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The salary range listed is the total compensation that includes base salary and potential monthly commission, with further details to be discussed during the interview process.
The Regional Sales Strategist is responsible for developing market-specific growth strategies that drive increased adoption of Sumitomo Rubber North America’s product portfolio within assigned Accounts.
This role also provides coaching and support to SRNA Territory Managers on strategic selling techniques and data-driven analysis.
Using market intelligence, sales data, and in-depth customer insights, the Regional Sales Strategist will identify, evaluate, and present growth opportunities to SRNA leadership and key Account stakeholders.
By leveraging comprehensive knowledge of SRNA’s sales processes, products, pricing, promotions, and market potential, this role will collaborate with internal teams and Accounts to build and execute strategic growth plans.
The strategist will establish clear performance goals, track progress, and communicate results regularly to Account leaders and SRNA Management through both in-person and virtual meetings.
Additional responsibilities include conducting market evaluations for new business prospecting and providing data-driven recommendations to support onboarding of new Accounts.
This position requires 70%+ travel.
ESSENTIAL JOB FUNCTIONS
* Account SKU and Market Management
* SKU Adoption Analysis
* New SKU Communication & Adoption
* Customer Sellout Data Management
* Market Analysis for Existing Customer Expansion
* Market Analysis for Prospecting
* AM (Account Manager) Interaction to Maximize Sales Closures
* Preparation of AMs for Key Sales Opportunities
* Business Intelligence Data Mining and Data Manipulation
* Product Strategy Support
* Channel Strategy Support
* Action Item Tracking and Follow-Up
Minimum of eight to ten (8–10) years of experience in a corporate sales environment, including at least five (5) years in outside sales preferably within the automotive industry and three (3) years in a leadership or management role with accountability for forecasting, budgeting, and achieving sales goals.
Bachelor’s Degree in Marketing, Business Management, or a related field from an accredited institution, or an equivalent combination of education and experience that demonstrates the ability to successfully perform the essential functions of the role.
Proficiency in Microsoft Office applications (Word, Excel, Outlook, PowerPoint) is required.
Must demonstrate strong mathematical competency, including calculations related to margins, markups, and percentages as they apply to pricing and sales.
Strong leadership capabilities, exceptional written and verbal communication skills, and effective interpersonal skills are essential.
This position requires the ability to travel up to 75% via air and automobile.
Must be able to stand, sit, walk, stoop, crouch, and use hands and fingers for extended periods.
Requires the ability to hear and speak clearly.
May involve reaching above shoulder height and below the waist, as well as lifting up to 100 pounds.
Must be able to participate in physically demanding outdoor activities and environments, including off-road desert and mountainous locations.
Work will occur across a variety of environments, including frequent travel by air and car, outdoor motorsport venues, entertainment facilities, restaurants, sporting environments, and standard office settings.
...
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Type: Permanent Location: Charlestown, US-IN
Salary / Rate: 124800
Posted: 2025-12-02 07:37:24
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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!
Deine Position
Als Manufacturing Quality Assurance (MQA) Manager Sterile Filling förderst Du aktiv die Umsetzung unserer Lean-Mindset Kultur unter Berücksichtigung der Pharma Technical Operations (PT) Behaviors und Lean-Methoden und lebst diese vor. Du förderst die Harmonisierung und kontinuierliche Verbesserung einzelner Prozesse und Vorgehensweisen in Abstimmung und Koordination mit den anderen Value Streams am Standort.
Be a coach! Operatives und strategisches GMP-Coaching aller Funktionen innerhalb und bei Bedarf ausserhalb des Bereichs übernimmst Du ebenfalls im Zuge deiner Tätigkeit.
Für Deine Aufgaben bist Du primär in Mannheim vor Ort.
Deine Aufgaben
* Du unterstützt aktiv die Patientenversorgung mit kommerziellen und klinischen Arzneimitteln durch Sicherstellung einer GMP-konformen und termingerechten Freigabe von Arzneimittelchargen.
Die Berücksichtigung der gesetzlichen, regulatorischen und Roche internen Vorgaben sind Dir hierbei besonders wichtig
* Zusammenstellung, Prüfung und Bewertung von Herstelldokumenten aus der eigenen Produktion und von anderen Standorten
* Die Bearbeitung und Qualitätsbewertung komplexer Abweichungen und geplanter Events (Changes, CAPA) übernimmst Du selbständig und leitest und koordinierst bei Bedarf das lokale Triage Team zur Bearbeitung und Root-Cause-Analyse (RCA) von Abweichungen innerhalb des verantworteten Bereichs
* Du übernimmst die Bearbeitung und Koordination von Abweichungen und geplanten Events (Changes, CAPA) in Zusammenarbeit mit anderen Partnern im Netzwerk (Multisite)
* Du vertrittst die Qualitätsaspekte des Value Streams und unterstützt aktiv Audits und Selbstinspektionen und nimmst daran teil.
Zudem übernimmst du die fachliche Vertretung des Standorts in globalen Qualitätsgremien oder bei Behörd...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-12-02 07:30:16
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Laborant:in EFZ Fachrichtung Biologie 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Laborant:in EFZ Fachrichtung Biologie
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Laborant:innen arbeiten in der Forschung, Entwicklung, Produktion, Kontrolle oder in der Diagnostik.
Sie planen und führen Versuche durch, überwachen deren Verlauf und erstellen Auswertungen.
Mit Fachrichtung Biologie untersuchst du Organismen, deren Aufbau und Entwicklung sowie ihre Wechselwirkung mit Wirkstoffen.
Dabei arbeitest du mit Mikroorganismen, Zellen und Pflanzen.
Du hilfst mit, die Art und Funktionsweise lebender Systeme auf verschiedenen Stufen zu ergründen: als ganze Organismen, in Zellkulturen, an isolierten Organen oder anhand isolierter Zellbestandteile und Biomoleküle.
Du arbeitest mit Messgeräten und verschiedenen Apparaturen und führst diverse Berechnungen durch.
Du beurteilst den Versuchsablauf und hältst die Vorschriften zur Arbeitssicherheit, zum Umweltschutz und zur Qualitätssicherung ein.
Was du mitbringen solltest:
- Gute Leistungen in den naturwissenschaftlichen und...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-12-02 07:30:02
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Logistiker:in EFZ 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Logistiker:in EFZ
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Diverse Standorte im Raum Schaffhausen
Hauptsitz: Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Logistiker:innen transportieren, lagern und verteilen Güter fachgerecht.
Bei uns arbeitest du in verschiedenen Lagern in einem Produktionsbetrieb.
Mit der Fachrichtung Lager bis du für die fachgerechte Bewirtschaftung von Waren zuständig.
Du nimmst diese in Empfang und kontrollierst und verbuchst sie anschliessend im Computersystem.
Mit Gabelstaplern oder komplexen Fördersystemen lagerst du die Güter in geeigneter Weise ein.
Wenn eine Bestellung eintrifft, kannst du die entsprechenden Waren für die Auslieferung oder den Versand vorbereiten, verpacken und beschriften.
Du wirst lernen die Lieferpapiere zu erstellen und die Fahrzeuge auf fachgerechte und sichere Art und Weise zu beladen.
Was du mitbringen solltest:
- Praktisches Verständnis
- Handwerkliches Geschick
- Organisationstalent
- Selbstständigkeit
- Zuverlässigkeit und Verantwortungsbewusstsein
- Ausdauer und Konzentrat...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-12-02 07:29:59
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Apprentice, Operations (Generalist)
Job Category:
Career Program
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
Als führendes Unternehmen in der Gesundheitsbranche bieten wir motivierten und talentierten Lernenden die Chance, ihr Potenzial zu entfalten und wertvolle Erfahrungen in einem innovativen und dynamischen Umfeld zu sammeln.
Unser Lernendenprogramm bietet eine vielfältige Palette an Möglichkeiten wie z.
B.
in einem globalen Netzwerk von Expert:innen zu arbeiten oder an innovativen Projekten mitzuwirken.
Wir legen Wert auf Vielfalt, Inklusion und persönliches Wachstum und bieten eine unterstützende und inspirierende Arbeitsumgebung.
Bewirb dich noch heute, um Teil einer dynamischen Unternehmung zu werden.
Standort:
Die Cilag AG in Schaffhausen wurde 1936 gegründet und ist seit 1959 Teil von Johnson & Johnson.
Der Standort fungiert als einer der wichtigsten Produzenten der Schweizer Pharmaindustrie und als bedeutender Arbeitgeber in der Region Schaffhausen.
Das Unternehmen stellt hochwertige pharmazeutische Substanzen und Produkte her, die Patienten auf der ganzen Welt zugutekommen.
Wir suchen DICH – Lehrstelle Chemie- und Pharmatechnologe:login EFZ 2026
Ausbildungsdauer:
3 Jahre
Abschluss:
Eidgenössisches Fähigkeitszeugnis Chemie- und Pharmatechnologe:login EFZ
Vorbildung:
Obligatorische Schule mit Grundanforderungen abgeschlossen
Ausbildungsort:
Cilag AG, Hochstrasse 201, 8200 Schaffhausen
Was du bei uns lernst:
Als Chemie- und Pharmatechnologe:login (CPT) stellst du mit automatisierten Fabrikationsanlagen chemische, biologische und pharmazeutische Produkte her.
Du bist verantwortlich für die Vorbereitung, Durchführung und Kontrolle des Produktionsprozesses.
Für die Produktionsprozesse planst und berechnest du die benötigten Mengen Rohstoffe und stellst diese entsprechend bereit.
Die Vorbereitung der Anlagen, bevor die Produktion gestartet werden kann, gehört ebenfalls zu deinen Aufgaben.
Mit einer Herstellvorschrift führst du die nötigen Arbeitsschritte sicher durch.
In bestimmten Prozessphasen ziehst du Produktmuster und analysierst diese im Labor.
Nach beendeter Produktion reinigst du die verwendeten Anlagenteile und führst anschliessend Funktionskontrollen, sowie kleinere Wartungsarbeiten durch.
Was du mitbringen solltest:
- Interesse an Mathematik, Chemie, Physik
- Handwerkliches Geschick
- T...
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Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-12-02 07:29:57
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Ardurra is seeking a full-time Senior Ecologist to join our team in Orlando, FL.
This role focuses on environmental permitting, regulatory compliance, and database management for transportation-related projects.
The ideal candidate will possess strong ecological assessment skills and a solid understanding of permitting requirements for both state and federal agencies.
Primary Function:
We are seeking a motivated and knowledgeable Sr Ecologist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout our Orlando Projects.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Review roadway plans to determine permitting requirements for minor and major transportation projects, including identification and assessment of wetlands and protected species affected, and assessment of stormwater impacts
* Prepare state and federal permit application packages that describe the site assessments, stormwater data, agency jurisdiction, the measures necessary to satisfy permit requirements, and summaries of meetings with the regulatory agencies
* Conduct wetland inventories and Environmental Assessments, including a focus on protected species
* Assist in preparing and reviewing reports in support of projects, including protected species, natural habitat, environmental impacts, biological evaluations, minor NEPA/NMSA, and related regulatory requirements and compliance guidelines
* Review documents for projects prepared by others, including pre-design environmental documents, permit application packages, exemption verifications, or need for additional wildlife surveys
* Perform QA/QC reviews to ensure completeness, accuracy, and conformity to established industry standards and local, state, or federal criteria
* Provide practical solutions to project challenges by applying accepted procedures and methodologies and collaborating with others
* Support the preparation of draft environmental scope, units, and staff hours for projects based on existing transportation permitting policies and guidelines
* Monitor project budgets and schedules to ensure profitability and timeliness of deliverables
* Mentor junior-level team members while being a positive leader for the team
* Contribute to business development efforts by supporting proposals and identifying new opportunities
Education and Experience Requirements:
* Bachelor’s degree in physical or natural sciences or a related field such as Environmental Science, Biology, or Ecology
* 10+ years of prior practical experience (or 7+ with a relevant Master’s degree)
* Familiarity or established relationships with FDOT, regulatory agencies, and other municipal clients is strongly preferred
* In-depth knowledge of FDOT and regulatory agency criteria, standards, and plans preparation requirements
*...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-12-02 07:25:34
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ERM is hiring Environmental Inspectors to oversee environmental compliance during the construction phase of our client’s transmission and distribution project in northern Nevada and southern Idaho.
This is a full-time (60-72 hours per week) limited-term role for a duration of 18 months, with the possibility of extension beginning in March 2026.
RESPONSIBILITIES:
* Preparing and conducting environmental training for construction personnel.
* Conducting field inspections, conducting environmental inspection of construction activities, and field survey work as directed.
* verifying that the limits of authorized construction work areas and locations of access roads are properly marked before clearing;
* Interacting with and serving as a point of contact with agency officials, regulatory agency staff, landowners, contractors, clients and other project members and conducting required agency notifications.
* Reviewing and implementing project documents and providing direction, support and critical judgment on environmental compliance issues.
* Providing technical leadership, support and direction to field staff. This includes the coordination of daily Environmental Inspector and Resource Monitor schedules and conducting morning construction meetings.
* Critically assessing environmental conditions in the field to evaluate potential environmental impacts from construction.
* Evaluating potential issues and concerns ahead of construction activities.
* Overseeing the proper implementation of mitigation measures.
* Conducting environmental sampling (hydrostatic test water, soil, etc.).
* Overseeing and verifying flagging and signage of waterbody and wetland boundaries, cultural and biological resources exclusion zones, refueling zones, or areas with special requirements within the construction work area.
* Inspecting and documenting compliance with a project's environmental requirements by preparing daily written inspection reports that provide up-to-date and consistent written and photo documentation of activities observed in the field.
* identifying, documenting, and overseeing corrective actions as needed to bring an activity back into compliance.
* identifying erosion/sediment control and soil stabilization needs.
* Participating in various construction meetings.
* Preparing documentation to support requests for variances from environmental permits.
* Evaluating restoration activities and conducting compaction testing as required.
* Compliance with ERM’s rigorous safety program.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
The role of an Environmental Inspector requires meticulous oversight by highly skilled individuals stationed in the field throughout construction to ensure compliance with federal, state and local environmental regulations.
Qualifications of individuals to be considered will include:
* BS or BA degree...
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Type: Permanent Location: Elko, US-NV
Salary / Rate: Not Specified
Posted: 2025-12-02 07:25:31
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ERM is hiring Field Biologists to conduct nesting bird surveys and surveys for special status species (plants and wildlife) for a large transmission and distribution program in northern Nevada and southern Idaho.
Successful candidates must be flexible and responsive to a changing work environment where schedules, site locations, and tasks fluctuate according to the needs of the project. This is a full-time (60-72 hours/week), limited-term role with a duration of 18 months and the possibility of extension.
RESPONSIBILITIES:
* Field biologist position to conduct pre-construction nesting bird and other special status species surveys and construction monitoring across the project area.
* Work locations are often remote and require Biologist to work independently.
* Monitoring involves coordination with construction crews and environmental inspectors and providing guidance for maintaining compliance with client requirements.
* 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:
The role of the Field Biologist requires meticulous oversight by highly skilled individuals stationed in the field throughout construction to ensure compliance with federal, state and local environmental regulations.
Qualifications of individuals to be considered will include:
* At least 2 years of Avian Biology and other Special Status Species experience required.
In addition to nesting birds, expertise should include more than one of the following species: pygmy rabbit, Burrowing Owl, Golden Eagle, Ferruginous Hawk,.
* Familiarity with nesting bird survey protocols and bird identification skills required.
* Electric Transmission and BLM experience 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), as well as Field Maps and Survey123 applications.
* 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.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area in remote locations.
Pay Transparency:
For the Field Biologist position, we anticipate the annual base pay of $74,825 – $93,600, $35.97/hr – $45.00/hr USD, lim...
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Type: Permanent Location: Elko, US-NV
Salary / Rate: Not Specified
Posted: 2025-12-02 07:25:29
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ERM is seeking an Environmental, Health and Safety Manager to work onsite at a key client in Kenosha, WI.
The ideal candidate will bring a wealth of technical capability and deep understanding of regulations, as well as business processes to help our client proactively address their EHS risks and challenges. This is a full-time (40 hours per week) limited-term role, with a duration of 12 months, extendable.
Responsibilities:
* Provide on-site health and safety support at client facilities such as training, review of change requests, incident investigations, and hazard reviews.
* Prepare technical reports and other deliverables.
* Achieve client’s expectations for scope, budget, schedule, and quality.
* Assist in the development of solutions to technical and regulatory issues and concerns.
* Design and implement corporate H&S strategies and programs for safety, compliance auditing, safety management systems, process safety and risk management, high-impact training, and general compliance support.
* Conduct training, field coaching, and assessment for safety performance improvement projects.
* Support, as needed, environmental, health and safety (EHS) compliance, environmental management system, sustainability, due diligence transaction, environmental compliance programs, contingency plans, multi-media permits, and reports for air quality, hazardous waste, spill prevention, storm water, and wastewater.
Requirements:
* BS/MS in safety, occupational health, engineering, or related science degree preferred.
* Minimum of 5 years relevant experience in working with significant industrial clients on regulatory compliance and sustainable H&S compliance programs, with emphasis on the manufacturing, pharma, and hi-tech sectors.
* Certification in field; CSP, CIH, PE, or similar registration is desirable but not required.
* Experience with LOTO, machine guarding and design reviews is required.
* Passionate about EHS performance improvement with substantial experience with practical implementation.
* Solid understanding of the relevant local, state, and federal regulations and how they apply to heavy industry and capital projects.
* Strong written and verbal communication skills and the ability to communicate effectively.
* Local candidates 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 b...
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-12-02 07:25:28
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
We are looking for an employee that is having a passion for quality and loves to operate in a very dynamic pharmaceutical production environment.
We are looking for an employee that likes to work with people and connects easily with our different business partners.
Job Description:
At the J&J IM SC Beerse site, different product types are being produced and released such as Steriles, Liquids & Creams and Transdermals.
The Beerse Site Quality Department ensures that all GMP activities of manufacturing, packaging, labelling, testing, release and distribution of Products at/from the Campus Belgium are carried out as required by GMP legislation.
Within this department, the QA Lab team is responsible to ensure compliance during the daily QC testing aspects in the lab.
The QA lab team is also responsible for release of excipients and packaging materials for further processing.
As QA Associate within the QA Lab team, you guarantee product quality by supporting investigations of non-conformances within the QC labs.
You will have quality oversight and support the investigation by connecting with all parties involved and documenting quality related decisions in a well-founded manner.
You ensure that root cause analysis, impact analysis and corrective and preventive actions are thoroughly carried out and documented.
Job Responsibilities:
Together with your team you support the daily quality operations within the quality control area:
• Ensure that deviations, CAPAs, Change Controls and trend reports are timely and properly investigated by providing quality, compliance and technical expertise such that the internal and external customer expectations are.
• Attend tier meetings within the QC Lab and QA Lab team.
• Prepare and attend QIP meetings.
• Perform check rounds in the QC laboratories and periodic witnessing of QC method execution.
• Establish and maintain strong working relationships with Business and Quality partners to ensure alignment of objectives and results and act as Quality Point of Contact.
• Support the quality oversight process of the operational activities by ensuring QA review and approval of GMP documentation.
• Ensure that deviations with potential impact on patient safety and/or product supply are properly escalated.
• Act as s...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:54
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Surgeons (Commission)
Job Category:
Business Enablement/Support
All Job Posting Locations:
Bydgoszcz, Kujawsko-Pomorskie, Poland, Poznan, Wielkopolskie, Poland, Warsaw, Masovian, Poland
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
CLINICAL ACCOUNT SPECIALIST (BIOSENSE WEBSTER)
Location: Poznań or Bydgoszcz
Contract: full-time
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
Purpose:
The Clinical Account Specialist will be responsible for: clinical support and promoting BW products among current and potential customers; developing professional education for end-users; effective and strong collaboration with sales team members; developing the business growth on the territory.
You will be responsible for:
* Provide every day in Hospital /EP Lab/ professional clinical & technical support, troubleshooting, and training to Physicians, Electrophysiology Lab Staff, Technicians, Nurses, and administrators staff regarding all aspects of the company’s systems and catheter equipment
* Understand and know clinical environment, competitor products – continuous development of the knowledge
* Serves as a troubleshooting resource during cases.
* Tailors’ product conversations to the audience to ensure proper understanding and optimal utilization.
* Demonstrates products features to meet customers’ unmet needs
* Become fluent in main types of arrhythmias
Qualifications / Requirements:
* University degree level or equivalent exper...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:43
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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:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
* Business Improvements ä¸å¡æ¹è¿
* Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
*       æ¯æè´¨éæ¹è¿æ´»å¨ï¼å¯¹äº§å/è¿ç¨è¿è¡æç»æ¹è¿åææ¬æ¹åã
* Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
*       è¯ä¼°ååæè´¨éå·¥å
·å项ç®çæææ§ï¼æ¯å¦PDCAï¼å
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* Conduct benchmarking to develop more effective methods for improving quality.
*       éè¿æ æ管çå¼åæ´ææçè´¨é管çæ¹æ³æåè´¨éã
* Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management.
*       å¼ååéçè´¨é管çæ¹æ³åºç¨äºè´¨éå·¥ç¨åè´¨éåè§çåå±ï¼è¿ç¨å¨æ°äº§å导å
¥å产åçå½å¨æ管çã
* Compliance/Regulatory åè§ç®¡ç
* Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc.
*       è¯ä¼°ååæç°æ产ååå¶ç¨æ¯å¦åè§ï¼æ¯å¦QSRsï¼ISO13485çæ³è§è¦æ±
* Champions compliance to applicable Global Regulations and standards (e.g.
QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
*       æ¯æå·¥åçå
å¤é¨å®¡æ ¸ï¼éµå®éç¨çæ³è§åæ å(ä¾å¦QSRs, ISO, ENåMDD)è¦æ±ã
* Conduct periodic line audits to assess for production controls such as lot segregation. Review results of area audits to ensure that corrective and preventive actions are adequate.
*       æ§è¡å¨æå®¡æ ¸è¯ä¼°ç产ç°åºæ¯å¦åè§ã审é
åºåå®¡æ ¸çç»æç¡®ä¿çº æ£åé¢é²æªæ½ææã
* New Product/Process Introduction æ°äº§å/å¶ç¨å¯¼å
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* Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.
* Â Â Â...
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:37
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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:
Cambridge, Massachusetts, 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 is currently seeking a Principal Scientist, Protein Design, to join our In Silico Protein and Antibody Design team within the Therapeutics Discovery organization, with a preference for this individual to be located at one of our sites in Spring House, PA, or Cambridge, MA.
Remote work options within the US may be considered on a case-by-case basis and if approved by the company.
This role presents an exciting opportunity to spearhead our molecular design and simulation initiatives, supporting and accelerating our drug discovery and development pipeline of protein-based therapeutics while collaborating with a passionate team of scientists and engineers.
Your work will be pivotal in building, evaluating, refining, and applying sophisticated computational approaches and infrastructures.
Your efforts will drive the discovery of complex molecules and expedite the development of protein therapeutics across various modalities and indications.
Key Responsibilities:
You will work closely with colleagues across the organization to design, develop and deliver on differentiated, best in class therapeutic molecules for a range of clinical indications spanning all therapeutic areas.
Qualified candidates will have a strong background in computational biology and a proven track record of seeing designs through experimental testing.
* Work directly with wet-lab scientists and therapeutic areas to design and optimize protein molecules for specific functions and properties, with a focus on antibody therapeutics.
* Collaborate with team members across Therapeutics Discovery on the planning, prioritization, and timely delivery of designs to support multiple concurrent programs
* Serve as an In Silico D...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:21
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Remote (US), Titusville, New Jersey, 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), a Johnson & Johnson company, is recruiting for a Postdoctoral Researcher which can be located remotely in the US.
The Data Science Analytics & Insights team within JJIM R&D develops innovative solutions using a variety of data sources across multiple different disease areas.
We are looking for an outstanding postdoc with a focus on Computer Vision (AI/ML Radiology).
Key Responsibilities:
* Conceive, develop, and implement analytics and AI/Machine learning radiology solutions to high-priority scientific problems
* Participate in cross-functional collaborations with external companies and internal scientific, clinical, and data science teams
* Shape internal/external collaborations and define the scope of research questions
* Extract insight from complex, unstructured radiology image or other imaging modalities data to improve drug discovery and healthcare (e.g., disease identification, patient stratification, disease insights)
* Clearly articulate highly technical methods and results to diverse audiences and partners to drive decision-making
Required Qualifications
* Ph.D.
degree in a quantitative discipline (e.g., artificial intelligence, computer science, applied mathematics, electrical engineering, or similar), or closely related field, completed within the past 3 years, or to be completed within the next 6 months.
* Demonstrated experience driving research in and applying Computer Vision techniques, such as Foundation models, Transformers, CNNs, Diffusion models, RNNs, GANs, and radiomics.
* Extensive experience with traditional Computer Vision applications, such as OpenCV, object detection, edge detection, image segmentation
* Extensive hands-on experience wi...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:07
-
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:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Professional
All Job Posting Locations:
Latina, Italy
Job Description:
MSAT Assistant Scientist (TD)
Johnson & Johnson is an American multinational company founded in 1886, a world leader in the development of products and devices for surgical therapies and pharmaceutical companies, as well as in the marketing of consumer products for personal hygiene, and is organized into three business segments: Pharmaceutical, Medical, Consumer.
Every day more than 120,000 employees work in 250 companies of the Group, located in 60 countries.
For the Italian production plant of Janssen (Borgo San Michele-Latina) we are looking for an ASSISTANT SCIENTIST to be hired with a TEMPORARY CONTRACT in the MSAT DEPARTMENT.
The person will be part of the team who manage MSAT LCM projects and will report to the MSAT Senior Manager (LCM) .
Main responsibility
The Assistant Scientist is in charge of:
- As Project Leader ensure planning and coordination of the activities in collaboration with the various departments involved in the implementation of the projects.
- Proactively identifying risks to define mitigation strategies.
- Assess the business impact, quality, compliance and safety involving stakeholders from other departments.
- Ensure compliance with the time of introduction, balancing the base business production needs.
- Ensure timely communication to MSAT Sr Manager and Global Functions to align with the production plans themselves.
- Ensure the timely availability of quality documentation for the project execution.
- Performs and/or support investigations for non-conformances in case of occurrence during project activities.
- Process Analytical Technologies, Multivariate Analysis & chemometrics application
Requirements
* Master’s degree in Engineering, Farmacy, CTF or Chemistry
* A minimum of 6 months experience in the pharmaceutical industry (Oral Solid production is preferred)
* Academic knowledge of lines, processes, materials and equipment for pharmaceutical process (oral solid pharma production competence is preferred).
* Fluent in English (B2 level and above)
* Good knowledge of quality, compliance and GMP related to manufacturing and packaging of pharmaceutical products.
* Basic experience in Project Management with ability to work in a multidepartment and dynamic environment an...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-12-01 07:16:06
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ERM is hiring a motivated hands-on Senior Environmental, Health and Safety (EHS) Consultant to join our growing Performance & Assurance technical team in Sunnyvale, California. This position is expected to involve working a minimum of 3 days on-site. This is a fixed-term, full-time role (40 hours a week) for a duration of 4 months, renewable.
The ideal candidate will have experience developing and supporting implementation of Cal/OSHA requirements, Standard Operating Procedures, Job Hazard Analysis/ Risk Assessments, Emergency Response Plans, Behavioral Safety Programs and Contractor Safety Management. Candidates should also have familiarity with research laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Oversee and direct team members to effectively manage tasks for on-time delivery and quality of their deliverables.
* Perform compliance audits to assess client compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as R&D laboratory safety, chemical safety, machine guarding, laser safety, robotics safety, hazardous materials use/storage/waste, EHS auditing.
* Develop and implement EHS compliance procedures, plans, permits, and reports.
* Manage tasks within assigned scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 7 years of applicable experience providing EHS support with an emphasis on health and safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to succeed in a fast-paced consulting environment, handling multiple assignments, meeting strict deadlines, and being able to re-prioritize tasks as-needed.
* Valid driver’s license and good driving record.
Pay Transparency:
For the Environmental, Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000– $97,400, $36.54/hr - $46.82/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on ...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2025-12-01 07:15:23
-
i2, a Harris Computer company, are seeking a Software Development Team Lead on a full-time, permanent, remote-working basis, in the UK.
We are seeking a skilled lead engineer with expertise in JavaScript, TypeScript & Node backend systems to drive the development and enhancement of our products and services.
In this role, you will also lead and manage a small team of 3–4 engineers, providing mentorship, guidance, and support to help them excel.
The candidate will play a key role in designing, developing, and maintaining a cloud-based service - and its surrounding ecosystem - that integrates data from various Open Source Intelligence (OSINT), digital forensics, commercial threat intelligence, and other critical data providers, enabling seamless access for i2 users.
The ideal candidate should possess a passion for creating efficient, scalable solutions, demonstrate expertise in building cloud-based services, and thrive in a collaborative, fast-paced environment.
This permanent position will be performed on a remote basis with a requirement to visit the i2 Office in Cambridge, UK as and when there is a business need to do so (circa 2 days per month).
What you will do
In performing this position, your core duties and responsibilities will include (but will not be limited to):
* Leading and managing a small team, encompassing the development of team members' skills and expertise through coaching, mentoring, and training, as well as performance management, succession planning, talent development, and creating a positive and inclusive team culture.
* In conjunction with the project manager oversee the planning, execution, and delivery of software projects, ensuring they are completed on time and within budget.
* Working closely with cross-functional teams, including UI/UX designers, architects, and product managers, to ship new services and full-stack features
* Being accountable for the technical feasibility of designs and optimizing solutions for maximum speed and scalability.
* Ensuring data security and platform compliance with relevant regulations and industry standards.
* Establishing robust monitoring, logging, and tracing systems to proactively detect issues and optimize performance APIs and the cloud services.
* Conducting thorough testing (automated and manual) to identify, fix bugs, and performance issues.
* Collaborating with Support engineers to troubleshoot and resolve complex customer issues, providing technical expertise and guidance to ensure timely and effective solutions.
* Staying up to date with the latest industry trends and technologies to ensure our applications are built using the best practices.
You will have
* Bachelor's degree with a minimum of 2:1 Computer Science, Information Technology, or a related field.
* Experience running small to mid-sized teams, including line management
* Demonstrable succ...
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Type: Permanent Location: London, GB-LND
Salary / Rate: Not Specified
Posted: 2025-11-29 07:27:55
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper & world-shaper.
Na Alcoa, você é uma parte essencial do nosso propósito: transformar o potencial bruto em progresso verdadeiro.
Esta é uma oportunidade para você trazer sua vasta experiência para a equipe e ajudar a moldar o futuro da sustentabilidade com inovações que mudam o mundo e tecnologias de baixo carbono.
Você tem o poder de moldar as coisas para torná-las melhores.
Sobre a função:
Alcoa está buscando profissional de Meio Ambiente para integrar nosso time na unidade de Juruti–PA.
Como Analista de Meio Ambiente Sênior, você terá papel estratégico na condução de processos de licenciamento de alta complexidade, garantindo conformidade legal e manutenção das licenças ambientais.
Você também será responsável pelo suporte à Gerência de Licenciamento Ambiental e por apoiar o time de Meio Ambiente.
As principais responsabilidades da função incluem:
* Conduzir e analisar processos de licenciamento ambiental complexos, assegurando a obtenção e manutenção das licenças vigentes;
* Garantir o cumprimento das condicionantes ambientais e requisitos legais aplicáveis às operações;
* Elaborar e revisar relatórios ambientais, assegurando qualidade e conformidade técnica;
* Apoiar tecnicamente vistorias realizadas por órgãos licenciadores e atuar em interface com órgãos ambientais nas esferas municipal, estadual e federal;
* Assessorar áreas internas sobre solicitações de novas licenças e em atendimento às condicionantes, promovendo governança e alinhamento;
* Monitorar indicadores (KPIs) da área e apoiar auditorias e comitês relacionados à temática ambiental.
O que você pode oferecer para a função:
* Formação Superior completo em cursos relacionados à área Ambiental, tais como: Geologia, Biologia, Ciências Ambientais, Gestão Ambiental, Engenharia Geológica, Engenharia Ambiental, Engenharia Florestal e afins;
* Sólida experiência em licenciamento ambiental, preferencialmente no Estado do Pará;
* Experiência em licenciamento ambiental em Mineração será considerado um diferencial;
* Conhecimento consolidado sobre Legislação Ambiental;
* Disponibilidade para residir em Belém-PA;
* Regime de Trabalho: Home Office.
O que está sendo oferecido:
* Nossa Essência e Cultura: somos movidos por valores sólidos - agimos com integridade, operamos com excelência, cuidamos das pessoas e lideramos com coragem;
* Segurança em Primeiro Lugar: a segurança não é apenas prioridade - é parte do nosso DNA.
Cada atividade começa e termina com o compromisso de proteger o que importa;
* Crescimento Profissional: oferecemos espaço para que você possa se desenvolver, explorar novas possibilidades e transforma...
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Type: Permanent Location: JURUTI, BR-PA
Salary / Rate: Not Specified
Posted: 2025-11-29 07:24:36
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Get to know us: NOVO Health Services offers linen management solutions to the healthcare industry.
NOVO Health keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen utilization by department to eliminate excess internal costs.
NOVO's wide range of service programs offer a variety of options to provide a seamless, single source distribution system.
NOVO's regional healthcare linen facilities are HLAC accredited and operate with state-of-the-art processing equipment and processes.
We are currently looking for a Soil Sorter, in our St.
Louis Healthcare Laundry facility. We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills. If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
MAJOR PURPOSE OF THIS JOB: Primary responsibility is for performing tasks in any of the production function areas in accordance with Novo Health Services Standard Operating Procedures.
Tasks include but are not limited to soiled linen separation, hand folding, ironing, operating washing and drying equipment and load building.
May perform some or all of the following duties depending on training and experience.
POSITION SUMMARY:
The Soil Room is responsible for removing soil from bags, sort and prepare for washing.
ESSENTIAL FUNCTIONS:
* Able to understand and follow Standard Operating Procedures (SOP’s).
* Open laundry carts and empty hamper bags onto sorting table.
* Sort linen by fabric type.
* Accurately weigh sorted loads and send linen to washers via negative air system as well as operate laundry equipment in either automatic or manual mode.
* Identify instruments, sharp items, hospital-owned linen and other foreign objects and place them in appropriate receptacles.
* Place empty laundry carts in cart wash and operate washing machinery.
* Deposit all instruments and other washable, returnable objects in wash rack and process through dishwasher or commercial washer, as well as wash all stainless basins.
* Completely clean and disinfect soil sort area at end of shift.
* Mentor / train fellow associates.
* Other duties as assigned.
What we can offer you as a full-time associate:
Competitive pay
Paid Holidays
Paid Time Off Program (PTO)
401(k) w/Employer Match
Flexible Spending Account (FSA)
Health Savings Account (HSA)
Medical, Dental, and Vision Programs
Basic Life/AD&D Insurance
Long-Term Disability (LTD)
Why work for Novo Health Services?
NOVO Health Services strives to be the employer of choice in the hospital sterile and hygienically clean linen industry.
To do that, we provide a safe, positive work environment where our associates experience tremendous growth and related opportunities for advancement.
Complete an on-line application at www.novoheal...
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Type: Permanent Location: St Louis, US-MO
Salary / Rate: Not Specified
Posted: 2025-11-29 07:17:47
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Zug, Switzerland
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.
Join us to advance the future of human health and take the first steps toward building a career with a purpose.
Position Overview - Tasks & Responsibilities:
As our Intern in Health Economics and Market Access (HEMA), you will play a key role in supporting our efforts to ensure access to our MedTech portfolio for patients who need it most.
Fully embedded in the Swiss MedTech team, you will contribute to shaping our health economic and reimbursement activities.
Your main tasks will be:
* Building of a database and executing reimbursement simulations across inpatient and outpatient tariff systems
* Analysis and visualization of medical coding and reimbursement changes relevant to JnJ’s MedTech portfolio
* Serving as the local point of contact for regional HEMA teams to ensure alignment with local business needs
* Collaborating with cross-functional teams to identify evidence gaps and supporting the development of new health economic tools and marketing materials
* Adaptation and communication of product value propositions to support our local sales force
Qualifications - Education and Experience:
* A completed bachelor's or ongoing master's degree in life sciences (biomedical sciences, pharmaceutical sciences, medicine) or a mathematical‑technical / computer‑science background with an interest in health economics
* Knowledge of the Swiss healthcare system
Qualifications - Skills:
* A high level of enthusiasm and a keen interest in the MedTech industry
* Excellent German, French or Italian, as well as very good English skills; other languages are a plus
* Excellent command of Microsoft Excel and common visualization tools (eg Power BI)
* Applied programming and data an...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-11-29 07:13:51
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Systems
Job Category:
Professional
All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom
Job Description:
About Orthopaedics
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 Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes.
The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.
Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.
We are searching for the best talent for the Quality Systems Analyst position to be in Leeds, UK.
Purpose:
This role is responsible for ensuring compliance with document control procedures and records management processes for the site.
This role must ensure that relevant documentation in the form of procedures and specifications are followed to guarantee compliance with Global Medical Device Standards and Regulations.
As a Quality Systems Analyst, you will:
* Perform Batch record review, correction, and associated document control activities, for Manufacturing and Customs products.
* Release of all Leeds production lots.
*...
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Type: Permanent Location: Leeds, GB-LDS
Salary / Rate: Not Specified
Posted: 2025-11-29 07:13:35
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Latina, Italy
Job Description:
A proposito di Innovative Medicine
La nostra esperienza in Innovative Medicine è ispirata dai pazienti, la cui conoscenza alimenta i nostri progressi scientifici.
I visionari come te lavorano in team che salvano vite sviluppando le cure del domani.
Unisciti a noi nello sviluppo di trattamenti, nella ricerca di cure e nel pionieristico percorso dal laboratorio alla vita, sostenendo i pazienti in ogni fase del percorso.
Per ulteriori informazioni, visitare il sito Web https://www.jnj.com/innovative-medicine
Stiamo cercando il miglior talento ne ruolo di Quality Control Technician basato a Latina.
Scopo:
Per il sito produttivo di Borgo San Michele (Latina) ricerchiamo candidati da inserire a TEMPO DETERMINATO di 12 MESI presso DIPARTIMENTO QUALITY CONTROL che abbiano la responsabilità di assicurare la conformità del prodotto alle norme e alle specifiche nazionali ed internazionali che regolano il settore farmaceutico sia dal punto di vista del controllo sul prodotto stesso sia dal punto di vista della documentazione ad esso legata.
La persona ricercata sarà responsabile delle seguenti attività:
* Eseguire, in accordo al proprio pacchetto training, alle procedure standardizzate ed alle direttive ricevute, tutte le operazioni necessarie per l’esecuzione di analisi chimiche, chimico-fisiche e microbiologiche utilizzando apparecchiature e strumentazioni di laboratorio.
* Assicurare l’esecuzione di test analitici definiti dai programmi su materie prime, semilavorati, prodotti finiti, stabilità di monitoraggio, sperimentali, controlli ambientali, cleaning validation, acque di stabilimento, nei tempi richiesti e secondo elevati standard di affidabilità, valutando la conformità e la validità dei risultati.
* Utilizzare in modo autonomo, secondo i programmi standardizzati, attrezzature ed apparecchi complessi; utilizzare unità di elaborazione dati.
* Eseguire correttamente i test di laboratorio attraverso lo studio dei principi elementari di teoria applicata ed alle buone norme di laboratorio (GLP), lo sviluppo dei calcoli numerici necessari nel corso del trattamento dei dati, proponendo idee e suggerimenti frutto delle proprie osservazioni e conclusioni.
* Assicurare la registrazione di tutti i dati relativi a metodologi...
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Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-11-29 07:13:31
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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:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Titusville, New Jersey, United States of America, Zug, Switzerland
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Technical Product Owner ERP Plan & Source, located in EMEA (preferred location Beerse BE or Switzerland CH).
This position has the potential to be located at another J&J facility within EMEA or in the US for the right talent.
At the 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.
Learn more at www.janssen.com and follow us @JanssenGlobal.
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.
As part of the Pharm Transcend Program, Technical Product Owner ERP Plan & Source, will be an active member of the Pharm Supply Chain JJT team, driving global standardization within Pharma of ERP technology solutions in the scope of Direct/Indirect Procurement, Supplier Management, MRP/Inventory Planning, Purchasing Master data Subcontracting, Intra & Intercompany stock transfer and OMP (Planning System) integration.
The position leads design, validation and delivery of SAP S/4 capabilities and data, aligned with business process needs.
The position governs the scope of the SAP S/4 template and drives template innovation and evolution through the deployments.
The Technical Product Owner ERP Plan & Source, role will take ownership of one or more of following scope areas:
* Direct/Indirect Procurement
* Supplier Management
* MRP/Inventory Planning
* OMP (Planning System) integration
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-11-29 07:13:08
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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:
MedTech Sales
Job Sub Function:
Capital Sales -- MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Chengdu, Sichuan, China
Job Description:
Supervises individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Leads processes and assignments for the Clinical Sales - Hospital/Hospital Systems team and supports organizational objectives and business goals.
Defines project terms to meet objectives and goals of the Clinical Sales - Hospital/Hospital Systems area.
Directs work flow for strategic plans and serves as a primary point of contact for the team.
Supervises individual contributors and/or Supervisors, and is accountable for conducting effective performance management.
Coordinates processes and assignments for supervisors and individual contributors to achieve sales goals.
Communicates information throughout the clinical sales area to ensure employees stay well-informed on product knowledge, launches, policies, and guidelines.
Supervises customer acquisition and retention process from identifying potential customers to maintaining positive relationships with existing customers.
Advises team on policies and procedures to ensure compliance and achievement of the organization's sales objectives for their designated area.
Responsible for managing operational aspects of their team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team goals within expected standards.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
Job is eligible for sales incentive / sales commissions.
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Type: Permanent Location: Chengdu, CN-51
Salary / Rate: Not Specified
Posted: 2025-11-29 07:13:04
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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:
Pharmaceutical Product R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Join us in Pharmaceutical Product Development and Supply (PPDS) as a Lab Systems & Data Lead within our Synthetics Development organization and play a pivotal role in reshaping how we develop small molecule medicine & therapies through innovative digital solutions for our scientists and engineers.
The CPRD organization focuses on the development of synthetic methodologies and processes for small molecules, oligonucleotides, peptides, antibody-drug conjugates and other emerging modalities.
CPRD aims to provide world-class production processes of active pharmaceutical ingredients (APIs) by enhancing efficiency, safety, and cost-effectiveness.
Its key objectives include refining synthetic routes, scaling up processes from the laboratory to commercial levels, ensuring regulatory compliance and minimizing environmental impact.
Your role will be vital in unlocking the power of data and enhancing our scientific lab systems.
As a key player in our digital transformation, you will drive the integration of data visualization, analytics, and AI/ML workflows to strengthen our data-driven decision-making culture.
You will also translate business opportunities into strategic system designs and oversee day-to-day system operations, focusing on adoption and the improvement of current workflows.
As our lab systems & data lead, you are the local operational lab system owner, and you will shape the lab systems strategy in line with our synthetics digital transformation strategy.
You will initiate and coordinate actions to build an integrated scientific data fabric, translating it into impactful end-user applications for our scientists and engineers to drive data-centric decision-making across different functional lab teams.
You will act as a digital change agent in our organization by ensuring that new users are effectively onboarded and trained in our digital tools.
You will drive change and empower others through knowledge sharing.
We invite you to be a part of shaping and redefining the future of Synthetic Molecule Research & Development and by joining our new synthetic extended digital leadership team you will be surrounded by passionate scientists & digital leaders and your contributions can truly make a diff...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-11-29 07:12:56
