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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:
Professional
All Job Posting Locations:
New Brunswick, New Jersey, United States of America
Job Description:
Employer: Janssen Research & Development, LLC
Job Title: Medical Writing Scientist
Job Code: A011.6201.6
Job Location: New Brunswick, NJ
Job Type: Full-Time
Rate of Pay: $127,000 - $145,000
Job Duties: Prepare regulatory documents to support development of novel pharmaceutical products in the oncology space.
Interpret, summarize, and present statistical and medical information concisely and clearly to ensure quality and accuracy of content in complex document types.
Author and coordinate clinical document preparation, including but not limited to Investigators Brochure, summary documents, clinical protocols, and Clinical Study Reports in alignment with internal standards, regulatory requirements, Medical Writing Style Guide, publishing guidelines, and team needs.
Proactively participate in cross-functional document planning and review meetings.
Ensure timely and high-quality completion of all assigned tasks, time reporting, training, and metrics database updates as required.
May telecommute.
Requirements: Employer will accept a Master's degree in Biology (Molecular/Cell), Biochemistry, Pharmacy, or related field and 2 years of experience in the job offered or in a Medical Writing Scientist-related occupation.
This job posting is anticipated to close on 6/11/2025.
Johnson & Johnson is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.
We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs.
If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
The anticipated base pay range for this position is :
$127,00...
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Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:26
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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:
Career Programs
Job Sub Function:
Post Doc – R&D Product Development
Job Category:
Career Program
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Contributes to projects and studies within R&D Product Development, with individual development opportunities tailored to the needs of the department and personal goals.
Continues to develop skillset from assignments and advanced training in area of relevant doctoral degree.
Develops comprehensive knowledge of the organization's R&D Product Development processes and policies.
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:19
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmacokinetics & Pharmacometrics
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Principal Scientist Bioanalytical Assay Development (LBA & LC-MS), BDDS
Johnson & Johnson Innovative Medicine is recruiting for a Principal Scientist, Bioanalytical Discovery & Development Sciences, located in Beerse, Belgium.
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, an inclusive work environment has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Guided by Our Credo, this value empowers our commitment to fostering a healthier and 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.
The Development PK team within Bioanalytical Discovery & Development Sciences (BDDS) Department at our research division in Beerse (Belgium) is seeking a bioanalytical assay development expert (Principal Scientist level) with hands-on experience in protein therapeutics (monoclonal Ab, ADCs, fusion proteins, etc) bioanalysis using both LBA and LC-MS approaches.
You will provide technical project leadership focused on the development of innovative bioanalytical assays to support J&J's pipeline.
You will be operating in a regulated bioanalytical lab that provides bioanalytical support for First-in-man clinical studies together with a highly collaborative team of scientists.
You wi...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:18
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Associate Analyst Quality Control to be in Raritan, NJ.
Purpose: Entry to developing individual contributor, who works under close supervision.
Assists staff in various processes in the Quality Control function.
Supports day-to-day laboratory activities such as sample management, supply ordering and receipt, and general housekeeping.
Assists with analysis, qualification/validation activities, and lab investigations.
Supports data review and metrics reporting.
Executes continuous improvement projects with supervision.
May execute testing under supervision.
You will be responsible for:
* Ensure testing is completed in compliance with all applicable procedures, standards, and current Good Manufacturing Practices regulations.
* Conduct analytical testing of final product samples submitted to the QC laboratories.
* Perform peer review/approval of laboratory data.
* Use electronic systems (LIMS, iLAB) for execution and documentation of testing.
* Build, review, and approve relevant QC documents, SOPs, and WIs.
Qualifications / Requirements:
Education:
* Minimum of a Bachelor’s or equivalent University Degree required; focused degree in Biology, Biochemistry, Microbiology, or related scientific field is preferred
Experience and Skills:
Required:
* 0 - 2 years of relevant work experience
* Knowledge and understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
* Experience performing one or more of the following cellular and/or molecular based techniques: qPCR, ELISA, Cell Culture, and/or Potency assays
* Experience with Manual Sample Processing
* Excellent written and verbal communication skills
Preferred:
* Experience in a Quality Control setting
* Experien...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:15
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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:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Cincinnati, Ohio, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
NOTE: Position is based in Cincinnati, Ohio
As a Co-op in the MD Quality and Compliance (Q&C) Digital Solutions organization, you will have the chance to:
* Use state of the art tools and take advantage of training courses offered at J&J.
* Collaborate with teams internal and external to the advanced analytics to implement customer-centric solutions for data analytics and process improvements
* Perform software development and validation to support medical device quality system digital solutions.
* Learn and apply various software development and lifecycle management techniques.
* Promote digital culture and capabilities across J&J medical devices
* Strengthen communication and leadership skills.
* Work with a diverse team of data scientists, analytics app developers, quality engineers, etc.
* Meet with Quality management to discuss risks and opportunities for the respective projects.
The Digital Solutions Co-op will:
* Have the opportunity to work at and support Ethicon, Inc in Cincinnati, Ohio
* Assigned to a team in one of the various franchises of each respective company.
* Work in MD Q&C Digital Solutions group.
* Report directly to, and receive assignments from, MD Q&C Digital Solutions Advanced Analytics Manager, while also working with the broader team for additional assignments.
* Participate in and/or lead on-campus activities such as learning comm...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:11
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Athens, Georgia, United States of America, Horsham, Pennsylvania, United States of America, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America
Job Description:
Janssen Supply Group, LLC, a member of Johnson & Johnson Innovative Medicine, is recruiting for a Sr.
Specialist, External Quality (Small Molecules).
The preferred location for this position will be in Horsham, PA or Titusville, NJ.
However, the role can also be located in Athens, GA or Tampa, FL.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
In this position you will provide end-to-end quality support for external manufacturers and strategic partners, ensuring consistent delivery of pharmaceutical products that meet or exceed safety, regulatory compliance, and product standards.
Key Responsibilities:
* Provide quality and technical support to ensure effective execution of quality systems at external manufacturing sites.
* Support the identification and resolution of quality issues and complaints, including review and approval of non-conformances and development of robust CAPA plans.
Support the escalation and issue management processes.
* Review and approve quality systems documentation, including batch documentation and product disposition, change controls, manufacturing instructions, quality agreements, specifications, validation documentation, and technical studies.
* Monitor quality performance through key performance indicators; analyze data to identify risks and drive implementation of mitigation plans.
* Build relationships with internal and external partners to meet patient supply requirements.
* Support external manufacturers to continuously improve processes and procedures focused on reliability, execution, and quality culture.
Support risk management initiatives necessar...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:09
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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:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States
Job Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for the Associate Clinical Account Specialist position to be in Cleveland and Columbus, OH.
.
Purpose:
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of the Electrophysiology’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding business goals.
You will be responsible for:
Under (e.g.
limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and corporate Johnson & Johnson, procedures and guidelines, the ACAS will:
* Attend all portions of the ACAS fellowship training program without exception.
* Engage in dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during training.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
* Prioritize and appropriately respond to re...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:07
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
Bangalore, Karnataka, India, Mumbai, India, PENJERLA, Telangana, India
Job Description:
The Associate Clinical Programmer is an individual contributor with basic knowledge of data structures, programming languages, and programming methods.
The associate supports data analyses and reporting and trial activities within clinical programming functional areas in accordance with departmental processes and procedures.
This position is a member of the programming team, capable of supporting activities of low complexity with appropriate guidance and may contribute to departmental innovation and process improvement projects.
Reviews specifications for mapping internal Data Review Model (DRM) for fit-for-purpose reporting consumption and ensures verification of DRM.
• Supports data cleaning by programming edit checks and data review listings and data reporting by creating data visualizations and listings for data management, medical monitoring, and central monitoring.
Completes programming trial activities of low complexity and/or criticality, with high quality and timeliness of deliverables.
• Designs and develops programs in support of clinical analysis and reporting activities.
• May support submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages.
• Performs activities in accordance with departmental processes and procedures.
• Performs appropriate quality control and verification in support of clinical analyses and reporting activities.
• Performs review and provides feedback on project requirements and documentation.
Education and Experience Requirements:
Bachelor’s degree or higher and/or equivalent in computer science, mathematics, data science/data engineering/analytics, public health, or other relevant scientific field (or equivalent theoretical/technical depth).
Experience and Skills Required:
• Basic knowledge of data structures and relevant programming languages for data manipulation, and statistical reporting which may include SAS, R, Python etc.
Knowledge of SAS is preferred for Clinical Programming role.
• Basic knowledge of processes, methods, and concepts relevant to programming.
• Experience working in a team environment preferred.
• Demonstrated w...
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Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:04
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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:
People Leader
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
Position Summary:
Manager Clinical Operations is accountable for the operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource allocation, adherence to timelines and budget, compliance with relevant Standard Operating Procedures (SOPs), policies, Health Care Compliance (HCC) and local regulatory requirements.
The Manager Clinical Operations supports Country Head in shaping and managing local organizational structure to ensure its optimal efficiency and demonstrates effective issue management.
The Manager Clinical Operations is responsible for overseeing resources at departmental level, providing managers and directors with the information they need to make decisions and is accountable for the monitoring of metrics, study budget and local vendors oversight at department level
This individual is responsible for line management of Local Trial Managers (LTM), Site Managers (SM), Clinical Trial Assistants (CTA) and/or other GCO staff, as required.
Oversees staff performance, development, training, project assignments, workload distribution and supports issue resolution with direct reports.
Ensures alignment of local goals with organizational objectives.
Drives innovative solutions and process improvements for the assigned therapeutic area(s), country, and GCO/Global Development (GD) overall.
Principal Responsibilities:
1 Provide line management to direct reports including setting goals and objectives, performance evaluation and talent development.
2 Evaluate and forecast resource needs for assigned portfolio and/or other specific area of responsibility, as required and agreed with local GCO management accordingly.
3 Responsible for deployment of the One Delivery Model through collaboration and oversight of vendors.
4 Accountable for the acquisition of new talents and development of human resources.
5 Guide direct reports in issue resolution and communication with involved stakeholders.
6 Lead organizational changes and effectively communicate on priority shifts as required.
7 Review and approve expenses in compliance with the company policies.
8 Demonstrate leadership behaviours in alignment with J&J Leadership Imperatives.
9 ...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-06-06 08:27:03
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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:
Nonclinical Safety
Job Category:
Scientific/Technology
All Job Posting Locations:
La Jolla, California, United States of America, Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal scientist, Data Scientist, Clinical Pathology & Safety Biomarkers to be in Spring House, PA and La Jolla, CA.
Purpose:
The Clinical Pathology & Safety Biomarkers (CPSB), Pathobiology, Preclinical Sciences and Translational Safety (PSTS), is seeking a highly motivated Principal Scientist to develop and conduct data analytics, visualization, and application of Artificial Intelligence/Machine Learning approaches in the CPSB laboratory.
The CPSB laboratory is a team of medical laboratory and biomarker scientists responsible for delivering on the PSTS translational safety biomarker vision of end-to-end (efficacy-to-safety, Discovery through Post-Marketing) across all J&J modalities and therapeutic areas.
The Principal Scientist will be responsible for applying data science approaches to analyze complex data-sets to drive key insights and support translational biomarker strategies.
The candidate will need to have a breadth of skills and knowledge to address key biological concerns and portfolio needs into meaningful data science questions and approaches to deploy relevant data analytics and visualization techniques.
The candidate is intellectually curious and will thrive in a dynamic, multidisciplinary and collaborative environment.
This role reports to the Head of the CPSB team.
You will be responsible for:
* Working closely with internal stakeholders (within CPSB and Pathobiology) and external partners (Scientific & In Vivo Strategies and Technology Research Systems) to understand and prioritize use cases and implement our Data Science roadmap for prioritized data science initiatives.
* Building a robust data infrastructure by cleaning, op...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-06 08:26:37
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ERM is hiring an onsite Construction Safety Specialist in Wilson, NC to support a key pharmaceutical client’s manufacturing facility project.
In this critical role, you will be responsible for providing on-site observation of construction activities from an EHS perspective, ensuring health and safety compliance with applicable regulations and existing company standards and contributing to an environment where employee health and safety is preserved. You will be present during all site activities and responsible for all health and safety activities.
This is a full-time (40+hrs/week), limited-term role for a duration of 1 year, renewable.
RESPONSIBILITIES:
* Engage with general contractor and subcontractors on behalf of owner’s representative.
* On-site observation of construction activities from an EHS perspective.
* Documentation of activities with respect to required EHS performance.
* Train on-site workers on EHS oversight program requirements.
* Train on-site subcontractors on EHS oversight program requirements.
* Help administer project directives given by the Client’s Environmental, Health, and Safety (EH&S) personnel throughout the project.
* Report on whether project staff and trade contractors are complying with the Client’s safety procedures and are working in accordance with the approved project-specific safety plan.
* Maintain required safety-related documentation on the project site including, but not limited to, safety orientation training, Job Hazard Analyses (JHA), SDSs, pre-task assessments, and toolbox talk summaries.
* Participate in daily pre-shift coordination meetings to include review of the day’s activities and associated hazards.
* Review and comment on the General Contractor’s JHAs with project trades and obtain signatures prior to commencement of work.
* Conduct daily site inspections, focusing on work site orderliness and compliance with safety procedures and protocols. Proposed corrections of safety deviations will be discussed with the General Contractor’s Safety Manager and provide support for corrective action implementation.
* Issue daily site observation reports for each site inspection.
REQUIREMENTS:
* Bachelor's degree in construction management, safety, or occupational health and safety, or a related degree preferred.
* 1+ years of full-time on-site experience in construction-specific project health & safety leadership.
* Certification in field; CHST, ASP/CSP, CIH, PE, or similar registration highly desirable.
* Strong knowledge of OSHA General Industry and construction standards.
* Strong commitment to safety, including implementing strict Health and Safety protocols.
* Completed training and certifications OSHA 30-hour construction (required), confined space entry training, and fall protection/prevention training (preferred).
* Strong initiative (self-starter), problem-solving and communicat...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-06-06 08:26:17
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America, US004 PA Malvern - 200 Great Valley Pkwy
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 Distinguished Scientist, Large Molecule Biologics to be in Malvern, PA or Spring House, PA.
Purpose:
Within the CMC group, you will lead multiple CMC Teams spanning from pre-NME through post-Approval, including Life Cycle Management (LCM).
This includes, but is not limited to, the creation and implementation of the development strategy, the adherence to the CMC 12 Stage process, approval by governance bodies, the identification and mitigation of CMC risks, the completion of required CMC regulatory documents and responses, creation and adherence to budget and timelines, and the delivery of clinical and launch drug supplies in accordance with development plans.
You will be the CMC point of contact with the Compound Development Team(s) (CDT) and Value Stream Teams (VST).
You will be responsible for:
* seeing opportunities for team or product development improvements across the TDS organization.
They may also support or lead teams in implementing initiatives to deliver organizational or process improvements.
* demonstrating behaviors consistent with the current Leadership Imperatives and will be mentoring and coaching CMC Team Members to improve their skills and contributions to the organization in collaboration with line management.
* focusing on development projects which may span multiple Therapeutic Areas (TAs) and/or Innovative Medicine Supply Chain (IMSC) and stages of development.
* Working in a multi-disciplinary, complex and innovative environment, with evidence of delivering results in this setting, including: In-depth experience and technical knowledge of the Large Molecule CMC protein and Bioconjugates (include Antibody Drug Conjugat...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-06 08:26:04
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ERM is hiring Environmental Inspector to oversee environmental compliance during the construction phase of a data center project in Frederick, MD.
This is a full-time (50 hours/week), limited-term role for a duration of 2 years.
RESPONSIBILITIES:
* Preparing and conducting environmental training for construction personnel.
* Conducting field inspections, monitoring and field survey work as directed.
* Interacting with and serving as a point of contact with agency officials, regulatory agency staff, landowners, contractors, clients, and other project members and conducting required agency notifications.
* Reviewing and implementing project documents and providing direction, support, and critical judgment on environmental compliance issues.
* Providing technical leadership, support, and direction to field staff. This includes participating in daily and weekly compliance and project management meetings with the Contractor, Owner, and Tennant.
* Critically assessing environmental conditions in the field to evaluate potential environmental impacts from construction.
* Evaluating potential issues and concerns ahead of construction activities.
* Overseeing the proper implementation of mitigation measures.
* Conducting environmental sampling (hydrostatic test water, soil, etc.).
* Overseeing and verifying flagging of wetland boundaries, cultural and biological resources exclusion zones, refueling zones, etc.
* Inspecting and documenting compliance with a project's environmental requirements by preparing daily written inspection reports that provide up-to-date and consistent written and photo documentation of activities observed in the field.
* Participating in various construction meetings.
* Preparing documentation to support requests for variances from environmental permits.
* Evaluating restoration activities.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
* Minimum of 5 years work experience in an environmental compliance position for a company in the environmental/construction industry or as an environmental consultant.
A minimum of 8 years of experience is required for individuals without a bachelor’s degree.
* Certification as an Environmental Specialist (CES), Erosion Sediment & Stormwater Inspector (CESSWI) Certified Professional in Erosion and Sediment Control (CPESC) or similar qualification required.
Willingness to obtain any of these certifications as soon as practicable, if not already held.
* Knowledge of relevant equipment, policies, procedures, and strategies to promote effective local, state, or national security operations for the protection of people, data, property, and institutions.
* Knowledge of the practical application of engineering science and technology including applying principles, techniques, procedures, and equipment to the design and production of various goods and services including building cons...
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Type: Permanent Location: Baltimore, US-MD
Salary / Rate: Not Specified
Posted: 2025-06-06 08:25:42
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Scientist, Antibody Discovery & Engineering
Join Elanco’s RBI Discovery Sciences team as a Scientist, Antibody Discovery & Engineering where you will be a key contributor to the discovery and optimization of novel biotherapeutics.
This position will be responsible for executing laboratory-based experiments to support monoclonal antibody drug discovery and engineering efforts in early research
Your Responsibilities:
* Conduct hands-on laboratory work for the discovery and engineering of monoclonal antibodies (mAbs)
* Collaborate with senior scientists and peers in a matrix environment to support the delivery of high-potential antibody therapeutics with optimized affinity and developability
* Communicate results effectively in written and oral form, including presenting findings at team meetings
* Maintain detailed electronic laboratory notebook and records of protocols, SOPs, etc.
What You Need to Succeed (minimum qualifications):
* Education: Master’s degree in Biology or related life sciences field (Biochemistry, Chemistry, Molecular Biology, Immunology) with 3-5 years of experience in the pharmaceutical and/or biotechnology industry, or Bachelor’s degree with 5-7 years of experience Strong background in molecular biology and biochemistry techniques, such as PCR, cloning, cell culture, ELISA
What will give you a competitive edge (preferred qualifications):
* Hands-on experience with display-based screening platform(s), such as phage, yeast, mammalian, or mRNA display
* Familiarity with antibody discovery workflows
* Understanding of antibody structure/function
Additional Information:
* Travel: Domestic & International Travel may be required (10%)
* Location: Global Elanco Headquarters - Greenfield, IN (New headquarters coming Q4 Indianapolis, IN)
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualif...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 123500
Posted: 2025-06-05 08:50:58
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SmartWorks is seeking a talented and motivated Technical Consultant who can balance their business knowledge, technical skills and strong interpersonal skills.
The Technical Consultant will interact with our customers, development teams and third-party software vendors to gather and document requirements, deploy applications and provide implementation support and training.
As a Technical Consultant, you will be required to travel throughout North America approximately 30% of the time when safe and appropriate.
While you're not traveling throughout Canada and the US, you will be able to work remotely from home or out of any of the Harris offices.
This role is available remotely within Canada and the US.
This role requires travel up to 30% in North America.
A valid passport is required.
What your new role will be:
* Design and implement SmartWorks solutions to meet customer requirements
* Integrate SmartWork’s application suite with 3rd party software interfaces
* Develop and maintain project documentation, standard operating procedures, and other documentation as required
* Lead or assist in training sessions with SmartWork’s customers and provide implementation support
* Act as a liaison between SmartWorks, customers, 3rd party vendors and industry consultants
* Provide consulting services based on knowledge of Smart Metering infrastructure and best practices on analysis of corresponding data
* Provide the Project Manager with regular updates on progress, issues and ideas for resolution, and successes
What we are looking for:
* Experience in the technical field (for example, Electric or Computer engineering, Computer Science) or a degree/diploma in the related field
* Strong grasp of SQL and one or more Enterprise Database Software such as SQL Server, Oracle etc
* Comfortable working in Linux and Windows
* Ability to travel in North America up to 30% of the time
* 5+ years of relevant work experience in software implementation
* Strong working knowledge of object-oriented design (C/C++ or Java)
* Previous experience in the Utilities industry
What will make you stand out:
* Possess strong analytical skills to understand requirements
* Demonstrate excellent verbal and written communication skills in English
* Can work independently, but most importantly, as a team player
* Demonstrate positive attitude and determination
* Previous experience in training customers and writing technical documents
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About us:
SmartWorks empowers utilities to navigate change and unleash the potential of the smart infrastructure.
At SmartWorks we are committed to delighting our cust...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 90000
Posted: 2025-06-05 08:50:35
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A New Era for the Aluminum Industry – ELYSIS
Carbon Free Aluminum
The ELYSIS™ technology is the greatest breakthrough in the aluminum industry since its beginnings in 1886.
Work is underway now to further develop this revolutionary new way to produce aluminum, eliminating carbon dioxide and all other greenhouse gas emissions from the traditional smelting process.
The ELYSIS process eliminates the use of carbon anodes, replacing those with proprietary materials.
It is the first industrial process that emits oxygen as its by-product and has the potential to transform an entire industry.
In 2018, two international aluminum producers, Alcoa and Rio Tinto, came together to form the ELYSIS joint venture with the provincial government of Quebec.
With support from the Canadian Government and Apple, the technology is progressing and is currently being designed to support the construction of new smelters or retrofits.
ELYSIS is headquartered in Montreal, with Technology Research & Development locations in Alma, Quebec, (Canada), in Jonquiere, Quebec, (Canada), in New Kensington, Pennsylvania, (United States), and in France.
Commercial quality metal produced by ELYSIS during the ongoing R&D process is already being used by Apple in a variety of products (The 16-inch MacBook Pro and the iPhone SE); Ab InBEV (cans); Audi (e-tron GT wheels produced by the RONAL Group), and Corona (cans).
Join the ELYSIS team in this exciting work!
About the location
The ELYSIS US Research & Development facility is located in the Alcoa Technical Center (ATC) in New Kensington, Pennsylvania. Located near Pittsburgh, the carbon-free smelting process was first developed at ATC, where a dedicated team is working to reinvent the aluminum industry for a sustainable future.
About the job
As the R&D Technician at the Alcoa Technical Center (ATC) in New Kensington, PA, you will directly contribute to a new era for the Aluminum Industry by working primarily on the ELYSIS project.
The ELYSIS process eliminates the use of carbon anodes, replacing those with proprietary materials.
It is the first industrial process that emits oxygen as its by-product and has the potential to transform an entire industry.
In this role, you will be responsible for running routine analysis on a primary material stream, while keeping safety, quality, and productivity standards.
The R&D Technician will lead all material diagnostic activities which are crucial to maintaining the ongoing quality expectations of the Elysis project.
The R&D Technician’s primary responsibilities include:
* Gain knowledge of Alcoa’s EHS standards, protocols, and tools to ensure that safety protocols are being followed accordingly.
* Efficiently managing sample queues and data collection in the thermal analysis lab including thermogravimetri...
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Type: Permanent Location: Alcoa Center, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-05 08:49:05
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy.
Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements.
Ensure provision of quality patient care while maintaining cost-effective clinical operations in accordance with all legal, compliance, and regulatory requirements and programs.
Adheres to all requirements of the FMCNA Compliance Program, and FMS patient care and administrative policies as the clinical leader, has the authority to make daily decisions to ensure continuity of care and patient and staff safety
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Manages the tactical execution of short- and long-term objectives through the coordination of activities with a direct responsibility for results, including costs, methods, and staffing.
* Provides leadership, coaching and development plans for all direct reports to maintain an engaged and productive workforce; partnering with Human Resources on employee matters.
* Technically proficient in the specific department and knowledge of industry practice and business principles.
Works on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current business trends.
Has a larger range within the department.
* Responsible for supporting and driving FMS quality standards through meeting all ESRD regulatory requirements and the practice of Quality Assessment and Improvement (QAI), including use of FMS QAI tools.
* Responsible for addressing and acting on adverse events and action thresholds.
* Oversees facility’s Home Therapies Program if applicable.
* Accountable for compliance with all applicable federal, state and local laws and regulations.
* Ensures all FMS Clinical Quality policies and procedures are communicated to and implemented by the facility staff.
* Maintains integrity of medical records and other FMS administrative and operational records.
* Complies with all data collections and auditing activities.
* Maintains facility environmental integrity, including safety.
* Experienced leadership required for multi-faceted environment; role primarily focuses on tactical execution.
Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.
* An individual contributor will have significant project/process responsibilities.
Program or project responsibility generally within the function.
* Follows processes and operational policies in selecting methods and techniques for obtaining solutions.
Interprets and recommends change to policies and establishes procedures that effect immediate organization(s).
* Decisions have an impact on work processes and outcomes.
Erroneous decisions or failure to achieve results will add costs and may impact the short-term goals of the organization.
* Frequent...
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Type: Permanent Location: Dallas, US-PA
Salary / Rate: Not Specified
Posted: 2025-06-05 08:48:33
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IFP Dry Tissue LCM Team leader, ASIA/Australia
Job Description
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
The IFP Dry Tissue LCM leader, Asia/Australia will be responsible for delivering the Innovation agenda and the Cost/margin transformation across all the Family Care tissue business and Professional tissue businesses for the ASIA + ANZ ABUs, supporting the growth acceleration and margin transformation in that region, which hosts three of the five focus markets for IFP (ANZ, Thailand, Taiwan).
This individual will report into the Dry Tissue LCM Senior Team Leader (based in UK), and will be an active participant & contributor of IFP Dry Tissue Platform Leadership team.
The individual will also serve as the go-to R&D partner for the ABU leadership in the region, facilitating seamless connection between the ABU and R&D leadership teams.
This role requires senior expertise in innovating on highly-commoditised categories like tissue, as well as solid experience in driving substantial cost & margin improvements through product, technology & process innovation, together with an exceptional understanding & knowledge of KC tissue manufacturing processes & facilities.
Role Overview & Primary Accountabilities:
* ANZ IFP markets. Partnering closely with the R&D innovation team to ensure seamless handover, and with PS counterparts to ensure successful start-up in mills. Also, leading complete end-to-end development & implementation of multiple local renovations for each of the individual countries within their region (with ANZ, Thailand & Taiwan making up 3 of the 5 focus markets for IFP).
Working across 7 mills (3xTaiwan, 1 Australia, 2xThailand, 1xMalaysia and several ECMs (Contract Manufacturing)
* Margin transformation & Cost management: Serve as regional R&D leader to develop the 0-3yr DTV (Design to Value) strategies, define key initiatives and execute the plan to ensure annual DTV targets are met/exceeded, partnering closely with Value stream teams, supporting the delivery of ~150Mn$/yr savings required from IFP to deliver Powering Care goal of 3Bn$ over 5 years
* Life Cycle Management: Lead and own all product Life Cycle Management activities to ensure strong business continuity & fast resolution of raw material or product related supply interruptions in partnership with Product supply together with ongoing work to mitigate such risks.
* Resource prioritization: Accountable to ensure team (6 FTE) is empowered and have clarity.
Team members located in: Australia, Thailand...
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Type: Permanent Location: Bangkok, TH-10
Salary / Rate: Not Specified
Posted: 2025-06-05 08:47:52
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eCommerce Growth and Analytics Trainee
Job Description
Your Job
The primary objective of the eCommerce Growth and Analytics Trainee will be to support and drive development of our eCommerce reporting capability through the building and maintaining of our key reporting dashboards.
These dashboards are a critical part of the team’s ability to assess the health of their individual accounts and identify opportunities to grow the eCom business across EMEA.
Development has been fast in this area with a number of new dashboards in place.
This role will need to maintain the pace of development, ensure data quality / accuracy, optimise the analytical output and continue to grow the impact of our reporting capability on our business.
You will need to work as a bridge between the eCommerce Team and the Data and Analytics team, supporting stakeholders and prioritisation in both areas.
Main areas of responsibility include:
* Support the creation, updating and maintenance of Power BI dashboards to monitor key ecommerce metrics.
* Support the creation and collation of monthly reporting decks for use by the eCom team and to be shared with Snr Management.
* Extract, transform and load data from various systems (SQL, Snowflake, SAP).
* Perform exploratory analyses in Excel, SQL, Python (pandas) to uncover trends, opportunities and areas for improvement in digital operations.
* Participate in A/B testing initiatives to refine product and sales strategies.
* Collaborate with Marketing, Analytics and Sales teams to translate business needs into actionable analytical solutions.
* Document processes, define metrics and help standardize reporting workflows.
About you
As a person and to be successful in this role, full proficiency in English is required (minimum B2+/C1 level)
You should be able to u these technical requirements:
* Power BI: comfortable with Power Query, writing DAX measures and crafting clear, effective visualizations.
* Excel (Advanced): pivot tables, advanced formulas and data modeling.
* SQL (Intermediate): able to write efficient SELECT queries, filter and aggregate data, and join tables in relational databases without getting lost in complex optimization details.
* Python (Intermediate): proficiency with pandas and matplotlib (or equivalent) for data wrangling and analysis.
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, 25% of people in the world use Kimberly-Clark products every day.
We know that these amazing Kimberly-Clark products wouldn’t exist without skilled workers, like you.
Here, you’ll use your skills to make some of the most helpful things for billions of people all around the world - all in a safe, stable, and caring environment.
While our products support better lives for billions of people around the world, o...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-06-05 08:47:45
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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:
Toronto, Ontario, Canada
Job Description:
Janssen Supply Group, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Manager, External Quality (Small Molecules)! This position can be performed in Titusville, NJ, Horsham, PA, Athens, GA or Toronto,Ontario CA.
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):
North America- Requisition #R-016448
Canada- Requisition #
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
As the world’s largest and most broadly-based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.
In this position you will provide end to end quality oversight for external manufacturers and strategic partners, ensuring consistent delivery of pharmaceutical products that meet or exceed safety, regulatory compliance, and product standards.
Key Responsibilities:
* Provide quality leadership and technical support to ensure effective execution of quality systems at external manufacturing sites
* Manage quality oversight in the selection, qualification, and ongoing monitoring of external partners
* Support the identification and resolution of quality issues and complaints, including facilitation of investigation process and development of robust CAPA plans.
* Review and approve quality systems documentation, including product disposition, manufacturing instructions, change controls, specifications, validation documentation, and technical studies.
* Monitor quality performance through the development of key performance indicators; analyze ...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-06-05 08:30:04
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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:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Cork, Cork, Ireland, Latina, Italy, Schaffhausen, Switzerland
Job Description:
Johnson & Johnson is currently recruiting for a Product Quality Vigilance Operations Analyst! This position can be located in Horsham or Malvern, PA, Raritan, NJ, Gurabo, PR, Beerse Belgium, Schaffhausen Switzerland, Cork Ireland or Latina, Italy.
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):
North America- Requisition #R-016619
Beerse Belgium, Schaffhausen Switzerland, Cork Ireland or Latina, Italy - Requisition #R-004014
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
As the world’s largest and most broadly-based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and ingenuity to profoundly change the trajectory of health for humanity.
Position Summary:
The position predominantly performs activities including trend analyses, signal detection and data analysis in the Product Quality Vigilance (PQV) organization.
This position leads efforts in support of the business as it develops and implements quality product-specific surveillance strategies.
Proactive, customer focused systematic detection and evaluation of potential signals from emerging trends in complaint data.
This position will be a key interface with the various product and business groups to ensure awareness of signals.
This is a hands-on position that will require an ambitious individual with excellent analytical, written and verbal communication skills.
You will have the opportunity to collaborate with business partners at all levels with multiple functional groups in an environment...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-06-05 08:30:04
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Reno, Nevada, United States, Santa Clara, California, United States of America
Job Description:
Job Description
Johnson & Johnson is hiring for a Field Clinical Specialist to join our team located in Reno, Nevada.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and drive.
* Present clinical study training materials based on investig...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-05 08:29:49
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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:
Manufacturing Product & Packaging Operations
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Global Cryopreservation & Cell Collection Director to join our Team!
Summary:
The CAR-T Global Cryopreservation and Cell Collection Director will be responsible for leading our new global team that will manage critical steps in our V2V supply chain for cell collection and cryopreservation of patient material.
This includes the onboarding and management of cryopreservation and apheresis sites; leading the SMEs for issue / impact of starting materials, material equivalency, and manuals; and serving as investigation leads.
This team will be structured to enhance operational performance for continuous improvement and drive the network strategy for cryopreservation.
Key Responsibilities:
* Lead Cryopreservation & GCC teams to manage aph and cryo operations, develop the talent pipeline and succession planning to ensure robust continuity within this team, and optimize the global footprint as we scale our volume and launch in new countries
* Drive performance and execution of cryopreservation strategy including platform metrics / reviews for Make Step #1 of our cell processing.
Proactive management of cryo network to prevent a constrained supply and provide sufficient availability for our aph slot bookings.
Identify and execute continuous improvement opportunities
* Partner closely with cross functional areas such as: Value Chain Management, MSAT, Autologous Platform (internal cryo operations), and PES to shape and implement the global cryopreservation strategy
* Lead escalations and strategy for external cryopreservation network.
This includes T2T meetings and decisions that align to our network strategy.
Qualifications
Education:
* Minimum of a Bachelor's Degree is required, MA/MBA preferred
...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-06-05 08:29:15
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Charleston, West Virginia, United States, Raleigh, North Carolina, United States, Santa Clara, California, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
This position is fully remote but you must reside within the Territory.
Purpose:
Established and productive individual contributor, who works under moderate supervision.
Helps implement projects, programs, and processes in support of the organization's overall Clinical Sales - Hospital/Hospital Systems strategy.
Applies practical knowledge of the Clinical Sales - Hospital/Hospital Systems field to administer best in class policies, procedures, and plans for the area.
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography.
Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs....
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-05 08:29:13
-
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 Systems
Job Category:
Professional
All Job Posting Locations:
Athens, Georgia, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson and Johnson is seeking for an Investigation Quality Leader, located in Athens, GA.
The Investigation Quality Leader is responsible to ensure the generation and completion of robust investigation reports (i.e Nonconformance and Root Cause investigations).
This includes, but is not limited to, providing quality, compliance, and technical feedback/ regarding quality and manufacturing investigations ensuring compliance to company policies while contributing to continuous improvement efforts.
Key Responsibilities:
* Lead/Participate in investigation processes such as initial triage, initial impact assessment, investigation strategy meetings, root cause and CAPAs alignment meetings.
* Write/review/approve investigation reports using a narrative based on process science and scientific knowledge that supports the identified root cause or most probable cause.
* Apply 6-sigma principles to the investigation process to identify root cause or most probable cause (5-why, 6M, affinity diagrams, brainstorming, etc.).
Applies critical thinking to discern relevant information to the investigation report.
* Contribute to the design of CAPAs aligned to root cause that are effective in preventing recurrences.
Assign CA-PA with reasonable timeframes, track due dates, reviews closing evidence and approves closure.
* Ensure that investigation process adheres to timelines to ensure approval in 30 calendar days.
Leads improvement process for the reduction of investigations and/or design of effective CAPAs.
* Approve investigations (initial impact assessment, investigation report) as delegated by supervisor.
* Responsible to follow J&J Innovative Medicine Policies, site procedures, Regulatory Agencies and Safety & Environmental regulations.
* Collaborate with other departments and team...
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Type: Permanent Location: Athens, US-GA
Salary / Rate: Not Specified
Posted: 2025-06-05 08:29:12
