-
SBA Communications is a leading independent owner and operator of wireless communications infrastructure, including towers, buildings, rooftops, DAS and small cells.
We offer a competitive benefits and compensation package and are looking for team members who will thrive in our dynamic environment.
We welcome your interest in SBA.
Let us know a little about you by checking all that apply:
* You are a self-starter.
* You are resourceful and thrive in a fast-paced environment.
* You have a strong work ethic.
* You are passionate and driven to achieve results.
* You are a team player who enjoys working in a collaborative environment.
* You continuously challenge yourself to find innovative ways to improve.
You may be a perfect fit.
At SBA, we operate with the highest sense of integrity and commitment to quality.
We focus on achievement and operate with responsiveness, timeliness and accountability.
Our culture of excellence incorporates working collegially, where every team member can contribute meaningfully and make a difference.
If you are ready to make an impact, join our team!
Job Profile Summary
The position will be responsible for leading the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the assigned region.
The position is responsible for researching and analyzing the site level internal and external data to create and implement a plan to optimize the performance of the international tower portfolio.
This position will work closely with other internal departments, including Site Leasing, Services, Sales, Real Estate, Legal, Accounting, Taxes, Mergers & Acquisitions, Business Development, solutions, technology, IT
and New Tower Builds and will present to the executive leadership regularly or as needed.
Your Next Career Opportunity – Principal Specialist, International Competitive Intelligence
The position will be responsible for leading the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the assigned region.
The position is responsible for researching and analyzing the site level internal and external data to create and implement a plan to optimize the performance of the international tower portfolio.
This position will work closely with other internal departments, including Site Leasing, Services, Sales, Real Estate, Legal, Accounting, Taxes, Mergers & Acquisitions, Business Development, solutions, technology, IT
and New Tower Builds and will present to the executive leadership regularly or as needed.
What You Will Do – Primary Responsibilities
Be the regional leader of the Competitive Intelligence (CI), Geographic Information Systems Group (GIS), and Revenue Defense projects for the International Competitive Intelligence area, which will include the review of all relevant business intelligence information, including extracting data from multiple servers (external an...
....Read more...
Type: Permanent Location: Boca Raton, US-FL
Salary / Rate: Not Specified
Posted: 2025-04-01 08:18:41
-
Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
*
*English version to follow
*
*
ELYSIS – Directeur(trice) global(e) approvisionnement
Une nouvelle ère pour l’industrie de l’aluminium – ELYSIS
Aluminium sans carbone
La technologie ELYSIS™ représente la plus grande avancée dans l’industrie de l’aluminium depuis 1886.
Des efforts sont présentement déployés afin de perfectionner cette nouvelle façon révolutionnaire de produire de l’aluminium, qui élimine le dioxyde de carbone et toutes les autres émissions de gaz à effet de serre du procédé conventionnel d’électrolyse.
Le procédé ELYSIS élimine l’utilisation d’anodes de carbone, en les remplaçant par des matériaux brevetés.
En tant que premier procédé industriel qui émet de l’oxygène comme sous-produit, il a le potentiel de transformer toute l’industrie.
En 2018, deux producteurs d’aluminium de calibre international, Alcoa et Rio Tinto, ont uni leurs forces afin de créer la coentreprise ELYSIS avec le gouvernement du Québec.
Bénéficiant du soutien du gouvernement du Canada et d’Apple, la technologie progresse et elle est actuellement conçue pour être utilisée aussi bien dans des projets de construction que de modernisation d’alumineries.
ELYSIS a son siège social à Montréal, avec des centres de recherche et de développement à Alma et à Jonquière, au Québec (Canada), ainsi qu’à New Kensington, en Pennsylvanie (États-Unis) et en France.
Du métal de qualité commerciale produit par ELYSIS durant le processus de R et D est déjà utilisé par Apple dans un éventail de produits (comme le MacBook Pro 16 po et l’iPhone SE), par AB InBev (canettes) et par Audi (roues du e-tron GT, fabriquées par le RONAL Group).
Joignez-vous à l’équipe d’ELYSIS !
À propos du poste
ELYSIS est à la recherche d’un(e) Directeur(trice) Global(e) des Approvisionnements hautement expérimenté(e), basé(e) à Montréal, Québec.
Relevant de la cheffe de la direction financière, il ou elle sera chargé(e) de gérer l’ensemble des achats de l’entreprise, en menant des initiatives stratégiques, en développant des solutions adaptées aux besoins de l’organisation et en dirigeant une équipe performante.
Principales activités et responsabilités :
* Gérer la fonction d'approvisionnement d'ELYSIS en respectant les normes de conformité et les meilleures pratiques établies pour l’achat de biens et services.
* Diriger les activités d'approvisionnement en fonction des besoins commerciaux de l’entreprise.
* Gérer et encadrer une équipe de professionnels dynamiques.
* Favoriser un environnement d'équipe positif, collaboratif et productif.
* Développer des stratégies pour la chaîne d'approvisionnement mondiale et apporter des ...
....Read more...
Type: Permanent Location: Montreal, CA-QC
Salary / Rate: Not Specified
Posted: 2025-04-01 08:18:30
-
Your Job
Georgia-Pacific, LLC is now hiring a Process Improvement Analyst (PIA) for our McDonough, GA Mailer's facility.The ideal candidate will be a self-driven individual with a passion for excellence in Safety, Continuous Improvement, Manufacturing, and Customer Focus.
The PIA is a key addition for the Mailer facility, responsible for improving the corrugated facility's manufacturing performance through technology implementation, raw material qualifications and production line enhancements.
It's the perfect opportunity for someone on a steep growth trajectory who is ready to stretch a little.
The PIA will normally work a weekday (M-F) 8a-5p shift with potential for coverage during off-shift hours as needed including potential Saturdays.
Our Team
Georgia-Pacific's Mailers is a part of the Packaging and Cellulose business, the Mailers business is expanding its product lines, working with key customers to create and launch one or more new products to complement our already thriving recyclable padded mailer business.
Watch a short 60 sec video to see what we do at Mailers: How We Make Mailers | Georgia-Pacific - YouTube
What You Will Do
* Identify and implement cost-saving opportunities after validation
* Assist with new product development and ensure compliance through the New Substance Request (NSR) process
* Facilitate the Change Request process by receiving requests, uploading them to the PLEX change module, monitoring approvals, and collaborating with requestors to update SOPs on SharePoint
* Assist the Product Quality Supervisor by:
* Maintaining accurate BOMs and Specifications in PLEX and keeping SOPs and OPLs updated in SharePoint.
* Training new plant personnel on current Product Quality procedures and updating all personnel on revised procedures.
* Collaborating with the Quality Manager to maintain training logs.
* Providing timely recommendations (Release/Scrap/Rework) for products on "Hold" using a risk management approach and entering resolutions into Plex.
* Managing lab equipment calibration and ensuring the R&D lab adheres to 6S standards.
* Supporting customer complaint resolution through collaborative root cause analysis and documenting in Plex
* Evaluating and testing incoming raw materials for specification adherence, documenting results, and facilitating early invoice payments for contractual price discounts
Maintain regular structured and informal communication with Product Quality Specialists, the R&D team, Quality Manager, and Operations team
Troubleshoot issues and develop Design of Experiments (DOE) to identify and resolve recurring manufacturing challenges
Who You Are (Basic Qualifications)
* Previous experience in a quality or process improvement role within a manufacturing/ industrial environment or lab setting
* Previous e xperience documenting procedures and data and communicating to technical and non-technical audiences
* Must ha...
....Read more...
Type: Permanent Location: McDonough, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-01 08:14:40
-
Safety Specialist PDS Primoris Distribution Services – Denton, TX
Job description
SUMMARY: Responsible for all area activities involving safety and compliance with company policy and regulatory requirements.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
· Responsible for performing field safety audits for all divisions and all products primarily in Denton Tx.
Area
· Perform accident and incident investigations and reporting as directed.
· Assists in documentation collection for driver qualification files while in the field.
· Assists in training functions.
· Investigates instances of non-conformance and facilitates the determination of the root cause.
· Provides input to management.
· Additional duties as assigned.
SUPERVISORY RESPONSIBILITIES - None
QUALIFICATIONS/EXPERIENCE
*Must be Bilingual (fluent in Spanish), OSHA 30 hours
*Some travel required for the position- up to 25%
· Risk management degree, safety professional certification, construction surface restoration, or utility construction experience preferred.
· Basic computer skills particularly Microsoft Office programs (Word, Excel and PowerPoint) for input and output of data.
· Knowledge of computers and Windows based software, or the ability and willingness to learn.
· Ability to identify and suggestion resolution of problems in a timely manner.
· Ability to coordinate multiple tasks simultaneously.
· Effective communication skills, both oral and written.
· Respond promptly to customer needs and resolve all issues satisfactorily.
· Maintain confidentiality at all times.
· Demonstrate accuracy and thoroughness in all tasks.
· Treat people with respect and uphold the organizational values.
· Follow policies and procedures, with attention to detail.
· Prioritize and plan work activities and use time efficiently.
· Ability to consistently meet or exceed deadlines.
· Ability to deal with frequent changes, delays or unexpected events.
· Effectively provide guidance, maturity and foster positive attitudes about the job and the company.
· Strong interpersonal skills with the ability to relate to all types of people.
· A demonstrated willingness to work hard and at times physically demanding work in the elements.
Some of the physical demands are:
1.
Must be able to lift 50 pounds on a daily and continual basis.
2.
Ability to drive on a stop and start basis daily and continually.
3.
Lifting, placing of materials, standing, walking – particularly on uneven surfaces, turning, stooping, kneeling, crawling, reaching, crouching, speaking and hearing are required continuously.
4.
Close vision is required for some functions and distance and peripheral vision is required for safety.
WORK ENVIRONMENT
· Employee will be subjected to both outdoor and indoor environments
EEO Statement:
We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, n...
....Read more...
Type: Permanent Location: Denton, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-01 08:11:32
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
Scientific/Technology
All Job Posting Locations:
BG001 Sofia, ES022 Janssen Madrid, GB006 High Wycombe, IN004 Bangalore, IN022 Hyderabad, KR010 Seoul Yongsan gu, Lisbon, Portugal, PH001 Cebu, PT002 Porto Office, RO001 Bucureşti, RS001 Novi Beograd, TR021 ACT Istanbul, Turkey
Job Description:
Manager, Local Medical Safety, Vendor Partnerships
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 Manager, Local Medical Safety (LMS) Vendor Partnerships to be located in Portugal, United Kingdom, Turkey, Spain, Serbia, Romania, Bulgaria, South Korea, Philippines, India, Costa Rica, Brazil, or Canada.
This position may require up to 5% travel.
Per our J&J Flex Policy, the expectation for this position is to work in office 3-4 days per week and work from home 1-2 days per week.
Purpose:
You will be responsible for establishing and furthering the relationship between Local Medical Safety teams and assigned vendors (global, regional, local) to ensure oversight to Local Medical Safety contracted services (e.g., individual case safety report handling, including translation, literature review, etc.), services-related or systems-related issue identification and resolution, establishment, modification and termination of Key Performance Indicators, invoice review, and other activities as needed. The Manager, LMS Vendor Partnerships is the primary point of contact among Local Medical Safety, Vendor, and GMO Strategic Procurement Office and GMS Business Management and Metrics.
This person will actively participate in all vendor oversight, operational, and governance meetings.
The person in this role, in partnership with Local Medical Safety Process, Systems, Oversight, and Regional Liaisons, will ensure solutions are applied globally and issues are assessed for global Local Medical Safety implications and solutions.
You will be responsible for:
* Vendor Relationship
+ Is a subject matter expert on the co...
....Read more...
Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-04-01 08:10:01
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Human Resources
Job Sub Function:
HR Business Partners
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Services, Inc.
is recruiting for a Human Resources Leader, Global Development, IM R&D, based in Raritan, NJ, Titusville, NJ, or Spring House, PA.
As a Business Unit HR Leader you will provide strategic HR partnership to our Delivery Unit organizations as part of Global Development, across all therapeutic areas in R&D to contribute to shaping business strategy, and drive aligned outcomes in these focus areas:
* Leverage internal and external insights to diagnose and design organizations optimized to achieve strategic goals
* Design and deploy data-driven talent strategies that curate the talent and capabilities required to deliver
* Shape and steward our culture and employee experiences that will attract, inspire, and retain top talent
* Accelerate performance through leadership coaching and team effectiveness
* Partner across our OneHR model to deliver on talent and organizational strategies
Core Responsibilities
Business strategy
* Fluent in key business strategies (even outside of people topics), as well as external market competitive landscape
* Represent OneHR and provide strategic input on business strategy
* Understand what the business needs (through diagnosis, analysis, data), including organizational health, and what the function must bring to meet those needs, leveraging the breadth of the OneHR model
* Partner with the business on how to ensure organization is optimally set up to deliver on business strategy inclusive of annual business planning and long-range financial planning (e.g., workforce planning)
* Lead and execute significant organizational design efforts, inclusive of partnership with ER/LR, legal reviews, work council strategy and engagement, and change management
Talent strategy and management
* Identify and diagnose talent needs of the business through strong business and analytical acumen and effective analysis
* Create and deploy talent strategy to attract, develop, reward, and retain talent, including robust succession-planned pipeline and critical capability building (e.g., digital)
* Own and drive talen...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-01 08:09:57
-
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: Sr.
Specialist - Downstream Operations Technician
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights incl...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2025-03-31 08:08:57
-
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!
职位描述：
1.负责礼蓝动保猪业务在川渝、云南的推广销售工作。
2.了解客户的需求，能为客户提供有竞争力和价值的解决方案。
3.完善经销商的管理，并帮助经销商开拓销售渠道。
4.提升礼蓝动保在市场的占有率和影响力。
职位要求：
1.本科及以上学历，畜牧兽医相关专业。
2.三年以上农场或动保行业销售工作经验，猪场工作经验尤佳。
3.主动积极，具备良好的沟通能力和独立的业务拓展能力。
4.具备良好的英语口语交流能力者优先。
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
....Read more...
Type: Permanent Location: Chengdu, CN-51
Salary / Rate: 149000
Posted: 2025-03-31 08:08:53
-
Coordonnateur R&D - Description du poste
Depuis 1980, PG SOLUTIONS, une filiale de Harris Computer, est un chef de file du marché québécois dans le domaine des solutions d'affaires et de gestion pour le domaine public et parapublic.
Notre mission est de concevoir, développer et déployer des solutions de gestion les plus performantes sur le marché afin de contribuer à l’atteinte des objectifs de gestion des organisations que nous desservons.
Présentation du poste
Tu es à la recherche d'une opportunité professionnelle stimulante au sein d'une entreprise novatrice et en pleine croissance ? Ce poste est fait pour toi !
En tant que Coordonnateur d’une équipe de développement, tu seras au cœur de notre mission d'innovation.
Tu participeras activement à la planification, à l’organisation et au suivi de toutes les activités de ton équipe.
Ton rôle sera essentiel pour analyser les opérations de développement, superviser les projets et proposer des méthodes de travail innovantes.
Avec ton leadership inspirant, tu guideras ton équipe vers l'excellence, en favorisant une approche axée sur le soutien et l'efficience.
Tu seras un pilier pour assurer la mobilisation et la motivation de ton équipe.
Nous recherchons une personne rigoureuse, curieuse et avide de nouveaux défis.
Si tu te reconnais dans cette description, cette opportunité est faite pour toi !
Tâches et responsabilités :
* Participer à l’analyse, la planification, la coordination et la supervision des activités nécessaires à l’atteinte de tous les objectifs des projets, en respectant les ressources allouées;
* Participer au suivi d’avancement des projets auprès de la direction R&D;
* Au besoin, répondre aux demandes complexes et décider des priorités quotidiennes des équipes;
* Assurer les bonnes relations entre les intervenants à tous les niveaux hiérarchiques;
* S’informer sur les bonnes pratiques et nouveautés dans le développement logiciel autant au niveau des processus que des langages;
Responsable du personnel de développement :
* Mesurer la « performance » des équipes (Engagement, respect des estimés, qualité);
* Définir, évaluer et gérer les objectifs, les compétences et les besoins de développement des membres des équipes afin de voir à leur croissance;
* Participer au recrutement de personnel;
* Mobiliser les équipes autour des objectifs et enjeux de l’entreprise.
Responsable des activités Scrum/Agile :
* Collaborer avec le « Product Owner » pour maintenir un carnet de produit sain et planifier les tâches des sprints en fonction de la capacité de l’équipe;
* Organiser et animer les réunions « Scrum / Agile » pour assurer une communication efficace au sein de l’équipe;
* Encourager l’autonomie de l’équipe et promouvoir une amélioration continue pour atteindre son plein potentiel;
* Guider l’équipe dans l’identificati...
....Read more...
Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 80000
Posted: 2025-03-31 08:08:25
-
Austin Industrial delivers premier maintenance, construction, and soft craft services to leading industrial companies across the U.S.
An industry leader for more than 60 years, we offer single-source solutions to our customers in the oil, gas, chemical, food, agriculture, power, and manufacturing industries.
Our team of employee-owners, equipped with innovative technology and optimized procedures, helps owners optimize safety, productivity, profit margins, and cost-efficiency.
This is a full-time maintenance job working 40 hours a week (4/10's). There is no per diem and no relocation funding.
Industrial Insulator
The Industrial Insulator will layout, fabricate, assemble, install and repair insulation and sheet metal around pipes, maintenance parts, fittings, equipment and systems.
Responsibilities
* Must be an experienced Industrial Insulator with 3 or more years of experience.
* Must be able to install temp mat and pads and install pipe covering and fittings (Calcium Silicate).
* Must have experience forming sheet metal materials around pipes, ductwork and industrial equipment.
* Must be able to install insulation and fittings, pipe cover and board materials, such as perlite and calcium silicate.
* Install sheet metal around insulated pipes with screws/ bands to protect the insulation from weather conditions or physical damage.
* Makes flat sheet metal layouts of finished parts, such as sheet metal "square-to-round" transitions, offsets, flashing, tapered elbows, transitional elbows, "Y" branches and compound fittings.
* Brush adhesives and mastic application to insulation material.
* Using tape measure or other measuring device, measure and cut metal material to specified size and shape for covering flat or round surfaces.
* Must be able to use hand tools and equipment to form, crimp, or roll metal in place.
* Must be able to perform work wearing personnel protective equipment.
Including but not limited to the following: rain gear, chemical protective clothing, supplied air and air purifying respirators, safety harness, fire resistant coveralls, hard hat, ear plugs and safety glasses.
* While performing the duties of this job, the employee is regularly required to have full range of mobility in upper and lower body, able to reach overhead, able to work in various positions, including, but not limited to, stooping, standing, bending over, sitting, kneeling, squatting; use hands to handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; work at heights, balance for extended periods of time. Must be able to climb ladders and lift a minimum of 50 pounds.
* Other duties as assigned.
Qualifications
Education – no minimum education requirements.
Experience - 3 years of Insulator experience.
Must pass drug screen and background check, as a condition of employment.
This is a full-time maintenance job working 40 hours a week (4/10's). There is n...
....Read more...
Type: Permanent Location: Orlando, US-FL
Salary / Rate: 26
Posted: 2025-03-31 08:03:29
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Submissions & Regulatory Intelligence Manager
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 Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programming, and global re...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:59:00
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
Bangalore, Karnataka, India, Beerse, Antwerp, Belgium, Leiden, South Holland, Netherlands, PENJERLA, Telangana, India
Job Description:
Submissions & Regulatory Intelligence Manager
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 Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programmi...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:57
-
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-000701
* Canada - Requisition Number: R-002921
* United Kingdom, Belgium, Switzerland - Requisition Number: R-002952
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.
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 provides 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 supporting documentation.
Ensure high quality and compliant labeling documents.
This role may collaborate with external partners.
* Contribute to and implement the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area and their development plans and status and knowledge of labeling aspects for the development of labeli...
....Read more...
Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:54
-
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:
Latina, Italy
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/
J&J Innovative Medicine is recruiting for a Analyst Quality Systems.
Principle responsibilities:
This role is part of the eLIMS Center of Excellence (CoE) Small Molecules (SM) and serves as a subject matter expert in the configuration and maintenance of master data within the eLIMS system.
This role supports key processes such as the release of pharmaceutical, raw, and packaging materials, as well as Certificate of Analysis (CoA) generation in translating specifications into the eLIMS system using current business processes.
The incumbent independently creates, maintains, and reviews high-quality master data, conducts system testing and supports the creation and updating of system-related documentation.
Additionally, the role identifies opportunities for process improvements and drives their implementation.
This role is responsible for managing and executing incoming requests promptly and effectively.
To ensure the accuracy and integrity of master data, it is essential to have a comprehensive understanding of the site’s master data requirements and laboratory processes.
Additionally, the position involves the creation of training materials to foster knowledge sharing within the team, and actively participates in the development of team members through training and continuous personal growth.
The individual in this role is expected to support various projects within QC Operations, which could include the implementation of iLAB (paperless lab execution program) initiatives, process harmonization and standardization, master data support for consumer products and contract manufacturing organizations (CMOs).
Furthermore, this position offers critical support to the Supervisor in managing COMET nonconformance investigations and proactively...
....Read more...
Type: Permanent Location: Latina, IT-LT
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:51
-
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:
Issy-les-Moulineaux, Hauts-de-Seine, France
Job Description:
En tant qu’acteur majeur du bloc opératoire, Johnson & Johnson MedTech développe et commercialise des dispositifs médicaux utilisés notamment en chirurgie générale, orthopédie, traumatologie, neuroradiologie et électrophysiologie.
Nous innovons en permanence pour apporter aux professionnels de santé des produits à la pointe de la technologie et des solutions innovantes qui visent à améliorer la qualité de vie des patients et répondre à leurs besoins.
Nous recrutons un(e) Spécialiste Qualité dans le cadre d'un contrat en alternance pour une durée de 12 mois à partir de septembre 2025 (Issy-les-Moulineaux (92))
Principales responsabilités :
* Être garant de la conformité du traitement des réclamations qualité et des vigilances relatives aux produits (dispositifs médicaux et médicaments) commercialisés par Johnson & Johnson MedTech, dans le respect de la réglementation française et européenne et des procédures de l’entreprise :
+ Recueil et enregistrement des réclamations qualité produits et signalements de matériovigilance et pharmacovigilance.
+ Contribution aux investigations en suivant les demandes d’informations complémentaires en lien avec les fabricants
+ Elaboration des réponses aux clients sur la base des conclusions d’investigations faites par le fabricant
* Contribuer à la mise en place et au suivi des informations et actions de terrain et de sécurité.
* Participer au maintien et au développement du système de Management de la Qualité en supportant l’exécution des processus suivants :
+ Gestion documentaire
+ Gestion des enregistrements qualité dans le respect de la protection des données personnelles
+ Participation aux audits et inspections
+ Suivi des Non-conformités et des CAPA
+ Gestion des changements
Qualifications
Formation :
* Formation scientifique, Management de la Qualité
Expérience et compétences :
Requis :
* Bon niveau d’anglais
* Connaissance de la réglementation française et européenne relative aux dispositifs médicaux
* Connaissance du système de management de la qualité
* Bonnes capacités relationnelles et...
....Read more...
Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:47
-
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:
Beerse, Antwerp, Belgium
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a (3 years) PostDoc position, located in Beerse, Belgium
To continue a rich legacy in the field of neuroscience, we are building on our proven track record of innovative precision discovery approaches with a long-term commitment to neurodegenerative and neuropsychiatric diseases.
Our scientists are an integral part of the Johnson & Johnson Innovative Medicine Research and Development community and conduct research in collaboration with a broad network of academic leaders in the field.
At Johnson & Johnson, we strive to attract passionate and talented scientists who can drive change and deliver real value to patients.
We focus on innovation, collaboration and impact and by working with us, you will discover a place where you can grow and realize your full potential.
Through our culture of recognition and motivation for exceptional work, we care for and value our employees, just as we do the patients we serve.
At our exciting scientific research site with an interdisciplinary team of scientists, our goal is to understand the dysfunctional neural pathways that underlie psychiatric and neurodegenerative disorders to implement precision therapies.
We now have the opportunity within the Department of Neuroscience to take up a 3-year postdoctoral research position to contribute to the evaluation and implementation of innovative, context-specific animal models of disease using cutting-edge and advanced analytics.
Key Responsibilities:
* Perform neurophysiological experiments, implement and validate novel technologies for EEG data collection and analysis in rodents.
* You will also have access to a
* Ability to independently plan, organize and prioritize own work to make the most effective use of time and resources emphasis on innovation, collaboration, and timely delivery of results.
* Seek innovative ideas that add value to the project activities and provide ad hoc support for coordinating operations with external preclinical imaging collaborators on combined EEG/MRI recording modalities.
* Act as a “team player” contributing to achievement of the project’s objectives, build effective collaborative working relationships with team members, understa...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:46
-
At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Business Improvements/ä¸å¡æ¹å
* Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
æ¯æè´¨éæ¹è¿ä¸¾æªï¼ä¾å¦è¿ç¨å产åç¹æ§ï¼ä»èå¾å°æç»æ§æ¹å/ææ¬æ¹åã
* Conduct benchmarking to develop more effective inspection methods for improving quality.
      æ§è¡åºåï¼ä¸ºäºæé«è´¨éå¶å®æ´ææçè´¨éæ£éªæ¹æ³ã
Compliance/Regulatory/åè§/æ³è§
* Support Quality Engineer to review/analyze whether current product and processes (including actions or decisions conducted) are in compliance to standards.
      æ¯æè´¨éå·¥ç¨å¸å¯¹å½å产ååæµç¨(å
æ¬æä½æå³ç)æ¯å¦ç¬¦åæ åè¿è¡æ¥ç/åæã
* Support Quality Engineer to conduct periodic line audits to assess for production controls such as lot segregation. Review results of area audits to ensure that corrective and preventive actions are adequate.
      æ¯æè´¨éå·¥ç¨å¸è¿è¡å®æçç产线审计以è¯ä¼°ç产æ§å¶ï¼å¦æ¹æ¬¡é离ãæ£æ¥åºå审计çç» Â Â æï¼ç¡®ä¿çº æ£åé¢é²æªæ½æ¯å
åçã
* Support Quality Engineer to ensure the documentation and business process compliance, such as: handle the documentation approval process in PLM system, support training system maintenance, ECR process in SAP, dashboard creation/update, data processing, sample retention etc.
åå©è´¨éå·¥ç¨å¸ç¡®ä¿æ件åä¸å¡æµç¨çåè§æ§ï¼ä¾å¦ï¼æ件å¨PLMç³»ç»çæ¹åæµç¨ãå¹è®ç³»ç»çç»´æ¤ãSAPç³»ç»ä¸ECRçæµç¨ãæ¥è¡¨å建ææ´æ°ãæ°æ®å¤çãçæ ·ççã
Product Quality, Control & Disposition and Performance Standards/产åè´¨éï¼æ§å¶&å¤ç½®åæ§è½æ å
* Supports activities related to the Material Review Board.
åå©MRBæå
³çæ´»å¨ã
* Support Quality Engineer to conduct actions of non-conformances, CAPAs and customer complaints.Â
åå©è´¨éå·¥ç¨å¸è¿è¡ä¸åæ ¼ãCAPAså客æ·æè¯çè¡å¨ã
* Support Quality Engineer for material identification, material segregation, and classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.åå©è´¨é...
....Read more...
Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:45
-
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:
Project/Program Management Group
Job Sub Function:
R&D Project Management
Job Category:
Professional
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New Brunswick, New Jersey, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for the role of Director, Global Functions, Data Science Digital Health. We have a strong preference for this hybrid position to be located at one of the following offices; Titusville, NJ; Raritan, NJ; New Brunswick, NJ; Spring House, PA; Horsham, PA; Cambridge, MA; or San Diego, CA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
At Johnson & Johnson Innovative Medicines R&D, the Data Science & Digital Health (DSDH) function is charged with applying analytic approaches to drug discovery and development across Therapeutic Areas.
We drive and shape internal and external collaborations, working across Janssen’s Therapeutic Areas and R&D functions, including Global Development and other areas.
The Global Functions, Data Science & Digital Health (GF, DSDH) group within the R&D Data Science organization has the accountability for full scale impact across the Development pipeline via AI/ML-driven site recommendation trial design optimization, real-world evidence (RWE) generation, digital endpoints, decentralized trials, and external policy, with the key pillars being:
* Manage the development of solutions for the purpose of driving Trial Acceleration & Optimization using data science, including but not limited to:
* Enrollment modeling, feasibility analytics, country footprint expansion, advanced AI/ML modeling for predictive site recommendations
* Leverage real-world data for pat...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:38
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Clinical Data Management
Job Category:
Professional
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
Submissions & Regulatory Intelligence Manager
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 Submissions & Regulatory Intelligence Manager (hybrid) located within commutable distance of High Wycombe, United Kingdom; Beerse, Belgium; Leiden, Netherlands; Bangalore or Hyderabad, India; Springhouse or Titusville NJ, United States.
Purpose:
Contributes to the Clinical Data Standards team as an individual contributor who is a developing subject matter expert, and who works independently with minimal supervision and who takes a leadership role in the collaboration with various internal and external partners.
Consults on projects, programs, and processes that span multiple related areas in support of the organization's overall Clinical Data Standards strategy.
Applies in-depth knowledge of Clinical Data Standards to install best in class policies, procedures, and plans for the area.
Ensures consistency of clinical data standards across clinical trials and in compliance with regulatory requirements.
The Submissions & Regulatory Intelligence Manager is responsible for providing significant expertise to the IDAR department (and GD if applicable) in clinical study data regulatory submission requirements and strategies.
Examples of this content are:
* Newly released or updated Regulatory Health Authority (RHA) and industry guidance documentation
* Identification of clinical study data submission information critical to IDAR submission processes and procedures, including providing an interpretation of such information if needed
* IDAR submission requirements and rules.
The position serves as the single Point of Contact for any stakeholder on data management, clinical and statistical programming, and global regulatory affairs, for data submission deliverable requir...
....Read more...
Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:37
-
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:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Pulmonary Hypertension, is recruiting for a Product Manager, HCP Access Marketing based in Titusville, NJ.
As part of Johnson & Johnson, we are working to create a world without disease.
Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us.
We bring together the best minds and pursue the most promising science.
We collaborate with the world for the health of everyone in it.
Johnson & Johnson PH is a leader in the field of pulmonary arterial hypertension (PAH).
Our portfolio of PAH treatments covers the spectrum of disease, from WHO Functional Class (FC) II through to FC IV, with oral, inhaled and intravenous medications.
This position is a critical part of the Johnson & Johnson PH U.S.
Lifecycle & Therapy Access Marketing team.
This position will be responsible for the development and execution of HCP access resources across the PH portfolio (OPSYNVI®, OPSUMIT®, and UPTRAVI®).
This role will report to the Product Director, Therapy Access & Lifecycle Marketing.
Key Responsibilities:
* Coordinate execution of pull through excellence approach to maximize access investments across the J&J PAH portfolio.
* Lead the development and execution of HCP access messaging and resources for an HCP audience in partnership with the SCG organization.
* Serve as program lead for the PH unbranded Access Speaker Bureau by managing all aspects of execution, including content development, speaker training and program logistics.
* Lead the execution of HCP Access initiatives across the PH portfolio based on business need including the development of non-personal promotion assets.
* Serve as the field sales POA planning lead for the Therapy Access & lifecycle marketing team.
Partner with Sales Learning & Development to create workshops and trainings to elevate access acumen of the field sales organization.
* Cultivate and identify HCP Access insights for the brand, market, and PH landscape in partnership with field-based Therapy Access colleagues, market research, competitive intelligence, and analytics.
* Work productively with external agencies and key internal groups within the organization (SCG, Advocacy, IT, Market R...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:22
-
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:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Titusville, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-000701
* Canada - Requisition Number: R-002921
* Belgium, United Kingdom, Switzerland - Requisition Number: R-002952
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 can be located in Raritan, NJ; Titusville, NJ; Horsham, PA.
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 provides 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 supporting documentation.
Ensure high quality and compliant labeling documents.
This role may collaborate with external partners.
* Contribute to and implement the global labeling strategy, including demonstrating an understandi...
....Read more...
Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:21
-
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:
Malvern, 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 Senior Scientist, Downstream Processing to be in Malvern, PA.
Purpose: This position will lead and perform purification process development for the antibody-based modalities within the API-Large Molecule group in Malvern, PA.
Primary responsibilities will include leading and participating in the design of experiments, executing the planned experiments, and optimizing the process steps to the target process scale.
This will include laboratory and occasional pilot-scale scale chromatography and filtration.
The candidate will lead the design and execution of development studies to identify and determine appropriate conditions and ranges of (critical) process parameters for chromatographic purification and separation and several types of filtration.
The candidate will record and analyze experimental data, verify data integrity and accuracy, interpret analytical characterization results, and report/summarize findings to the project team, and also draft technical documents and perform technology transfer to collaboration partners.
The candidate should have experience with computational modeling/simulations and knowledge of downstream application.
The candidate is expected to work in a team environment as well as contributing individually to meet project timeline and objectives.
You will be responsible for:
* Lead and perform process development for the antibody purification processes.
* Lead, design and execute planned experiments which will include laboratory and occasional pilot-scale chromatography and filtration.
* Lead, design and execute development studies to identify and determine appropriate conditions and ranges of (critical) process parameters for chromatographic purification & separation an...
....Read more...
Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:18
-
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:
IE004 Barnahely
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
Job Description:
We are searching for the best talent for the Quality Control Analyst role to be in Cork, Ireland.
Purpose:
The QC analyst role is responsible for carrying out tasks and projects related to equipment, lab utilities and testing procedures at Janssen Sciences Ireland (JSI) as required by Good Manufacturing Practice (GMP).
Partners with other departments to ensure that all QC testing activities are completed in an efficient manner.
You will be responsible for:
* Achieves competency in laboratory methods and procedures.
* Trains other QC analysts in laboratory methods and procedures when required.
* Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
* Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.
* Writes, executes, reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
* Performs routine and non-routine analytical testing activities.
* Review and approval (where appropriate) of laboratory test results.
* Ensures that testing and results approval are completed within agreed turnaround times.
* Writes and reviews laboratory TMs, SOPs, TMDs and WIs as directed by company policy.
* Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
* Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Specialist, QC Team Leader and Manager.
* Deals with Quality Issues in an accurate and timely manner.
* Maintains and develops knowledge of analytical technology as well as cGMP stan...
....Read more...
Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:17
-
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:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Clinical Research Manager for Shockwave Medical Inc.
The position is fully remote
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Position Overview
The Clinical Research Manager is responsible for the day-to-day management of a global clinical study.
The Clinical Research Manager will be accountable for project management activities, oversight of multiple vendors and for conducting a global clinical study in compliance with applicable clinical and regulatory standards and in alignment with the business needs.
This work is accomplished with minimal oversight, requires frequent contact with internal and external customers and is critical to the success of the business.
Essential Job Functions
* Responsible for organizing, communicating and evaluating team objectives for clinical studies
* Participates in study design and study preparation activities
* Development of clinical trial documentation including clinical trial protocol development, case report form (CRF) development, IRB/Ethics submissions
* Participates or leads the process to evaluate and select potential investigators and sites
* Participates or leads the process to evaluate and select potential vendors as applicable
* Conducts or oversees site visits as required (pre-study, initiation, interim and close-out visits) to ensure protocol compliance, accurate and thorough data collection, and appropriate study conduct
* Develops site training tools, interprets clinical data, manages investigational sites, develops tracking tools and performs other clinical activities as needed during clinical study conduct
* Leads clinical study teams focused on conducting clinical programs consistent with applicable re...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:13
-
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:
Clinical Quality
Job Category:
People Leader
All Job Posting Locations:
New Brighton, Minnesota, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring a Senior Manager, Clinical Quality Assurance, to join our team! This is a fully remote role, with flexibility to be based anywhere within a reasonable commute to a major airport.
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 Sr.
Manager, Clinical Quality Assurance will provide GCP and compliance-related oversight and audit of internal and external Clinical Studies in process, support and update procedure compliance with applicable regulations and oversee clinical affairs initial and ongoing vendor audits as needed.
This work is accomplished with minimal oversight, requires frequent contact with internal and external customers and is critical to the success of the business.
Essential Job Functions
* Act as a Clinical Quality Lead on clinical trials by supporting project team compliance with national and international regulatory standards and guidance for medical devices
* Develop and manage audit management plans and audit strategy for ongoing clinical trials
* Prioritize audit strategies for GCP programs
* Coordinate, plan and conduct internal system au...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-03-31 07:58:04
