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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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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 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
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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, 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:
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
-
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
-
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
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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
Your Department and Team:
The Analytical Development and Quality Control (ADQC) unit is located in the Gene Therapy Development Center (GTDC) in Penzberg, Germany.
The ADQC department consists of 40 - 50 persons working to develop and implement novel analytical technologies for pre-clinical studies until market authorization and launch of gene therapeutic modalities.
The sub-team focusing on analytical ultracentrifugation (AUC) technologies consists of one subject matter expert (SME) and one part-time analyst.
We are looking for a highly motivated scientist (m/f/d) with a specific focus on/ or interest in analytical ultracentrifugation technologies for the testing and characterization of gene therapy vectors.
Key Responsibilities:
* Scouting, evaluation, development and implementation of innovative, cutting edge analytical ultracentrifugation technologies and workflows for the analysis and characterization of viral vectors (predominantly rAAV) for gene therapeutic applications
* Driving and advancing the science to characterize and quantify viral vectors with a highly enthusiastic and agile, interdisciplinary team
* Independent, self-organized hands-on execution of experiments: method development, equipment qualification and assay validation under GMP requirements as well as testing
* Contribution to the development and definition of control and testing strategies for gene therapy vectors (e.g.
rAAV payload, full/ empty ratio, process related impurities)
* Independent interpretation, evaluation, and documentation of data and the generation of analytical reports in accordance with current regulations
Who you are:
* You have a track record and knowledge (theoretical as well as hands-on) in analytical ultracentrifugation technologies such as e.g.
MWL-AUC method, operating Optima-AUC, UltraScan, Sedfit software solutions, as well as developing and applying respective IT and data management tools
* You have knowledge in the area of gene therapeutic modalities (AAV, Lentiviruses, etc.).
* You have knowledge and experience with principles of GMP (e.g.
data integrity, equipment qualification, assay validation)
* You have a high degree of self-motivation, responsibility, result-orientation and you are an excellent team player
* You are fluent in English and German language skills (written and spoken)
Advantages:
* Flexible time management
* 2092 Euro salary per month for a full-time internship > 3 months
* Reduce...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-15 08:07:23
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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:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Aachen, North Rhine-Westphalia, Germany, Berlin, Germany
Job Description:
Über Kardiovaskulär
Angetrieben von Innovationen an der Schnittstelle von Biologie und Technologie entwickeln wir die nächste Generation intelligenter, weniger invasiver und personalisierter Behandlungen.
Sind Sie begeistert von der Verbesserung und Erweiterung der Behandlungsmöglichkeiten von Herz- und Gefäßerkrankungen? Sind Sie bereit, in einem Team mitzuarbeiten, das die Art und Weise, wie wir Menschen heilen, neu erfindet?
Unser Team entwickelt führende Lösungen für die Wiederherstellung des Herzens, die Elektrophysiologie und den Schlaganfall.
Werden Sie ein Teil einer stolzen Tradition der kontinuierlichen Verbesserung der Standards für die Versorgung von Schlaganfall-, Herzinsuffizienz- und Vorhofflimmern (AFib)-Patienten.
Begleiten Sie uns auf unserem Weg, während wir Medizinprodukte weiterentwickeln und den Übergang von der Forschung ins echte Leben ermöglichen – immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/medtech
Wir suchen aktuell einen Clinical Educator/Consultant (m/w/d), innerhalb der Region Berlin Süd
Spannende Aufgaben warten auf Sie:
* Patientenbetreuung: Verbesserung der Patientenergebnisse durch eine fachgerechte Ausbildung und Beratung des medizinischen Personals.
* Betreuung aller Kliniken, in denen Patienten mit Impella® Produkten behandelt werden.
* Reportings von klinisch relevanten Daten, Dokumentation von Ergebnissen und eine enge Zusammenarbeit mit unseren Teammitgliedern und Vertriebskollegen.
* Klinische Beratung: Durchführung von Trainings zur Steigerung der klinischen Auslastung und Leistung unserer Kunden.
Verwaltung von Schulungen für unsere neuen und bestehenden Kunden.
* Training/klinische Demos: Unterstützung bei der Koordination von klinischen Demos vor Ort.
Ihr Profil:
* Erfolgreich abgeschlossene klinische oder klinisch-technische Ausbildung, idealerweise als Gesundheits- bzw.
Krankenpfleger(in) oder Kardiotechniker(in) / Klinischer Perfusionist(in).
* Mehrjährige Berufserfahrung in der direkten Patientenbetreuung auf Intensiv- oder Pflegestation, im OP oder im HKL.
* Überzeugendes Auftre...
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-04-15 08:07:19
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Ardurra is currently hiring a Hydrologist/Hydraulic Engineer/Civil Engineer to join our office in Phoenix, Arizona.
Summary
In this role, you will have the opportunity to be a part of the growing Ardurra family in the Drainage Engineering Group.
You will help to evaluate drainage and design a wide variety of exciting drainage projects throughout the Southwest region.
This includes projects supporting drainage for roadway, land development, commercial/industrial developments, parks, and municipal facilities as well as drainage studies/design for public agencies.
Work/life balance is important at Ardurra, once you have been established in this role, there is a potential for a hybrid work schedule mutually agreed upon by your supervisor.
Primary Function
* Provide design and help evaluate a variety of civil engineering projects (both public and private) to support our Drainage Engineering Group.
* Perform drainage calculations using various softwares, and/or equations.
* Frequent collaboration with other engineering departments (transportation, public works, water/wastewater, site civil and surveying).
* Assist with client interface, budgets, and schedules, and executes on time/on budget project delivery.
* Assist with preparing project proposals, scope/fees, and RFP responses.
* Help plan, organize, and supervise design activities for a variety of complex civil engineering projects (e.g., a multi-structure facility requiring frequent interface and collaboration with various consultants and disciplines).
* Prepare drainage design plans, base files, and reference files using Auto CAD software.
* Coordinate with project design team members, clients, contractors, subconsultants, and permit agency representatives regularly.
* Prepare and review technical engineering reports and calculations.
* Facilitate and collaborate during project construction administration by interacting with the construction team/GC, reviewing Shop Drawings/submittals, and addressing RFIs.
Education and Experience Requirements
* 0 to 5 years of related professional experience in Civil Engineering, Water Resources and/or Drainage field.
* Drainage design experience is desired and preferred, including drainage softwares.
* Engineer-in-Train (EIT) certification preferred but not required.
* Professional Engineer (PE) license in AZ will be a plus.
* Education: bachelor’s degree in civil engineering, or related field, from an accredited university or college.
* Proficient working knowledge of applicable software, such as, Microsoft Office, AutoCAD Civil 3D, and Bluebeam.
* Strong communication skills both written and verbal.
* Strong organizational, analytical, and problem-solving skills.
* Highly self-motivated, able to work both independently and in a collaborative environment.
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our...
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Type: Permanent Location: Phoenix, US-AZ
Salary / Rate: Not Specified
Posted: 2025-04-15 08:06:02
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The Sr.
Director of Sales – Animal Nutrition is responsible for driving profitable growth within the business unit.
This includes connecting, developing, and maintaining key customer relationships across the value chain, such as dairy farm operators, nutritionists, and distributors to maximize both the push and pull of dairy ingredients.
The role also involves setting objectives, leveraging internal and external resources, reviewing progress, and making necessary mid-course corrections to achieve the plan. The position will contribute directly to the coaching, mentoring, and developing of the growing sales team, ensuring all are equipped with the right tools to contribute effectively and execute against business plans.
Additionally, this position will partner with the senior leadership team to develop business unit strategies, focused on optimizing enterprise results.
ESSENTIAL DUTIES and RESPONSIBILITIES:
* Develop and implement sales and marketing programs for each of the key product lines within the branded, private label and custom product portfolio.
* Engage with the most senior level of customer organizations to support new business development and growth within existing customers, promoting strong customer service practices and pricing and purchasing policies.
* Develop distribution for the product lines through appropriate distribution channels including animal health distributors, feed companies and independent distributors.
* Evaluate operating results ensuring growth objectives are met as well as create, implement, and track benchmark metrics.
* Build upon culture within the team through leadership aligned with the Actus Nutrition’s values.
* Help recruit, retain, and build a high functioning sales and technical services teams to support strategic growth initiatives.
* Participate in appropriate industry events and states associations.
Promote good stewardship in the communities served and promote healthy customer and supplier relationships.
QUALIFICATIONS:
* 8-10 years of senior sales/sales leadership experience in an animal feed/nutrition organization
* Demonstrated experience and knowledge in business development, strategic analysis, new product launches, with the requisite financial and analytical skills
* Excels in fast-paced, entrepreneurial, results-driven organization
* Superior business acumen with demonstratable analytical skills
* A business builder’s perspective, thought process, and executional capability
* Consensus builder that possesses the ability to develop and implement programs to address specific issues and achieve organizational goals
* Outstanding communication skills.
Demonstrated ability to effectively visualize, understand, and persuasively communicate what Actus Nutrition and its technologies can bring to dairy farmers, distributors, and nutritionists
* Possess influence, diplomacy, and evaluative problem-solving skills to...
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Type: Permanent Location: Eden Prairie, US-MN
Salary / Rate: Not Specified
Posted: 2025-04-14 08:15:42
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
We are searching for the best talent for a Laboratory EHSS Specialist to be in Leiden, Netherlands!
Join our dynamic team at Janssen Biologics as we seek a hardworking Laboratory EHSS Specialist in our Quality Control department! This is a fantastic opportunity for someone who is enthusiastic about safety and environmental regulations and is eager to make a positive impact in laboratory environments.
As a key member of our small, dedicated team, you will help develop and implement safety protocols that ensure a safe and compliant workplace.
We value ownership, accountability, and results, and we're looking for someone who can inspire a culture of safety among our lab personnel.
You'll also have the chance to build a wide network across the QC organization and JBV site, encouraging collaboration and innovation.
Come be part of something great!
You will be responsible for:
* Lead investigations into safety incidents, ensuring root cause analysis and timely reporting, while handling safety metrics for the QC laboratories.
* Act as an advisor on safety issues, participating in meetings and assessing EHSS topics related to lab changes and new materials.
* Review lab processes and equipment for EHS compliance and assist in preparing safety documentation such as Safety Data Sheets and procedures.
* Conduct regular safety audits, Gemba walks, and inspections to identify hazards and ensure compliance with EHS standards and regulations.
* Develop and deliver engaging safety training for laboratory staff, promoting standard methodologies and encouraging a collaborative safety culture.
Qualifications/Requirements:
* Hold (at minimum) a HBO or bachelor’s degree in Safety Management, Industrial Hygiene, Environmental Sciences, Life Sciences, or a related field, with proven expertise in (laboratory) safety and environmental health.
* Possess proven understanding of (laboratory) safety regulations, hazardous materials handling, and waste management.
* Demonstrate excellent written and oral communication skills in English, with proficiency in Dutch being a plus, to optimally train and engage diverse teams.
* Exhibit proactive leadership and project management skills, capable of driving safety initiatives across depart...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-04-14 08:14:11
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Product Development Testing
Job Category:
Business Enablement/Support
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a R&D Technician II to join our team located in Santa Clara, CA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
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.
The R&D Technician II will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases.
The R&D Technician II will participate on multiple cross-functional development teams that manage projects from concept through commercialization.
Perform and support a variety of development and engineering activities, which mainly focus on disposable devices prototyping, fabrication and testing.
Will work directly with other R&D technicians and R&D engineers to complete duties described below.
Essential Job Functions
* Generate functional prototype from design concepts and assist the transfer of R&D product build to manufacturing
* Support product builds through all R&D project phases, providing feedback on assembly process
* Assist other technicians, assemblers and engineers on procedures and product assembly
* Assist engineers with product and process development and improvement
* Perform testing to support design, process, and ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-14 08:14:10
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Vous voulez contribuer à des projets d’envergure et avoir un impact sur le monde qui vous entoure ?
Intégrer Janssen, la division Pharmaceutique de Johnson & Johnson, le leader mondial dans le domaine de la santé et du bien-être (140 000 collaborateurs dans le monde et 265 entreprises présentes dans 60 pays), c'est participer à l’amélioration de la santé en étant au plus près des besoins des patients.
Rejoindre notre équipe en charge de la Communication, des Affaires Publiques et de la RSE, c’est vous épanouir dans une entreprise à taille humaine tout en bénéficiant des expertises et des opportunités d’un grand groupe.
Alternance en Communication et RSE H/F
Localisation : Issy-les-Moulineaux
Date de démarrage : Septembre 2025 (12mois)
Projets Environnement & RSE :
* Mobilisation et accompagnement des collaborateurs sur les sujets RSE (production de supports de communication, animation des réseaux sociaux en interne, campagnes de sensibilisation, etc.)
* Rédaction des réponses aux questions RSE des appels d’offres hospitaliers
* Soutien aux projets et actions de réduction des impacts environnementaux
* Participation aux instances de gouvernance RSE
Communication aires thérapeutiques (50%)
Soutien et accompagnement de l’équipe Communication des Aires Thérapeutiques dans la préparation et réalisation de leur actions/campagnes de communication en interne comme en externe, plus particulièrement :
* Accompagner l’équipe sur la mise en place d’événements en interne (comme les Journées Mondiale / les mois de sensibilisation, des conférences inspirantes…)
* Site internet Janssen.fr – mise à jour de l’ensemble des pages dédiées aux produits
* Création de contenu pour Yammer et les réseaux sociaux (soutien à la gestion de nos calendriers réseaux sociaux LK, Twitter)
* Soutenir l’équipe du Pole de la communication des Aires Thérapeutiques sur la mise en place d’actions de relations presse ou le suivi de campagnes de disease awareness…
* Participer activement à des événements externes comme les conférences de presse / interviews, événement de relations publiques pour une meilleure appréhension et compréhension de notre en...
....Read more...
Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-04-14 08:14:06
