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ERM is looking for a hands-on Consulting Associate, Environmental Engineering, Geology, or Science to join our growing team.
Working under the direction of project managers and partners, the successful candidate will work on a wide variety of site investigation, remediation, compliance, and hazardous waste management projects throughout office service area; however, opportunities for travel throughout the United States and globally may also occur.
This is a great opportunity to work with ERM's technical experts to implement the latest investigation and remediation technologies as well as more sustainable approaches, while building the required experience to obtain your professional registration.
RESPONSIBILITIES:
* Conduct field work, including soil, sediment, groundwater, surface water, soil vapor, and indoor air sampling, aquifer testing, drilling oversight and soil logging, soil boring and monitoring well installation, well development, purging and sampling, remedial and wastewater treatment pilot tests, and remedial system operation and maintenance.
* Assist in groundwater and wastewater system performance monitoring.
* Perform Phase I and II environmental assessments to support property transfer transactions.
* Compile and evaluate data and assist in report preparation.
* Prepare environmental compliance work plans, permits, and reports for air quality, hazardous waste, spill prevention, storm water, and wastewater.
* Assist in ensuring compliance with all federal, state and local regulations.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Bachelors in geology, hydrogeology, engineering, environmental science or related environmental discipline; Masters a plus.
Minimum 3.0 GPA.
Or equivalent experience.
* Recent graduate to 2 years of experience.
* Willingness/interest in field assignments; ability to perform field work standing or walking for full field days.
* Strong commitment to safety, including following established Health and Safety protocols.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to work independently and as part of a team.
* Detail-oriented with solutions and results-oriented aptitude and hands-on trouble-shooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
* Ability to lift at least 40 pounds
* 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.
* 40-hour OSHA HAZWOPER certification a ...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:20:42
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Associate, Immunochemistry
The Quality Assistant performs bio-analytical testing (primarily ELISA) on various sample types (raw materials, in-process, release, stability) following regulatory guidelines (9CFR, EU, VICH) and company SOPs.
This role involves initiating, executing, and completing assays while ensuring timely communication with supervisors regarding testing progress, compliance, or scheduling challenges.
Additionally, the Quality Assistant maintains a safe work environment and adheres to GMP documentation practices, with further duties assigned based on experience level.
Your Responsibilities:
* Performs ELISA and PCR testing on in-process, release, and stability samples.
* Prepares reagents and maintains calibrated equipment essential for testing.
* Analyzes test results and reports data using designated software systems.
* Manages inventory, orders necessary kits/supplies, and monitors critical reagent consumption.
* Reviews, updates standard methods, and collaborates with relevant personnel (QC Media Kitchen, Senior Scientists, Supervisors, Managers, Directors) for support and problem-solving.
What You Need to Succeed (minimum qualifications):
* Bachelor’s degree in scientific discipline (e.g., Biology, Biochemistry, Microbiology, etc.) (preferred), Associate degree with laboratory experience, or equivalent laboratory experience in lieu of degree
* Strong understanding of scientific principles, basic lab techniques and immunochemistry processes.
* Ability to performs and document work following established methods, SOP's, GLP/GCP and/or cGMP.
What Will Give You the Competitive Edge (preferred qualifications):
* Problem solving within the scope of responsibilities with some guidance from Supervisor.
* Strong ability to document lab results / data in a lab notebook following applicable regulations.
Additional Information:
* Laboratory work: 80% Lab work, Documentation 20%
* Location: Fort Dodge, Iowa
Don’t meet every single requirement? Studies ...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:25:18
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Director – Internal Manufacturing Procurement
As Global Director Internal Manufacturing Procurement, you will lead a team responsible for strategic sourcing and procurement activities across Elanco’s global manufacturing operations, focusing on Raw Materials, Packaging, and Consumables categories.
In this pivotal role, you’ll report to the Senior Director of Internal Manufacturing, Logistics, and R&D, collaborating closely with stakeholders to optimize costs, enhance quality, and manage supplier relationships effectively.
Your Responsibilities:
* Lead and manage a global team of 4-8 procurement professionals specializing in strategic sourcing for Raw Materials, Packaging, and Consumables categories, ensuring alignment with Elanco’s business objectives to reduce costs, improve quality, and manage procurement risks.
* Drive continuous improvement initiatives by actively seeking and implementing cost reduction and avoidance opportunities across procurement activities, leveraging market insights and strategic supplier partnerships.
* Develop and operationalize comprehensive sourcing strategies and options aimed at enhancing efficiency, mitigating risks, and achieving cost savings, collaborating closely with cross-functional teams to secure approval and execute plans effectively.
* Oversee team to ensure strong management of contractual agreements with key suppliers to ensure robust commercial relationships; map risks and opportunities while fostering strong partnerships with internal stakeholders, including strategy, engineering, and site teams, to drive innovation and operational excellence
* Oversee market analysis and maintain a strong understanding of the supply base to identify potential sourcing solutions, and oversee the preparation and execution of RFIs, RFPs, and tender projects, and prepare team members to lead complex negotiations for products and services to optimize value and terms.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s degree in busines...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-04-16 08:25:17
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Process Operator – Product Finishing
As a Process Operator for Product Finishing, you will play a key role in the granulating, blending, and bagging of animal health products.
In this role, you'll be responsible for meeting departmental goals, ensuring quality, quantity, and cost targets while maintaining safety, compliance, and industry standards.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Operate large-scale processing equipment and troubleshoot issues as they arise.
* Drive a fork truck and handle 60-pound bags as part of routine operations.
* Ensure all production operations align with cGMP and ISO 9000 standards.
* Follow proper documentation, verification guidelines, and safety procedures.
* Suggest and implement safety and process improvements to enhance efficiency.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience operating industrial processing equipment and working in a manufacturing environment.
* Top 2 skills: Troubleshooting and problem-solving skills
What will give you a competitive edge (preferred qualifications):
* Familiarity with fork truck operation.
* Experience in the animal health or related industry.
* Previous experience with cGMP and ISO 9000 standards.
* Strong initiative and ability to work independently.
Additional Information:
* Location: Clinton, IN Manufacturing Site\
* 12-Hour Rotating Shift (Days/Nights)
This position is a fixed duration employee with a one-year contract, annually renewable for up to 4 years with a potential for a full-time position, based on individual performance and business needs.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: 23
Posted: 2025-04-16 08:24:58
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At EVRAZ, our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
Job Description and Responsibilities
We are currently seeking a Safety Supervisor to join our Pueblo, Colorado team. As a Safety Supervisor you will ensure employee safety, OSHA compliance and EVRAZ Pueblo Safety Program Compliance.
EVRAZ is committed to maintaining and promoting a safe, healthy and injury-free environment. It is required for all jobs.
* Employee engagement regarding safety programs, concerns, and compliance
* Audit and inspect various safety programs and processes including fire extinguishers, fall protection, eye wash stations, incident investigation, and safety permits
* Provide technical safety support to assigned mill and work in conjunction with entire safety department to ensure proper application of and compliance with regulatory, plant, and mill requirements
* Participate in the tracking and communication of mill safety statistics
* Conduct safety training
* Participate in the safety improvement and risk assessment processes related to the EVRAZ Business System continuous improvement program.
* Other duties as assigned
Requirements
* High school diploma or equivalent, 2- or 4-year college degree with an emphasis in occupational health and safety preferred
* Valid Driver’s License
* 2 years of occupational health and safety experience and training, with experience in a manufacturing facility preferred
* Safety program management experience and training, with experience in a manufacturing facility preferred
* Experience supervising in a union environment preferred
* Knowledgeable of OSHA regulations
* Must be available to be on call and assist personnel in times of emergency and business needs
* Ability to professionally communicate, in written and verbal forms, with all levels of our organization
* Strong leadership skills
* Functional knowledge in Microsoft Excel, Access, Word, PowerPoint
* Proven ability to professionally organize, engage, and motivate teams for safe, high-quality results and maximum productivity
* Ability to effectively manage change
COMPENSATION
* $75,000 – $80,000
Open & Closing Dates: 1/16/25 - 5/15/25
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be elig...
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Type: Permanent Location: Pueblo, US-CO
Salary / Rate: Not Specified
Posted: 2025-04-16 08:24:56
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* Recent dialysis experience required
PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy.
Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements.
Ensure provision of quality patient care while maintaining cost-effective clinical operations in accordance with all legal, compliance, and regulatory requirements and programs.
Adheres to all requirements of the FMCNA Compliance Program, and FMS patient care and administrative policies as the clinical leader, has the authority to make daily decisions to ensure continuity of care and patient and staff safety
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Manages the tactical execution of short- and long-term objectives through the coordination of activities with a direct responsibility for results, including costs, methods, and staffing.
* Provides leadership, coaching and development plans for all direct reports to maintain an engaged and productive workforce; partnering with Human Resources on employee matters.
* Technically proficient in the specific department and knowledge of industry practice and business principles.
Works on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current business trends.
Has a larger range within the department.
* Responsible for supporting and driving FMS quality standards through meeting all ESRD regulatory requirements and the practice of Quality Assessment and Improvement (QAI), including use of FMS QAI tools.
* Responsible for addressing and acting on adverse events and action thresholds.
* Oversees facility’s Home Therapies Program if applicable.
* Accountable for compliance with all applicable federal, state and local laws and regulations.
* Ensures all FMS Clinical Quality policies and procedures are communicated to and implemented by the facility staff.
* Maintains integrity of medical records and other FMS administrative and operational records.
* Complies with all data collections and auditing activities.
* Maintains facility environmental integrity, including safety.
* Experienced leadership required for multi-faceted environment; role primarily focuses on tactical execution.
Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.
* An individual contributor will have significant project/process responsibilities.
Program or project responsibility generally within the function.
* Follows processes and operational policies in selecting methods and techniques for obtaining solutions.
Interprets and recommends change to policies and establishes procedures that effect immediate organization(s).
* Decisions have an impact on work processes and outcomes.
Erroneous decisions or failure to achieve results will add costs and may impact the short-term...
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Type: Permanent Location: Linwood, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-16 08:22:55
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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.
About the role
The Global Decarbonisation Director is responsible for overseeing and coordinating the implementation of Alcoa’s Decarbonisation Plan.
In this role, you will lead and manage decarbonisation initiatives across our global operations.
This requires collaboration with a wide range of stakeholders, including internal teams, external consultants, and regulatory bodies, to optimise decarbonisation pathways and drive associated strategies.
You will work across global operations to develop and execute complex projects, ensuring effective coordination, clear communication, and strategic planning to achieve successful outcomes.
Reporting to Vice President, Capital, you will:
* Help drive opportunities to reduce GHG Emissions through influencing of key stakeholders and execution of the global decarbonization roadmap, with the ultimate objective to achieve Alcoa’s global decarbonisation ambitions in a timely and cost-effective manner.
* Provide Alcoa knowledge and management support to drive decarbonisation activities for the global operations.
This will include coordinating and ensuring alignment between Operations and Corporate functions, including Refinery of the Future, Centres of Excellence, and the Sustainability function.
* Own the global Decarbonisation Roadmap, including overseeing stage gate development and execution of initiatives, with a line of sight to marry up with emerging and future technologies and opportunities.
* Be the link between Alcoa’s Corporate Sustainability function and the global operations teams engaging directly with the Climate Change Director to ensure continued alignment with the overall climate strategy.
* Provide decarbonisation program management expertise, problem analysis and decision-making skills to fast-track execution of the roadmap and develop further recommendations for decarbonisation opportunities.
* Lead the development and execution of the priority projects in conjunction with existing and new operating teams to achieve critical outcomes for the operations.
* Ensure all projects and outputs are based on strong commercial and technical understanding of our assets (Mining, Refining and Smelting).
* Work closely with the Corporate Affairs team to secure support, funding and available subsidies for projects.
* Use a combination of technical and commercial acumen to solve complex commercial and strategic issues and then articulate these to internal stakeholders to strengthen understanding of the issues.
* Build an understanding and awareness in the global operations of decarbonisation trends and financial implications for the water and energy areas of the business.
* Implement rigorous and measurable project management and ...
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Type: Permanent Location: Montreal, CA-QC
Salary / Rate: Not Specified
Posted: 2025-04-16 08:22:25
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PURPOSE AND SCOPE:
The Field Service Technician performs client-site installation, service and maintenance on company manufactured and/or distributed equipment within the assigned regional area(s). The incumbent provides technical support in the diagnosis of operational and/or technical issues of applicable equipment. The Field Service Technician performs all responsibilities in compliance with company policies and procedures intended to meet health and safety, compliance and regulatory guidelines.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Performs all assigned equipment installation, service and/or maintenance in compliance with company policies and procedures.
* Provides high level technical in-service support for cross-divisional teams and/or customers as requested.
* Handles various confidential patient and/or health information in compliance with company policies and procedures, HIPAA, and other regulatory requirements.
* Ensures data accuracy and integrity within applicable systems throughout the documentation process of all completed services performed.
* Processes applicable documentation and corresponding parts in compliance with company policies and procedures on a routine basis.
* Maintains field service inventory in compliance with management recommendations; ensuring accountability for the usage and/or dispersal of assigned inventory.
* Maintains assigned company vehicle, credit card(s) and other business accounts in compliance with company policies and procedures.
* Contributes to the improvement of ongoing operations within the assigned function(s) to maximize efficacy and efficiency in alignment with company goals and objectives.
* May be required to provide cross-coverage of additional regional area(s) to meet business needs.
* Assists with various projects as assigned by direct supervisor.
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
* The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
+ Participation in the District On Call Technician (DOCT) and National After Hours On Call Technician (NACT) call rotations required.
+ Must be available for inclusion in a rotating 24-hour call coverage schedule.
+ Must be available to work overtime as required.
+ Exposure to blood borne pathogens and/or hazardous materials possible.
+ Routinely lift and/or move up to 70 pounds.
* Extensive travel may be required.
EDUCATION:
High School Diploma required; Associate’s Degree desirable; and Bachelor’s ...
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Type: Permanent Location: St Louis, US-MO
Salary / Rate: Not Specified
Posted: 2025-04-16 08:22:19
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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
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein.
Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Was macht unseren Bereich aus:
Der Bereich Produktion Chemie innerhalb des Geschäftsbereiches Diagnostics Operations Penzberg ist der wichtigste Produzent qualitativ hochwertiger Einsatzstoffe für die Diagnostik-Division von Roche.
Es erwartet Sie eine vielseitige, interessante und verantwortungsvolle Aufgabe innerhalb des Bereiches der chemischen und biotechnologischen Produktion.
Hier werden Reagenzien und Einsatzstoffe für alle Geschäftsbereiche und vor allem die In-vitro-Diagnostik mehrerer Roche-Geschäftseinheiten hergestellt.
Ergänzen Sie unser Team:
Wir sind der Betrieb der chemisch/biotechnologischen Produktion und sind stolz darauf, für nahezu alle Einheiten im Roche Konzern viele wichtige Produkte zu liefern.
Aktuell sind in der Abteilung Produktion Biosubstanzen und Nukleotide knapp 80 Mitarbeitende in den Produktionsbetrieben und im Analytik-Labor beschäftigt.
Unsere Gruppe ist für die analytische Inprozess-Kontrolle (IPK) aller Produktionsbetriebe innerhalb der Hauptabteilung zuständig.
Außerdem unterstützen wir die Betriebe bei Troubleshootings und gewährleisten somit einen hohen Qualitätsstandard der hergestellten Einsatzstoffe.
Unser Team zeichnet sich durch Vielfalt aus, angefangen von den Jahren an Berufserfahrung über den Ausbildungshintergrund bis hin zur Freizeitbeschäftigung.
Wir gehen gerne auch einmal die Extra-Meile, sind offen für neue Ideen und vergessen dabei nicht den Spaß an der Arbeit.
Es erwartet Sie ein abwechslungsreiches und eigenverantwortliches Aufgabengebiet:
* In Ihrem Aufgabengebiet unterstützen Sie die chemischen Produktionsbetriebe mit der Durchführung von Inprozess-Kontrollen unter Verwendung verschiedenster analytischer Methoden und Geräte (z.B.
HPLC, Spektralphotometrie, TOC-Analysen, NMR, MS) im Labor.
* Sie sind zuständig für die selbstständige Vorbereitung und Durchführung chemischer und enzymatischer Analysen nach vorliegenden Vorschriften.
* Die Dokumentation Ihrer Arbeitsabläufe entsprechend den gültigen Qualitätsanforderungen ist ein wichtiger Bestandteil Ihrer Aufgabe.
Wir suchen genau Sie:
* Sie bringen eine erfolgreich abgeschlossene Ausbildung als Che...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-16 08:10:04
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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:
Supply Chain Manufacturing
Job Sub Function:
Multi-Family Supply Chain Manufacturing
Job Category:
People Leader
All Job Posting Locations:
Leiden, Netherlands, Ringaskiddy, Cork, Ireland
Job Description:
Janssen Supply Chain is recruiting for a Global Lead, Site Engineering Biotherapeutics to be located in Leiden, Netherlands, Zug or Schaffhausen, Switzerland or Cork, Ireland.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Switzerland - Requisition Number: R-001569
Netherlands, Ireland -R-009372
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
#Li-Hybrid
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
That’s why for more than 130 years, we have sought to keep people well at every age and every stage of life.
Today, as the world’s largest and most broadly- based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, build healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and resourcefulness to profoundly change the trajectory of health for humanity.
Position Summary:
The Global Lead, Site Engineering Biotherapeutics will be a key member of the Global Engineering Leadership Team, responsible for supporting and executing the engineering strategy across all Biotherapeutics manufacturing sites.
This role will be pivotal in enhancing operational excellence, asset reliability, and technical standardization while ensuring alignment with network strategy and global engineering priorities.
The role will support global engineering initiatives, ensuring alignment with evolving business needs and technological advancements.
It will require strong stakeholder management and influencing leadership skills to collaborate across Manufacturing, Quality, MSAT, Facilities, EHS and the broader global engineering function.
#Li-Hybrid
Key Responsibilities:
* Global Engineering...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:57
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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:
Santa Rosa, California, United States of America
Job Description:
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
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for QA Technician III to be in Santa Rosa, CA.
The Quality Technician III is responsible for assuring that company products have been manufactured, inspected, and tested using company approved procedures.
Work with manufacturing and QA to implement solutions to quality related problems.
Description of Work
Perform a wide variety of audits, inspections, checks, tests, and sampling procedures to ensure quality of manufactured goods and adherence to quality procedures.
Maintain “qualified” status on all quality audits, inspections, testing, and equipment procedures.
Coordinate training/cross-training of new and/or existing employees.
With direction from supervisor, coordinate quality activities (i.e., inspections, testing, audits) based on manufacturing and/or Research & Development activities.
Alert supervisor and/or department engineer of any situation that prevents the Quality Technicians from achieving optimum efficiency.
Work with department engineers on development/modification of test methods for new and/or existing products.
Write and update inspection procedures and checklists as required.
Propose document changes, as necessary, to supervisor or engineers to ensure GMP compliance.
Check lot history records for completeness, accuracy, and conformance to SOP.
Monitor calibration and maintenance of all test equipment and fixtures and operation of equipment.
In partnership with manufacturing, implement visual standards and limit samples related to WIP and final inspection of product.
Maintain thorough knowledge of all testing related to set-up, in-process, final inspection, and lot release testing.
Support implementation of corrective actions related to internal/external audits.
Required Skills & Experience
* High school diploma
* 5+ yea...
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Type: Permanent Location: Santa Rosa, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:55
-
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 – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America, US059 DC Washington - 1350 I St NW
Job Description:
Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc.
located in Washington.
DC.
This position is fully remote and you must be located n the DC area.
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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and dr...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:51
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, 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/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
This position is fully remote and you must live in the West Virginia area
Purpose:
Established and productive individual contributor, who works under moderate supervision.
Helps implement projects, programs, and processes in support of the organization's overall Clinical Sales - Hospital/Hospital Systems strategy.
Applies practical knowledge of the Clinical Sales - Hospital/Hospital Systems field to administer best in class policies, procedures, and plans for the area.
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography.
Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs.
The Territory Manager is responsible for case coverage in catheter labs while w...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:47
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Internal Lab to be in Malvern, PA
Purpose:
The Analytical Scientist will act as an analytical Subject Matter Expert (SME) and have various responsibilities centered around internal lab-based development projects.
This will be a laboratory-based role and will require the ability to work independently, be self-motivated, be collaborative, build analytical capability, and operate in a cross-functional environment.
You will be responsible for:
* Identifying, developing, qualifying, validating, implementing analytical methods for raw materials and related in-process samples (e.g., bioreactor samples and formulations).
Support Chemistry, Manufacturing and Controls (CMC) development studies, material qualification, Quality Control (QC) release testing, and investigations.
* Overseeing internal method development activities including LC/MS, GC/MS, ICP/MS, XRF, FTIR-ATR, spectroscopic methods.
* Designing and carrying out experiments in support of analytical characterization of raw materials.
Building analytical capability, including evaluation of new instruments and methods.
Supporting enhanced characterization and data analysis, including statistical modeling.
* Collaborating within TDS Material Sciences, Active Pharmaceutical Ingredient (API) Protein Upstream and Downstream teams on testing plans.
Establishing raw materials controls in-process and formulation design.
* Leading method development projects and participate in scientific meetings to share knowledge and foster a culture of scientific thinking.
Ensuring the accurate and timely preparation of technical reports.
Providing guidance toward development of specifications for various materials including cell cult...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:14
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Malvern, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist to be in Malvern, PA
Purpose:
Material Sciences is a technical, scientific department within the Therapeutics Development and Supply (TDS) organization.
We are expanding our team to strengthen our technical capability around raw materials used in our Biotherapeutics portfolio.
The Analytical Scientist will act as an analytical Subject Matter Expert (SME) and have various responsibilities centered around external analytical development activities.
You will be responsible for:
* Identifying, developing, qualifying, validating, implementing analytical methods for raw materials and related in-process samples (e.g., bioreactor samples and formulations).
Support Chemistry, Manufacturing and Controls (CMC) development studies, material qualification, Quality Control (QC) release testing, and investigations.
* Overseeing external method development activities at global network of contract labs (CROs).
* Designing and carrying out experiments in support of analytical characterization of raw materials.
Building analytical capability, including evaluation of new instruments and methods.
Supporting enhanced characterization and data analysis, including statistical modeling.
* Collaborating within TDS Material Sciences, Active Pharmaceutical Ingredient (API) Protein Upstream and Downstream teams on testing plans.
Establish raw materials controls in-process and formulation design.
* Leading method development projects and participate in scientific meetings to share knowledge and foster a culture of scientific thinking.
Ensure the accurate and timely preparation of technical reports.
Providing guidance toward development of specifications for various materials including cell ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:14
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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:
Neuss, North Rhine-Westphalia, Germany
Job Description:
Zur Unterstützung unseres Teams suchen wir zum nächstmöglichen Zeitpunkt einen Werkstudent (m/w/d) für den Bereich L&D Organizational Transformation (19Std/Woche)
In dieser Position unterstützt du unser Team bei der Implementierung unserer transformativen Learning & Development Projekte, erstellst bedarfsorientiert digitale Lernmaterialien und bist an der Evaluation unserer Maßnahmen beteiligt.
Aufgabenprofil:
· Du arbeitest zusammen mit unseren L&D Managern, die unterschiedliche transformative Projekte entwickeln und implementieren – je nach Projekt und Bedarf unterstützt Du in den relevanten Aktivitäten
· Die Erstellung von Lernmaterialien (Präsentationen, Trainingsvideos etc.) im Kontext der genannten Projekte sowie auf Basis individuellen Bedarfs erstellst Du eigenverantwortlich
· Du stellst sicher, dass wir für alle unsere Aktivitäten Daten zur Evaluation dieser generieren, regelmäßige Auswertungen darauf basierend erhalten, und dass sich unser Evaluationsmodell entsprechend den Anforderungen weiterentwickelt
Voraussetzungen:
· Du studierst ein naturwissenschaftliches Fach, Pharmazie, Medizin, Psychologie, Pädagogik, Erwachsenenbildung, Sozialwissenschaften oder eine andere Richtung mit Bezug zum Bereich Learning & Development
· Du hast eine Affinität für Training, Coaching, digitale Lernformate und/ oder Personalentwicklung
· Dir fällt es leicht, mit anderen zu kommunizieren und im Team zu arbeiten
· Auch in hektischen Phasen behältst Du den Überblick
· Du bist ein Organisationstalent und arbeitest strukturiert, systematisch und präzise – gleichzeitig fällt es Dir leicht, bei Bedarf schnell den Fokus auf ein neues Thema zu lenken
· Du bist selbstständig sowie verantwortungsbewusst
· Du kennst Dich mit den MS Office Anwendungen gut aus (insbesondere PowerPoint und Teams)
· Eine Arbeit im hybriden Setting ist Dir vertraut und macht Dir Freude
· Gute Englischkenntnisse in Wort und Schrift runden Dein Profil ab
Was bieten wir Dir?
· Ein tolles Team, in dem die Zusammenarbeit Spaß macht
· Die Möglichkeit, Berufserfahrung in einem erfolgreichen Pharma-Unternehmen zu sammeln, das Teil des weltweit größten Gesundheitskonzerns ist
· Viele Einblicke in Personal- und Train...
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Type: Permanent Location: Neuss, DE-NW
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:10
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands, Sassenheim, Netherlands
Job Description:
THE OPPORTUNITY
As part of the JSC Laboratories situated at the Janssen Biologics Manufacturing site in Leiden, the QC Microbiology department is essential in ensuring the safety and quality of our products.
We rigorously test for microbial contaminants at every stage, from raw materials to finished products, using advanced techniques like sterility testing.
Our department not only guarantees compliance with industry regulations but also fosters trust among consumers, ensuring that every product is safe for use.
By collaborating with other teams, we integrate microbiological safety into the entire production process, making us a key player in delivering high-quality products.
We are looking for a Senior Supervisor to lead the Microbiology group and oversee day-to-day operations.
Responsibilities & Accountabilities
As a Senior Supervisor, you:
* will lead a team of 8-12 individuals and be directly accountable for their performance and development through structured conversations.
You will set objectives aligned with the JSC Lab Organization business strategy to ensure your team's effectiveness.
* will define and oversee the execution of testing activities, ensuring compliance with cGMP and safety regulations.
Additionally, you will ensure that all necessary elements for testing—such as materials, equipment, and trained personnel—are in place to complete tasks in a timely manner.
* will have primary accountability for planning, organizing, and supervising daily tasks within the team, ensuring a smooth transfer of activities via SmartQC.
* will ensure that assays are performed to meet required quality and quantity standards, setting priorities to resolve any conflicting situations within the JSC Lab Organization.
You will oversee monitoring and reporting of critical activities (e.g., process delays in testing) and implement relevant action plans independently.
* will be responsible for the proper coordination of investigations at the team level to achieve swift resolutions in compliance with GMP principles.
* will follow up on key performance indicators (KPIs), including but not limited to 5S/housekeeping, invalid assay rates, training status, and lead time for test results.
* will...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:04
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
People Leader
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Basic purpose of the role
* Leading the EH&S organization for Janssen Biologics (JBV) site in the Netherlands (NL).
This consists in deploying, leading, and implementing EH&S strategies, policies, plans, procedures for JBV.
Key outcome is ensuring the EH&S team has taken all needed EH&S precautions to assure continuous, EH&S reliable & compliant supply chain, research & development activities, and is continuously improving in the field of EHS.
* Familiar with the annual company /division goals and aware of how he/she can influence these through his/her performance.
* Results achieved through effective leadership of the JBV EH&S team and through effective collaboration / influencing key leadership teams on the JBV EHS team as well as with J&J global EH&S.
All their needs/ improvements to be balanced with global/ local context.
The EH&S lead decides how to convert these in a lean, results oriented, compliant EHS approach.
* Responsible for developing and coordinating site EHS&S infrastructure to help GM & Site Management to ensure compliance with legislative and J&J requirements.
* Partner with Site LT to establish and implement site EHS&S strategy and Management Action Plan (MAP) in alignment with the J&J requirements.
* Responsible for site EHS&S department including budget (OPEX &CAPEX)
* Coach and mentor line management to take ownership of EHS&S.
* Ability is to reach outside J&J and represent the JBV EH&S team when meeting with governmental inspectors for the site.
Key Responsibilities
* Shared responsibility with site General Manager for EHS&S performance at the site.
Responsibility to provide advice to Site Manager for EHS&S performance at the site.
* Partner with local Management to develop and implement a site MAP to address EHS&S program deficiencies and ensure EHS&S regulatory compliance.
* Build effective working relationships with staff and key stakeholders including corporate EHS&S function and regulatory authorities.
* Develop EHS&S objectives for the site - auditing, analyzing, documenting, reporting on their implementation / effectiveness to management via dashboards, reports & management re...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:48
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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:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for an Sr Data Scientist- Shockwave Medical- Remote to join our team.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
We are seeking a proactive and curious Sr.
Data Scientist with a passion for transforming data into actionable insights.
The ideal candidate possesses experience working with a global team where they can optimize existing systems to help answer end users questions through data insights.
This role is an exceptional opportunity to be a pioneer in a company that is embarking on its data science journey.
You will play a pivotal role in shaping our data infrastructure, ensuring it is primed for leveraging data science effectively, and actively contribute to the company's success in a rapidly evolving landscape.
Essential Job Functions
* Utilize programming languages such as Python and R, along with the Snowpark analytics engine, to extract, transform, and analyze data from various sources.
* Database management.
* Clean, manage, and ensure the integrity of data to facilitate analysis.
* Develop dashboards and reports using Power BI to communicate findings and ins...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:41
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
* 2024 Best Places to Work – #1 in Health Industry
* Competitive salary package, flexible work practices, award winning benefits
* Continuous training and development
* Focus on Johnson & Johnson Innovative Medicine’s exciting Lung Cancer portfolio
* Location: New South Wales
THE OPPORTUNITY
Due to team expansion, you could be the next MSL/Senior MSL to join a high impact team where you will represent the scientific face of the company, engaging in communication with healthcare practitioners to translate the latest exciting scientific and clinical evidence into clinical practice.
This role will be based in the field where you will build strong, trusted peer-level relationships with thought leaders, clinical investigators and healthcare decision makers.
This is also an opportunity to be at the forefront of a revolution in oncology. At Johnson & Johnson, we have a market-leading oncology portfolio with exciting new therapies in the pipeline, all designed with a singular vision: to eliminate cancer.
Join us and play a pivotal role in delivering transformational therapies that have the power to redefine the standard of care, fundamentally changing the lives of patients with cancer.
RESPONSIBILITIES
You will collaborate externally and internally to identify actionable insights and help shape the current and future treatment landscape in Lung Cancer, to ultimately improve patient outcomes.
* Establish and maintain trusted partnerships with KOLs and HCPs to address research, educational, and clinical needs aligned with business priorities.
* Communicate clinical and scientific data effectively, translating evidence to enhance patient outcomes.
* Maintain in-depth scientific and therapeutic knowledge, including Johnson & Johnson products and other companies’ products for the relevant disease state.
* Work within a cross-functional team to align and execute on medical strategies and deliver value to healthcare professionals, patients, and other external partners.
* Identify and address medical education needs through presentations, responses to inquiries, and the development and delivery of educational activities.
* Create and implement KOL Engagement pl...
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Type: Permanent Location: North Ryde, AU-NSW
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:36
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ERM is seeking an energetic and knowledgeable Senior Consultant, Climate Change join our growing corporate sustainability and climate change advisory services practice.
The person will report to Partners in Manhattan, NY, but the role is hybrid/remote and remote locations will be considered.
This is an excellent opportunity for an experienced professional looking to play a key role working with an expert consulting team on interesting climate advisory projects for Fortune 500 and privately held clients.
In this role, you will be a key contributor to a team developing and growing ERM’s corporate sustainability and climate change business.
ERM delivers a wide range of climate change services including strategy development, policy and regulatory analysis, greenhouse gas emissions target setting, and peer benchmarking.
We help clients, including global companies, electric and natural gas utilities, and financial institutions, develop and implement climate change programs across a broad range of industry sectors and contribute to climate, clean energy, and clean transportation policy development.
This is an excellent opportunity for an experienced professional looking to play a key role working with an expert consulting team on leading-edge climate advisory projects for Fortune 500 and privately held clients.
Responsibilities:
Managing Clients and Projects
* Demonstrates expertise in understanding climate and energy policy, identifying climate change risks and opportunities, and conducting policy and technical analyses.
* Supports development of climate change strategy, action planning, and/or modeling of and setting science-based targets.
* Thinks strategically in order to influence decision-makers and outcomes.
* Expertise in electric and natural gas utilities, transportation electrification, or air and climate regulation a plus.
* Effectively coaches colleagues to deliver high-quality outputs based on complex source material.
* Demonstrates strong project management skills and oversight through the project lifecycle, including scoping, budget and delivery.
* Demonstrates strong analytical skills, excellent writing and presentation skills, and a mastery of client communication.
* Builds strong and trusted relationships with clients and/or business partners.
Teamwork and Organization
* Demonstrates strong people management skills; particularly the ability to support, coach and celebrate others in order to advance employee engagement and achieve results.
* Mentors junior staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Identifies, evaluates, cultivates and manages partnerships and relationships with senior clients, external stakeholders and key opinion leaders.
* Effectively collaborates internally to bring our services to existing clients.
* Enhances ERM’s capability to sup...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:16
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ERM seeks a motivated Principal Technical Consultant, EHS to join our team in Raleigh or Charlotte, NC. This is an excellent career opportunity to work with an expert consulting team on challenging EHS management projects for large power clients.
Access to ERM's national compliance experts provide knowledge sharing of best practices across the industry and ongoing learning opportunities for our team.
RESPONSIBILITIES:
* Provides technical direction and oversight for functional areas such as biology, chemistry, and environmental services in relation to water programs for power generation facilities.
Duties may include developing technical procedures, designing tests and experiments, investigation and resolving technical problems.
* Prepares thorough and accurate technical plans and reports, correspondence, documentation, calculations, and models with the ability to conduct analysis and recommend process enhancements and standards relative to area of water resources and hydro licenses/permits.
* Develops positive working relationships with clients to effectively coordinate work activities. Demonstrates effective oral and written communication skills. Maintains accurate records and files.
* Maintains good working relationship and communication with client managers and support personnel to meet the analytical and technical needs of the client’s generation stations.
* Skilled in the practices of researching scientific issues, evaluating alternatives, making sound recommendations and preparing and presenting recommendations.
* Provides backup to the client in the areas of report generation, client interfaces, and other Program Manager responsibilities for a hydro license compliance programs.
* Stays current with issues in both the industry and regulatory communities in relation to water resources, aquatic monitoring programs, etc.
* Support ERM Partners-in-Charge and other Project Managers to effectively manage and deliver projects.
* Effectively steward and build client relationships leading to repeat business.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in chemistry, biology, environmental science, engineering or related discipline.
Or equivalent experience.
* 6+ years of consulting experience.
* Excellent communication, interpersonal, MS Office computer, and analytical skills; experienced in writing comprehensive technical reports.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
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 a...
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Type: Contract Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:14
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ERM is seeking a motivated Consultant, Environmental Scientist to join our global consulting firm in our Cincinnati, OH office.
As a consultant at ERM, you will gain a wealth of experience across different sectors, clients, geographies and services, all of which will help shape your future career path at ERM. In this role, you will work closely with Project Managers on a variety of projects in the energy industry including renewable energy and electric transmission. ERM's collaborative culture provides knowledge sharing of best practices and ongoing learning opportunities for our consultants, allowing you to build your own individualized career path.
RESPONSIBILITIES:
* Provide technical assistance on environmental impact assessments and sustainability-related projects.
* Prepare plans, permits, and reports for wetlands, storm water, NPDES, and wastewater programs.
* Perform environmental compliance assessments and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Conduct field work, including ecological field studies.
* Provide general environmental compliance support to clients, including on-site assistance, as needed.
* Compile and evaluate data and assist in report preparation.
* Perform project tasks within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Support ERM Partners-in-Charge and Project Managers to deliver exceptional client value on projects.
REQUIREMENTS:
* BS in biology, environmental studies, or related science degree.
* 2+ years of relevant environmental experience.
* Strong commitment to safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Strong hands-on spreadsheet and database comprehension.
* Detail-oriented with mechanical aptitude and hands-on troubleshooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
* 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.
* Ability to lift up to 30 pounds.
* 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 solu...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:14
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Primary Function
At Ardurra, the Senior Recruiter is a blend of a strategic and detailed hands-on role responsible for applying and participating in enhancing talent resources solutions that align with our growing organization’s goals and supporting our culture and a great employee work environment.
Our company’s organic growth and acquisitive growth strategies require a successful Senior Recruiter to have a deep understanding of both technical and business aspects to identify and address hidden issues that may impede the company’s talent acquisition success.
Strong collaboration and communication skills are essential to effectively interact with hiring managers and candidates at all levels and to positively influence organizational and/or regional outcomes.
The Sr.
Recruiter works in a collaborative culture, identifying and delivering high performing candidates within the Architectural, Engineering, and Construction (AEC) industry.
Serving as a trusted advisor to internal business teams, guiding the hiring process in a highly competitive industry.
This includes offer negotiation, understanding the psychology of selling and hiring, navigating non-compete agreements, and managing external recruiting agencies.
The ideal candidate will have experience in a professional services or engineering, architectural and construction organization.
The right candidate will be energized by the talented individuals who make up our entrepreneurial workforce.
Primary Duties
* Manage full life-cycle recruitment including creating search strategies, actively sourcing candidates, pre-screening, interviewing and presenting qualified candidates to hiring managers, negotiating offers and facilitating the hiring processes
* Involvement on all aspects of the hiring process, including hiring strategies, recruitment cycle timing and guidance on best practices and sourcing trends
* Build relationships and communicate consistently and proactively throughout the recruitment process to ensure all participants in the hiring process are updated and well informed
* Create a positive candidate experience throughout the entire recruiting process
* Creation of offer letters and keeping candidate files updated
* Update and maintain administrative responsibilities such as applicant tracking system data entry and Excel report
* Follows compliance standards throughout process
Education and Experience Requirements
* Bachelor’s Degree plus 7 plus years of related recruiting experience or equivalent
* Solid experience recruiting for positions in Engineering required (Transportation, Water/Wastewater, Environmental, Structural or Civil)
* Architectural, Engineering, and Construction (AEC) industry experience (required)
* Experience with LinkedIn Recruiter and working within an ATS (required)
* Must have successful track record in sourcing passive candidates
* Creative sourcing techniques and cold c...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-16 08:07:38
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About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Overview
Serves as a key role within the Merz Aesthetics Clinical Research and Development team, the Clinical Scientist is responsible for contributing scientific and strategic expertise to our global clinical programs.
Liaising with cross-functional study teams, this position requires a highly motivated, scientifically driven leader to contribute to the development of clinical strategy including study design and execution, and data analysis and interpretation, delivering clear, consistent, and comprehensive results toward the registration of new aesthetic products and/or novel aesthetic indications.
What you will do:
* Accountable for contributing scientific expertise to the trial design phase of clinical projects under development:
+ Provide scientific and strategic input across various stages of clinical development to achieve market approval for new products and/or novel indications.
o a.
Duties performed as a member of a cross-functional team of internal and external experts and in support of the medical director.
o b.
Projects are focused on devices, drugs, biologics, and/or other products for human use.
o c.
Projects may span from in-development to post-marketing studies and products.
+ Coordinate and integrate data and information from a variety of sources (e.g., internal and external studies, research documentation, and published literature) to support various clinical development initiatives.
+ Consolidate input from internal and external contributors to develop appropriate key messaging.
+ Provide scientific guidance and technical expertise within teams, across departments, and across functions by providing strategic, actionable direction, creating a strong sense of team unity and identity, and providing positive, constructive feedback.
+ Proactively identify and troubleshoot study-specific issues, competing priorities, and clinical or scientific challenges; propose and enact solutions, developing contingency plans as needed.
+ Ensure effective, accurate, and timely communication of key issues and progress to the team and senior management.
+ Support planning and preparation for internal and external stakeholder meetings (e.g., workshops/summits, investigator meetings, scientific advisory boards, and regulatory meetings).
* Accountable for authorship of various clinical documents, i...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-15 08:29:25
