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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:
Workday Associate B
Job Category:
Non-Standard
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson is currently seeking a Quality Control – Micro analyst to join our CAR-T Hub located in Beerse.
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/.
CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, Janssen has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories will be operated from the existing Janssen Beerse site.
The QC Micro analyst, CAR-T Europe is responsible for preparing and conducting testing of the different samples taken during the production process.
You are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
The candidate will be part of the weekend team, working on Saturday and Sunday.
Working hours will be from 6am to 6pm.
Possibly preceded by training period in week regime.
You will be responsible for:
* Perform analytical testing in compliance with all applicable specifications, procedures, GMP regulations.
* Maintain a safe work environment in compliance with all applicable environmental, health, and safety regulations.
* Perform peer review of laboratory data.
* Author and update SOPs, WIs and Protocols to support daily operations of the lab using the Document Management System.
* Support laboratory related investigation records and CAPAs.
* Assist in the execution of internal audits.
* Provide input to functional laboratory meetings.
* Provide input and take actions as a QC representative at cross-...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-30 08:41:02
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Mexico & Brasil - Requisition Number: R-015573
United Kingdom - Requisition Number: R-014669
Portugal, Spain, Poland - Requisition Number: R-015574
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Medical Affairs – Delivery Unit, Lead, Trial Delivery Manager (TDM) is responsible for the execution of study-level activities, creating and updating trial-specific documents, vendor oversight & delivery, compound training, and other activities.
The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery.
The TDM might have responsibilities cross different trial types (such as Company Sponsored, Investigator Initiated, and Collaborative Studies), within different Therapeutic Areas, in a local, regional, or global setting, depending on the business need.
Principal Responsibilities:
* Create and update critical trial-specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product [IMP] related documentation).
* Manage vendor set up and management of day-to-day study vendor activities, including set-up, SOW
* creation and budget oversight.
* Responsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibilit...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-30 08:39:46
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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: 2025-05-30 08:39:43
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
The Associate Statistical Programmer is an individual contributor with knowledge of statistical programming methods, languages and data structures who supports data analysis and reporting activities within the Statistical Programming functional area in compliance with departmental processes and procedures.
This position is accountable for the development, verification, and documentation of code used for the analysis and reporting of clinical data and is responsible for the timeliness and quality of assigned deliverables supporting clinical projects and submissions.
This position is a member of a programming team, capable of supporting programming activities of low to medium complexity with appropriate guidance.
In addition, the Associate Statistical Programmer may contribute to departmental innovation and process improvement projects.
* Designs and develops statistical programs in support of clinical research analysis and reporting activities.
* Performs appropriate quality control and verification in support of assigned clinical research analysis and reporting activities.
* Maintains statistical programming documentation as appropriate.
* Completes programming tasks of low to medium complexity with high quality and timeliness of deliverables.
* Performs activities in accordance with departmental processes and procedures.
* Collaborates effectively with statistical programming and cross-functional team members and counterparts to achieve project goals.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team..
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-30 08:39:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Translational Discovery & Development Biomarkers
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Director, Biomarker - Aging and Metabolism to be in Spring House, PA.
Purpose:
This individual will play a critical role in driving biomarker strategy and advancing translational research efforts to support drug discovery and development.
This position leverages deep expertise in preclinical and clinical biomarkers to accelerate the development of novel therapeutics targeting age-related degenerative diseases, including cardiovascular pathology, thrombosis, and sarcopenic obesity.
Additionally, this role contributes to Johnson & Johnson therapeutic strategies across neuroscience, immunology, and oncology.
You will be responsible for:
• Biomarker strategy to support sarcopenic and aging-related diseases, collaborating across J&J’s Cross-Therapeutic Area (TA) Small Molecule, Biologics, and MedTech teams.
• Drive biomarker development efforts for early- and late-stage drug candidates, ensuring robust clinical translation.
• Provide scientific and strategic leadership, supporting cross-functional teams and external research collaborators.
• Oversee preclinical and clinical biomarker implementation, integrating cross-TA exploratory efforts to evaluate novel assets and repurpose J&J pipeline candidates.
• Biomarker support for the regulatory filing of macitentan 75 in pulmonary arterial hypertension.
• Maintain scientific leadership, fostering innovation, collaboration, and visibility through publications, external engagement, and strategic partnerships.
• Strategic Impact: The Biomarker Director – Aging & Metabolism plays a vital role in shaping preclinical and clinical development strategies t...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-30 08:39:28
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Lima, Peru
Job Description:
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Senior MSL Inmunology to be in Lima, Perú.
Purpose:
Personnel in the field responsible for the education of health professionals; scientific exchange with key opinion leaders; acts as a contact center for regional clinical programs.
Provide clinical support to internal colleagues.
Develops and implements the clinical strategy plan within a geographic region.
MSLs are also responsible for incorporating competitive intelligence input from the field into internal strategy meetings
You will be responsible for:
• Provide and implement plans for medical matters, including the identification of critical pathways and monitoring of projects.
• Establish and provide strategic leadership for Medical Affairs, develop and execute initiatives for upcoming and / or new compounds in the portfolio.
o Work with the Medical Affairs team and implement launch readiness and life cycle programs for products.
• Function as a scientific expert in the field for internal and external clients within areas of expertise such as clinical, scientific and Pharmacoeconomics.
o Plan, organize and implement medical and product education events for selected physician groups.
o Provide scientific support to opinion leaders, community physicians, researchers, and other healthcare providers
o Provide medical training to independent researchers / physicians and company personnel on specific and specific topics.
o Respond to requests for scientific information individually or through group discussions, discussion of the concepts of...
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Type: Permanent Location: Lima, PE-LIM
Salary / Rate: Not Specified
Posted: 2025-05-30 08:39:27
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Bogotá Distrito Capital, Colombia
Job Description:
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses.
You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for Senior MSL Inmunology to be in Bogotá, Colombia.
Purpose:
Personnel in the field responsible for the education of health professionals; scientific exchange with key opinion leaders; acts as a contact center for regional clinical programs.
Provide clinical support to internal colleagues.
Develops and implements the clinical strategy plan within a geographic region.
MSLs are also responsible for incorporating competitive intelligence input from the field into internal strategy meetings
You will be responsible for:
• Provide and implement plans for medical matters, including the identification of critical pathways and monitoring of projects.
• Establish and provide strategic leadership for Medical Affairs, develop and execute initiatives for upcoming and / or new compounds in the portfolio.
o Work with the Medical Affairs team and implement launch readiness and life cycle programs for products.
• Function as a scientific expert in the field for internal and external clients within areas of expertise such as clinical, scientific and Pharmacoeconomics.
o Plan, organize and implement medical and product education events for selected physician groups.
o Provide scientific support to opinion leaders, community physicians, researchers, and other healthcare providers
o Provide medical training to independent researchers / physicians and company personnel on specific and specific topics.
o Respond to requests for scientific information individually or through group discussions,...
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Type: Permanent Location: Bogotá Distrito Capital, CO-DC
Salary / Rate: Not Specified
Posted: 2025-05-30 08:39:25
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
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
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 Scientist, Molecular Analytics to be located in Spring House, PA.
Purpose: We are seeking a motivated and high performing Senior Scientist to join the Cell and Genetic Medicines group within Therapeutics Discovery (TD) to support the development of CAR T cell therapy programs.
In this role, you will perform molecular assays to evaluate both viral and non-viral engineered CAR T cells at the genomic and transcriptomic levels. The successful candidate will have experience with advanced analytical skills to assess the efficiency and fidelity of targeted gene delivery along with quantification of various RNA species.
Success in this position will require both the ability to independently complete lab responsibilities and to effectively collaborate within a cross-functional team.
This role is an exciting opportunity to join a diverse and ambitious discovery team and to work with innovative technology to create life-changing therapies for patients.
You will be responsible for:
* Developing and performing analytical assays to evaluate genomic outcomes following transgene delivery to primary human T cells.
* Leading projects to characterize and quantify various RNA species from transgenic and endogenous genetic elements.
* Advancing projects by performing molecular biology techniques such as DNA/RNA extraction and quantification, qPCR, ddPCR, and next-generation sequencing (NGS).
* Staying current on the latest scientific and technological advancements in the gene editing field, incorporating new knowledge into ongoing projects, and proposing new areas of investigation.
* Analyzing data, preparing reports, and effectively communicating resu...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-30 08:38:48
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
People Leader
All Job Posting Locations:
Geel, Antwerp, Belgium
Job Description:
Within Johnson & Johnson Innovative Medicine Supply Chain, we are recruiting a QA Director Commercial API (M/F/X) as member of our Quality team overseeing Small Molecule Active Pharmaceutical Ingredients (SM-API) based in Geel, Belgium.
J&J Innovative Medicine Supply Chain Geel serves as Centre of Excellence for the development and manufacturing of SM-API used in treatments that improve the health and lifestyle of people worldwide.
The Supply Chain Quality (SCQ) team supports the Geel site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of SM-API guaranteeing reliable supplies in compliance with applicable regulations.
As QA Director you lead a team of QA managers and professionals responsible for the quality oversight and timely release of API’s manufactured at the commercial Launch & Grow facilities of the Geel site ensuring compliance with applicable regulations.
You act as QA Point of Contact ensuring quality oversight of the API production plants.
You encourage your team and business partners to continuously strengthen the Quality and Compliance Culture at the site.
You act as a leader who provides strategic direction and fosters an environment of innovative thinking.
Under your leadership, you ensure that the GMP activities as manufacturing, packaging, labelling, testing, release, storage, importation and distribution are carried out as required by legislation.
Job Description:
* Lead a team of QA managers and professionals by supporting, coaching and developing team members in reaching quality, business and personal objectives.
* Establish and maintain strong working relationships with Business Partners in Supply Chain as well as local and global Quality partners to ensure alignment of objectives and results.
Strengthen the Quality Culture in the supporting departments by providing coaching and/or training on cGMP requirements.
* Act as QA Point of Contact for commercial API ensuring timely release in compliance with global regulations and J&J quality requirements.
* Represent Quality in review meetings governing Quality and Compliance metric and operational business performance of the Quality Unit.
Identify trends and define actions ensuring continuous improvement of the Qua...
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Type: Permanent Location: Geel, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-30 08:38:22
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ERM is hiring a motivated hands-on Environmental Health and Safety (EHS) Consultant to support our key technology client onsite in Southbay San Francisco, CA.
This is a full time (40 hours a week), limited-term role with a duration of 6 months, extendable.
The ideal candidate will have experience developing and supporting implementation of OSHA requirements, Standard Operating Procedures, Health and Safety Plans, Job Hazard Analysis, Emergency Response Plans, Risk Assessment processes, Behavioral Safety programs and Contractor Safety Management. Candidates should also have familiarity with lab safety requirements, waste management (hazardous, non-hazardous, universal, electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Perform compliance and system audits to assess project compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as machine guarding, laser safety, robotics safety, Chemical/Lab Safety, Hazardous Materials, EHS auditing, and ISO 14001/18001/45000 Management Systems.
* Develop EHS compliance procedures, plans, permits, and reports.
* Manage tasks within scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 2 years of experience providing EHS support with an emphasis on health and safety.
* Existing certification or working towards certification as Certified Industrial Hygiene (CIH) and/or Certified Safety Professional (CSP/ASP) certification a plus.
* Demonstrated understanding of regulatory compliance and reporting processes.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Valid driver’s license and good driving record.
* Familiarity with ISO 14001, OHSAS 18001, and/or 45001 preferred but not required.
Pay Transparency:
For the Environmental Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000 – $97,410, $36.53/hr - $46.83/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors, including, b...
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Type: Permanent Location: San Francisco, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-30 08:38:13
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Bioanalytical Scientist
Join Elanco’s RBI Discovery Science team as a Senior Bioanalytical Scientist, where you'll play a key role in developing and validating cutting-edge bioanalytical assays to support the advancement of our biologic's portfolio, including therapeutic proteins and vaccines.
You’ll combine hands-on laboratory expertise with strategic leadership, working across internal teams and managing collaborations with external CROs.
This role offers an exciting opportunity to innovate, lead cross-functional initiatives, and contribute to the development of new bioanalytical technologies, driving products from discovery to clinical development.
We’re looking for expertise in ligand-binding assays (e.g., MSD, ELISA), cell-based assays, immunogenicity assessments, and ideally, assay automation.
A strong background in large molecules like monoclonal antibodies and complex proteins is highly desired.
Success in this role will require a collaborative mindset, leadership skills, and a proven ability to solve problems and communicate effectively in cross-functional environments.
Your Responsibilities:
* Lead the development, validation, and optimization of bioanalytical assays (e.g., MSD, ELISA, cell-based) for therapeutic proteins and vaccines.
* Independently design, execute, troubleshoot, and interpret laboratory studies, contributing directly to data generation and analysis.
* Manage and mentor junior scientists, fostering talent and ensuring excellence in internal and external (CRO) bioanalytical activities.
* Oversee CRO activities, including assay transfer, study monitoring, data review, and issue resolution, ensuring timelines and data quality.
* Drive innovation by developing creative solutions for bioanalytical challenges and implementing new technologies and platforms.
* Collaborate across teams (Discovery, PK, Pharmacology, Toxicology, Clinical) to align on assay design, development, and implementation.
* Design and execute assays for PK/TK studies, immunogenicity assessments (incl...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 171000
Posted: 2025-05-29 09:41:52
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Accounts Payable Analyst I - (Global Business Services)
Job Description
Accounts Payable Analyst I - (Global Business Services)
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.
Role Overview & Primary Accountabilities:
* Execute payment for vendor and expense claims. Ensure expenditures are duly paid.
* Attend queries from Query Management Team
* To perform First Strike Report to prevent duplicate payment
* Review and coordinate vendor master maintenance, vendors payment, blocked payment, aging reports and supporting documents.
* Payment Forecast to Treasury Team
* Support back up plan & ad-hoc tasks.
* Ensuring appropriate internal controls in place.
* Support and execute continuous improvement (CI) initiatives to streamline existing accounts payable processes.
* Perform analysis & trouble shoot exceptions to drive KPI results.
* Support internal & external audit query to Team Leader.
* Support in operation meeting.
* Support SME for APAC (within team's portfolio)
* Responsibilities include issue resolution and engage in process improvement AP projects.
* AP Project sustainability with improvement idea.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make flexibility work for both you and th...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-29 09:39:11
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POSITION SUMMARY: The Chemical Process Operator is responsible for assisting in the repair process and production of manufactured parts of exceptional quality.
PRIMARY DUTIES AND RESPONSIBILITIES: 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. The duties and responsibilities regularly performed for this position are:
* Blending of surfaces and applying or removing excess material with hand tools or machinery
* Set-up and use of various machines, fixtures and tools.
* Part modification to specifications
* Mixing production materials
* Must follow production specifications at all times
* Embrace/implement continuous improvement and lean principles in all activities
* Maintain department safety and housekeeping standards
* Ensure compliance with Quality Control Manual (QCM)
* Must be aware of ISO – Total Customer Satisfaction (TCS) quality requirements
* Ensure compliance with Company RSM, must be aware of ISO/TCS quality requirements
* Adhere to all Company health, safety and environmental policies while performing job duties
* Adhere to and promote Corporate Code of Ethical Standards
* Regular and reliable attendance
* Performing other tasks in the facility as needed
EDUCATION AND WORK EXPERIENCE:
* High School Diploma or GED preferred
* Previous metal working experience preferred but not required
* Must be able to read, write and speak in English.
* Must be able to follow oral and written instructions.
* Ability to use handheld measuring tools.
* Ability to work effectively individually or as part of a team.
COMPUTER SKILLS
Basic computer skills including Microsoft Outlook and familiarity with Microsoft packages.
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Type: Permanent Location: Carson City, US-NV
Salary / Rate: Not Specified
Posted: 2025-05-29 09:33:53
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Job Summary
Responsible for ensuring our patients, families, visitors, as well as employees have a wonderful experience by cleaning and maintaining your assigned area within Nicklaus Children's Hospital and its properties.
Working here is about making a difference in the lives of children every day.
Job Specific Duties
* Cleans/maintains assigned work area by gathering materials, refill carts, trash removal, disposing red bags, disinfecting bathrooms (including showers, sink and toilet) and dusting.
* Cleans/Disinfect emergency spills and debris immediately.
* Ensures equipment is in good working order.
* Removes and properly disposes of trash and soiled linen.
* Replenishes supplies and linen.
* Reports safety hazards and defects immediately.
* Provides excellent customer service to all patients, visitors, and internal customers.
* Performs special cleaning procedures such as terminal cleanings when needed (deep cleaning using bleach, wipe walls, clean underneath bed, high dust, change curtains).
* Pull supplies from shelf and prepare cart.
Minimum Job Requirements
* Level II Background Check
* Prior work experience.
Knowledge, Skills, and Abilities
* High school education or equivalent preferred.
* Housekeeping and/or maintenance experience preferred.
* Floor care experience preferred.
* Able to communicate to request supplies and writes identifying information.
* Able to comprehend verbal and written instructions in English.
* Able to relate cooperatively and constructively with clients and co-workers.
* Ability to follow simple instructions to accomplish repetitive tasks.
* Excellent customer service skills.
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Type: Permanent Location: Miami, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-29 09:29:37
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Georgia-Pacific is actively seeking an Product Compliance Manager-International for our Building Products Gypsum products.
This is an exciting opportunity for an individual who is passionate about product compliance and wants to make a significant impact in a leading company.
As the International Product Compliance Manager, you will be instrumental in building international product compliance administrative programs, managing product testing, and supporting product standard and industry initiatives.
Join us as we transform the compliance capabilities of our building products division!
About the Role:
In this high-level compliance support role, you will focus on ensuring our building products meet the necessary compliance standards in European markets.
By leveraging resources, tools, and a commitment to excellence, you will create value and drive compliance efforts that keep Georgia-Pacific at the forefront of the industry.
Your unique contributions will be key to our success.
This is a remote role with travel to European markets.
Responsibilities:
* Provide expert compliance support, focusing primarily on European market requirements.
* Assess building codes and certification program applicability to our products.
* Determine country-specific requirements and ensure they align with our products.
* Seek, obtain, and maintain necessary certifications.
* Develop and maintain ongoing compliance programs.
* Design and implement test plans for building products in the European market.
* Engage with trade and test standard organizations that influence the European market.
* Collaborate with the broader compliance team to leverage learnings from the North American market
(Basic Qualifications):
* Understanding of building and technical standards relevant to the European market.
* Proficiency in Microsoft Office Suite (Teams, Word, PowerPoint, Outlook, Excel).
* Ability to travel approximately 20% to Europe and North America.
What Will Put You Ahead:
* Knowledge of European test standards and certifications, as well as Oceania (AUS/NZ) standards.
* Experience in fire or roof assembly testing.
* Proficiency in English and Spanish, French, or German.
* Familiarity with gypsum products
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-05-29 09:28:37
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Come grow with us! Georgia-Pacific has an immediate need for a Product Compliance Engineer at the Building Products Decatur Technical Center (DTC) in Decatur, GA.
The Product Compliance Engineer will lead product compliance administrative programs, manage product testing and support product standard and industry initiatives.
The product compliance engineer role will help transform the product compliance capability of building products division! Bring your skills, passion, and willingness to learn and grow in a dynamic team environment!
The Decatur Technical Center primarily focuses on Georgia-Pacific building products Research & Development, Technical Service, and Product Compliance efforts.
As a market leader, Georgia-Pacific has the resources, tools, assets, and commitment for you to be a successful contributor and create value.
At Georgia-Pacific, your unique abilities and contributions will be instrumental to our team & business.
If you aspire to use your skills and passion to create value as a Product Compliance Engineer, we are interested in learning more about you!
The successful Candidate will demonstrate:
* Strong processes development skills
* Strong interpersonal and communication skills
* Ability to balance multiple priorities.
* Strong decision making skills and highly self-motivation
* Strong attention to detail
* Ability and desire to learn and grow
What You Will Do
* Own and manage 3 rd party testing process & program
* Perform product testing needs assessment and establish Scope of Work for all new product testing programs
* Plan resource deployment for testing
* Mange test report document control system
* Support manufacturing facility 3rd party compliance audit program
* Manage renewals and submissions of product evaluations and certifications
Own and manage all existing product evaluation reports and product certifications
* Participate in select standards activities/org (e.g.
ASTM)
* Lead compliance document control projects
Who You Are (Basic Qualifications)
* Bachelor Degree (BS) in engineering (chemical, civil, etc.), environmental studies/policy, chemistry or science field OR building products experience in one or more of the following areas:
* Lab / Product / Quality testing
* Product Stewardship
* Building code interpretation
* Product renewals
* Compliance audits
Experience with Microsoft Office Suite (i.e.
Teams, Word, PowerPoint, Outlook, Excel)
What Will Put You Ahead
* Project Management experience
* Gypsum board manufacturing knowledge, or Gypsum product knowledge, or
Building Code & building product compliance knowledge
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
Th...
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Type: Permanent Location: Decatur, US-GA
Salary / Rate: Not Specified
Posted: 2025-05-29 09:28:36
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
The Opportunity:
The Global Medical Collaboration Leader (GMCL) is a medical, field-based role working across countries and affiliates to accelerate the development and delivery of medicines to patients through effective medical customer engagement across the lifecycle of a molecule/Disease Area (Obesity).
The GMCL:
* Acts as a strategic field-based medical partner for global teams and affiliate colleagues
* Understands the needs and supports strategic and tactical planning across the Disease Area (DA) lifecycle
* Serves as an above-country medical expert, establishing scientific collaborations and value-based partnerships
* Supports medicines and disease areas from early development through to post-approval
What will you be working on:
As a field-based GMCL, you will have 5 key responsibilities but not limited to:
Develop and Facilitate External Network & Relationships, Championing ONE Roche
* Establish and maintain valued relationships with key external stakeholders, acting as the face of Roche and ambassador in new Disease Areas
* Drive scientific knowledge exchange and medical education activities, identifying opportunities for medical initiatives and partnerships to support the ICX strategy for optimal customer experience
* Execute activities with customer centricity, staying updated on relevant developments and trends, including Digital Health and personalized medicine
Engage, Educate, and Partner with Investigators to Expedite Clinical Program Delivery
* Work closely with global and affiliate teams to ensure coordinated identification, selection, and engagement of clinical trial sites, championing a ONE ROCHE approach
* Drive scientific engagement with clinical trial sites to support patient recruitment and retention, while suggesting innovative approaches to design, recruitment, and data collection
* Gather investigator feedback to optimize clinical development performance and customer experience, contributing to identifying data gaps and supporting access activities
Provide Real-Time Insights and Ground-Level Understanding of Disease Area Across Countries
* Partner with internal colleagues to define the insights collection strategy and execute activities to address knowledge gaps through various methods such as advisory boards and external surveys
* Map and profile external stakeholders to inform and build engagement plans aligned with customer needs and pre...
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Type: Permanent Location: Baden-Wurttemberg, DE-BW
Salary / Rate: Not Specified
Posted: 2025-05-29 09:22:50
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
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 Kingdom - Requisition Number: R-016401
Belgium, Netherlands, Spain, Poland, Ireland - Requisition Number: R-013644
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
The Clinical Project Manager is responsible for the creation and management of a subset of Studies within the Medical Affairs Deliver Unit Portfolio.
They will collect, consolidate, and report budget, timeline and FTE actuals vs.
plan and will identify potential issues for the trial through active management of the study schedule.
Major Duties & Responsibilities
* Create, manage, and maintain study schedules in PLW + For company Sponsored and Collaborative Studies; create initial study costing and support initial OOPS management up till FPI.
* Assure Clinical timelines in PLW align to mCTMS and to latest assumptions.
Ensure proper resource demand is reflected
* Develop scenarios in PLW for budget, timeline, and FTE forecasting, while generating situational operational scenarios.
* Collect, consolidate, and report financial, timeline and resource data for governance approvals and external funding partnerships. Manage scope control, FTE and OOP variances.
+ Provide necessary Portfolio Data Insights to the TA leads
* Provide necessary Portfolio Data Insights to the TA leads
* Provide support to Finance, Business Partners and Commercial Stakeholders
Additional Responsibilities may Include:
* Mentor & support onboarding of new team members, particularly those in Trial Management.
* Foster employee engagement, inclusion, and Credo Behaviors.
Principal Relationships:
Internal: Trial Delivery Leader, Trial Delivery Manager, Program Management Leaders, Clinical Trial Assistants, DAS Leaders, Trial Management Directors, representatives of Delivery Operations, representatives of other GD and non-GD Functions and Clin...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:52
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-008331
* Canada - Requisition Number: R-009630
* Belgium - Requisition Number: R-009644
* United Kingdom - Requisition Number R-009647
* Switzerland - Requisition Number: R-009649
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and will be located in Allschwil, Switzerland.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
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 Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labe...
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Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:43
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-008331
* Canada - Requisition Number: R-009630
* Belgium - Requisition Number: R-009644
* United Kingdom - Requisition Number R-009647
* Switzerland - Requisition Number: R-009649
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and will be located in High Wycombe, United Kingdom.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
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 Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary o...
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:42
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Toronto, Ontario, Canada
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-008331
* Canada - Requisition Number: R-009630
* Belgium - Requisition Number: R-009644
* United Kingdom - Requisition Number R-009647
* Switzerland - Requisition Number: R-009649
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and will be located in Toronto, Canada.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
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 Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the support...
....Read more...
Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:41
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-008331
* Canada - Requisition Number: R-009630
* Belgium - Requisition Number: R-009644
* United Kingdom - Requisition Number R-009647
* Switzerland - Requisition Number: R-009649
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Director, Global Labeling Product Leader.
This position is a hybrid role and will be located in Beerse, Belgium.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
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 Associate Director, Global Labeling Product Leader will be responsible for the following:
* Lead the development, revision, review, agreement, and maintenance of primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents (labeling text for EU, US)) for assigned compounds.
* Make recommendations and provide advice and guidance about labeling content, processes, timelines, and scientific integrity. Coordinate the resolution of any labeling issues with potential impact on the primary or derived labeling, or the support...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:40
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Finance
Job Sub Function:
Financial Planning & Analysis
Job Category:
Professional
All Job Posting Locations:
Markham, Ontario, Canada
Job Description:
We are searching for a Senior Finance Analyst Compliance, to be located in Markham, ON (200 Whitehall Dr).
This is a 12 month contract position.
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
Purpose:
* Review the Risk Control Matrix (RCM) and identify control owners
* Ensure each control has appropriate SOP documentation and complete/improve where necessary
* Educate control owners of any potential gaps and work with them to develop processes and appropriate tracking for proof of performance
* Partner with Internal Audit and in some cases global control owners to align on control ownership
* Periodic progress reports to Sr.
Manager
Qualifications / Requirements:
* Successful completion of a Bachelor's degree in a financial discipline or business
* In progress towards or successful completion of an Accounting designation (i.e.
CPA, CMA, CGA or CA) or MBA
* 4+ years of relevant experience in general accounting
* Understand and apply internal control and SOX compliance
* Advanced knowledge of Microsoft Excel (i.e.
pivot tables, macros and v-lookups)
* Working knowledge of SAP and TM1
* Strong accounting skills and understanding of accounting principles
* Attention to detail and ability to maintain a high level of accuracy in preparing and entering financial control information.
* Effective analytical and problem-solving skills, plus demonstrates drive and a willingness to take ownership for tasks and responsibilities
* Effective communication, collaboration and influencing skills
* Demonstrate sound work ethics, respect, team building, and cultural sensitivity and awareness
* This is a hybrid position that requires candidates to work in the office a minimum of three days per week.
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Type: Permanent Location: Markham, CA-ON
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:14
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Professional
All Job Posting Locations:
Istanbul, Turkey
Job Description:
Position Summary:
An Associate, Site Manager is an entry level site management role with typically 0-2 years of experience.
This role serves as the primary contact point between the Sponsor and the Investigational Site.
An Associate, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
Responsibilities may include assisting with site selection, site qualification assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
The Associate, Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to process improvement and training.
Some supervision from a more Senior, Site Manager (Senior SM or Lead SM) to help provide guidance to Associate, Site Manager.
Principal Responsibilities:
1 Acts as primary local company contact for assigned sites for specific trials.
2 May participate in site feasibility and/or Site Qualification Visit.
3 Attends/participates in investigator meetings as needed.
4 Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
Responsible for the implementation of analytical risk-based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
Occasionally may require assistance or oversight from Lead, Site Manager or LTM.
5 Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timef...
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Type: Permanent Location: Istanbul, TR-34
Salary / Rate: Not Specified
Posted: 2025-05-29 08:58:06
-
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:
Marketing
Job Sub Function:
Marketing Insights & Analytics
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America
Job Description:
We are searching for the best talent for a Manager, Forecasting – TECVAYLI® to be located in Horsham, PA.
About Oncology
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 Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
We lead where medicine is going and need innovators with an unwavering commitment to results.
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
Purpose: The Manager, Forecasting – Tecvayli position is responsible for generating, integrating, and translating insights and analytics into growth opportunities that shape decisions and drive organizational action.
This highly visible position will partner closely with senior brand stakeholders for TECVAYLI®, serving as a trusted advisor for informing demand forecast, attainment, performance, market dynamics, and evaluation of business strategies, and as a result, shares accountability for business results.
You will be responsible for:
* Lead brand forecast modeling, tracking, identification of risks & opportunities, and shaping articulation of performance story to senior leadership
* Drive innovation through objective analyses that uncover findings and insights across disparate data sets, enabling organizational decision making and action within brands
* Proactively identify enhancements to forecast modeling, process improvements/efficiencies, new data sources, and leading indicators that will increase accuracy and maximize time spent on high value projects
* Facilitate Integrated Business Planning (IBP) process and alignment across brand stakeholders to deliver latest thinking forecasts to business
* Embed insights from Strategic Insights & Analytics peers (integrated analytics, market research, competitive intelligence) into forecasting cycles to enhance decision making
* Apply basic consulting skills, including consultative l...
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Type: Permanent Location: Horsham, US-PA
Salary / Rate: Not Specified
Posted: 2025-05-29 08:57:46
