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Your Job
Georgia-Pacific is now hiring for a Converting Production Leader for our Operations Department in the Plattsburgh, NY Mill.
This Leader is responsible for providing leadership with accountability for all hourly employees on the shift, safety, and environmental compliance.
They will also coach, train and develop personnel in safety, quality, production, problem solving and technical skills.
This role will have roughly 12 direct reports and will report to the Operations Manager.
The shift for this position is 12 hour rotating shifts that fluctuate from 2 weeks of day shift to 2 weeks of night shift.
Our Team
The Plattsburgh Tissue Mill is situated on the shores of Lake Champlain in the Northeast region of upstate New York and is rich in history.
GP made its historic entry into the world of consumer paper products when it purchased this facility in 1963 as GP's first tissue mill.
Georgia-Pacific's Plattsburgh facility uses state of the art innovation and technology to manufacture Quilted Northern Ultra Plush Tissue.
What You Will Do
* Build and develop capability of on-shift personnel
* Be a business partner with Manufacturing Engineers in their respective areas
* Ensure safety and environmental ownership and compliance
* Identify and correct unsafe conditions and acts, recognizing positive safety performance as well as individual and team contributions to a safer workplace
* Lead operational and shift maintenance initiatives in accordance with the Asset Strategy to achieve maximum asset capability
* Provide performance feedback and coaching: appraising performance and providing feedback as needed
* Assist in resolving complaints and issues; hold employees accountable in a fair and consistent manner, and communicate issues and results daily
* Act as a positive change agent for continued transformation and improvement
* Develop and foster an environment where employees are contribution motivated
* Work within the bounds of a union contract (USW)
Who You Are (Basic Qualifications)
* Continuous improvement experience
* Knowledge and experience with reliability systems and work processes
What Will Put You Ahead
* Bachelor's Degree or higher in Engineering or Paper Science
* Experience initiating, executing, commissioning and starting-up capital projects
* Experience managing product systems
* Leadership experience with responsibility for direct reports
For this role, we anticipate paying $85,000 to 100,000 per year.
This role is eligible for variable pay, issued as a monetary bonus or in another form.
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 ...
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Type: Permanent Location: Plattsburgh, US-NY
Salary / Rate: Not Specified
Posted: 2025-06-02 08:09:08
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Your Job
The desired candidate must demonstrate customer focus as well as strategic & economic thinking, possess good problem-solving skills, and enjoy collaborating across the organization.
This position supports all control systems (DCS, PLC, VFDs, Instrumentation, etc) throughout the mill and will be responsible for designing and implementing control improvements while working with others to maintain and troubleshoot the mill's control systems.
Our Team
Georgia-Pacific is seeking a Process Control Engineer to join our team at the Big Island, Virginia Mill.
Big Island is located near Lynchburg in central Virginia.
What You Will Do
• Support process operations (your customer) by troubleshooting installed systems to improve the effectiveness and efficiency of these systems.
• Partner with operations to implement new technologies that support advanced manufacturing.
• Work closely with mill personnel to identify opportunities and solve problems
• Be involved in the controls and automation design, implementation, and support of hardware and software systems for mill process equipment i.e.
ABB DCS/QCS systems and Rockwell PLCs, drives, and instrumentation.
• Develop and lead projects to migrate away from end of life control systems.
• Act as project resource for new instrumentation or control/automation systems.
• Implement, design, and configure advance process control strategies.
Maintain functional design specifications for process control systems.
• Support optimization and Advanced Process Control efforts.
• Support of the mill safety program both personally and through observation.
Who You Are (Basic Qualifications)
• Bachelor's degree or higher in engineering field plus internship/coop experience in controls-related assignment OR industrial experience working as an electrical or instrumentation technician.
What Will Put You Ahead
• Experience in the Pulp and Paper industry.
• Degree in Electrical Engineering or similar
• Experience with ABB DCS (AC800M, Bailey) platforms
• Experience with control system network topology (i.e.
Ethernet, EthernetIP, ProfiNET)
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
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based...
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Type: Permanent Location: Big Island, US-VA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:57
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Your Job
DEPCOM Power Inc.
is looking for a Site Manager to join the team in Fort Stockton, TX.
The Site Manager will support the O&M team on the Alamo & Pearl Utility Solar Site.
Our Team
The fast-growing DEPCOM Power O&M group is a collaborative, safety-oriented team that operates our customer's industrial solar power generating sites.
The O&M group rounds out the DEPCOM Engineering, Procurement, Construction (EPC) group's capability to give our customers the support they need from designing to the daily operations for industrial solar sites.
What You Will Do
* Oversee daily operations at the project site, ensuring adherence to safety protocols and project timelines.
* Communicate effectively with contractors, team members, and stakeholders, providing updates and addressing any concerns.
* Document daily site activities, including progress reports, safety inspections, and any incidents or challenges.
* Utilize Microsoft Excel to create and maintain project reports, track key performance indicators, and analyze data.
* Set up and facilitate meetings with contractors, project stakeholders, and team members to ensure alignment and resolve issues.
* Manage the team's expense reports and ensure accurate tracking of time worked by team members.
* Collaborate with the project management team to support contractor onboarding and performance evaluations.
* Identify challenges on-site and proactively seek solutions to optimize operations and efficiency.
* Assist in the coordination and management of resources, equipment, and materials necessary for project completion.
* Ensure compliance with all regulatory requirements and company policies related to site operations.
* Serve as the primary point of contact for customer inquiries and concerns, ensuring high levels of satisfaction and responsiveness.
Who You Are (Basic Qualifications)
* Previous experience in a team environment
* Experience with Microsoft Office ( Word, PowerPoint)
What Will Put You Ahead
* Previous experience in a leadership role within Utility Scale PV Solar
* Experience with PV systems utility scale operations & maintenance
* Knowledge of inverters, tracker systems & communications
* Knowledge of Medium Voltage (MV) and High Voltage (HV) power distribution equipment
* Knowledge of Commercial, Industrial and Utility Power Plant Operations
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.
This position is not eligib...
....Read more...
Type: Permanent Location: Fort Stockton, US-TX
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:55
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Your Job
Georgia-Pacific is looking for a Paper Machine Gatekeeper to join our team in Brewton, AL.
The Gatekeeper plays critical role in our organization and asset maintenance work process.
People in this role work with and through other mill leaders to balance competing maintenance priorities, forecasting spend plans, while focusing on the long-term success of operations within their departments and beyond.
Our Team
The Brewton Mill is an integrated paper mill producing product for Dixie® plates and various GP and external corrugated box facilities.
Brewton is located in south central Alabama, about an hour from Mobile, AL, Pensacola, FL, and the beautiful beaches of the Gulf Coast.
To learn more about Georgia-Pacific's packaging business please visit: www.gppackaging.com and view the video How Paper Is Made! Our culture is defined by the Principle Based Management™ philosophy which guides everyday decision making and provides employees with opportunities to contribute and personally benefit from the value they create.
What You Will Do
• Optimize value creation by managing maintenance and miscellaneous operations spend for the Paper Machine area.
• Actively participate in Mill Spend Evaluation meetings, presenting the planned and unplanned spend on a weekly and monthly basis.
• Actively participate in Work Prioritization meetings to ensure proper work is scheduled for execution.
• Review submitted work requests for need, accuracy, correct accounting codes daily.
Convert work requests to work orders and send to planning or execution as needed.
• Manage existing contracts, invoices, and accruals for correctness.
• Monitor Work Process Status & Aging dashboards and keep up to date.
• Effectively manage many high priority tasks / projects with a sense of urgency.
• Review and follow up on emergency work execution to ensure completeness and if follow up work is required.
• Manage forecast for Extraordinary Maintenance needs /spend plans as well as baseline spend and full year spend plans.
• Work with the team to review and analyze loss analysis and asset tracking data to identify equipment reliability and performance issues (gap analysis) and develop improvement plans.
• Help develop long-term reliability and asset strategies.
• Collaborate with manufacturing engineers, maintenance team members, and department leaders on critical equipment strategies.
• Ensure reliability activities are scheduled based on resource availability and priority.
Provide technical support on both capital and non-capital projects.
Who You Are (Basic Qualifications)
• Experience working within a manufacturing, industrial or military environment.
• Experience leading and facilitating meetings.
• Ability to respectively challenge co-workers at all levels of the organization when necessary.
• Ability to work collaboratively in fast paced 24/7 manufacturing environment, including multitasking and prioritization.
•...
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Type: Permanent Location: Brewton, US-AL
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:50
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Your Job
The Paper Area Manufacturing Leader will be responsible for leading the day-to-day operations of our two paper machines at the Brewton mill.
This will include leading a team of 6 salaried direct reports and indirect responsibility for the entire paper team of 160+ employees.
They will partner closely with, act as a strategic thought partner, and report to the Paper Production Leader.
Our ideal candidate will aspire for continued career growth and advancement, beyond this opportunity.
This position will provide strategic and tactical leadership to achieve key objectives in safety, environmental compliance, reliability, production, quality, and cost.
The successful candidate will utilize problem solving skills while focusing on safely improving productivity and reducing cost through process/equipment optimization and operator knowledge/skill improvement with a high sense of urgency.
Our Team
The Brewton mill is located in south central Alabama about an hour from Mobile, AL, Pensacola, FL, and the beautiful beaches of the Gulf Coast.
The team is made up of 450 employees who produce white top linerboard and solid bleached sulfate (SBS) paperboard.
The SBS material is used to make GP's Dixie plates.
White top linerboard is used in production of corrugated containers and displays.
This position is an opportunity to be part of a rapidly expanding organization with tremendous growth potential.
The most recent $160M capital investment is expected to be completed in late 2024.
The Brewton mill was also the first fully integrated pulp and paper mill in the US to receive an Energy Star designation from the U.S.
Environmental Protection Agency.
To learn more about Georgia-Pacific's packaging business please visit: www.gppackaging.com and view the video How Paper Is Made! Our culture is defined by the Principle Based Management™ philosophy which guides everyday decision making and provides employees with opportunities to contribute and personally benefit from the value they create.
Learn more about our Brewton facility and employees here: We Are: Brewton
What You Will Do
• Providing leadership through application of Koch's Principled Based Management (PBM) philosophy to achieve superior results.
• Drive a culture of safety and environmental excellence through critical hazard identification, risk reduction and risk mitigation.
• Work with Area Leader and other leaders to coach and develop employees.
• Lead teams in the identification, development, evaluation and implementation of safety, quality, and /or cost reduction initiatives and projects that has the highest value to the operation to drive continuous improvement.
• Demonstrate ownership for planning outages and routine maintenance.
• Understand, communicate, and align goals in the areas of safety, quality, production, and reliability.
• Drive process and equipment modifications that result in improved product quality, reduced variation, and higher customer satisfact...
....Read more...
Type: Permanent Location: Brewton, US-AL
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:49
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Senior Retail Media / eCommerce Solution Architect
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.
In this role, you will:
* Lead digital shelf ecosystem architecture, development, integration, implementation and operations in collaboration with the content, Ad Tech and data & analytics product teams.
* Manage features timelines, budgets, and resource allocation for digital shelf.
* Provide technical support to internal stakeholders on digital shelf related tools and processes.
* Identify and resolve technical issues related to content syndication, data mapping, and platform integrations.
* Manage data mapping, validation rules and data quality checks to ensure accurate product listing in collaboration with the data & analytics product teams and downstream application owners.
* Analyze digital shelf performance metrics to identify areas for improvement.
* Develop and implement strategies to optimize content delivery and product discoverability on the digital shelf.
* Develop and maintain automated workflows to syndicate product content to various retailer websites and marketplaces in collaboration with Content Solution Architect.
* In collaboration with legal, privacy and compliance, ensure that all architectural designs comply with CPRA/CCPA, GDPR, and other data privacy regulations.
* Stay current with industry trends in digital experience platforms and architecture, applying relevant advancements to improve solutions.
About Us
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.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new i...
....Read more...
Type: Permanent Location: Buenos Aires, AR-B
Salary / Rate: Not Specified
Posted: 2025-06-02 08:08:47
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Your Job
Georgia-Pacific's Plywood facility located in Taylorsville, Mississippi is now hiring for Production Utility Associates.
Compensation:
* $20.05 per hour
* $1.50 shift differential for night shift
* This role is eligible for variable pay
You will work as a part of a team committed to safety and production excellence.
There are opportunities for long-term growth and fulfillment in a supportive environment.
You will be able to contribute to a team that encourages critical thinking, driving initiative, and working collaboratively.
Our Team
Georgia-Pacific employees strive for safety and health excellence while achieving an injury-free workplace.
Georgia-Pacific's Building Products business is consistently among the nation's top suppliers of building products to large warehouse retailers and building materials dealers.
To learn more about our Building Products division, visit http://www.buildgp.com .
What You Will Do
* Maintain strict adherence to safety rules and regulations, to include wearing safety equipment
* Perform basic housekeeping responsibilities throughout the mill
* Continuous knowledge development through shadowing and training in various roles
* Perform basic operator care and preventive maintenance tasks
* Engage in tasks such as lifting, walking, climbing, stooping, pushing and/or pulling for twelve (12) or more hours a day
* Work in a hot, cold, humid, noisy, industrial environment
* Work around dust, oil, grease, chemicals, and other substances
Who You Are (Basic Qualifications)
* Experience in a farming, carpentry, construction, warehouse, military, production or manufacturing environment
What Will Put You Ahead
* At least one (1) or more years of experience in a farming, carpentry, construction, warehouse, military, production or manufacturing environment
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
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more tha...
....Read more...
Type: Permanent Location: Taylorsville, US-MS
Salary / Rate: Not Specified
Posted: 2025-06-02 08:07:43
-
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:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
People Leader
All Job Posting Locations:
Beijing, China
Job Description:
1.
 Principal Duties and Responsibilities (General Summary, essential functions and authorities, etc.)
    主è¦å·¥ä½èè´£ï¼åºæ¬æ¦åµï¼ä¸»è¦åè½ï¼æéçï¼
ï§Â   Align with company and commercial strategy, direct, develop and manage project registration activities focused on the define registration (and renewal) strategy, registration project plan, supervision on project execution and delivery.
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¬å¸åä¸å¡çç¥ï¼æ导ãå¼åå管ç项ç®æ³¨åå·¥ä½ï¼çéäºå¶å®æ³¨åï¼å延ç»æ³¨åï¼æç¥ã注å项ç®è®¡åï¼çç£é¡¹ç®æ§è¡ä¸äº¤ä»ã
ï§Â   Manage day-to-day operation to ensure registration related projects/programs progress.
Review and approve required information for the registration dossier and technical requirement document.
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³é¡¹ç®/计åçæµç¨å¦¥åå®æ½ã审æ¹æ³¨åèµæåææ¯è¦æ±æ件æéä¿¡æ¯ã
ï§Â   Assign and allocate resources and actively oversee departmental (team) projects.
Provides managerial leadership & direction to assigned team allowing appropriate prioritization of resources to achieve goals.
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许éå½çèµæºä¼åé
置以å®ç°ç®æ ã
ï§Â   Interact and proactively forge new relationships with external partners, including global regulatory functions, quality, R&D, manufacture and commercial partners, Effectively communicates with franchise and local cross functional leaders.
ï§Â   ä¸å
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¨çæ³è§é¨é¨ãè´¨éãç åãç产ååä¸ä¼ä¼´äºå¨å¹¶ç§¯æ建ç«æ°å
³ç³»ãåæ»é¨åå½å°è·¨èè½é¨é¨è´è´£äººæææ²éã
ï§Â   Establish and maintain relationship with NMPA and other authorities, manage and maintain clear and effective internal-external communication channel.
ï§Â   ä¸NMPA以åå
¶ä»ç管é¨é¨å»ºç«å¹¶ç»´æè¯å¥½å
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-å¤é¨ä¹é´çæææ²éæ¸ éãÂ
ï§Â   Provide regulatory support for cross functional departments and cultivate company regulatory compliance environment.
ï§Â   为跨èè½é¨é¨æä¾æ³è§æ¯æï¼å¹¶è¥é...
....Read more...
Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-06-02 08:05:02
-
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:
Shanghai, China
Job Description:
Principal Duties and Responsibilities (General Summary, essential functions and authorities, etc.)
主要工作职责（基本概况，主要功能，权限等）
* 法规事务专员由其直线经理监督管理。法规事务专员负责多个法规事务项目的计划、执行和交付，以实现公司重大目标。法规事务专员负责在直线经理的监督管理下计划并执行所分配项目的注册工作；负责协调不同跨职能部门之间的工作，包括研发、生产、质量、医学事务、临床、法务以及其他职能部门，以满足项目注册之需要。本职位要求具备相应的法规和产品知识、一定的协调能力、沟通能力与执行能力，这些都会直接影响业务部门的运营结果。
RA Specialist is under the supervision from their line manager.
They will be responsible for planning, execution, and delivery of multiple RA projects to achieve significant company goals.
RA Specialist plan and execute the registration activities for assigned projects under their line manager’s supervision.
They coordinate activities of various cross-functional departments including research & development, manufacturing, quality, medical, clinical, legal, and other functions to meet the needs of project registration.
This role requires regulation and product knowledge, coordination, communication skills and execution which directly impact the operational results of the business unit.
* 主要职责/任务（以时间的百分比表示）：
* Key responsibilities/tasks （indicate estimated % of time spent where possible）：
* 70% 产品注册准备和执行。
* 70% Product registration preparation & execution.
* 10% 制定注册项目计划。
* 10% Develop registration project plan.
* 10% 为法规合规工作提供支持。
* 10% Support regulatory compliance activities.
* 10% 法规信息收集、解读和政策制定。
* 10% Regulatory intelligence collection, interpretation and policy shaping.
* 职责/主要衡量指标：
* Accountabilities/Key measures：
* 根据注册（以及延续注册）策略和注册项目计划，计划并执行项目注册工作。
* Plan an...
....Read more...
Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-06-02 08:05:01
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Leiden, South Holland, Netherlands
Job Description:
Scientist, Quality Control
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to create 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/.
Johnson & Johnson Services Inc., a member of the Johnson & Johnson Family of Companies, is recruiting a QC Scientist.
This position will be located in Leiden, Netherlands.
The Leiden Quality Control (QC) Leiden department is a Business Unit within the Leiden site, a biotherapeutics and vaccines manufacturing site belonging to the Johnson & Johnson Supply Chain.
The Leiden QC department is responsible for raw material, in-process, and release testing for products manufactured at the site.
Additionally, the Leiden QC department has a unique global responsibility and exposure by being the stability testing hub for large molecule products within the Johnson & Johnson Supply Chain, and by partnering with multiple Contract Manufacturing Organizations to perform the release testing.
The department is structured in different testing laboratories and supporting teams, which are divided based on specific techniques and/or expertise.
The Scientist will be part of the testing teams within the Quality Control (QC) department, acting as the scientific responsible person to support the analytical testing aspects associated with Drug Substance and Drug Product manufacturing.
This role involves troubleshooting of analytical methods, ensuring smooth entry of new methods into QC, proactively making improvements to test methods to stimulate executional excellence, managing product related deviations, leading investigations and analytical method transfers, and providing subject matter expertise for new equipment.
Additional responsibilities include participating as a Subject Matter Expert (SME) in internal and external audits, writing observation responses, and developing the next generation QC Scientists.
The Scientist...
....Read more...
Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Employer: Auris Health, Inc.
Job Title: Senior Regulatory Affairs Specialist, Program Lead
Job Code: A011.485
Job Location: New Brunswick, NJ
Job Type: Full-Time
Rate of Pay: $135,000 - $160,000
Job Duties: Author regulatory submissions and support product development stages to help the organization achieve US and international regulatory (NPD) approval goals.
Support health authority communications and contribute to strategy development.
Manage, prepare, and submit regulatory submissions required for device approvals and registrations in the US and globally.
Oversee SME resources preparation of submission deliverables to meet regulatory requirements or other project objectives.
Correspond and collaborate with international J&J colleagues on international approval efforts.
Conduct regulatory evaluation of changes to Auris devices in accordance with requirements of commercial/operating geography and generate the required regulatory submission.
Anticipate program risk and make recommendations for mitigations.
Function as a Regulatory Affairs subject matter expert on new product introduction and lifecycle management supporting cross functional partners including clinical, marketing, and engineering through design control activities.
Conduct reviews and provide expert regulatory feedback on specifications, device testing, risk management, and other relevant documentation in accordance with regulatory requirements and positioning for regulatory submission.
Assist research personnel, application specialists, and risk management specialists to ensure clinical research and clinical evaluations are performed in accordance with regulatory requirements.
Support quality system and technical file/design dossier audits.
Translate and simplify problems of considerable scope and complexity into manageable tasks with measurable requirements.
May telecommute.
Requirements: Employer will accept a Master's degree in Pharmacy Administration, Biomechanical Engineering, or related field and 4 years of experience in the job offered or in a Senior Regulatory Affairs Specialist, Program Lead-related occupation.
This job posting is anticipated t...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:55
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Cincinnati, Ohio, United States of America, Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson is recruiting a Senior Financial Analyst.
This position is based in Cincinnati, OH or Raritan, NJ.
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
The Senior Financial Analyst role is essential in developing deals for our US Surgery customers as well as developing creative pricing programs and solutions to grow our overall business.
A successful candidate will learn how the business directly interacts with the administration and clinical staff at the hospital systems.
Key Responsibilities:
* Leads the creation of financial models for customer deals in close connection with Offer Development, Account & Key Account Management teams.
* Fully owns and presents financial models at Pricing Committee meetings when requested.
* Develop a deep understanding of End User sales and how pricing decisions impact overall value for both the business and the customer
* Partners closely with Brand Marketing finance teams and Gross to Net teams to bring greater transparency to pricing decisions and impacts to overall business results.
* Works directly on, and shapes complex analytical pricing & marketing projects.
* Ability to independently manage timelines and deliverables to ensure customer response expectations are met.
* Presents ad hoc analyses and presentations for management as unique customer situations arise.
Qualifications:
* Minimum of a bachelor's degree required, preferably a major in Accounting, Finance or other related field
* At least 3 years of work experience in accounting, finance or related field required.
* Strong Excel and PowerPoint skills
* This position is based in Cincinnati, OH or Raritan, NJ and 10% of t...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:54
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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:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Istanbul, Turkey
Job Description:
We are looking for a skilled and proactive Senior Financial Analyst to join our finance team.
This role is instrumental in driving financial performance and ensuring compliance with accounting standards.
The ideal candidate will collaborate with various business partners to provide strategic insights that support decision-making and enhance financial management.
Key Responsibilities:
* Monthly & Quarterly Reporting: Prepare and submit comprehensive close reports to meet organizational policies and deadlines, ensuring accuracy and transparency.
* Budgeting & Forecasting: Actively participate in the budgeting process and rolling forecasts, contributing valuable insights to enhance the financial planning framework.
* Internal Reporting: Monitor and track actual costs against budget, providing regular updates and insightful analyses to key stakeholders.
* Strategic Development: Collaborate with business partners to develop strategic business cases, offering financial insights and recommendations to drive organizational goals.
* Compliance Assurance: Ensure adherence to accounting policies and internal requirements, fostering integrity in all financial practices.
* Metric Management: Manage and monitor key performance indicators (KPIs), providing detailed tracking reports to facilitate performance assessment.
* Project Participation: Engage in local and regional special projects, including systems implementations, process improvements, and strategic data analysis.
Provide ad hoc support as needed.
Requirements:
* Bachelor’s or master’s degree in Business Administration, Accounting, or a related field.
* 3-5 years of experience in finance, preferably within the pharmaceutical industry; experience in a Reputable Audit Company is a plus.
* Strong understanding of accounting fundamentals, financial control, budgeting, and reporting processes.
* Proficiency in accounting software (SAP BPC, FM, FI, and CO) and advanced Excel skills.
* Excellent command of both oral and written English.
* Compliance-oriented with a strong commitment to ethical financial practices.
* Strong communication and analytical skills and a proactive mindset.
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Type: Permanent Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:47
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Ciudad Juarez, Chihuahua, Mexico
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Senior Trainer to be in Ciudad Juarez.
Purpose:
Along with the Training Coordinator, the trainer ensures that all manufacturing associates are trained to the corresponding specifications / procedures, as established in the training curriculum.
· Execute New Hire Orientation activities (NHO) as required.
· Assign exams to assess the training effectiveness.
· Document training activities and verify documentation related to training.
· Supports the development of programs and materials for the effectiveness of training for manufacturing personnel.
· Support in the maintenance of department files.
· Maintains reports and department records (matrix, records, reports, etc.)
· Supports manufacturing associates in solving machine and product / process problems.
· Supports manufacturing activities related to training as required.
· Participates in Site's safety initiatives.
· Know and comply with all safety regulations established by the company.
You will be responsible for:
In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Along with the Training Coordinator, the trainer ensures that all manufacturing associates are trained to the corresponding specifications / procedures, as established in the training curriculum.
* Execute New Hire Orientation activities (NHO) as required.
* Assign exams to assess the training effectiveness.
* Document training activities and verify documentation related to training.
* Supports the development of programs and materials for the effectiveness of training for manufacturing personnel.
* Support in the maintenance of department files.
* Maintains reports and department records (matrix, records, reports, etc.)
* Supports manufacturing associates in solving machine and product / process problems.
* Supports manufacturing...
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Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:46
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Leiden, Netherlands
Job Description:
Are you ready to take on a unique and exciting opportunity as a Specialist QA – GMP Quality Systems Compliance? Johnson & Johnson is seeking a highly motivated individual to join our team in Leiden, Netherlands with an unlimited contract.
This is your chance to be part of a world-class organization that is committed to innovation and delivering flawless quality in everything we do.
As the Specialist QA – GMP Quality Systems Compliance, you will play a crucial role in ensuring that our operations meet the highest standards of quality and compliance.
You will have the opportunity to work with a team of exceptional professionals and contribute to the success of our goals.
Ensures a professional, up to date, high quality level of JBV’s core Quality Systems and its application of these systems to maintain and improve the compliance status of JBV’s processes and systems in line with the regulatory, JBV, Janssen Supply Chain and J&J standards.
Develops and updates quality systems and procedures when appropriate.
Advises Q&C Management and the executing departments regarding compliance issues and ensure resolution.
Essential Job Duties and Responsibilities GMP Specialist
Acts as a Center of Expertise for GMP core quality systems.
Maintains and improves GMP core quality systems, ensuring that the JBV quality systems are compliant, state-of-the-art, and efficient.
Ensures consistency in the quality systems across processes and departments.
Has an outstanding knowledge of GMP regulations, Janssen and J&J standards and translates these requirements in JBV systems that are compliant.
Is responsible for the Inspection Readiness program for the quality systems under his/her responsibility ensuring that JBV is in compliance with the GMP regulations and has a high First Time Pass for all regulatory inspections.
Performs internal audits as a (lead/team) auditor.
Identifies critical areas for improvement through audits and assessments and prioritizes and executes the compliance improvements initiatives resulting from this.
Uses appropriate assessment tools (e.g., PE, Lean, Risk Management principles) in assessing the status of current quality processes and in introducing improvements.
Ensures that quality initiatives are implemented effectively across all relevant...
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Type: Permanent Location: Leiden, NL-ZH
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:42
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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:
Supply Chain Planning
Job Sub Function:
Demand Planning
Job Category:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
Johnson & Johnson MedTech is recruiting for a Senior Demand Planner.
This position is located in Markham, ON Canada.
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
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
As a Senior Demand Planner, you will play a key role in the Sales & Operations Planning Process to drive the alignment among Supply Chain, Finance, and Commercial functions for the reliable demand forecast.
You will drive the monthly cadence of the S&OP Cycle (Demand Review, Supply Review) and will contribute to the maturity of the Demand Planning process towards IBP (Integrated Business Planning).
You also work closely with the Supply Planning team to deliver the outstanding service level, optimize inventory, and reduce obsolescence.
In addition, you are the key linkage point with the Global Planning organizations ensuring End-to-End visibility and synchronicity between global and local supply chain.
Responsibilities:
* Lead the Canadian S&OP process for the assigned portfolio of products aiming to align Commercial and Supply Chain plans.
* Own critical metrics related to product portfolio (OTIF, forecast accuracy, NPI on-time launch and Life Cycle Management) and contributes to other supply chain related measurements (Inventory, obsolescence and write-offs)
* Review statistical forecast generated and provide input on changes that may be required.
Collaborate with functions such as Sales, Marketing, Commercial Operations, and Finance to identify and incorporate market intelligence (events) into the demand forecast.
* Proactively identify and resolve directly or through business partnership any issue affecting the product flow.
* Collaborate with global supply chain teams on projects affecting the product portfolio and/or the supply network.
* Partner with the Field Assets Management team to find opportunities and implement solutions for field assets optimization - if applicable.
* Ensure positive rel...
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Type: Permanent Location: Markham, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:42
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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:
Sales Enablement
Job Sub Function:
Sales Operations & Administration
Job Category:
People Leader
All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, West Chester, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for a Senior Manager of Commercial Operations Systems to be in Raynham, MA, West Chester, PA or Palm Beach Gardens, FL.
About Orthopaedics
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.
Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Purpose:
We are seeking a dynamic and experienced Senior Manager of Commercial Operations Systems to lead our key technology strategy and deployment initiatives within our Orthopaedics business.
This role will focus on the strategic alignment and deployment of technology solutions that drive operational efficiency and enhance sales and commercial effectiveness.
In this role, you will have the opportunity to lead the strategy, design, and delivery of new and innovative technologies, as well as enhancements to existing technologies, that will modernize the experience for our commercial teams.
These include field inventory management systems, set tracking capabilities, and ERP upgrades.
The role will interface with several connected organizations, providing the opportunity to gain exposure to the broader Orthopaedics organization.
Key Responsibilities
* Strategic Leadership: Develop and execute a comprehensive technology strategy for Orthopaedics Sales and Commercial Operations, ensuring alignment with overall business objectives.
* Business Process Ownership: Provide guidance and serve as subject matter expert on business requirements that Information Technology partners will use...
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Type: Permanent Location: Raynham, US-MA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:39
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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:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Toronto, Ontario, Canada
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 Site Manager (Clinical Research Associate).
This position is a field-based role covering primarily the Greater Toronto Area, Ontario; occasional travel outside of this province as needed. Ideally, the Associate Site Manager should be located in the Greater Toronto Area.
Purpose:
As an Associate Site Manager (Clinical Research Associate), you will be part of the Global Clinical Operations (GCO) Canada team and will be responsible for study site management through the assessment/selection, initiation, maintenance and closure phases of a clinical trial (Phase 1 – 4 trials).
You will be responsible for:
* You are the primary point of contact for the study site; liaison with study teams.
* Your responsibilities include actively identifying and driving patient recruitment strategies at assigned sites.
* You are responsible for monitoring the study/site according to GCP standards and J&J GCO SOPs, both on-site and with remote contacts.
This includes source document verification, Investigator Site File (ISF) review and accurate drug accountability.
* You will provide site training, during site initiation and ongoing, to ensure compliance with all required regulations, SOPs, trial-specific tools and systems, and specialized procedures.
* You will ensure resolution of site-specific issues and will partner closely with investigator and site staff to meet all study timelines.
* You will work closely with the local study operations team to resolve protocol and site-specific issues.
* You will use and maintain the clinical trial tracking system (CTMS) and update the electronic Trial Master File (TMF) as required.
Qualifications / Requirements:
* Bachelor of Science, R.N., or equivalent degree in Biologica...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:37
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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:
Medical Affairs Group
Job Sub Function:
Medical Affairs
Job Category:
Scientific/Technology
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
About Immunology
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.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
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 Associate Director, Global Medical Affairs Execution in our Global Commercial Strategic Organization (GCSO) Immunology Medical Affairs organization to be located in Horsham, PA.
Purpose:
The Associate Director, Global Medical Affairs Execution supports the strategic objectives of the J&J Innovative Medicine Immunology Global Medical Affairs (GMAF) team.
This individual will partner within designated Immunology disease areas ensuring execution of GMAF data generation and dissemination strategies in support of the GMAF Immunology team.
You will be responsible for:
* Partner with GMAF Leaders in preparing robust strategies (including integrated evidence generation plans) for compounds in development that reflect prioritized regional needs and support medical launch excellence
* Global Medical Affairs Team management and coordination
* Development and execution of globally funded medical strategies (i.e.
advisory boards, steering committees, external data landscapes, internal training, etc.)
* Development and execution of comprehensive scientific engagement strategies and congress plans (i.e.
manage internal congress websites, pre/post congress meetings, onsite HCP meetings, etc.)
Qualifications / Requirements:
* A minimum of a Bachelor’s degree is required, an advanced degree preferred
* A minimum of 6 years of relevant work experience is required
* Experience in a medical, clinical or scientific environment is required
* Project leadership and strong organizational skills are ...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:35
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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:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
PL002 Iłżecka
Job Description:
Position Summary:
Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations.
Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts.
Principal Responsibilities:
• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator-initiated studies through direct negotiation with clinical trial sites or via oversite of a Clinical Research Organization responsible for contract negotiations.
• Responsible for delivery on established targets/measurements.
Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical trial agreements and other relevant legal documents as they relate to various clinical projects.
Ensure that contractual terms and provisions are in compliance with corporate process, systems, and strategies.
• Provide specialized support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.
• Analyze investigator grants for fair market value aligned with regional knowledge and the J&J grant pricing guidelines, and based on adequate scope of work, clinical trial protocol and other clinical trial information.
Participate in and/or lead the approval escalation of grants as appropriate.
• Work with the global CCS team as necessary to review and analyze contractual terms and conditions in order to reach acceptable language.
Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions and communicate such to stakeholders.
Liaise with CCS management and functional CCS support teams, legal, Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and escalate issues as appropriate.
• Work proactively to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the in...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:27
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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:
Finance
Job Sub Function:
Accounting
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:
Johnson & Johnson Innovative Medicine Supply Chain (IM SC) is recruiting for a Senior Financial Analyst IMSC NA PIC COE, supporting our North America Inventory team.
The preferred locations for the role are Titusville, NJ, Raritan, NJ or Horsham, PA.
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/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
This supply chain finance position with Innovative Medicine will be responsible for activities within the North America PIC COE.
The role's focus is to consolidate gross-to-net North America inventory for both actuals and forecast cycles.
This requires the analyst to build and maintain strong relationships within NA IMSC finance by providing accounting expertise and leadership.
The key to this role is to partner with local finance teams as well as work closely with IMSC affiliates, IMPO (Janssen Business Services/JBS), and IM Global Tax Planning ensuring that Supply Chain and Affiliate Gross Profit (AGP...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:25
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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:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson is recruiting for a Senior Financial Analyst located in Horsham, Pennsylvania or Titusville, New Jersey, to support ongoing financial systems and process alignment activities.
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/
Role Description:
The Systems and Process Senior Financial Analyst role will primarily focus on supporting various aspects of the overall Innovative Medicine Finance, Financial Systems Landscape, to ensure information is produced in a standardized way, while also providing local business insights to support and influence data driven decisions.
This includes financial close support, data analytics for system troubleshooting, data management, system security, compliance, business projects, and system enhancement and optimization initiatives.
These responsibilities require building effective cross functional partnerships for coordinating, supporting, and leading assigned projects and phases of other projects for US Innovative Medicine Finance as well as contributing to corporate wide standardization initiatives within Global Finance.
Business partners include GFS, Commercial Finance, Financial Reporting, Tax, Supply Chain Finance, Global IT, Systems Security, Corporate and other project management personnel.
This role will also partner within US Innovative Medicine Finance and other functional areas, when applicable, to document and analyze current business, financial and data utilization practices leveraging process excellence tools.
Responsibilities:
* Knowledge expert in financial system integrations ensuring accurate system structures to enable financial processes.
* Identify and implement efficiency opportunities leveraging current systems or ado...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:20
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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:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Facilities – Operations, binnen onze afdeling “Engineering & Property services” beheert de kritische gebouwen, HVAC, nutsvoorzieningen (stoom, koelmedia, verwarmingsmedia, watersystemen, perslucht, hoogspanning…) en installaties (stoomvormers, koelcellen, luchtgroepen, clean rooms, magazijnen...) op de sites te Beerse, Geel, Olen, Merksem, La Louviere, Courcelles en Gent; vanaf de centrale productie en distributie tot in de chemische, farmaceutische productie- en R&D-gebouwen en Advanced Therapy labo’s.
Voor de groep welke verantwoordelijk is voor de onderhoudsystemen en compliance methodieken, voor de uitbating van kritische installaties/systemen/services op de verschillende Belgische campussen, zijn we op zoek naar een Senior Compliance Engineer:
Doel:
* Het managen van de compliance methodieken binnen E&PS.
* Expert in de levenscyclus voor computer system validation, level 1 tot en met level 4 systemen, binnen E&PS.
* Coordineren van de compliance status van verschillende services, zoals programma soft services beheer, pestcontrole, cleaning.
* Bewaken van de uitbestede services, operationele compliance en projectkwalificaties gedragen door commissioning en kwalificatie.
* Opvolgen van het inspectie readiness programma voor de E&PS organisatie.
* Expertise in de processen zoals mappingen, certificatie, calibratie en andere.
* Aanspreekpunt voor de verschillende compliance programma’s komende van J&J en E&PS globaal naar implementatie.
* Ondersteunen van andere E&PS sites, op vraag.
U bent verantwoordelijk voor:
* Ownership over het horizontaal proces “compliance”.
+ Coordineert de periodieke meeting met de Compliance Engineers uit de operationele zuilen;
+ Beheerder van het ontwikkelings- en overleg model voor de compliance methodieken.
* Aanspreekpunt computer system validation voor de bestaande E&PS systemen en de nieuwe ontwikkelingen.
+ Beheerder, vanuit het escalatie model, over de bestaande ticketten van de computer systemen;
+ Evalueert en ondersteunt nieuwe ontwikkelingsvragen vanuit E&PS.
* Coordineren en ondersteunen van de compliance activiteiten van de verschillende E&PS services tot een inspectie re...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:15
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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:
Legal & Compliance
Job Sub Function:
Health Care Compliance
Job Category:
Professional
All Job Posting Locations:
Bucureşti, Romania
Job Description:
Senior Health Care Compliance Specialist
Location: Romania
Full-Time - permanent contract
SUMMARY:
The Health Care Compliance Senior Specialist supports Health Care Compliance Programs to ensure business practices and activities are in compliance with related Johnson & Johnson internal guidelines, local laws and regulations and anticorruption laws, including the Foreign Corrupt Practices act.
Therefore, the candidate supports planning, trainings, assessments, testing & monitoring and other varied Health Care Compliance functions.
This position reports directly to the Health Care Compliance Officer.
Position is located in Bucharest and supports the Health Care Compliance Program in Romania.
PROFILE:
* Requires strong communication, organizational and analytical skills
* Proven track record in delivering results, self-starter and ability to manage complexity it is a must
* Industry related experience preferred, experience in the Pharmaceutical or Consumer industries
* Ability to work independently and in a detailed manner
* Ability to manage conflicts in an open and constructive manner
* Ability to work well between functions and across all levels of the business and effective time management skills are essential
* Understands the J&J Credo based culture and able to make things happen through managing a broad set of J&J Credo based values
* Background may include Compliance, Medical Affairs, Regulatory
* Fluent in English language
ESSENTIAL DUTIES AND RESPONSIBILITIES:
The Health Care Compliance Senior Specialist will work with Health Care Compliance Officer (HCCO) - to implement the company’s compliance program on various activities, which may include but not limited to the following:
* Assist HCCO in the update and implementation of all HCC policies (SOPs) and procedures on an ongoing basis.
* Support the HCCO in the implementation of education, training, and regular communications in compliance to all covered employees, including local sales, marketing, medical affairs, finance, HR, supply chain at the local level.
* Prepare the report of unplanned deviations, consolidate data & metrics relevant to Risk Assessment process and support HCCO in managing day-to-day inquiries, al...
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Type: Permanent Location: Bucureşti, RO-B
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:09
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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:
Business Support
Job Sub Function:
Administration & Secretarial
Job Category:
Business Enablement/Support
All Job Posting Locations:
Amersfoort, Utrecht, Netherlands
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Administrator to be in Amersfoort!
The Administrator Service Center plays a crucial role in ensuring the smooth and efficient operation of the organization by managing administrative tasks, coordinating office activities, and providing support to various departments.
The primary goal of this position is to facilitate a well-organized and productive work environment so that the organization can achieve its objectives.
You will be responsible for:
* Office Management: Supervise daily office operations and ensure a clean and organized work environment.
Manage office supplies, equipment, and facilities to meet the needs of the staff.
* Communication and Correspondence: Manage incoming and outgoing communications, including emails, phone calls, and written correspondence.
* Record and Data Management: Maintain accurate records, files, and databases.
Assist with data entry and retrieval, ensuring the confidentiality and integrity of information.
* Support to Management: Provide administrative support to executives and managers.
Help prepare reports, presentations, and documentation as needed.
* Teamwork: Collaborate with various departments to facilitate cross-functional communication and cooperation.
Qualifications/Requirements:
* Secondary education; additional training or certification in office management or a related field is a plus.
* Full proficiency in Dutch and English, both written and spoken, at a professional level is required.
* Proven experience in administrative roles, with a successful track record in effectively managing office operations and familiarity with common office software and tools.
* Strong verbal and written communication skills to effectively connect with individuals at all levels within the organization.
* Outstanding organizational and multitasking skills with a focus on accuracy and completeness.
*...
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Type: Permanent Location: Amersfoort, NL-UT
Salary / Rate: Not Specified
Posted: 2025-06-02 08:04:02
