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Your Job
Location: Neenah, WI
Georgia-Pacific is seeking a talented Mechanical Product Design Engineer to join our Technical Center in Neenah, WI.
You will be a key contributor to developing innovative dispensing solutions for the consumer products business by collaborating with cross-functional teams to solve complex engineering challenges.
If you're passionate about creativity, designing new products from the ground up, and continuously improving existing designs, we want to hear from you.
What You Will Do
* Design and development of electro-mechanical devices from concept through product lifecycle, ensuring robust and reliable solutions.
* Collaborate closely with business leaders, project engineers, electrical and test engineers, quality managers, and designers to deliver market-leading products.
* Develop and execute product validation and verification test plans to guarantee performance and reliability.
* Use SolidWorks CAD software to create detailed product designs that minimize build and test iterations through effective modeling and engineering analysis.
* Support ongoing product improvements and troubleshooting throughout the product lifecycle.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in Mechanical Engineering
* Strong problem-solving skills
* Product design experience
* Proficiency in 3D CAD design
What Will Put You Ahead
* Proficiency in SolidWorks CAD software.
* Experience with plastic part design for injection molding .
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Our Benefits
Our goal is for each employee, and their families, to live fulfilling and healthy lives.
We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most.
Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and m...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-08 08:11:28
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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:
Finance LDP
Job Category:
Career Program
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
The Finance MBA Leadership Development Program (LDP) Internship is a full-time 10-week program where MBA students are responsible for leading project(s) that support strategic business initiatives within the Finance function. Internship assignments may include Financial Planning & Analysis, Commercial Finance, Supply Chain Finance, Research & Development Finance or Corporate Services.
Intern assignments will be within the J&J operating companies, supporting either Medical Technology, Innovative Medicine, or Corporate Services Sectors. The MBA Internship positions are typically located in or near New Brunswick, Raritan, Titusville, NJ or Horsham, Spring House, PA.
Successful candidates will possess the ability to work independently, and have strong problem solving, organizational, communication and analytical skills.
Interns will participate in organized activities, including live trainings to build J&J business acumen, networking with peers and senior leaders, opportunities to experience company culture and build understanding of career opportunities within J&J.
The Finance MBA LDP Intern program is one of the primary sources of talent for the full-time Finance MBA Leadership Development Program (MBA LDP). The Finance MBA Leadership Development Program (MBA LDP) is a four-year program designed to successfully develop a pipeline of future leaders for Johnson & Johnson through a combination of diverse rotational assignments, targeted training, and continuous coaching and development.
The anticipated base pay for this position is $51/hour, but will be based on candidate’s program year, discipline, degree and/or experience.
This position is overtime eligible.
Co-Ops/Interns may be eligible to participate in Company employee benefit programs such as medical insurance, sick time, and holiday pay in accordance with the terms of the applicable plans.
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
Ineligibility for severance.
#JNJFinance
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:30
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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:
Procurement
Job Sub Function:
Category
Job Category:
Professional
All Job Posting Locations:
São Paulo, Brazil
Job Description:
Johnson & Johnson is currently recruiting for a Manager Procurement, IT Procurement.
The position can be based out of Titusville, NJ, Raritan, NJ, New Brunswick, NJ, or Sao Paulo, Brazil, Tampa, FL.
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/
Position Overview
This role will be accountable for building robust and relevant category strategies that are strongly aligned to the business needs and market dynamics.
This individual will also serve as global Supplier Relationship manager to some strategic suppliers and ensure maximum value and innovation from those partnerships. The role works directly with the business, J&J technology team, key suppliers, Global Services and the broader Procurement function.
Key Responsibilities:
* Understand the JJ Technology priorities and devise category strategies that advance those priorities.
* Collaborate with business leaders and Service Delivery team to ensure Procurement strategies meet the business needs, and are adopted within the business
* Identify industry trends that Procurement must incorporate in its category strategies to ensure sustainable relevance to the business
* Partner with the Category and Service Delivery teams in the execution of strategic sourcing events, negotiations and contract lifecycle management
* Develop and maintain strong strategic relationships with key suppliers
* Deliver against savings, innovation and other performance targets for the organization in the role’s area of responsibility and ensure target achievement
Qualifications
* A Bachelors Degree is required, and an MBA or other advanced degree is desirable.
* Minimum 5 years related experience is required (preferably in Procurement, Business Operations or Supply Chain)
* Influencing skills - Able to persuade others ...
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Type: Permanent Location: São Paulo, BR-SP
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:29
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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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
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
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):
* United States - Requisition Number: R-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in High Wycombe, United Kingdom.
The Manager, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling ...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland
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
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):
* United States - Requisition Number: R-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in Allschwil, Switzerland.
The Manager, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling and target lab...
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Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:25
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
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):
* United States - Requisition Number: R-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager, Global Labeling Product Leader.
This position is a hybrid role and will be located in Beerse, Belgium.
The Manager, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeling and target labeling.
* Contri...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:25
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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:
Laboratory Operations
Job Category:
Business Enablement/Support
All Job Posting Locations:
Yokneam, Haifa District, Israel
Job Description:
About Johnson & Johnson MedTech Cardiovascular:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for a R&D Technician role, to join our team located in Yokneam, Israel.
Purpose: We are looking for a skilled and innovative technician to join our Haifa Tech Incubator team, working on the development of next-generation medical technologies.
This is a high-impact, hands-on role at the intersection of system integration, catheter technologies, and rapid prototyping in a fast-paced and multidisciplinary environment.
The ideal candidate is creative, detail-oriented, and experienced in both mechanical and electrical domains, with a strong passion for innovation and problem-solving in medical device development.
You'll be instrumental in transforming advanced research concepts into tangible, manufacturable solutions.
You will be responsible for:
* Assembly and soldering of miniature components and high-fidelity prototypes
* Support development of futuristic concepts and system-level integration
* Work closely with Haifa Tech Incubator engineers on fast prototyping and iteration
Qualifications and Requirements:
* Proven experience in electronics assembly and implementation, preferably in the medical device industry
* Skilled in micro-assemblies and precise manual work
* Strong soldering skills, especially with small components and fine wires
* Certification in soldering technologies – required
* Minimum 3 years of experience in electronics or hardware-focused companies
* Ability to manage multiple tasks simultaneously
* Str...
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Type: Permanent Location: Yokneam, IL-HA
Salary / Rate: Not Specified
Posted: 2025-09-08 08:06:07
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
Milano, Italy
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 an Experienced Specialist Local Medical Safety to be in Milan.
Purpose
We ensure that the local Pharmacovigilance (PV) system is handled in compliance with local regulations and company policies/procedures at local, regional, and global levels and in accordance with any PV agreements with third party business partners.
We support activities related to the pharmacovigilance regulatory requirements of Marketing Authorization Holders (MAH) and/or study sponsors, as applicable.
You will
Ensure the management of the local Pharmacovigilance (PV) system as described and in accordance with any PV agreements with third party business partners.
Ensure pro-active Benefit Risk Management throughout product life cycle by translating global safety data to insights and actions, and tailoring to local specificities and needs.
Conducting local benefit-risk activities to ensure pro-active benefit-risk management
Icsrs's management and oversight
Ensuring local collection, review, reporting, reconciliation, and follow up of Individual Case Safety Reports (ICSR) and implementation of the local literature process.
Maintain active involvement in day-to-day ICSR management related activities and maintain oversight of corresponding vendor activities as required.
Aggregate reports
Leading Preparation, review, tracking and timely submission of aggregate reports to all relevant local authorities or other official bodies, where applicable.
Local Safety compliance
Providing insights into ICSR inbound and outbound compliance metrics, perform ICSR reconciliations and leading actions as needed.
Acting as a CAPA content owner and subject matter authority, owning actions as required.
Performing or coordinating procedural document review and improvement, conducting impact assessments as required on l...
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Type: Permanent Location: Milano, IT-MI
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:52
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Plant Management
Job Category:
People Leader
All Job Posting Locations:
Woburn, Massachusetts, United States of America
Job Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for an Associate Director of Sensor Operations.
Purpose: The Sensor Operations Leader is a role targeted at improving the stability of J&J Heart Recovery's Sensor Supply, working closely with research and development team, supply chain and production operations.
You will be responsible for:
* Sustain a Patients First, winning culture of excellence in execution, continuous improvement, and communication within production facilities. Demonstrated ability to think globally.
* Manages other Managers, Supervisors, and/or individual contributors in a matrix environment, and is accountable for conducting effective performance management and meaningful career development conversations.
* Collaborates cross-functionally to coordinate Manufacturing Assembly improvement initiatives.
* Develop training programs to facilitate cross training of manufacturing personnel, employee development, and quality systems compliance.
* Ensure compliance with ISO13485, GMP, FDA, OSHA regulations
* Assure timely delivery of product per agreed-to build plan to internal and finished goods customers
* Monitor work, alter schedules to meet unforeseen conditions, control flow of work to ensure maximum use of available capacity and effective use of labor, tools and equipment
* Provide prompt problem solving for key issues, driving through from root cause identification, containment, problem resolution, and ensuring repeat issues are avoided
* Act as a team role model and change ...
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Type: Permanent Location: Woburn, US-MA
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:48
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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:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, 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 Technical Fellow (Director), Advanced Therapies - MSAT to be in Raritan, NJ, Titusville, NJ, Malvern, PA, or Spring House, PA.
Purpose:
The Technical Fellow serves as a subject matter expert (SME) in CAR-T manufacturing and Quality Control analysis, playing a pivotal role in ensuring the quality and safety of cellular therapies.
This position is critical in addressing challenges that arise when non-conforming products or deviations are generated during the manufacturing process, which can impact patient treatment.
The Technical Fellow actively engages with healthcare providers to navigate these challenges, facilitating clear communication and collaborative problem-solving.
In addition to direct interaction with healthcare providers, the Technical Fellow curates and analyzes manufacturing case studies to expedite the release of drug products.
This role requires deep expertise in key areas, including apheresis collection, cryopreservation, cell processing, quality control testing, and quality release processes.
The Technical Fellow provides insights to both internal manufacturing teams and external partners, ensuring adherence to the highest standards of quality.
The Technical Fellow is also an integral member of various site/network operational teams, including planning, release, clinical/commercial rapid response teams, safety management, and site escalations.
In this capacity, they contribute to the development of robust strategies that maintain the validated state of cell therapy processes while supporting lifecycle management initiatives involving new technologies, automation, and technology transfer.
Finally, this role serves as a key thought leader and scientific expert driving manufacturing trend investigation teams towards root c...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:36
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Non-Standard
Job Sub Function:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Contributes to assigned team at J&J.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:29
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, 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
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):
* United States - Requisition Number: R-020573
* Belgium - Requisition Number: R-021550
* United Kingdom - Requisition Number R-021551
* Switzerland - Requisition Number: R-021552
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager, Global Labeling Product Leader.
This position is a hybrid role and can be located in Raritan, NJ; Titusville, NJ; or Horsham, PA.
The Manager, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the supporting documentation.
Ensure high quality and compliant labeling documents.
* Contribute to and participate in the global labeling strategy, including demonstrating an understanding of competitors in the therapeut...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:26
-
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:
Nonclinical Safety
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, 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
Johnson & Johnson Innovative Medicine R&D is recruiting for a Distinguished Scientist, Nonclinical Safety Leader within Preclinical Sciences and Translational Safety (PSTS). This position is a hybrid role and will be located in Spring House, PA.
As a Distinguished Scientist, Nonclinical Safety (NCS) Leader, you will collaborate with innovative and diverse scientists to support projects in our large and varied portfolio that spans multiple therapeutic areas and includes innovative modalities. In this vital role you will provide toxicology leadership for all aspects of discovery and development projects, with flexibility to specialize or work across stages of development, therapy areas, and modalities. You will also collaborate with discovery scientists to identify and nominate candidate molecules, and with development teams to bring these molecules to humans and ultimately through global registration.
Principal Responsibilities:
* Lead PSTS project teams of nonclinical safety and Pharmacokinetic (PK) scientists, ensuring efficient information transfer within the team.
* Serve as the NCS representative for global project teams, providing toxicology expertise and interfacing with senior management.
* Create target risk assessments and develop plans to screen for and mitigate potential risks; analyze toxicology and safety pharmacology studies, contextualizing results for human safety and preparing nonclinical safety assessments.
* Contribute to issue-resolution teams by generating hypotheses and investigative strategies.
* Accountable for global regulatory nonclinical documents and health authority responses to support clinical trials and compound registrations.
* Participate in medical safety teams, signal detectio...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:24
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Hangzhou, Zhejiang, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
â¢Â      Actively identify, develop, and engage key KOLs at regional level.
â¢Â      Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
â¢Â      Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
â¢Â      Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
â¢Â      Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
â¢Â      To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
â¢Â      To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
â¢Â      To organize and moderate advisory boards in cooperation with TA groups.
â¢Â      To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
â¢Â      To collect insights from external customers and feedback timely to shape Brand/medical strategy    Â
Scientific Communication Effectiveness with external/internal customers
â¢Â      To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
â¢Â      To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
â¢Â      Support medical affairs program and activities at local and regional level.
â¢Â      Ensure program implementation 100% in compliance.    Â...
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Type: Permanent Location: Hangzhou, CN-33
Salary / Rate: Not Specified
Posted: 2025-09-08 08:05:20
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Quality Control Inspector
Location: Houston, Texas
Overview:
Bray International is seeking a skilled Quality Control Inspector to join our team in a fast-paced industrial manufacturing environment.
If you are passionate about ensuring product quality and have at least four years of experience in quality inspection, we encourage you to apply.
This is an exciting opportunity to contribute to a leading company in the industrial valve and actuator industry.
Key Responsibilities:
* Perform incoming inspections on purchased parts, subassemblies, and finished products to ensure compliance with engineering drawings and customer standards.
* Review Material Test Reports (MTR) and Certificates of Conformance (CofC) against relevant standards.
* Analyze Non-Conformance Reports (NCR) to identify trends and generate Corrective Action Reports (CAR) as needed.
* Create Non-Conformance Reports and other departmental reports as assigned.
* Evaluate issues and make initial recommendations for corrective actions to supervisors.
* Investigate failures to determine root causes and propose remedial actions.
Qualifications:
* Minimum of four years’ experience in quality control within the industrial manufacturing sector.
* Experience with Positive Material Identification (PMI) preferred.
* Proficient in computerized record-keeping and standard software applications.
* Strong written and verbal communication skills.
* Skilled in using and calibrating precision measuring equipment (e.g., micrometers, height gauges, calipers, dial indicators, bore gauges).
* Knowledge of ISO 9001:2008/2015 and API standards.
* Ability to analyze and determine the best inspection methods for product conformity.
* Proficient in interpreting engineering drawings and understanding Geometric Dimensioning and Tolerancing (GD&T).
* Experience with Coordinate Measuring Machines (CMM).
* Ability to manage multiple tasks in a fast-paced environment while meeting delivery requirements.
* High School Diploma or equivalent required.
Physical Demands:
* Must have 20/20 vision (correctable) without color blindness.
* Ability to lift up to 20 pounds.
Note: Immigration sponsorship is not offered for this position.
Why Work for Us?
At Bray International, we are a global leader in providing industrial valves, actuators, and related control products.
We are known for our innovative flow control solutions and are looking for individuals who share our commitment to excellence, integrity, and collaboration.
What We Offer:
* Career Growth: We offer numerous opportunities for advancement within the organization.
* Comprehensive Benefits: Enjoy benefits such as:
+ Life, medical, dental, and vision insurance
+ Paid holidays and vacation
+ 401(k) plan with matching contributions
* Healthy Work Environment: We provide a smoke-free, drug-free workplace to ensure a sa...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-07 08:13:52
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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: Senior Research Scientist, Non-Clinical Safety & Toxicology
We are seeking an experienced non-clinical toxicology / safety scientist to join the Global Non-Clinical Development team in Global Clinical Development.
As the Senior Research Scientist, Non-Clinical Safety & Toxicology you will be responsible for, or will assist with, human (user & consumer) safety and target animal safety program strategy and execution at all phases of global veterinary pharmaceutical drug/product and feed additive research and development, product safety assessments, and support for marketed products.
This role applies toxicology and immunology expertise to assess safety risks across the full product lifecycle, from early development through commercialization.
Responsibilities include evaluating potential safety concerns related to product design, manufacturing changes, deviations, or consumer complaints that could impact animal safety or end-user health.
The role involves preparing Product Safety Assessments (PSAs) for products in development, production, or on the market, and compiling medical and toxicological data to assess potential health risks for consumers and end users.
Your Responsibilities:
* Independently design, organize, monitor, report, and resolve issues related to outsourced in vitro and in vivo safety/toxicology studies, utilizing external CROs and/or consultants as needed.
These studies may involve typical rodent and non-rodent species.
Target animal safety evaluations may include companion animals (dogs and cats) as well as food-producing animals (e.g., cattle, pigs, chickens).
* Conduct literature reviews and author expert reports, position papers, safety and hazard/risk assessments, and other strategic scientific, technical, or medical evaluations to address safety considerations for veterinary drugs (small molecules and biologics), feed additives, excipients, E&L substances, impurities, or other chemicals.
* Provide internal expert guidance, including expert statements, health-based exposure limits (e.g., PDEs, OELs...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-07 08:10:19
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program..
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Adell, Wisconsin facility and after 60 days of training, would support the New Holstein, WI and Boscobel, WI facilities.
Position would be based out of Adell.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits
* Maintain required wastewater discharge permits, renewals, and related documentation.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager. Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs. Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks. Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations. Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corp...
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Type: Permanent Location: Norfolk, US-NE
Salary / Rate: Not Specified
Posted: 2025-09-07 08:05:06
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Nous sommes à la recherche d’un·e Chef d’équipe – Assurance Qualité Logicielle pour rejoindre notre équipe dynamique.
Relevant directement du Vice-président à la Recherche et au Développement, vous jouerez un rôle central dans l’assurance de la qualité, de la fiabilité et de la performance de nos produits.
À la tête d’une équipe composée de 5 spécialistes QA, vous serez responsable de l’encadrement, de la motivation et du développement professionnel de vos collaborateurs.
Vous veillerez à la mise en œuvre et au respect des meilleures pratiques de l’industrie en matière d’assurance qualité.
Vous superviserez l’ensemble des processus de tests automatisés, assurerez le maintien d’une pyramide de tests équilibrée et garantirez que chaque nouvelle version de nos produits respecte nos standards d’excellence.
Votre objectif : des livraisons impeccables, à chaque fois.
Responsabilités principales:
* Assumer la responsabilité complète de la qualité des livraisons logicielles.
* Définir et implanter les meilleures pratiques de l’industrie en matière d’assurance qualité logicielle.
* Élaborer et mettre en œuvre des stratégies de test robustes, incluant une pyramide de tests bien équilibrée (tests unitaires, d’intégration, end-to-end, etc.).
* Superviser l’équipe QA : définir les objectifs, évaluer les compétences, identifier les besoins de développement et soutenir la croissance professionnelle des membres.
* Identifier, documenter et suivre les anomalies et défauts logiciels.
* Collaborer étroitement avec les équipes de développement, produit et opérations pour résoudre les problèmes et améliorer les processus.
* Assurer la conformité aux normes de qualité internes et externes.
* Réaliser des tests de performance, de sécurité, de compatibilité et de régression.
* Produire des rapports de test clairs et formuler des recommandations pour l’amélioration continue.
* Prioriser les éléments à automatiser dans le cadre du processus CI/CD (intégration et déploiement continus), incluant les tests QA, afin d’assurer des livraisons fiables jusqu’en production.
Qualifications requises:
* Minimum de 10 ans d’expérience en assurance qualité logicielle, dont plusieurs années dans un environnement Agile/DevOps.
* Diplôme en informatique, en génie logiciel ou dans un domaine connexe.
* Expérience significative en assurance qualité logicielle, idéalement dans un environnement Agile/DevOps.
* Maîtrise des méthodologies de test (manuelles et automatisées) et des outils associés.
* Solides compétences en gestion d’équipe, leadership et communication.
* Capacité à travailler sous pression, à gérer les priorités et à respecter les échéanciers.
* Une bonne maîtrise du français et de l’anglais est requise car le titulaire du poste aura à communiquer fréquemm...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-09-06 08:34:29
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A division of Harris, InHANCE is seeking a highly motivated and skilled Business Development Representative to join our dynamic team and drive the growth of our software in the utility market.
As a market leader in utility management solutions, we provide innovative software that optimizes billing processes, enhances customer self service, and improves utility management efficiency.
This remote role welcomes candidates anywhere in Canada and the US.
Up to 25% of travel within the United States is required for demos and trade shows.
Candidates based in Canada must hold a valid passport to travel.
What your impact will be:
* Reporting to the Director of Sales & Marketing, the Business Development Representative will be responsible for generating a healthy pipeline of inbound prospects and converting the prospects to customers, as well as proactively seeking outbound opportunities to drive revenue to exceed sales targets.
* In performing this role your core duties and responsibilities will include (but will not be limited to):
* Identify and target potential customers within the specified water utility sector to expand our customer base and overall market presence.
* Research and analyze the utility industry to understand market trends, customer needs, and competitive landscape.
* Develop and implement effective business development strategies to generate leads, nurture prospects, and close deals.
* Cultivate strong relationships with key stakeholders, including utility companies, municipalities, local governments and utility management agencies.
* Conduct product demonstrations and presentations to showcase the value of our utility solutions.
* Collaborate with the marketing and sales teams to develop compelling marketing materials, campaigns, and sales pitches.
* Represent the company at industry events, conferences, and trade shows to promote our software and network with potential clients and partners.
* Negotiate contracts and agreements with clients, ensuring a win-win outcome for both parties.
* Stay updated on industry regulations, technological advancements, and best practices to ensure our software remains competitive and relevant.
* Manage all lead and opportunity data within the Salesforce CRM solution.
* Provide regular reports on sales performance, market insights, and business development activities to the management team.
What we are looking for:
* Proven track record in business development, sales, or a similar role, with 5+ years of direct experience selling to municipalities and local government.
* Proven track record of self generating leads and pipeline.
* Excellent communication, negotiation, and presentation skills.
* Ability to build and foster strong relationships with clients and partners.
* Self-driven, proactive, positive, and goal-oriented mindset with the ability to work independently and as part of a team.
* Hunter ...
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Type: Permanent Location: Springfield, US-IL
Salary / Rate: Not Specified
Posted: 2025-09-06 08:34:27
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At Elanco (NYSE: ELAN) â 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.
Weâre driven by our vision of âFood and Companionship Enriching Lifeâ and our approach to sustainability â the Elanco Healthy Purpose⢠â 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, youâll 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 animalsâ lives better makes life better â join our team today!
Role: Principal Data Scientist
Responsibilities:
* This role supports the needs of the Global Analytics & Insights team, part of the Corporate Strategy Team, with a focus on providing Advanced Analytics (to include statistical modeling, regression analyses, market basket, churn modelling methods) to work on program/promotion design and ROI post program.
Additional project-based work around price elasticity, mixed market modelling, segmentation, game theory modelling and predictive analytics (e.g., customer lifetime value) will be in scope.
The overarching goal of all work will be to find efficiencies in current promotional spend and optimize future business activities.
* This position is responsible for managing all aspects of project-based analyses including data preparation, analysis design, implementation using appropriate methods & results presentation.
* Leading readouts and review with internal customers.
* Lead discussions with customers to uncover needs, design and deliver analytics solutions.
Enable measurement and improved effectiveness of rebates, media spend, pricing and sales force activities leveraging statistics and data science techniques.
* Collaborate with internal stakeholders, descriptive analytics team and cross-functional teams to solve business problems, propose efficiencies and innovative approaches.
* Constantly innovate in data science domain, constantly bringing new expertise to the team and adding to team knowledge
* Guide the junior members on technical and functional aspects, problem formulation, approach design, model building, model refinement and selection, reviewing and storyboarding the results.
* Consistent, constant alignment with all members of team in Greenfield, Indiana.Â
* Maintain an environment open to change and innovation, recognizing improvements in existing tools and anticipating new technologies to deliver world class analytics and maximize effectiveness
Minimum Qualification:
* Education: Bachelorâs Degree in quantitative or management field.
(Masterâ...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-09-06 08:33:39
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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 /Environmental Monitoring Technician
Environmental Monitoring / QC Technician Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine environmental monitoring of the manufacturing facilities and associated utilities, as well as microbiology analysis.
Your Responsibilities:
* Conducts Environmental Monitoring: Performs routine and non-routine sampling of manufacturing environments (air and surfaces) and utilities (WFI, USP Water, Pure Steam, Clean Compressed Air).
Maintains gowning qualifications for sterile environments.
* Ensures cGMP Compliance: Upholds cGMP, safety, and environmental standards within the QC lab, generating accurate and compliant data.
Participates in internal assessments and audits.
* Performs Microbiological Testing: Executes routine and non-routine analyses of raw materials, in-process materials, finished goods, and stability samples.
Conducts a variety of microbiology tests, including bioburden, sterility, and microbial identifications.
* Supports Investigations and Deviations: Assists in the investigation of out-of-specification/out-of-trend results, environmental monitoring excursions, and deviations.
Contributes to the preparation of Certificates of Analysis.
* Develops and Maintains QC Methods: Assists in developing, qualifying/validating, and transferring new test methods.
Contributes to the writing and revision of testing methods, specifications, SOPs, and validation protocols/reports.
Maintains lab inventory and performs routine equipment maintenance and cleaning.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma/GED with 5years experience, BA or BS degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or closely related field, or comparable experience.
* Experience: Technical skills in Environmental Monitoring to include, but not limited to, monitoring of manufacturing environment and utilities.
* Excellent c...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 27
Posted: 2025-09-06 08:33:37
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EHS Leader
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Position Summary:
Provide functional leadership to ensure the KCPX Pilot Facility implements EHS (Environmental, Health & Safety) systems that meet Kimberly-Clark Best Practices and federal and state regulatory requirements.
The incumbent will provide leadership for continuous improvement in all EHS activities in support of achieving a loss-free environment.
In this role, you will:
* Provide leadership in safety and environmental loss prevention.
This requires establishing strategies and processes that directly support the implementation of the EHS Maturity Model program deliverables.
* Responsible for implementing strategies & initiatives that achieve site EHS objectives and results in the continuous improvement of site EHS processes.
* Create and foster programs that lead to the creation of a culture where safety is recognized as a value and team members are motivated to develop and to use safe work habits.
* Benchmark and implement Leader Standard Work and other KC site EHS best practices.
* Ensure site compliance with Wisconsin OSHA, EPA, NFPA, and other federal and state mandated safety regulations.
* Lead the team that implements site-wide safety and environmental initiatives which will include such programs as hazardous energy control, machine safeguarding, ergonomics, risk reduction strategies and other EHS programs as required to reach safety objectives.
* Identify, evaluate and coordinate implementation of new methods and approaches to accelerate safety and environmental improvement at the KCPX facility.
* Lead incident investigations at site and ensure 4-step problem solving is followed and root causes are identified with assignable corrective actions.
* Lead the site EHS Steering Committee meetings
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by Yo...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-06 08:31:14
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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. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) process.
...
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Type: Permanent Location: Kansas City, US-MO
Salary / Rate: Not Specified
Posted: 2025-09-06 08:30:08
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The Missons, Concepts and Capabilities (MCC) division of Applied Research Associates, Inc.
(ARA) is looking for a Chemical Analyst.
This position provides operational, research and development, and training support along with subject matter expert advice and decision support to the Defense Threat Reduction Agency (DTRA) as part of its 24/7/365 Technical Reachback Support program.
The ideal candidate will apply subject matter expertise and problem-solving skills to develop, integrate, test, verify, validate, and apply Chemical, Biological, Radiological, Nuclear, and (high yield) Explosives (CBRNE) software/scenarios based on experiments and predicted phenomena using theoretical and computational methods.
The candidate will work closely with other members of the multi-disciplinary Reachback team.
Required tasks include performing complex engineering, scientific modeling and analyses, providing scientific reports, and technical assessments to military decision makers.
Each Technical Reachback team member is cross trained on all models and undergoes a rigorous certification process on the use of our CBRNE models before becoming an active member of the Reachback team.
The successful candidate will be team-oriented and possess strong multi-tasking abilities.
In addition, this position requires the use of models in all areas of CBRNE.
Tasks also include the presentation of modeling results and decision support aids to both internal and external customers in the form of written reports and oral presentations.
* Reviewing current research in various and potentially diverse subject areas for familiarity and relevance
* Providing general knowledge and chemical-related subject matter expertise to government agencies and first responders
* Assisting in the development of program plans, timelines, and technical documents
* Attending technical and programmatic meetings in which you coordinate responses from scientific community members and review the assembled materials for technical accuracy, consistency, and completeness
* Willingness to be cross-trained to provide modeling and information across the CBRNE spectrum
Required Qualifications:
* MS in Chemistry or a related field with a minimum of 3 years of experience
* Able and willing to work rotating shifts (every three months) in support of 24/7/365 operations
* Must be a US Citizen
* Hands-on experience using computer-based software to develop structurally sound and comprehensive models that account for all structural components
* Active US DoD Secret or Top Secret clearance
* Strong communication skills, both orally and verbally, technical presentation, teamwork mentality, graphic visualization, and Microsoft Office proficiency skills
Desired Qualifications:
* Experience working with organizations within DTRA or the DoD as well as other government agencies
* Experience in Combating Weapons of Mass Destruction (WMD) threats or CBRN threa...
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Type: Permanent Location: Fort Belvoir, US-VA
Salary / Rate: Not Specified
Posted: 2025-09-06 08:23:40
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Applied Research Associates, Inc.
(ARA) is seeking a Staff Scientific Data Analyst to join the Health Effects, Analytics, Risk, and Technology (HEART) located in Raleigh, NC.
The candidate will support physiological modeling for exposure risk assessment in support of the National Institutes of Health (NIH) Division of Program Coordination, Planning, and Strategic Initiatives (DPCPSI).
The successful candidate will be on a new team supporting the NIH DPCPSI Office of Research Innovation, Validation and Application (ORIVA).
Working at ARA, there will be opportunities to work with a multi-disciplinary team focused on toxicology, physiological modeling, and risk assessment.
Responsibilities include but are not limited to:
* Data development, analysis and evaluation, including cleaning and analyzing data and utilizing methods (e.g., knowledge graphs to explore chemical-biological effect relationships).
* Routinely review, evaluate, curate, and integrate data from relevant databases (e.g,NCATS N3C, NCI CRDC, ToxRefDB, ToxCast, ExpoCast, DSSTox, CEBS, IUCLID, MassIVE and others).
* Ensure data integrity including preparing program guidelines, performing necessary data checks and managing datasets and data documentation.
* Ensure customer satisfaction by providing high quality deliverables and anticipating needs.
Position Requirements:
* Masters in bioinformatics, mathematics, statistics, computational linguistics, computer science, data science, or other relevant field with 4 years or PhD with 0 years.
* Expertise in NAMs or a related scientific field.
* U.S.
Citizenship Required.
* Capable of fundamental programming for data analysis, survey data analysis, and data management.
* Providing quality assurance on deliverables and timely delivery.
* Excellent verbal and written communications skills.
COMPANY INFORMATION:
Applied Research Associates, Inc.
is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems in the physical sciences.
The company, founded in Albuquerque, NM, in 1979, currently employs over 2,353 professionals and continues to grow.
ARA offices throughout the United States and Canada provide a broad range of technical expertise in defense technologies, civil technologies, computer software and simulation, systems analysis, environmental technologies, and testing and measurement.
The corporation also provides sophisticated technical products for environmental site characterization, pavement analysis, and robotics.
At ARA, employees are our greatest assets.
The corporation realizes that employee ownership spawns greater creativity and initiative along with higher performance and customer satisfaction levels.
ARA gives employees the tools, training, and opportunities to take more active roles as owners.
The culture is challenging and innovation and experimentation are the norm.
Emplo...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-06 08:20:48
