations, and best practices.
· Parasite Management: Assist in developing and implementing external and internal parasite management strategies for beef operations, working collaboratively with veterinarians and producers to optimize animal health and productivity.
· Account Growth Identification: Identify and evaluate opportunities for account growth within the beef sector, conduct market research and analysis to identify potential new clients and expand existing relationships.
· Veterinary Clinic Networking: Build and maintain strong relationships with veterinary clinics, acting as a liaison between Elanco and the veterinary community to foster collaboration and knowledge sharing.
· Collaboration with Key Account Managers and Technical Consultants: Work alongside experienced Key Account Managers, Veterinarian Technical Consultants, and Nutritionist Technical Consultants to gain valuable insights into account management, technical advising, and industry best practices.
Professional Development Opportunities:
This internship is designed to foster professional growth in various areas, including:
· Clinical Skills Development: Enhance clinical skills through hands-on experience and mentorship from experienced veterinarians.
· Interpersonal Skills Enhancement: Develop strong communication and interpersonal skills by interacting with clients, colleagues, and industry professionals.
· Business Analytics Exposure: Gain exposure to business analytics and ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 27
Posted: 2025-10-09 08:42:21
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Cuxhaven liegt direkt an der Nordsee, der Elbe sowie am Nationalpark Wattenmeer (UNESCO Weltnaturerbe) und ist das größte deutsche Seeheilbad.
Mit einem stark wachsenden Tourismus (mehr als 4 Millionen Übernachtungen pro Jahr) gehört Cuxhaven zur Metropolregion Bremen / Hamburg.
IHRE AUFGABEN UND VERANTWORTLICHKEITEN
* Schnittstelle QA und Process Team, erster Ansprechpartner für das Process Team in qualitätsrelevanten Fragen
* Durchführung von Qualitätssicherungsmaßnahmen bei der Aufrechterhaltung und Sicherstellung der GMP-konformen Produktion, wie z.B.
bei Risikoanalysen, Prozessvalidierungen und Qualifizierungen, sowie Prozessoptimierungen
* Unterstützung und Beratung des Process Teams bei der Erstellung und Bewertung von Abweichungen, Änderungen und weiteren relevanten Themen wie z.B.
SOP- und PQR-Erstellung, Vor- und Nachbereitung von Inspektionen
* Coaching und Training der Process Team-Mitglieder zum Qualitätsstandard, z.B.
GMP-Schulungen, Ursachen- und Risikoanalysen
* Unterstützung bei Kontakten zu Aufsichtsbehörden und Inspektionen durch Aufsichtsbehörden sowie Unterstützung bei Kundenkontakten und Kundenaudits, Sicherstellung der "all time inspection readiness" im Verantwortungsbereich
* Verantwortlich für die Sicherstellung des korrekten GMP-Status, kontinuierliche Verbesserungen und Überwachung der Qualifizierungs- und Validierungsprozesse im Bereich
* Überprüfung und Genehmigung von Dokumenten
* Umsetzung von Operational Excellence-Management und einer Kultur der kontinuierlichen Verbesserung
* Unterstützung und Mitwirken bei Projekten
WAS SIE MITBRINGEN
* Abgeschlossenes naturwissenschaftliches oder technisches Studium oder eine vergleichbare Qualifikation
* Praktische Erfahrung in der GMP-ausgerichteten pharmazeutischen Industrie im Bereich QA oder in der sterilen bzw.
aseptischen Produktion sind von Vorteil
* Sehr gute schriftliche und mündliche Kommunikationsfähigkeiten (Deutsch und Englisch)
* Fähigkeit zu eigenständige...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: 49750
Posted: 2025-10-09 08:42:20
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The Capabilities, Analysis and Development (CAD) division of Applied Research Associates, Inc.
(ARA) has an outstanding opportunity for an exceptional Nuclear Systems Analyst with experience identifying, characterizing, and assessing state nuclear weapons programs and the threats, developments, and trends associated with those programs.
This position provides Defense, Service, and Interagency audiences with timely and accurate assessments of adversary nuclear programs, strategic threats, and weapons-related S&T developments.
This position routinely contributes to Defense Intelligence Enterprise deliverables, including but not limited to foundational assessments, warning reports, technical briefings, and other analytic documents.
The position collaborates with the Intelligence Community, Defense Department, national labs, and academia to address nuclear-related threat issues.
The Nuclear Systems Analyst provides guidance to less experienced staff, reviews the work of others, authoritatively contributes to multi-functional analytic teams, and maintains currency in understanding relevant nuclear-related technologies, trends, and threats.
The position is expected to understand and articulate official government analytic positions during customer engagements and represent Defense Intelligence Enterprise analytic units as directed.
Required Qualifications:
* Master’s degree and 6+ years of experience conducting intelligence cycle functions and/or creating intelligence reports, assessments, or deliverables; or 17 years of same experience without a Master’s degree.
* Experience with intelligence analysis, including employing multi-INT databases to develop analytic assessments and briefings.
* Demonstrated knowledge of state nuclear programs, strategic weapons developments, and WMD-related proliferation and procurement.
* Practical understanding of the technical requirements necessary to develop and deliver nuclear weapons.
* Understanding of global technology control, arms-control, and nonproliferation efforts associated with nuclear and strategic weapons (CTBT, FMCT, New START).
* Familiarity assessing consequence management variables associated with nuclear weapons use and radiologically contaminated environments.
* Working familiarity with established Intelligence Community directives, standards, and tradecraft documents.
* Demonstrated ability to work effectively within or lead a team of peers, as well as excellent interpersonal and communications skills.
* Ability to communicate complex analyses at a level comprehensible to diverse military audiences and senior-level government representatives.
* Ability to clearly express in writing, technical analysis results and program characterizations.
* Word, Excel and PowerPoint proficiency.
* Active TS/SCI clearance.
Desired Qualifications:
* Advanced degree and/or technical training related to nuclear engineering, physics...
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Type: Permanent Location: Reston, US-VA
Salary / Rate: Not Specified
Posted: 2025-10-09 08:29:18
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The Missons, Concepts and Capabilities (MCC) division of Applied Research Associates, Inc.
(ARA) is looking for a Chemical Analyst.
This position provides operational, research and development, and training support along with subject matter expert advice and decision support to the Defense Threat Reduction Agency (DTRA) as part of its 24/7/365 Technical Reachback Support program.
The ideal candidate will apply subject matter expertise and problem-solving skills to develop, integrate, test, verify, validate, and apply Chemical, Biological, Radiological, Nuclear, and (high yield) Explosives (CBRNE) software/scenarios based on experiments and predicted phenomena using theoretical and computational methods.
The candidate will work closely with other members of the multi-disciplinary Reachback team.
Required tasks include performing complex engineering, scientific modeling and analyses, providing scientific reports, and technical assessments to military decision makers.
Each Technical Reachback team member is cross trained on all models and undergoes a rigorous certification process on the use of our CBRNE models before becoming an active member of the Reachback team.
The successful candidate will be team-oriented and possess strong multi-tasking abilities.
In addition, this position requires the use of models in all areas of CBRNE.
Tasks also include the presentation of modeling results and decision support aids to both internal and external customers in the form of written reports and oral presentations.
* Reviewing current research in various and potentially diverse subject areas for familiarity and relevance
* Providing general knowledge and chemical-related subject matter expertise to government agencies and first responders
* Assisting in the development of program plans, timelines, and technical documents
* Attending technical and programmatic meetings in which you coordinate responses from scientific community members and review the assembled materials for technical accuracy, consistency, and completeness
* Willingness to be cross-trained to provide modeling and information across the CBRNE spectrum
Required Qualifications:
* MS in Chemistry or a related field with a minimum of 3 years of experience
* Able and willing to work rotating shifts (every three months) in support of 24/7/365 operations
* Must be a US Citizen
* Hands-on experience using computer-based software to develop structurally sound and comprehensive models that account for all structural components
* Active US DoD Secret or Top Secret clearance
* Strong communication skills, both orally and verbally, technical presentation, teamwork mentality, graphic visualization, and Microsoft Office proficiency skills
Desired Qualifications:
* Experience working with organizations within DTRA or the DoD as well as other government agencies
* Experience in Combating Weapons of Mass Destruction (WMD) threats or CBRN threa...
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Type: Permanent Location: Fort Belvoir, US-VA
Salary / Rate: Not Specified
Posted: 2025-10-09 08:29:17
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Nous sommes la plus grande marque d’hôtels de luxe au monde, et nous en sommes extrêmement fiers.
En tant qu'ambassadeurs d'InterContinental, nous perfectionnons notre expertise depuis des décennies, accueillant nos invités dans un cadre de luxe inégalé et créant des atmosphères chaleureuses pour ceux qui souhaitent explorer différentes cultures.
Chaque établissement cultive un style et une ambiance uniques, offrant à nos invités un séjour extraordinaire, où chaque moment est conçu pour Inspire Incredible des expériences uniques.
Certifié Great Place to Work depuis 2020, InterContinental Genève offre un environnement de travail inclusif et stimulant.
La diversité de notre équipe est essentielle à notre succès, et nous encourageons chacun à développer son potentiel grâce à des opportunités de mobilité interne et des formations continues.
Un petit aperçu de ton quotidien.
Chaque jour est différent, mais tu seras surtout :
* Assurer les tâches d’ouverture du service et préparer l’affectation des chambres.
* Planifier, gérer, encadrer et contrôler le travail des équipes de femmes de chambre et portiers.
* Contrôler la bonne tenue des chambres et suites, locaux et lieux publics.
* Inspecter les offices pour s’assurer de leur propreté, leur bon état et leur approvisionnement.
* Préparer les inventaires pour maintenir un niveau de matériel adéquat.
* Répondre aux plaintes et aux demandes spéciales pour s’assurer de la satisfaction optimale de nos clients.
* Effectuer des briefings, des réunions d’étages et des évaluations.
* S'assurer que tout le personnel est bien formé et qu'il dispose des outils et des équipements nécessaires pour s'acquitter efficacement de ses tâches.
* Remplir tous les documents et effectuer les tâches de clôture du service.
* Promouvoir le travail d'équipe et la qualité de service par la communication quotidienne et la coordination avec les autres services.
* S’acquitter, des tâches liées à l’entretien des chambres (faire les lits, passer l’aspirateur, etc.) pendant la saison basse.
* Se conformer et s’assurer du respect des standards de l’établissement.
Ce dont nous avons besoin de votre part
Issu d’une formation hôtelière, vous justifiez d'une expérience significative (minimum 1 ans) sur un poste équivalent, acquise dans un établissement de même catégorie (4 ou 5 étoiles / +250 chambres).
Vous parlez couramment français et anglais.
La maîtrise d’une autre langue étrangère d’un de nos marchés cibles (Allemagne, Chine, Italie, Moyen Orient, Pays-Bas, Espagne, Russie) est un véritable atout.
La maîtrise du système OPERA est également un plus.
Doté d’un excellent sens relationnel et d’un sens du détail poussé, vous faites preuve d’adaptabilité, de rigueur et de flexibilité.
Vous devrez nous apporter votre passion, votre dynamisme et nous faire part...
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Type: Permanent Location: Genève, CH-GE
Salary / Rate: Not Specified
Posted: 2025-10-09 08:21:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Financial Planning & Analysis
Job Category:
People Leader
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
The North America Global Functions IT team is recruiting for a Lead Finance Analyst, NAM Global Functions IT (MedTech) to support the MedTech IT function team.
This role is located in Titusville, 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. Learn more at https://www.jnj.com/.
The Finance Lead will be pivotal in owning the Financial Planning, Forecasting, and Reporting for IT across both the US and Canada for the sector.
This position provides analytics and insights to Commercial, R&D and Supply Chain IT business partners in collaboration with PMO and Global Functions Finance.
The successful candidate will lead a team of 2.
Key responsibilities will include the following:
* Lead all forecast planning/actual close cycles
* Conduct reviews with business partners
* Provide leadership in driving IT strategies to achieve financial targets
* Provide ad-hoc analytics/support to business partners by applying performance and data driven insights and metrics to identify new opportunities, efficiencies, or solutions to meet business needs.
This includes challenging the status quo, demonstrating business / financial acumen, systems linkages and value stream mapping skills to drive continuous improvement.
* Key finance contact for NA with opportunities for cross-regional collaboration with global partners
* This position will provide leadership, guidance, and oversight to one SFA and one FLDP.
The Finance Lead will focus on strong people leadership through coaching and development of the team by clearly aligning short term and long-term goals and by collecting and providing timely feedback
Qualifications:
* A minimum of a bachelor’s degree is required, preferably with a major in Accounting, Economics or Finance.
* A minimum 4 years of ...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Human Resources
Job Sub Function:
Health Services
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for Occupational Health Nurse
Position Summary
Entry to developing individual contributor, who works under close supervision.
Services are provided under the mentorship or supervision of a Sr.
Occupational Health Nurse or Health Services & Resources Supervisor and general direction of the designated physician (as required by law).
Provides occupational health nursing, medical, and integrated services consistent with the policies, guidelines, objectives, and content of the Johnson & Johnson Occupational Health program.
Adheres to established privacy, safety, and confidentiality regulations.
Principal Responsibilities
Provides nursing services and emergency (first-aid) treatments to employees who become ill or suffer an accident on company premises, arranging for transportation to another care provider, if needed.
Notifies all concerned.
* Participates as an active member of the First Aid/Emergency Response Team.
* Under supervision of a physician, administers medications and performs various minor treatments or therapies for injured or ill employees.
Administers injections for allergies and for overseas travel as directed by the physician.
* Provides various preventive health evaluations and tests in accordance with the company Health Services program protocols.
* Conducts health profiles, health evaluations and other services within the integrated employee Health Services & Resources strategy including but not limited to health promotion education, health screenings, drug screenings.
* Promote well-being resources a...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
People Leader
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The MSL Head, Medical Science Liaison Head in Oncology leads a large and multi-level organization of highly qualified MSLs, and Field Directors to provide fair balanced and objective scientific information and education to health care professionals and to internal partners as required by scientific and business needs.
This position requires the MSL Head to set and implement the vision for a fast growing organization while also effectively collaborating with key internal and external stakeholders.
The MSL Head is responsible for leading an Oncology Medical Science Liaison (MSL) national organization of MSLs and Field Directors, in providing scientific, research, and educational support to health care professionals and internal partners related to the current and future Janssen Oncology products as required by scientific and buisines needs.
The MSL head will also set and implement the vision for the organization and TA field strategy while also collaborating closely across the value stream of internal and external stakeholders.
The primary role of the MSL Head is to set organizational strategy for their disease area and national organization and implement their strategic vision.
They will also provide support, coaching and development to Field Directors utilizing the compency model, routine feedback, and Leadership concept coaching.
The MSL Head will also provide coaching, along with development assessment and guidance for the MSLs within their organization.
* The MSL Head will lead the development and execution of strategies for the engagement of opinion leaders (nation, region...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:34
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Alabama (Any City), Alabama (Any City), Arizona (Any City), Arkansas (Any City), California (Any City), Colorado Springs, Colorado, United States of America, Connecticut (Any City), Danvers, Massachusetts, United States of America, Delaware (Any City), Florida (Any City), Georgia (Any City), Idaho (Any City), Illinois (Any City), Indiana (Any City), Iowa (Any City), Kansas (Any City), Kentucky (Any City), Louisiana (Any City), Maine (Any City), Maryland (Any City), Michigan (Any City), Minnesota (Any City), Mississippi (Any City), Missouri (Any City), Montana (Any City) {+ 23 more}
Job Description:
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for a Manager, Global Clinical Compliance. This is a remote role available in the continental USA.
Purpose: The Manager, Global Clinical Compliance is responsible for ensuring that clinical studies are executed in accordance with applicable international, federal, and local regulations, Good Clinical Practices (GCP), and Abiomed internal Standard Operating Procedures (SOPs).
She/he will serve as a resource for clinical study teams to instill regulation awareness and promote a constant state of inspection readiness, inclusive of identifying potential risks and advising on solutions to ensure high quality clinical evidence is generated in support of clinical study tactical plan objectives.
She/he will conduct routine quality checks of clinical studies to ensure that quality records are accurate, complete, and contemporaneous.
She/he will take an ownership role of the Clinical Quality System, ensuring alignment with regulations, GCP, and corporate quality standards; levera...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:32
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Limerick, Ireland
Job Description:
Role Title: Graduate Quality Engineer
Intake: September 2026
Location: Limerick
About the Johnson & Johnson Graduate Programme:
The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites.
It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business.
The Successful Candidate will have the opportunity to:
* Develop relevant technical skills within their area of expertise.
* Cross functional exposure both on site and within Campus Ireland.
* Regular one to ones and feedback to support your on-going development.
* Personal development and effectiveness training.
* Skills development in influencing & communication.
* Project and Project Management experience.
* Introduction to new and innovative technologies.
* Exposure to Senior Management Team.
* Continuous professional development program with a recognised qualification.
Roles & Responsibilities
The Graduate Quality Engineer position is focused on providing quality engineering support within a high volume, fully automated manufacturing environment.
* Provides product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes
* Utilizes medical device industry and process excellence standards in daily quality operations, including good manufacturing practices (GMP) and international organization for standardization (ISO).
* Addresses and corrects product and process complaints.
* Responsible for supporting the activities of Operations/Engineering/information management in building quality into our products and assuring compliance to the pertinent regulations while at the same time attaining operational effectiveness
* Supports and executes upgrades to Quality System
* Support QA programs in assuring compliance to the pertinent regulation
* Support lead cost and technical improvements under the departments’ continuous improvement program.
* Project Management - provide timely and accurate reporting on project activities.
* Actively particip...
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Type: Permanent Location: Limerick, IE-LK
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:27
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯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.â¯Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Chez Johnson & Johnson, nous pensons que la santé est essentielle.
Notre force en termes d'innovation dans les soins de santé nous permet de construire un monde dans lequel nous contribuons à prévenir, à soigner et à guérir les maladies complexes, où les traitements sont plus intelligents et moins invasifs, et où les solutions sont personnalisées.
Grâce à notre expertise en matière de thérapies innovantes et de technologie médicale, nous avons une position unique pour innover aujourd'hui sur tout le spectre des solutions de santé afin de réaliser les progrès de demain et d'agir en profondeur pour la santé de l'humanité.
Pour en savoir plus, consultez le site https://www.jnj.com
Vision Care est la division des lentilles de contact du Groupe Johnson & Johnson.
ACUVUE® est le n° 1 mondial des lentilles de contact, distribué dans plus de 70 pays dans le monde.
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Vision Care recrute un/e Analyste Business Intelligence en stage pour ses 2 marchés, France et Benelux.
Stage dâune durée de 6 mois - début du stage Janvier 2026
Localisation : Issy-Les-Moulineaux
En tant que membre de l'équipe Business Intelligence & Analytics, vous accompagnerez le groupe dans l'analyse approfondie de nos marchés et dans la gestion de la performance de nos produits grâce à des reportings clairs qui facilitent la prise de décisions et la réalisation d'études de marché.Dans ce cadre, votre rôle sera :
*  Ãlaborer et créer des supports de formation dynamiques pour favoriser lâutilisation efficace de nos outils tels que Sales Force, Tableau et Showpad, dans le but dâaccroître la productivité commerciale.
* Rassembler, nettoyer et organiser des données provenant de différentes sources pour garantir leur précision et leur pertinence.
* Collaborer avec les analystes et les responsables pour réaliser des études de marché, en fournissant des analyses approfondies et des recommandations ciblées.
* Développer des visualisations attrayantes et des rapports complets pour communiquer clairement les informations essentielles et les résultats auprès de lâéquipe et des parties prenantes.
* Travailler en harmonie avec les équipes techniques en Europe pour concevoir et améliorer les flux de donnÃ...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-10-09 08:20:20
