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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:
Beerse, Antwerp, Belgium, Leiden, Netherlands
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-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
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 Director, Global Regulatory Leader.
This position is a hybrid role and can be located in Beerse, Belgium or Leiden, Netherlands.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Profile (for global programs as assigned).
* In interacting with the Health Authorities, lead and/or participat...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:07
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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:
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-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
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 Director, Global Regulatory Leader.
This position is a hybrid role and will be located in High Wycombe, United Kingdom.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Profile (for global programs as assigned).
* In interacting with the Health Authorities, lead and/or participate in meet...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:06
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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:
Istanbul, Turkey
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 Medical Safety Specialist.
This position will be located in Istanbul, Turkey.
Essential Job Duties and Responsibilities
The position is responsible for supporting the compliance of LOC Safety activities of TURGAN cluster by mainly focused on Turkiye, covering medicinal products, with local regulations, company policies, and global standards, including any Product vigilance agreements with third-party partners.
It involves assisting in establishing and maintaining effective Pharmacovigilance and Risk management systems and supporting the oversight of the products within its responsibility.
The role includes contributing to the proactive management of Benefit Risk Management throughout the product life cycle, tailoring actions to local needs.
Additionally, it involves aiding in safety reporting requirements as needed by Marketing Authorization Holders (MAH) and study sponsors, as applicable.
Safety Management & Reporting
Oversight and Providing Input
* Support Data-generating Activities: Assist in overseeing data-generating activities to ensure appropriate review and reporting processes are included in project documents for reporting potential Adverse Events (AEs), such as patient support programs, market research surveys, and internet sites, as applicable.
Provide support to the Hub for Related Research Activities (RRA) activities, where applicable.
* Vendor Contracts: Ensure, in collaboration with the Hub if applicable, that all vendor contracts have appropriate Pharmacovigilance language incorporated and that these contracts are archived in the global system, as applicable.
* Product Portfolio Oversight: Support the oversight of the full product portfolio and establish links with local management and key stakeholders.
Assist in overseeing the safety ...
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Type: Permanent Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:18
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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:
Manufacturing Engineering
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
Johnson and Johnson Innovative Medicines is recruiting for the Advanced Therapies Manufacturing Science and Technology (MSAT) organization! We are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
Are you interested in joining a team that is positively impacting patients' lives by growing and scaling our high quality cell and gene therapy products? Apply today for this exciting opportunity to be part of the team!
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-031792
Belgium: Requisition Number: R-032748
RESPONSIBILITIES:
This is a hybrid/remote role available in multiple cities within the United States or Belgium.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from any location to apply.
The Head, Lifecycle Management is accountable for the lifecycle of products for the MSAT advanced therapies organization.
This role provides technical and strategic leadership in support of a broad set of technology initiatives to enable new product manufacturing modalities, manufacturing technology, process control, process understanding, facility design, and network strategy. They are responsible for leading global cross-functional and cross-sector teams to develop and implement high value technical solutions for growth, reliability, compliance and efficiency of product value chains end-to-end through cutting edge solutions and insights.
ESSENTIAL FUNCTIONS:
* Own the advanced therapies product technology roadmaps; lead cross-functional and cross-sector teams in the strategic development of high value solutions required to achieve goals in technology, science, faciliti...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:16
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
The Lead Clinical Data Manager will be responsible with leading all aspects of clinical data management associated with data cleaning and quality review processes for assigned projects.
S/he ensures clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets.
POSITION DUTIES & RESPONSIBILITIES:
Reporting to the Manager, Data Management this individual will:
* Mentor, train and supervise junior associates as needed in clinical data management processes and procedures
* Independently lead several complex trials
* Lead CRF design, review and validation of clinical database, including management of CRO activities in this area as assigned if required
* Be responsible for creation of data management plans and other data management documentation as needed
* Monitor progress and conduct of their respective projects, including all data cleaning and QC activities to ensure all remain on target to project timelines partnering as appropriate with Clinical Operations, Franchise and other BSDM functions
* Lead, coordinate, facilitate and manage all data management activities from initiation of protocol through database lock, partnering as appropriate with Clinical Operations, Franchise and other BSDM functions for their respective projects
* Proactively organize and manages ongoing data review throughout study conduct, including being responsible for the correction of errors and discrepancies management for the life of a project
* Proactively identify and address issues that may impact the quality of the data, deliverables or timelines
* Be responsible for identification of data handling processes for non-CRF data, including lab data and image handling
* Work with BSDM leadership, and leadership in Clinical Operations and Franchise to develop project management plans for trial execution including timelines milestones and budgets
* Lead efforts co-ordinating with Medical Affairs organization to facilitate data coding and safety reviews as needed
* Independently lead new data management initiatives and contribute towards process improvement, data standards and efficiency gaining initiatives within data...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:54
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Customer Management
Job Sub Function:
Technical Field Service
Job Category:
Business Enablement/Support
All Job Posting Locations:
Kansas City, Missouri, United States, Santa Ana, California, United States of America, Springfield, Missouri, United States
Job Description:
Johnson and Johnson Vision is recruiting for a Field Specialist.
The position will be located in Kansas City/Springfield, MO.
This position will require frequent travel on short notice.
Candidate must reside in the Kansas City / Springfield, MO.
or surrounding areas.
Candidate must have the ability to work in home office 25% & in field 75%.
Valid US Driver’s license required.
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.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Under limited supervision and in accordance with all applicable federal, state, and local laws and regulations, as well as Johnson & Johnson corporate procedures and guidelines, this position will be responsible for the following:
RESPONSIBILITIES:
* Provides technical support to physicians, nurses and other medical professionals on company products and services.
* Installs, maintains, and repairs complex electro-mechanical medical lasers and oth...
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Type: Permanent Location: Santa Ana, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:43
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Jacksonville, Florida, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Tampa, Florida, 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-027240
* Toronto, Canada - Requisition Number: R-029840
* United Kingdom - Requisition Number R-029838
* Belgium, Spain - Requisition Number: R-029842
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 Clinical Operations Learning and Training.
This position is a hybrid role and can be located in Spring House, NJ; Horsham, PA; Raritan, NJ; Titusville, NJ; San Diego, CA; Jacksonville, Florida; Tampa, Florida.
The Clinical Trial Learning and Training (CTLT) organization develops and implements training strategies and designs for clinical trial training and Global Clinical Operations (GCO) functional role-based global onboarding programs.
This includes determining training needs, developing, and implementing strategic learning initiatives, and leveraging resources to deploy the training plan.
CTLT delivers impactful learning and training programs that address gaps and build capabilities to meet future needs while ensuring compliance with relevant Regulations, Standard...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:42
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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:
Supplier Quality
Job Category:
Professional
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
Abiomed, part of Johnson & Johnson MedTech, is recruiting for a Supplier Quality Engineer II to be located in Danvers, MA.
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
Abiomed, part of Johnson & Johnson MedTech, is a leading provider of medical devices that provide circulatory and respiratory support, with a mission of recovering hearts & saving lives.
Abiomed’s “Patients First!” culture drives our skilled workforce and strong relationships with clinicians.
Our innovative product portfolio and robust pipeline provide us the incredible opportunity to bring lifesaving technology to more patients around the world than ever before.
Founded in 1981, Abiomed has a proven track record for growth, integrity and innovation.
I Am Abiomed | I Am Heart Recovery | Patients First!
ABIOMED is redefining success while reshaping heart recovery.
Here, new ideas are welcomed and encouraged, learning is constant, and our dynamic setting enables positive people to do profoundly important work.
The Supplier Quality Engineer II is responsible for cross-functional Quality Assurance, Quality Management/Compliance and activities associated with all Abiomed products and processes with a focus on supplier for the Danvers plant.
This role involves hands-on project management, collaboration with multi-functional teams, and ensuring that supplier qualification processes align with quality standards and company objectives.
Primary Duties and Responsibilities:
* Develop and implement Supplier qualification plans, including risk assessments, quality audits, and performance evaluation
* Establish and communicate clear quality standards and criteria for new suppliers
* Collaborate with engineering and procurement teams to define specifications and expectations for supplier performance
* Develop project plans outlining milestones, timelines, and resource requirements for new supplier qualification projects
* Implement projects efficiently, ensuring alignment with overall business objectives an...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:42
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Jinan, Shandong, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• 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.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• 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.
• 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.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance. ...
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Type: Permanent Location: Jinan, CN-37
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:39
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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:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, 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-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
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 Director, Global Regulatory Leader.
This position is a hybrid role and can be located in Titusville, NJ; Raritan, NJ; or Spring House, PA.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Pr...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Planning
Job Sub Function:
End-to-End Planning
Job Category:
People Leader
All Job Posting Locations:
Diegem, Flemish Brabant, Belgium
Job Description:
Johnson & Johnson is currently seeking “Global Supply Network Planning Manager” join our TEAM.The role is based in in Belgium (Diegem), Germany ( Norderstedt) , India (Pune), Brazil (San Jose Dos Campos) and Mexico (Juarez).
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/.
About J&J MedTech
At Johnson & Johnson MedTech, we unleash diverse healthcare expertise, purposeful technology, and a passion for people to transform the future of medical intervention and empower everyone to live their best life possible.
For more than a century, we have driven breakthrough scientific innovation to address unmet needs and reimagine health.
In surgery, orthopedics, vision, and interventional solutions, we continue to help save lives and create a future where healthcare solutions are smarter, less invasive, and more personalized.
Summary
The Global Supply Network Planning Manager is responsible for network planning, managing and delivering accurate worldwide demand and replenishment forecasts, service levels and inventory for all value streams sourced out of the assigned Region / Manufacturing Site.
You will provide leadership and guidance on the demand and supply planning processes that drives cost-effective stock availability.
Key Responsibilities
* Manages the global service levels to customers and drives the inventories to entitlement levels.
Responsible for achieving on time in full (OTIF) at allocation targets and driving continuous improvements in this area.
* Responsible for achieving backorder targets and driving continuous improvements in this area.
* Leads different Sales and Operations Planning Process or S&OP meetings (Supply and Demand focused end-to-end Planning) for the Value Streams assigned.
* Responsible for ide...
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Type: Permanent Location: Diegem, BE-VBR
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:35
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Human Resources
Job Sub Function:
Health Services
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
OCCUPATIONAL HEALTH PHYSICIAN / Emerging Occupational Health Leader – Internal prevention service Janssen Pharmaceutica NV
Location: Based at Beerse, Belgium
Contract: Full Time
Johnson and Johnson, Janssen Pharmaceutica NV has an exciting opportunity for an occupational health physician or emerging OH leader to join our world class internal employee health and wellbeing community, based in Beerse, Belgium.
Johnson and Johnson is one of the most innovative Pharmaceutical and Medtech companies in the world. With over 6300 employees across Belgium, our national, multi-location service serves our world class community across J&J in Belgium.
Working with us as part of J&J in the Benelux, you’ll be part of an organization which is the no.
1 investor in pharma R&D and no.
1 private investor in R&D in all industries.
Our top capabilities include early product development, manufacturing, logistics, patient access, and commercialization as well as full suite of corporate, supportive functions.
As a healthcare company and to support our high-performance thriving teams, we take the health and wellbeing of our employees very seriously.
To drive health protection, wellbeing support and proactive healthy performance, our team is recruiting an extra occupational health physician or emerging Occ Health leader.
The responsibilities & the impact YOU will have:
* You join a team of doctors and nurses where focus on qualitative service delivery and compliance with local regulations and J&J policies is key.
* You are an occupational health physician with interest in a broad variety of occupational health risks and are eager to contribute to and support the mental wellbeing and high performance of our world class employees.
* We are excited to hear from an emerging or aspirational OH team leader, especially if you have the desire to learn and become our next departmental or national service leader
* Alongside the execution of our medical surveillance programs, you give direction and support the team during emergency interventions.
* You contribute to the ongoing evolution of our critical employee support processes and first-class work practices related to medical surveillance, reintegration after illness, emergency response or m...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:34
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Strategy & Corporate Development
Job Sub Function:
Change Management
Job Category:
Professional
All Job Posting Locations:
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
We are searching for the best talent for an Associate Director, Global Development Strategy & Operations to be based in Titusville, NJ.
Purpose:
The Associate Director, Global Development (GD) Strategy & Operations, is responsible for assisting with planning and coordinating GD business operations communications.
They will liaise with communications stakeholders to ensure a coherent and aligned strategy across the organization.
They will be accountable for equipping people managers and employees within GD with clear communications – written and in live forums – regarding topics that include business operations updates, goal-setting, process and procedures, and beyond.
They will also provide additional support to the Director as needed.
This role will partner with appropriate stakeholders, including the GD Global Communications Leader, GD Strategy & Operations Leader, and Business Growth, Innovation & Advocacy Head, to help develop and align on a holistic internal and external communications strategy, approach and plan that supports the overall GD goals and objectives, embeds change, strengthens culture, and implements key ways of working.
This role will partner with other stakeholders and functions as needed to help drive clarity and efficiencies across the communications continuum.
The Associate Director, GD Strategy & Operations, will be responsible for drafting high-quality, engaging content for various internal channels, including websites, newsletters, and other avenues as needed, ensuring consistent messaging and branding across all platforms.
They will also be accountable for managing distribution lists and maintaining standards for internal communication.
This role will also contribute to establishing metrics and key performance indicators ...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:32
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biological Research
Job Category:
People Leader
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
We are searching for the best talent for an Associate Director, Cellular & Mechanistic Pharmacology located in Spring House, PA.
Purpose: Translational Bioscreening is a newly formed team within the Multiomics Discovery function of Discovery Technologies & Molecular Pharmacology (DTMP).
We contribute to the progression of cross-modality drug discovery projects from target identification to clinical development.
Join our team! We’re looking for a talented scientific leader with an immunology background, deep expertise in disease biology and cellular pharmacology, and a passion for finding innovative therapeutics to treat diseases with high unmet medical need.
You will be responsible for:
* Lead development of innovative cell-based assays for immunology-focused projects to identify and evaluate targets, and to progress hits and lead molecules.
* Act as a key liaison between DTMP and program teams, driving project strategy and execution, in partnership with cross-functional colleagues.
* Lead efforts to integrate translational and mechanistic biology with novel AI/ML methods to enable the discovery of novel therapeutics
* Manage and mentor a team of lab scientists.
* Analyze and present data at program team meetings, in-house seminars, leadership meetings and external scientific conferences, and publish research in high-quality journals.
Qualifications/Requirements:
Education:
* Ph.
D.
in Immunology, cell biology or equivalent with a minimum of 8 years of experience in a pharmaceutical industry setting developing and applying novel cellular assays is required.
Experience/Skills:
Required:
* Proven track record in leading immunology-focused drug discovery programs across diverse modalities, in an industry setting.
...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:30
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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:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
* Business Improvements ä¸å¡æ¹è¿
* Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
* æ¯æè´¨éæ¹è¿æ´»å¨ï¼å¯¹äº§å/è¿ç¨è¿è¡æç»æ¹è¿åææ¬æ¹åã
* Review/analyze the effectiveness of PDCA, Six Sigma, Kaizen, Lean Techniques and/or other improvement tools and programs.
* è¯ä¼°ååæè´¨éå·¥å
·å项ç®çæææ§ï¼æ¯å¦PDCAï¼å
è¥¿æ ¼çï¼æ¹åï¼ç²¾çææ¯å/æå
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* Conduct benchmarking to develop more effective methods for improving quality.
* éè¿æ æ管çå¼åæ´ææçè´¨é管çæ¹æ³æåè´¨éã
* Supports the development of quality engineering and quality compliance with the right skill sets for new product introductions, and product life cycle management.
* å¼ååéçè´¨é管çæ¹æ³åºç¨äºè´¨éå·¥ç¨åè´¨éåè§çåå±ï¼è¿ç¨å¨æ°äº§å导å
¥å产åçå½å¨æ管çã
* Compliance/Regulatory åè§ç®¡ç
* Review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards such as the QSRs, ISO 13485, etc.
* è¯ä¼°ååæç°æ产ååå¶ç¨æ¯å¦åè§ï¼æ¯å¦QSRsï¼ISO13485çæ³è§è¦æ±
* Champions compliance to applicable Global Regulations and standards (e.g.
QSRs, ISO, EN and Medical Device Directive (MDD) requirements) including providing support during internal and external audits.
* æ¯æå·¥åçå
å¤é¨å®¡æ ¸ï¼éµå®éç¨çæ³è§åæ å(ä¾å¦QSRs, ISO, ENåMDD)è¦æ±ã
* Conduct periodic line audits to assess for production controls such as lot segregation. Review results of area audits to ensure that corrective and preventive actions are adequate.
* æ§è¡å¨æå®¡æ ¸è¯ä¼°ç产ç°åºæ¯å¦åè§ã审é
åºåå®¡æ ¸çç»æç¡®ä¿çº æ£åé¢é²æªæ½ææã
* New Product/Process Introduction æ°äº§å/å¶ç¨å¯¼å
¥
* Partners with R&D and other cross functional partners to ensure the proper application of design controls, risk management and the investigation/correction of design failures/challenges.
* åè°ç ååå
¶ä»çè·¨é¨é¨åä½ç¡®ä¿ç¸å
³é¢åè´¨é管çå¯æ§ãæ¯å¦è®¾è®¡ç®¡çï...
....Read more...
Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:15
-
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 ...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:02
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Cuxhaven liegt direkt an der Nordsee, der Elbe sowie am Nationalpark Wattenmeer (UNESCO Weltnaturerbe) und ist das größte deutsche Seeheilbad.
Mit einem stark wachsenden Tourismus (mehr als 4 Millionen Übernachtungen pro Jahr) gehört Cuxhaven zur Metropolregion Bremen / Hamburg.
IHRE AUFGABEN UND VERANTWORTLICHKEITEN
* Schnittstelle QA und Process Team, erster Ansprechpartner für das Process Team in qualitätsrelevanten Fragen
* Durchführung von Qualitätssicherungsmaßnahmen bei der Aufrechterhaltung und Sicherstellung der GMP-konformen Produktion, wie z.B.
bei Risikoanalysen, Prozessvalidierungen und Qualifizierungen, sowie Prozessoptimierungen
* Unterstützung und Beratung des Process Teams bei der Erstellung und Bewertung von Abweichungen, Änderungen und weiteren relevanten Themen wie z.B.
SOP- und PQR-Erstellung, Vor- und Nachbereitung von Inspektionen
* Coaching und Training der Process Team-Mitglieder zum Qualitätsstandard, z.B.
GMP-Schulungen, Ursachen- und Risikoanalysen
* Unterstützung bei Kontakten zu Aufsichtsbehörden und Inspektionen durch Aufsichtsbehörden sowie Unterstützung bei Kundenkontakten und Kundenaudits, Sicherstellung der "all time inspection readiness" im Verantwortungsbereich
* Verantwortlich für die Sicherstellung des korrekten GMP-Status, kontinuierliche Verbesserungen und Überwachung der Qualifizierungs- und Validierungsprozesse im Bereich
* Überprüfung und Genehmigung von Dokumenten
* Umsetzung von Operational Excellence-Management und einer Kultur der kontinuierlichen Verbesserung
* Unterstützung und Mitwirken bei Projekten
WAS SIE MITBRINGEN
* Abgeschlossenes naturwissenschaftliches oder technisches Studium oder eine vergleichbare Qualifikation
* Praktische Erfahrung in der GMP-ausgerichteten pharmazeutischen Industrie im Bereich QA oder in der sterilen bzw.
aseptischen Produktion sind von Vorteil
* Sehr gute schriftliche und mündliche Kommunikationsfähigkeiten (Deutsch und Englisch)
* Fähigkeit zu eigenständige...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: Not Specified
Posted: 2025-09-10 08:37:13
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Company Overview:
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: Analyst – PV Case Processing
As an analyst in PV Case Processing, you will be responsible for managing adverse event reports, ensuring data accuracy, and maintaining compliance with global pharmacovigilance regulations and timelines.
The role involves data entry, assessing seriousness and causality, and ensuring the completeness and quality of cases for regulatory submission.
Effective communication skills, knowledge of regulations, and the ability to manage multiple priorities are essential.
The Analyst must demonstrate Elanco core values, adaptability, and commitment to high-quality standards in all tasks.
Your Responsibilities:
* Responsible for data entry, seriousness assessment and causality assessment of adverse event reports in the PV database
* Identify issues in case processing that may result in a delay in submission and escalates issues to management as appropriate.
* Develop an understanding of pharmacovigilance regulations and comply with internal and external timelines for managing adverse events and product complaint case processing, and case submission processes as appropriate.
* Typical case processing activities include (but not limited to):
...
....Read more...
Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:37:02
-
Job Category:
Intern
Job Family:
Student Intern
Job Description:
Schreiber Foods is looking for motivated and talented engineering students to join us as interns for the upcoming Summer 2026 across our manufacturing plants in the U.S. We have opportunities in the following communities: Michigan (Grand Rapids), Missouri (Carthage, Clinton, Monett, Mt.
Vernon), Pennsylvania (Shippensburg), Texas (Stephenville), Utah (Logan, Smithfield), Wisconsin (Green Bay, Richland Center, West Bend).
Relocation Assistance is provided if relocating 50 miles or more for this internship.
This is a paid internship with an hourly rate of pay: $22.00
Our Engineering Internship Program offers an exciting opportunity to gain hands-on experience in a food manufacturing environment. Interns will work closely with skilled engineers, contributing to projects that have a direct impact on our operations and success. We offer internship opportunities in various areas of engineering, allowing you to specialize based on your interests and career aspirations.
Interns will also participate in our company Internship Program which includes Executive Speakers, Social & Networking Events and Career Branding & Professional Development.
What you’ll do:
Manufacturing & Process Engineering:
* Focus on the optimization of manufacturing processes.
* Work on process improvements in efficiency, productivity, process capability, risk, and cost reduction.
* Collaborate with cross-functional teams to design and implement efficient manufacturing workflows.
What you need to succeed:
* Completed Sophomore-level status or higher toward a BS degree in an Engineering or Engineering Technology program (Electrical, Automation, Mechanical, Chemical, Engineering Physics or Manufacturing preferred).
Students must be enrolled as student during the time of the internship (Recent or previous graduates will not be considered).
* Willingness to relocate for Summer of 2026.
* Ability to work a minimum of 10 weeks during the Summer of 2026.
* Ability to work 40 hours/week during the summer.
* Strong analytical and problem-solving skills.
* Excellent communication and teamwork abilities.
* Interest in pursuing a full-time career in the areas listed above.
* Ability to take ownership of assignments and complete them on time and accurately.
* Desire to grow and take on new opportunities.
* Reliable transportation.
Schreiber Foods strives to do good through food every day.
Based in North America, we’re a customer-brand leader in cream cheese, natural cheese, process cheese, beverages and yogurt.
Our more than 10,000 employees and presence on five continents enable us to be an essential ingredient in our customers’ success.
With annual sales of more than $7 billion, we partner with the best retailers, restaurants, distributors and food manufacturers around the globe.
We also recognize our responsibility to do good in ...
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Type: Contract Location: Green Bay, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-10 08:36:15
-
Sr.
Plant Finance Manager - Warren
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.
The initial focus of this position will involve working with Supply Chain Accounting to ensure manufacturing cost and product costing design for the Warren site.
This collaboration is crucial in establishing accurate cost structures and product costing methodologies to support the operations at the Warren site.
By aligning with Supply Chain Accounting and other support teams, the position can contribute to optimizing cost management and financial processes within the manufacturing and Logistics operations.
When Warren site is operational, this role will transition to provide leadership for all finance-related activities and internal controls at the site. As a key source of senior financial expertise within the site leadership team, this position plays a crucial role in ensuring that the plant's financial accounting results and systems adhere to the Corporation's policies and procedures.
The individual will offer business counsel to the plant and supply chain leadership team to develop and execute effective strategies aimed at achieving the desired financial and business outcomes.
Moreover, the role involves driving cost-saving programs that optimize Total Delivered Cost over both short- and long-term horizons while ensuring the plant financial strategies and objectives are aligned with business unit and enterprise objectives.
In this role, you will:
* Exhibit strong financial and business acumen as well as strategic financial analysis and leadership
* Lead, develop, and manage activities responsible for finance, internal controls, mill services, energy, & plant systems where applicable
* Lead the development of strategies, objectives, and execution plans that optimize total delivered cost
* Lead operating reviews & drive cost management with plant team
* Lead annual plant budget, target setting process, and quarterly forecast process for plant team
* Supports major appropriation analysis for investment tied to future plant strategy
* Provide input into new, or improving existing processes, standards, or operational plans in support of mill results
* Maintain strong, safe working conditions and drive a people-based safety culture consistent with plant and staff objectives
* Lead and develop the talent of the site operations team & Financial Analyst supporting the plant
* Provide oversight and leadership for all plant controls (Cycle Counts, Archer Requirements, Intern...
....Read more...
Type: Permanent Location: WARREN, US-OH
Salary / Rate: Not Specified
Posted: 2025-09-10 08:33:49
-
LTI, Inc. is looking for individuals who possess a positive attitude and who are customer driven to join our team! At LTI, Inc.
we specialize in the transport of liquid- and dry-bulk commodities throughout the Pacific Northwest and Western Canada. For over 75 years, we have proudly served our customers’ transportation requirements and the needs of our employees. This is not a safety sensitive position.
Primary Function: Responsible for developing transportation pricing strategies, preparing rates and quotes, and monitoring financial performance with the Business and Development team in a fast-paced environment.
Why Work for LTI, Inc.
* Compensation: $80k to $110k
* Retirement Plan: 50% of the first 6% contributed matched + an additional 3% of your compensation regardless of your participation following one year of service.
* Discretionary Bonus(s)
* Additional Compensation: Cell Phone allowance stipend
* Paid Time Off/Extended Leave: 17 days of PTO annually to new employees, days increase with years of service + 6 days annually of Extended Leave.
* Holidays: 8 paid Holidays a year
* Benefits: Employees (and their families) may opt into medical, dental, vision, and basic life insurance. Long Term Disability Coverage, AD&D Insurance, and Employee Assistance Programs + flexible spending arrangements are offered.
* Schedule: Monday through Friday onsite
Qualifications
* Bachelor’s degree in business, supply chain management, logistics, accounting, finance, economics, or three years of related experience preferred.
* Proficient in MS Office suite (Outlook, Word, Excel, PowerPoint, Teams) and other analytical tools.
* Demonstrates refined analytical thinking, abstract reasoning, and thoughtful use of mathematics.
* Communicates complex ideas clearly in both written and spoken forms.
* A mindful approach grounded in analysis, curiosity, and a dedication to detail.
* Openness to learning and using new technologies.
* Demonstrates a positive attitude and a strong commitment to contributing within a collaborative team environment.
This role does not offer sponsorship for work authorization.
External applicants must be eligible to work in the US.
What You Will Be Doing
* Develop and implement transportation pricing strategies in alignment with company policy, prepare rates and quotes aligning with financial objectives set by the executive team.
* Analyze and respond to Requests for Proposals (RFPs), special pricing inquiries, and support managers in business development to maximize margins.
* Create, update, and maintain pricing models, cost models, and associated metrics to evaluate operational costs and recommend pricing actions.
* Monitor market trends and the competitive environment to provide recommendations on pricing adjustments and strategic opportunities.
* Oversee the organization and upkeep of all pricing-related documentati...
....Read more...
Type: Permanent Location: Seattle, US-WA
Salary / Rate: 95000
Posted: 2025-09-10 08:33:21
-
LTI, Inc. is looking for individuals who possess a positive attitude and who are customer driven to join our team! At LTI, Inc.
we specialize in the transport of liquid- and dry-bulk commodities throughout the Pacific Northwest and Western Canada. For over 75 years, we have proudly served our customers’ transportation requirements and the needs of our employees. This is not a safety sensitive position.
Primary Function: Responsible for developing transportation pricing strategies, preparing rates and quotes, and monitoring financial performance with the Business and Development team in a fast-paced environment.
Why Work for LTI, Inc.
* Compensation: $80k to $110k
* Retirement Plan: 50% of the first 6% contributed matched + an additional 3% of your compensation regardless of your participation following one year of service.
* Discretionary Bonus(s)
* Additional Compensation: Cell Phone allowance stipend
* Paid Time Off/Extended Leave: 17 days of PTO annually to new employees, days increase with years of service + 6 days annually of Extended Leave.
* Holidays: 8 paid Holidays a year
* Benefits: Employees (and their families) may opt into medical, dental, vision, and basic life insurance. Long Term Disability Coverage, AD&D Insurance, and Employee Assistance Programs + flexible spending arrangements are offered.
* Schedule: Monday through Friday onsite
Qualifications
* Bachelor’s degree in business, supply chain management, logistics, accounting, finance, economics, or three years of related experience preferred.
* Proficient in MS Office suite (Outlook, Word, Excel, PowerPoint, Teams) and other analytical tools.
* Demonstrates refined analytical thinking, abstract reasoning, and thoughtful use of mathematics.
* Communicates complex ideas clearly in both written and spoken forms.
* A mindful approach grounded in analysis, curiosity, and a dedication to detail.
* Openness to learning and using new technologies.
* Demonstrates a positive attitude and a strong commitment to contributing within a collaborative team environment.
This role does not offer sponsorship for work authorization.
External applicants must be eligible to work in the US.
What You Will Be Doing
* Develop and implement transportation pricing strategies in alignment with company policy, prepare rates and quotes aligning with financial objectives set by the executive team.
* Analyze and respond to Requests for Proposals (RFPs), special pricing inquiries, and support managers in business development to maximize margins.
* Create, update, and maintain pricing models, cost models, and associated metrics to evaluate operational costs and recommend pricing actions.
* Monitor market trends and the competitive environment to provide recommendations on pricing adjustments and strategic opportunities.
* Oversee the organization and upkeep of all pricing-related documentati...
....Read more...
Type: Permanent Location: pasco, US-WA
Salary / Rate: 95000
Posted: 2025-09-10 08:33:20
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About the Company
Vantage Group Holdings Ltd.
(Vantage) was established in late 2020 as a re/insurance partner designed for the future.
Driven by relentless curiosity, our team of trusted experts provides a fresh perspective on our clients’ risks.
We add creativity to tech-enabled efficiency and robust analytics to address risks others avoid.
Vantage provides specialty re/insurance through its operating subsidiaries in Bermuda and the U.S.
Vantage has approximately 365 colleagues in both the United States and Bermuda.
We have offices in Chicago, IL, Norwalk, CT, Arlington, VA, Boston, MA, New York, NY, Atlanta, GA and Hamilton, Bermuda.
Additionally, we are a highly geographically diverse workforce with colleagues based in 35 states and counting.
We fully support work flexibility including remote and hybrid work arrangements.
About the role:
The Actuarial Analyst, Pricing Operations & Portfolio Management will play an important role in the Vantage’s Insurance business by supporting the Insurance Pricing and Portfolio Management functions.
These functions, overseen by the Chief Pricing & Portfolio Actuary, are tasked with tracking, analyzing, and reporting key pricing and underwriting metrics.
The Insurance Leadership Team rely on this work as they make decisions for the future of Vantage Insurance.
The successful candidate will work alongside the Head of Pricing Operations & Strategy and the Chief Pricing & Portfolio Actuary to maintain and run models, tools, and processes to ensure the Pricing & Portfolio Management functions are fit for purpose and scalable.
They will take ownership of established pricing operations and portfolio management work.
They should have a keen attention to detail, enjoy solving problems, and proactively contribute to improving pricing operations and portfolio management.
This position will be part of the Insurance Pricing Team and will report to the Head of Pricing Operations & Strategy.
The Pricing Operations & Strategy function has the Pricing Team as their first-line customers.
The other members of the Pricing Team are the business unit pricing actuaries, the Head of Pricing Operations & Strategy, and the Chief Pricing & Portfolio Actuary.
The Pricing Team’s core customers are the Insurance Leadership Team and the underwriting business units.
We prefer this position to be filled by a candidate able to work 2-3 days per week in the West Hartford, Connecticut, office.
However, we are flexible in terms of location, with both remote and in-office options available for the right candidate.
The base salary expectation for this role is between $80,000 and $110,000.
Actual base salary for the selected candidate may be higher commensurate with candidate experience and expectations.
Additionally, Vantage offers its colleagues performance-based bonus potential, strong health & welfare benefits, retirement plans with company match, competitive time off plans, a highly flexible work environment, and much mor...
....Read more...
Type: Permanent Location: West Hartford, US-CT
Salary / Rate: 95000
Posted: 2025-09-10 08:32:57
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Overview: The Surgical Sales Representative is responsible for the sale and ongoing support of the Company's product(s) in a specified region or major geographical area.
Responsibilities:
* Create demand for Sight Sciences products within both company and industry-compliant guidelines
* Develop effective sales presentations to differentiate product(s) compared to current surgical glaucoma offerings with Ophthalmic surgeons within the assigned territory
* Analyze data and manage territory to create an effective business plan, including regular sales forecasting
* Maintain knowledge of current trends in the industry and competitive products
* Manage territory budget and resource
* Complete administrative paperwork in a timely manner and provide reports to the Manager regarding established average call activity and feedback from physicians
* Attend various sales training workshops, sales meetings, national/regional conferences, and relevant trade shows
* Maintains direct contact with customers before and after the sale:
+ Pre-sale: Responds to customer inquiries to determine appropriate product literature and pricing schedules; influences production and shipping schedules
+ Post-sale: Responds to customer inquiries (RMA, status, delivery, etc.).
Resolves production scheduling and shipping or invoicing problems; determines the validity of warranty claims and schedules repair resources
* Support company goals and objectives, policies, and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic or international requirements
* Maintain a professional and credible image with key physicians, distributors, consultants, vendors, and co-workers
Skills/Qualifications:
* 5+ years of sales experience, with preferably a minimum of 3 years of medical sales experience in ophthalmology, with a proven track record of success
* Successful sales track record in the medical device industry
* Strong relationship-building skills
* Strong sales presentation skills
* Ability to work independently and as well as within a strong team environment
* Bachelor’s Degree or equivalent experience
* Valid driver's license to travel to customer locations
* Required residence in territory geography
#LI-Hybrid
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Milwaukee, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-10 08:28:32
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Overview: The Surgical Sales Representative is responsible for the sale and ongoing support of the Company's product(s) in a specified region or major geographical area.
Responsibilities:
* Create demand for Sight Sciences products within both company and industry-compliant guidelines
* Develop effective sales presentations to differentiate product(s) compared to current surgical glaucoma offerings with Ophthalmic surgeons within the assigned territory
* Analyze data and manage territory to create an effective business plan, including regular sales forecasting
* Maintain knowledge of current trends in the industry and competitive products
* Manage territory budget and resource
* Complete administrative paperwork in a timely manner and provide reports to the Manager regarding established average call activity and feedback from physicians
* Attend various sales training workshops, sales meetings, national/regional conferences, and relevant trade shows
* Maintains direct contact with customers before and after the sale:
+ Pre-sale: Responds to customer inquiries to determine appropriate product literature and pricing schedules; influences production and shipping schedules
+ Post-sale: Responds to customer inquiries (RMA, status, delivery, etc.).
Resolves production scheduling and shipping or invoicing problems; determines the validity of warranty claims and schedules repair resources
* Support company goals and objectives, policies, and procedures that comply with FDA Quality System Regulations (QSR), ISO 13485, and any other applicable domestic or international requirements
* Maintain a professional and credible image with key physicians, distributors, consultants, vendors, and co-workers
Skills/Qualifications:
* 5+ years of sales experience, with preferably a minimum of 3 years of medical sales experience in ophthalmology, with a proven track record of success
* Successful sales track record in the medical device industry
* Strong relationship-building skills
* Strong sales presentation skills
* Ability to work independently and as well as within a strong team environment
* Bachelor’s Degree or equivalent experience
* Valid driver's license to travel to customer locations
* Required residence in territory geography
For Illinois, the base salary range for this position is $93,750-$120,000 (highly qualified) a year.
The Company maintains highly competitive, performance-based compensation programs.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
....Read more...
Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2025-09-10 08:28:30
