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Join our growing Cardiology team as an experienced Echo Tech!
New hire generally starts between $44.95-$56.35/hour, and placement in the range is based on an evaluation of experience.
Schedule: Flexible three days a week (M-F), 10-hour shift 7am to 6pm - NO nights, NO weekends, NO call!
Location: 87th Ave location
As an Echo Tech you will:
* Perform transthoracic echocardiograms on patients (including 2D, m-mode, PW, CW and color Doppler) and obtain the highest quality of images possible.
* Perform both stress echoes and pharmacological stress echocardiograms and obtain the highest quality of images possible.
* Perform Bubble Studies and obtain the highest quality and images possible.
* Perform Strain Imaging if ordered or at technicians' discretion.
* Use Contrast if ordered or at technicians' discretion.
* Provide preliminary findings from exams and accurately completes exam worksheets including measurements and calculations.
* Individual interaction with and treatment of patients during exams, with special attention to privacy needs.
Patient positioning is done with consideration of patient's ability to comply.
Requirements:
* Completion of an accredited program in Cardiovascular Technology or Diagnostic Medical Sonography required.
* Current certification in Adult Echocardiography within one year of hire or transfer (ARDMS-RDCS or CCI-RCS) required.
* Minimum three years of experience performing and interpreting 2D, M-Mode, Doppler Echocardiograms and stress echocardiograms required.
* Current Health Care Provider BLS CPR certification.
* Knowledge of current accepted Echocardiography principles, practices, and techniques, including cardiac anatomy, physiology, and pathophysiology required
Pay Range:
$44.09 - $66.15
The above information is intended to indicate the general nature and level of work required in this position.
It is not designed to contain or be interpreted as a comprehensive description of all duties, responsibilities, and qualifications required of those assigned to this job.
We offer a competitive Total Rewards Program.
Eligibility for benefits is dependent on factors such as position type and FTE.
Benefit-eligible employees qualify for benefits beginning on the first of the month following one month of employment.
Vancouver Clinic offers medical, dental, vision, life insurance, AD&D, long term disability, health savings account, flexible spending account, employee assistance program, and multiple supplemental benefits (voluntary life, critical illness, accident, hospital indemnity, identity theft protection, legal services, etc.).
We also offer a 401k retirement plan, with employer contributions after your first year of employment.
Benefits-eligible employees accrue PTO and Personal Time based on hours worked and State worked, totaling 120 hours in the first year for full time staff and 200 hours in the first year for full time supervisors and above, incr...
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Type: Permanent Location: Vancouver, US-WA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:12
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Werde Lagermitarbeiter / Kommissionierer für Briefe und Pakete in Dreieich
Was wir bieten
* 16,60 € Tarif-Stundenlohn inkl.
50% Weihnachtsgeld
* + 25% Nachtzulage steuerfrei schon ab 20:00 Uhr (bis 6:00 Uhr)
* Weitere 50% Weihnachtsgeld im November
* Bis zu 332 € Urlaubsgeld
* Du kannst sofort befristet in Teilzeit starten, ab 10 Stunden/Woche
* Ein krisensicherer Arbeitsplatz, bezahlte Einarbeitung, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Kostenlose Ausstattung, wie z.B.
Sicherheitsschuhe und Schutzhandschuhe
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Teamleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote, wie z.B.
Rabatte bei Mobilfunkanbietern, Fitnessstudios, Modemarken etc.
Deine Aufgaben als Kommissionierer bei uns
* Bedienen der Kommissionieranlagen
* Heranholen und Zuführen der Briefbehälter und Pakete
* Abnahme und Abtransport der Briefbehälter
* Unsere Schichten: Mo.- Sa.
* Frühschicht von 07:00 Uhr bis 09:00 Uhr
Was du als Lagermitarbeiter bietest
* Du arbeitest zuverlässig und bist engagiert
* Du kannst anpacken und hast Spaß an körperlicher Arbeit
* Du kannst dich auf Deutsch unterhalten
* Du arbeitest gern im Team
Werde Kommissionierer bei Deutsche Post DHL
Als Kommissionierer in unserem Lager sorgst du dafür, dass unsere Briefe pünktlich ankommen! Bei uns sind auch Quereinsteiger oder Studenten herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Lagerhelfer, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#kommissionierer
#werdeeinervonunslagerhelfer
#jobsNLFrankfurt
....Read more...
Type: Contract Location: Dreieich, DE-HE
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:12
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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:
Packaging Design Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Schaffhausen, Switzerland
Job Description:
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 Senior Packaging Engineer to be based in Schaffhausen, Switzerland.
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 & Puerto Rico - Requisition Number: R-035182
Italy & Belgium - Requisition Number: R-036150
Switzerland- Requisitions Number: R-036183
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
As a Primary Packaging Lifecycle Engineer, you will have the unique opportunity to contribute to the ongoing lifecycle management of primary container closure systems, dosing devices, and critical secondary packaging materials in our Janssen Supply Chain network.
Your technical expertise and problem-solving skills will be vital in ensuring flawless packaging solutions for our pharmaceutical products
Responsibilities:
* Investigate the suitability of packaging materials and devices for pharmaceutical products, ensuring compatibility, protection, safety, and processability.
* Lead root cause investigations, develop improvement plans, and prepare technical documents.
* Facilitate changes by following the change control procedure, assuming roles such as change owner, assessor, or action item owner.
* Introduce innovative techniques to improve process efficiency and quality.
* Collaborate with external suppliers and receiving sites to develop robust packaging processes.
* Provide technical expertise for the design and technology transfer of primary p...
....Read more...
Type: Permanent Location: Schaffhausen, CH-SH
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:10
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Packaging Design Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Latina, Italy
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Senior Packaging Engineer to be based in Latina, Italy or Belgium.
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 & Puerto Rico - Requisition Number: R-035182
Italy & Belgium - Requisition Number: R-036150
Switzerland- Requisitions Number: R036183
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
As a Primary Packaging Lifecycle Engineer, you will have the unique opportunity to contribute to the ongoing lifecycle management of primary container closure systems, dosing devices, and critical secondary packaging materials in our Janssen Supply Chain network.
Your technical expertise and problem-solving skills will be vital in ensuring flawless packaging solutions for our pharmaceutical products
Responsibilities:
* Investigate the suitability of packaging materials and devices for pharmaceutical products, ensuring compatibility, protection, safety, and processability.
* Lead root cause investigations, develop improvement plans, and prepare technical documents.
* Facilitate changes by following the change control procedure, assuming roles such as change owner, assessor, or action item owner.
* Introduce innovative techniques to improve process efficiency and quality.
* Collaborate with external suppliers and receiving sites to develop robust packaging processes.
* Provide technical expertise for the design and technology transfer of primary packag...
....Read more...
Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:06
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ABOUT US
Hoffmaster Group Inc, is an industry leader producing the most complete line of specialty disposable tabletop products for over 70 years.
Hoffmaster competes in three distinct business segments - Foodservice, Consumer, and E-Commerce.
Our products can be found in thousands of retailers, restaurants, hotels, and more.
As a customer centric company, we strive to deliver innovative solutions to both our customers and the ultimate end users of our products.
This Innovation is a key part of what we do here at Hoffmaster, and we continue to drive the industry forward by investing in our employees and state-of-the-art technology.
All new employees are eligible for a $1500 sign on bonus!! Tell your family and friends...
PRIMARY PURPOSE OF THE ROLE
Rewind Operators run our rewinder machines to rewind paper into different sizes and lengths.
This position requires operating the machine in safe manner while following established safety policies, properly tracking the raw materials used and the finished good produced, and keeping the machine at 5S standards.
An Operator must be able to work overtime when required and perform other duties as assigned by their supervisor or team lead.
ESSENTIAL JOB DUTIES
* Efficiently operate the assigned rewinder machine in a safe manner, meeting daily established production goals
* Efficiently perform machine make-readies
* Accurately report daily production of machine
* Read and interpret a manufacturing order to ensure finished product meets specifications
* Effectively troubleshoot machine issues and make adjustments as needed
* Work overtime as necessary to cover other shift operators and meet overall production demand
* Ensure correct product (raw materials, sizes, ink colors, quantities, etc.) are being manufactured
* Document and quality check output of machines to ensure consistency and quality
* Wear appropriate PPE and conduct work with a safety-focused mindset, follow all company safety policies
* Report any unsafe acts or conditions to the supervisor or lead person
* Maintain 5S standards
KNOWLEDGE
Required Skills/Abilities
* Knowledge of industrial manufacturing equipment; paper converting and/or rewinding preferred
* Knowledge of best practices and procedures for machine operation
* Skill in oral and written communication
* Basic math skills required
* Skill in working well with others / teamwork
* Ability to flexible, self-directed, and motivated to improve processes
* Ability to be patient and adaptable to unforeseen changes
* Ability to work overtime when needed
* Ability to communicate effectively with team members
* Ability to come to work prepared, on-time, and with a positive attitude
Education
Min/Preferred
Education Level
Description
Preferred
High School or GED
Preferred
Vocational / Technical
Related certifications (Lean Manufacturing, 5S, etc.)
Years ...
....Read more...
Type: Permanent Location: Sparks, US-NV
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:03
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Primary of the Purpose
The Process Engineer will be responsible for designing, implementing, and improving manufacturing processes to ensure efficient production and product quality.
This role involves collaborating with cross-functional teams, identifying and building robust processes around equipment run-ability as well as driving initiatives to enhance product reliability and customer satisfaction.
This individual can also perform work associated with the design, building, repair, and maintenance of manufacturing plants and their machinery along with managing small - medium new equipment and product launches including trials
Essential Job Duties
Process Improvement & Optimization:
* During new equipment and product launches, analyze and identify opportunities to improve production processes, reducing waste, enhancing efficiency, and lowering costs.
* Use methodologies such as Lean, Six Sigma, and Kaizen to streamline operations.
* Develop and implement process control plans, procedures, and facilitate new equipment & product launches within manufacturing sites.
* Gathers and analyzes data from relevant sources to identify trends and implement changes to improve operating efficiency of facility, lower costs, and improve safety and quality performance.
* Provides technical support through problem resolution (Root Cause Analysis), preventive/predictive maintenance, and asset optimization, etc.
* Creates and modifies procedures as needed to maximize equipment and maintenance operations.
* Maintains a basic knowledge of the latest developments and technologies relative to machine reliability, asset management, and maintenance operations.
* Assists with New Product Development.
Collaboration & Reporting:
* Work closely with production, design, and supply chain teams to resolve quality issues and improve product/process design.
* On new product and equipment launches, develop key performance indicators (KPIs) for quality, process efficiency, and yield.
* Prepare detailed reports on launch trials, quality metrics, and improvement activities for management review during new equipment and product launches.
Training & Support:
* Facilitate training and guidance to production teams on quality standards, process improvements, and best practices for new product & equipment launches.
* Ensure that quality standards are integrated into all stages of product development and manufacturing.
* Provides active support and participation in safety-related projects as an active member of the Hoffmaster safety culture.
* Follows and maintains all Food Safety, GMP, and HACCP Guidelines.
* Performs other duties as assigned.
Required Skills and Abilities
* Bachelor's degree in Industrial Engineering, Mechanical Engineering, or a related field.
* Minimum of 3 years of experience in process engineering, quality engineering, or manufacturing operations.
* K...
....Read more...
Type: Permanent Location: Oconto, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:02
-
ABOUT US
Hoffmaster Group Inc is an industry leader producing the most complete line of specialty disposable tabletop products for over 70 years.
Hoffmaster competes in three distinct business segments - Foodservice, Consumer, and E-Commerce.
Our products can be found in thousands of retailers, restaurants, hotels, and more.
As a customer centric company, we strive to deliver innovative solutions to both our customers and the ultimate end users of our products.
This Innovation is a key part of what we do here at Hoffmaster, and we continue to drive the industry forward by investing in our employees and state-of-the-art technology.
All new employees are eligible for a $1500 sign on bonus!! Tell your family and friends...
PRIMARY PURPOSE OF THE ROLE
Sleeter Operators run our Sleeter machines to produce various sizes of baking parchment sheets.
This position requires operating the machine in safe manner while following established safety policies, properly tracking the raw materials used and the finished good produced, and keeping the machine at 5S standards.
An Operator must be able to work overtime when required and perform other duties as assigned by their supervisor or team lead.
ESSENTIAL JOB DUTIES
* Efficiently operate the assigned sheeter machine in a safe manner, meeting daily established production goals.
* Efficiently perform machine make-readies
* Accurately report daily production of machine
* Read and interpret a manufacturing order to ensure finished product meets specifications
* Effectively troubleshoot machine issues and make adjustments as needed
* Work overtime as necessary to cover other shift operators and meet overall production demand
* Ensure correct product (raw materials, sizes, ink colors, quantities, etc.) are being manufactured
* Document and quality check output of machines to ensure consistency and quality
* Wear appropriate PPE and conduct work with a safety-focused mindset, follow all company safety policies
* Report any unsafe acts or conditions to the supervisor or lead person
* Maintain 5S standards
KNOWLEDGE
Required Skills/Abilities
* Knowledge of industrial manufacturing equipment; paper converting and/or printing machinery preferred
* Knowledge of best practices and procedures for machine operation
* Skill in oral and written communication
* Basic math skills required
* Skill in working well with others / teamwork
* Ability to flexible, self-directed, and motivated to improve processes
* Ability to be patient and adaptable to unforeseen changes
* Ability to work overtime when needed
* Ability to communicate effectively with team members
* Ability to come to work prepared, on-time, and with a positive attitude
Education
Min/Preferred
Education Level
Description
Preferred
High School or GED
Vocational / Technical
Related certifications (Lean Manufacturing, 5S, etc.)
Years ...
....Read more...
Type: Permanent Location: Sparks, US-NV
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:01
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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 Writing
Job Category:
People Leader
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:
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 Manager, Regulatory Medical Writing to support one or more of our therapeutic areas in within the X-TA Regulatory Medical Writing unit, Integrated Data Analytics & Reporting (IDAR) business.
The position may be in the UK (High Wycombe), Belgium (Beerse), Netherlands (Leiden) or the United States (Raritan, Springhouse or Titusville).
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 position is Hybrid (3 days onsite weekly).
Remote work options may be considered on a case-by-case basis and if approved by the company
Are you ready to join our team? Then please read further!
You will be responsible for:
* Preparing and finalizing all types of clinical documents independently within and across therapeutic areas (TAs).
* Leading in a team environment.
Working with a high level of independence and taking a lead role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking.
May consult with more senior colleagues on complex situations.
* Lead and actively participate in setting functional tactics/strategy as needed.
* Oversee the work of external contractors
* Leading or setting objectives for others on team projects and tasks, eg, leading process working groups.
* Guiding or training cross-functional team members on processes and best practices.
* Potentially leading project-level/submission/indication writing teams.
* If a lead writer for a program/compound (or submissions, indications, or disease areas): act as the primary point of contact ...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:00
-
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 Writing
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Leiden, South Holland, Netherlands
Job Description:
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 Manager, Regulatory Medical Writing to support one or more of our therapeutic areas in within the X-TA Regulatory Medical Writing unit, Integrated Data Analytics & Reporting (IDAR) business.
The position may be in the UK (High Wycombe), Belgium (Beerse), Netherlands (Leiden) or the United States (Raritan, Springhouse or Titusville).
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 position is Hybrid (3 days onsite weekly).
Remote work options may be considered on a case-by-case basis and if approved by the company
Are you ready to join our team? Then please read further!
You will be responsible for:
* Preparing and finalizing all types of clinical documents independently within and across therapeutic areas (TAs).
* Leading in a team environment.
Working with a high level of independence and taking a lead role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking.
May consult with more senior colleagues on complex situations.
* Lead and actively participate in setting functional tactics/strategy as needed.
* Oversee the work of external contractors
* Leading or setting objectives for others on team projects and tasks, eg, leading process working groups.
* Guiding or training cross-functional team members on processes and best practices.
* Potentially leading project-level/submission/indication writing teams.
* If a lead writer for a program/compound (or submissions, indications, or disease areas): act as the primary point of contact and champion for medical writing activities for the clinical team.
Responsible for planni...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-03 08:36:00
-
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 Writing
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Dublin, Ireland, Imperia, Italy, Issy-les-Moulineaux, France, Leiden, South Holland, Netherlands, Madrid, Spain, Neuss, North Rhine-Westphalia, Germany
Job Description:
At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives.
We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.
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, Regulatory Medical Writing within our Integrated Data Analytics & Reporting (IDAR) business.
This role will support one or more of our therapeutic areas within the X-TA Regulatory Medical Writing area.
This position is open globally and may be in Europe (eg, United Kingdom, Ireland, Belgium, Netherlands, Germany, France, Spain, Italy), in addition to North America (eg, Spring House, PA, Raritan, NJ, or Titusville, NJ).
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.
This can be a hybrid (3 days in office and 2 remote) OR Remote role available in all countries listed above.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
Are you ready to join our team? Then please read further!
You will be responsible for:
* Leading compound/submission/indication/disease area writing teams independently.
* May have additional major responsibility with supervision.
* Cross-functional, cross-TA, or cross-J&J initiative/collaboration.
* Larger organizational responsibility (eg, manage a subset of TA).
* Preparing and finalizing all types of clinical documents, taking a proactive or lead role in terms of content and scientific strategy.
Working with a high level of independence and taking a lead role on with respec...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:59
-
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 Writing
Job Category:
People Leader
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:
At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives.
We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.
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, Regulatory Medical Writing within our Integrated Data Analytics & Reporting (IDAR) business.
This role will support one or more of our therapeutic areas within the X-TA Regulatory Medical Writing area.
This position is open globally and may be in Europe (eg, United Kingdom, Ireland, Belgium, Netherlands, Germany, France, Spain, Italy), in addition to North America (eg, Spring House, PA, Raritan, NJ, or Titusville, NJ).
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.
This can be a hybrid (3 days in office and 2 remote) OR Remote role available in all countries listed above.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
Are you ready to join our team? Then please read further!
You will be responsible for:
* Leading compound/submission/indication/disease area writing teams independently.
* May have additional major responsibility with supervision.
* Cross-functional, cross-TA, or cross-J&J initiative/collaboration.
* Larger organizational responsibility (eg, manage a subset of TA).
* Preparing and finalizing all types of clinical documents, taking a proactive or lead role in terms of content and scientific strategy.
Working with a high level of independence and taking a lead role on with respect to timing, scheduling, and...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:59
-
Howmet Aerospace Inc.
(NYSE: HWM), headquartered in Pittsburgh, Pennsylvania, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries.
Our primary businesses focus on jet engine components, aerospace fastening systems, titanium structural parts and forged wheels.
With $7.4 Billion in revenue in 2024, our products play a crucial role in enabling fuel efficiency and lightweighting, contributing to our customers' success and making a positive impact on the world.
To learn more about the way Howmet Aerospace Inc.
is advancing the sustainability of our customers, markets, and communities where we operate, review the 2024 Environmental Social and Governance report at www.howmet.com/esg-report .
Follow: LinkedIn , Twitter , Instagram , Facebook , and YouTube .
Equal Opportunity Employer:
Howmet is proud to be an Equal Employment Opportunity employer.
We are committed to creating an inclusive environment for all employees.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other applicable legally protected characteristics.
If you need assistance to complete your application due to a disability, please email TalentAcquisitionCoE_Howmet@howmet.comBasic Qualifications
* Bachelor's degree from an accredited institution.
* A minimum of three years of experience in a manufacturing environment with increasing responsibility, including supervisory experience.
* This position entails access to export-controlled items and employment offers are conditioned upon an applicant's ability to lawfully obtain access to such items.
* Employees must be legally authorized to work in the United States.
Verification of employment eligibility will be required at the time of hire.
Visa sponsorship is not available for this position.
Preferred Qualifications
* Direct experience with lean manufacturing and continuous improvement initiatives, including participation in Kaizen projects.
* Six Sigma Green Belt or Black Belt certification.
* Experience in Material Resource Planning (MRP) and Six Sigma methodologies.
* A minimum of five years' experience in a manufacturing environment.
Howmet Engines is a world-class producer of aero engine and industrial gas turbine components, including airfoils, rings, disks, and forgings.
We excel in vacuum-melted superalloys, machining, performance coatings, and hot isostatic pressing for high-performance parts that enable the next generation of quieter, more fuel-efficient aero engines and cleaner power generation.
Howmet Dover Casting is a world-class supplier of complex, investment-cast turbine airfoils and other components for the aircraft engine and industrial gas turbine industries.
Howmet Dover Alloy is a world-class supplier of vacuum and air-melted nickel- and cobalt-based supera...
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Type: Permanent Location: Dover, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:58
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Howmet Aerospace Inc.
(NYSE: HWM), headquartered in Pittsburgh, Pennsylvania, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries.
Our primary businesses focus on jet engine components, aerospace fastening systems, titanium structural parts and forged wheels.
With $7.4 Billion in revenue in 2024, our products play a crucial role in enabling fuel efficiency and lightweighting, contributing to our customers' success and making a positive impact on the world.
To learn more about the way Howmet Aerospace Inc.
is advancing the sustainability of our customers, markets, and communities where we operate, review the 2024 Environmental Social and Governance report at www.howmet.com/esg-report .
Follow: LinkedIn , Twitter , Instagram , Facebook , and YouTube .
Equal Opportunity Employer:
Howmet is proud to be an Equal Employment Opportunity employer.
We are committed to creating an inclusive environment for all employees.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other applicable legally protected characteristics.
If you need assistance to complete your application due to a disability, please email TalentAcquisitionCoE_Howmet@howmet.comQualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education and/or Experience
* Bachelor's degree from an accredited institution in Engineering
* Minimum of 1 internship, preferably in aerospace or 6 months of related experience
Howmet Fastening Systems (HFS) is seeking an Engineer I at our City of Industry, CA location.
Howmet Aerospace Inc.
(NYSE: HWM), headquartered in Pittsburgh, Pennsylvania, is a leading global provider of advanced engineered solutions for the aerospace and transportation industries.
Our primary businesses focus on jet engine components, aerospace fastening systems, titanium structural parts and forged wheels.
With $7.4 Billion in revenue in 2024, our products play a crucial role in enabling fuel efficiency and lightweighting, contributing to our customers' success and making a positive impact on the world.
To learn more about the way Howmet Aerospace Inc.
is advancing the sustainability of our customers, markets, and communities where we operate, review the 2024 Environmental Social and Governance report at www.howmet.com/esg-report .
Follow: LinkedIn , Twitter , Instagram , Facebook , and YouTube .
Born from many well-known and long-standing brands, Howmet Fastening Systems, headquartered in Torrance, California, is the premier designer and manufacturer of aerospace and indust...
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Type: Permanent Location: City of Industry, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:57
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Werde Lagermitarbeiter / Kommissionierer für Briefe in Langenselbold
Was wir bieten
* 16,60 € Tarif-Stundenlohn inkl.
50% Weihnachtsgeld
* + 25% Nachtzulage steuerfrei schon ab 20:00 Uhr (bis 6:00 Uhr)
* Weitere 50% Weihnachtsgeld im November
* Bis zu 332 € Urlaubsgeld
* Du kannst sofort befristet in Teilzeit starten, ab sofort mit 17,5 Stunden/Woche Dienstag bis Samstag
* Ein krisensicherer Arbeitsplatz, bezahlte Einarbeitung, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Kostenlose Ausstattung, wie z.B.
Sicherheitsschuhe und Schutzhandschuhe
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Teamleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote, wie z.B.
Rabatte bei Mobilfunkanbietern, Fitnessstudios, Modemarken etc.
Deine Aufgaben als Kommissionierer bei uns
* Heranholen und Zuführen der Briefbehälter
* Abnahme und Abtransport der Briefbehälter
* Unsere Schichten:
+ 05:00 Uhr bis 08:30 Uhr
Was du als Lagermitarbeiter bietest
* Du arbeitest zuverlässig und bist engagiert
* Du kannst anpacken und hast Spaß an körperlicher Arbeit
* Du kannst dich auf Deutsch unterhalten
* Du arbeitest gern im Team
Werde Kommissionierer bei Deutsche Post DHL
Als Kommissionierer in unserem Lager sorgst du dafür, dass unsere Briefe pünktlich ankommen! Bei uns sind auch Quereinsteiger oder Studenten herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Lagerhelfer, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#kommissionierer
#werdeeinervonunslagerhelfer
#jobsNLFrankfurt
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Type: Contract Location: Langenselbold, DE-HE
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:56
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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:
Clinical Development & Research – MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
JOB DESCRIPTION
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 Neuroscience team tackles the world’s toughest brain health challenges including Alzheimer’s disease, Parkinson’s disease, myasthenia gravis, major depressive disorder, bipolar disorder, and schizophrenia.
This patient-focused team helps address some of the most complex diseases of our time.
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
The Study Responsible Physician (SRP) is responsible for design and execution of Ph3 studies in neurologic disorders.
The SRP is a critical member of a cross-functional clinical team led by a Clinical Lead, and provides active medical and scientific contribution to the team. The SRP provides input and helps with the clinical development plan, the development of the clinical trial protocol, clinical trial materials including protocol training, content of clinical study reports and relevant documents for regulatory filings. The SRP provides critical oversight of the medical safety of patients in the clinical trial through frequent and detailed medical data reviews, adverse event and medical history codings, review and coding of protocol deviations, and frequent site interactions to ensure protocol compliance, data quality, and patient safety.
Team matrix interactions of the SRP include project management, finance, legal, quality assurance & compliance, clinical supplies, regulatory affairs, data management, medical writing, biostatistics, global safety, global medical affairs, clinical operations, and other scientific and business-related disciplines. The SRP may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area.
ESSENTIAL FUNCTIONS:
* Responsible for medical monitoring/reporting and compan...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Technology Enterprise Strategy & Security
Job Sub Function:
Security & Controls
Job Category:
Scientific/Technology
All Job Posting Locations:
Seoul, Korea, Republic of
Job Description:
Do you want to be part of an organization that is thriving on a diverse company culture, celebrating the uniqueness of our employees and committed to inclusion? Then join us! We are proud to be an equal opportunity employer.
We are searching for the best talent for Sr.
Manager, Chief Information Security Officer.
The Sr.
Manager, CISO (Chief Information Security Officer) enables a framework of robust security and governance for assessing risks to eliminate threats and takes accountability for Korea business operations in the challenging business landscape and evolving compliance regulations.
As a senior manager, the CISO is responsible for establishing and maintaining a company-wide information and security management program to oversee the protection of people, assets and technology from malicious attacks and to ensure that information assets are adequately protected to meet local privacy and security regulations.
The CISO also serves as a focal point for all assurance activities related to the confidentiality, integrity and availability of customer/patient, business partner, employee and business information in compliance with the J&J Information Asset Protection Policies.
A key element of the CISO's role is working with executive management to determine acceptable levels of risks for the organization.
Key Responsibilities:
- Appointed to local South Korea CISO for cross sector J&J Korea companies and will follow below roles and responsibilities as defined by South Korea Privacy and Security Laws:
* Establish, manage, and operate information security management system.
* Analyze, assess, and improve information security weaknesses.
* Prevent and respond to data breach or data incidents as a focal reporting point for any security related incidents.
* Prepare preventive information protection measures, design, and implement security measures, etc.
* Review of information security risk.
* Carry out other vital measures for information security as required by Korea PIPA and Network Act, including ISMS certification, annual information security public disclosure to the Ministry of Science & ICT, cybersecurity insurance.
- Leading the response to inquiries or investigations from ...
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Type: Permanent Location: Seoul, KR-11
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:53
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Anasco, Puerto Rico, United States of America
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 Manufacturing Engineer Co-Op to be in Añasco, PR.
* The typical Co-op term is from January to December, 2026
* Full time requirement (40 hours per week)
Purpose:
The Project Engineer will play a key role in supporting the Project Management Office (PMO) by providing technical expertise, coordinating project execution activities, and ensuring alignment with established PMO processes.
This role bridges engineering knowledge with project governance, supporting project managers in planning, execution, reporting, and continuous improvement of portfolio management practices.
You will be responsible for:
* Ensure compliance with PMO standards, methodologies, and reporting requirements.
* Maintain accurate project data within portfolio management tools (e.g., Planisware, MS Project, Power BI, PMO SharePoint).
* Support stage-gate reviews, project audits, and portfolio reporting cycles.
* Prepare and deliver project status reports and presentations for stakeholders and leadership.
* Provide technical insights to support decision-making during portfolio prioritization and resource allocation.
* Contribute to the development and refinement of PMO processes, templates, and best practices.
* Identify opportunities for efficiency in project delivery and portfolio reporting.
* Support lessons learned sessions and implementation of corrective actions.
* Performs activities of process/product validation.
* Knowledge of process validation (IQ/OQ/PQ) and familiarity with statistical analysis, preferred.
* Ensuring compliance with all regulatory, safety, and environmental requirements.
* Ability to assess issues and opportunities, establish priorities, and act with a sense of urgency.
Qualifications / Requirements:
* Completion of Undergraduate Freshman year at accredited University is required.
* Currently pursuing a bachelor’s d...
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Type: Permanent Location: Anasco, US-PR
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:42
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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:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
People Leader
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson Innovative Medicine (J&J IM), a pharmaceutical company of Johnson & Johnson is recruiting for a Director, R&D Data Science – Product Mastering, Consent & Preference Management.
This position has a primary location of Titusville, NJ but is also open to Spring House, PA or Cambridge, MA. This position requires up to 25% travel.
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
Position Summary
The Director, Product Mastering and Consent & Preference Management leads the strategy, governance, and operationalization of patient-centric master data across R&D.
This role is responsible for ensuring that patient, consent, and preference data are accurate, complete, traceable, and accessible across the enterprise, enabling trusted data use in clinical development, real-world evidence generation, and regulatory submissions.
As part of the R&D Data Science & Digital Health – Data Strategy & Products team, the Director will define and implement best-in-class approaches for patient mastering and consent and preference management.
This includes harmonizing patient identifiers across systems, establishing clear stewardship practices, and embedding privacy and compliance requirements to support ethical and responsible use of patient data.
Key Responsibilities:
Patient Master Data Strategy & Execution
* Lead the design and delivery of a forward-looking patient mastering strategy that ensures consistent, high-quality, and fit-for-purpose patient and participant data across R&D.
* Develop and maintain a unified patient master that connects patient, account, and clinical study data for seamless interoperability.
Consent & Preference Management
* Establish frameworks and tools for capturing, managing, and tracking patient c...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:34
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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:
Non-Standard
Job Sub Function:
Fixed Term Employee
Job Category:
Non-Standard
All Job Posting Locations:
Chiyoda, Tokyo, Japan
Job Description:
Job Summary:
The Supply Chain Finance Contractor will be supporting the activity at Plant located in Fuji, Japan.
This position reports to the Finance Manager of Innovative Medicine Supply Chain (IMSC) Japan and has close interaction with local departments and international business partners.
Key Responsibilities:
* Support Financial Planning & Analysis of the plant, including expenses, headcount, capital for budget cycle.
* Prepare analysis & management report to departments including capital/ investment proposals and Cost Improvement Project.
* Perform month end close activities related to Cost Accounting.
* Develop and maintain standard costs of finished goods and production components in SAP; maintain periodic cost rolls/updates.
* Support in maintaining and improving processes and compliance controls associated with manufacturing costs and inventory valuation.
* Support in preparation of actual vs.
plan analysis related to manufacturing costs, inventory, and expense information.
Work location:
Based in Tokyo. Potential day trips to Fuji Plant.
Qualifications - External
* Bachelor degree in Finance/Accounting or equivalent with professional certification such as CPA, CMA
* 5+ years of accounting experience
* Knowledge of SAP and cost accounting will be at advantage
* Fluent in English and Japanese, written and verbal
* Good analytical skills with strong focus on accuracy and attention to detail
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Type: Permanent Location: Chiyoda, JP-13
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:26
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Packaging Design Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Guaynabo, Puerto Rico, United States of America, Horsham, Pennsylvania, United States of America, Malvern, Pennsylvania, 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
We are searching for the best talent for a Senior Packaging Engineer to be based in Guaynabo PR.
Alternative locations include Horsham, Pennsylvania, Malvern, Pennsylvania, Springhouse, Pennsylvania, and Titusville, New Jersey.
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 & Puerto Rico - Requisition Number: R-035182
Italy & Belgium - Requisition Number: R-036150
Switzerland- Requisitions Number: R-035182
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
As a Primary Packaging Lifecycle Engineer, you will have the unique opportunity to contribute to the ongoing lifecycle management of primary container closure systems, dosing devices, and critical secondary packaging materials in our Janssen Supply Chain network.
Your technical expertise and problem-solving skills will be vital in ensuring flawless packaging solutions for our pharmaceutical products
Responsibilities:
* Investigate the suitability of packaging materials and devices for pharmaceutical products, ensuring compatibility, protection, safety, and processability.
* Lead root cause investigations, develop improvement plans, and prepare technical documents.
* Facilitate changes by following the change control procedure, assuming roles ...
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Type: Permanent Location: Guaynabo, US-PR
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:21
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Manufacturing
Job Sub Function:
Multi-Family Supply Chain Manufacturing
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America, Wilson, North Carolina, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Vice President, Global Lead Biotherapeutics Engineering located in Wilson, North Carolina or Raritan, New Jersey.
The Vice President, Global Lead Biotherapeutics Engineering is a vital leadership role entrusted with shaping the technical future and operational excellence of our biotherapeutics network across multiple global sites.
This leader oversees the successful execution of large-scale capital projects, drives regulatory compliance, and builds resilient, sustainable capabilities that enhance performance in a tightly regulated environment.
In this role, the VP will be responsible for developing and overseeing engineering strategies and governance models, while ensuring flawless execution across all internal biotherapeutics manufacturing sites.
A core responsibility will be leading the development of multi-site CAPEX plans, aligning investment priorities with business and site strategies, and ensuring disciplined capital allocation.
Working in close partnership with cross-functional global leads, site management, and platform stakeholders, the successful candidate will serve as a key influencer shaping engineering direction and execution across the biotherapeutics network, driving technical consistency, mitigating risk, and enabling operational excellence at scale.
Strategic Engineering Leadership and Capital Planning:
• Define and execute the long-term engineering vision for the biotherapeutics network, ensuring alignment with MTO strategy and enterprise priorities.
• Lead the development of multi-site capital investment strategies and Long-Range Financial Plans (LRFP) to enable growth, innovation, and supply resilience.
• Shape and oversee global engineering masterplans for facilities, utilities, and infrastructure, ensuring optimal lifecycle management of assets.
• Champion best-in-class engineering solutions that improve productivity, sustainability, and cost efficiency across the network.
• Drive business case development, CAPEX justification, and disciplined capital allocation to maximize value creation.
• Ensure successful delivery of a diverse por...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:13
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Werde Postbote für Pakete und Briefe in Emleben bei Gotha
Was wir bieten
* 17,40 € Tarif-Stundenlohn inkl.
50% Weihnachtsgeld
* Weitere 50% Weihnachtsgeld im November
* Bis zu 332 € Urlaubsgeld
* Du kannst ab sofort befristet in Vollzeit starten, 38,5 Stunden/Woche
* Möglichkeit der Auszahlung von Überstunden und zusätzlichen Vergütung durch bspw.
freiwillige Rufbereitschaft
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Kostenlose Bereitstellung von hochwertiger Arbeitskleidung
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für die Zustellung
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Postbote bei uns
* Zustellung von Brief- und Paketsendungen mit zur Verfügung gestellten Hilfsmitteln
* Auslieferung an 5 Werktagen (zwischen Montag und Samstag)
* Sendungen im Durchschnitt unter 10 kg
* Zustellung mit unseren Geschäftsfahrzeugen, bspw.
vollelektrische Fahrzeuge
Was du als Zusteller bietest
* Du darfst einen Pkw fahren
* Du kannst dich auf Deutsch unterhalten
* Du bist wetterfest und kannst gut anpacken
* Du bist zuverlässig und hängst dich rein
Werde Postbote bei Deutsche Post DHL
Als Postbote bringst du den Menschen in deinem Bezirk Brief- und Paketsendungen.
Dabei lässt du dir von keinem Wetter die Laune verderben.
Auch Quereinsteiger oder Studenten sind bei uns herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Fahrer, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#werdeeinervonunspostbote
#jobsNLErfurt
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Type: Contract Location: Emleben, DE-TH
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:10
-
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:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
Scientific/Technology
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
We are searching for the best talent for a Technical Product Owner.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Responsibilities:
* Shape the squad vision / roadmap and steer the squad in delivering products / platforms features / work oriented around business impact
* Shape and prioritize backlog, utilizing business expertise and understanding of customer needs, translate requirements into user stories & acceptance criteria
* Balance business value with technical feasibility while prioritizing stories and features, optimizing cost and improving delivery efficiency
* Act as the “voice of the customer” within the squad to ensure the squad “builds the right thing”
* Plan resourcing for the squad (i.e.
new role, change in role), create ASOE requests, interview, select and onboard members to join the squad
* Accountable for shaping and hitting squad OKRs
* Work closely with Product/Platform Manager to establish the products’ business value and support messaging, comms and customer outreach as necessary
* Ensure the products / features / work meets relevant security, privacy & compliance standards
* Drive continuous improvement across the product lifecycle
* Drive engagement with third parties to support delivery of squad objectives
* Drive selection of solution options, work with the Lead Engineer to assess tech elements of the solution prior to user testing
* Facilitate release planning, sprint planning and demos with stakeholders
* Interact with other Squads within the Product / Platform as part of synch...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:35:06
-
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:
Pharmaceutical Sales
Job Sub Function:
Sales – Immunology (Commission)
Job Category:
Professional
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
We are searching for the best talent for an Immunology Sales Specialist-Rheumatology to support clients in the Riverside & Palm Springs, CA territory.
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
As the Immunology Sales Specialist, you will:
* Be responsible for attaining sales objectives, presenting complex clinical and business information on Janssen Biotech's immunology products and services to an audience of office and institutional based Dermatology healthcare professionals, government agencies, professional and patient groups, health plans and others involved in the decision-making process.
* Use discretion and judgment to execute the franchise and company brand strategy and tactics within the assigned customer segment, which may include physicians within specialty medical practices and their staff, specialists within local hospitals, clinics, and pharmacists within a specific geographic area.
* Influence decision makers and influencers within assigned customers to support the use of the company's products in the treatment of relevant disease states by developing and applying clinical and business expertise, and effective selling skills.
* Execute marketing strategies at the local level, leveraging resources appropriately and working successfully with company team members and counterparts to share ideas and information to enhance business results.
* Build customer loyalty by identifying and cultivating relationships with key decision makers at the local level who can influence decision making within the healthcare provider systems.
Required ...
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Type: Permanent Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-03 08:34:59
-
Werde Starkverkehrsunterstützung als Postbote für Pakete und Briefe in Eisenach
Was wir bieten
* 17,40 € Tarif-Stundenlohn inkl.
50% Weihnachtsgeld
* Anteilig Weihnachtsgeld im November
* Du kannst ab September befristet in Vollzeit starten, 38,5 Stunden/Woche
* Möglichkeit der Auszahlung von Überstunden und zusätzlichen Vergütung durch bspw.
freiwillige Rufbereitschaft
* Ein krisensicherer Arbeitsplatz, garantierte Gehaltssteigerung gemäß Tarifvertrag und pünktliche Gehaltszahlungen
* Möglichkeit der Sprachförderung
* Kostenlose Bereitstellung von hochwertiger Arbeitskleidung
* Ausführliche Einweisung (bezahlt) – wir machen dich fit für die Zustellung
* Unbefristete Übernahme und Entwicklungsmöglichkeiten (bspw.
Standortleiter) bei guten Leistungen und offenen Positionen möglich
* Attraktive Mitarbeiterangebote wie z.B.
arbeitgeberfinanzierte betriebliche Altersvorsorge, Fahrradleasing, Rabatte bei Mobilfunkanbietern, etc.
Deine Aufgaben als Postbote bei uns
* Zustellung von Brief- und Paketsendungen mit zur Verfügung gestellten Hilfsmitteln
* Auslieferung an 5 Werktagen (zwischen Montag und Samstag)
* Sendungen im Durchschnitt unter 10 kg
* Zustellung mit unseren Geschäftsfahrzeugen, bspw.
vollelektrische Fahrzeuge
Was du als Zusteller bietest
* Du darfst einen Pkw fahren
* Du kannst dich auf Deutsch unterhalten
* Du bist wetterfest und kannst gut anpacken
* Du bist zuverlässig und hängst dich rein
Werde Postbote bei Deutsche Post DHL
Als Postbote bringst du den Menschen in deinem Bezirk Brief- und Paketsendungen.
Dabei lässt du dir von keinem Wetter die Laune verderben.
Auch Quereinsteiger oder Studenten sind bei uns herzlich willkommen, denn du zählst, wie du bist!
Wir freuen uns auf deine Bewerbung als Fahrer, am besten online! Klicke dazu einfach auf den 'Bewerben'-Button – auch ganz ohne Lebenslauf.
MENSCHEN VERBINDEN, LEBEN VERBESSERN
#werdeeinervonuns
#werdeeinervonunspostbote
#jobsNLErfurt
....Read more...
Type: Contract Location: Eisenach, DE-TH
Salary / Rate: Not Specified
Posted: 2025-10-03 08:34:56
