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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:
Business Intelligence
Job Category:
Professional
All Job Posting Locations:
Birkerod, Capital, Denmark, Oslo, Norway
Job Description:
Are you a strategic thinker with a passion for data? Do you thrive on transforming complex information into clear, actionable insights that drive business growth? If so, we invite you to explore this exciting opportunity to lead Business Intelligence (BI) across the Nordics at Johnson & Johnson Innovative Medicine.
As Nordic BI Manager, you’ll be at the heart of our data-driven decision-making.
You’ll lead key forecasting workstreams, shape the development of BI solutions for our prioritized brands, and build insight strategies that connect data across therapeutic areas.
Your ability to identify correlations, model scenarios, and translate analytics into business impact will be central to our success.
You’ll also play a key leadership role—coaching a team of BI analysts, collaborating with country leadership teams, and leading the roadmap and budget for BI deliverables such as Market Research, Reporting, and Competitive Intelligence.
Key Responsibilities:
* Drive and lead our key forecast workstreams (BP & LRFP) from a BI point of view
* Lead, develop and shape the development of out BI solutions related to our prioritized brands
* Own or lead the operational BI work in one or more TA's
* Lead and drive the strategy and roadmap for one or more key BI deliverables and CoE areas (e.g.
Market Research, Reporting, CI).
Own the budget of those area(s)
* Drive the development of the BI group and coaches direct reports in their roles
* providing relevant inputs via patient-based models to guide the LRFP and BP submissions of selected TAs (where applicable)
* Help strategic important Country Leadership Teams to investigate strategic questions by delivering insights to key business questions
We’re looking for someone with a master’s degree or equivalent experience or equivalent in a relevant field such as Data Science, Business Analytics, Economics, or Engineering.
You are experienced in Business Intelligence (6-8 years)—ideally within the pharmaceutical industry—and have a strong command of quantitative analysis, data modeling, and strategic insight development.
People leadership experience and fluency in English are needed.
Beyond technical skills, we value ...
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Type: Permanent Location: Birkerod, DK-84
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:27
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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:
Ciudad de Mexico, Mexico, Monterrey, Nuevo León, Mexico
Job Description:
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 the disease state and complex medical problems
o Have scientific and competitive intelligence incorporating contributions to the strategic plan.
• Collect requests on:
o Proposals to support educational activities
o Physician requests for researcher-initiated studies in accordance with company guidelines
o Any medical and scientific research related to therapeutic areas of expertise
o Disease and product training
• Provide feedback and intelligence on the market environment, promotional and clinical strategies, competition
• Ensure compliance with local regulations and the company's internal Compliance policies in their daily work.
• ...
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Type: Permanent Location: Ciudad de Mexico, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:25
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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:
Environmental Health, Safety (EH&S) and Facilities Services (FS)
Job Sub Function:
Environmental Health & Safety
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Manager, EH&S to join our team located in Titusville, NJ.
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
Under the direction of the Environmental, Health & Safety (EH&S) Enterprise organization, this candidate will be primarily responsible for managing all aspects of environmental, health and safety (EH&S) for the J&J Titusville, Horsham and Aviation Operations locations.
This role will have responsible for managing EH&S operations to assure compliance with federal, state, and local EH&S regulations, as well as Johnson & Johnson EH&S Standards.
Additional responsibilities include project and site support for Americas Office and Road Safety organization, supervision of associated direct reports or contracted resources, and EH&S compliance support for Innovative Medicine Field Sales teams reporting into the commercial teams. This role will also partner with the site leadership teams to establish and implement an EH&S strategy and Corrective and Preventive Actions (CAPAs) in alignment with the J&J Enterprise EH&S organization.
Key relationships
This leader will work closely with various internal and external stakeholders.
* Internal: J&J site leadership teams and commercial leadership, Facilities/Contracted Partners, Employee, Health & Wellbeing and J&J Enterprise EH&S organization and SAFE FLEET, Fleet SMEs.
* External: Regulators, 3rd party consultants/assessors and contractors.
Key Responsibilities
* Provide leadership and manage EH&S responsibilities for Titusville, Horsham and Aviation operations locations.
* Partner with site management to proactively identify, develop and implement Corrective & Preventive Actions (CAPAs) to address EH&S program deficiencies and ensure EH&S regulatory compliance.
* Monitor the progress of ...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:16
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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:
Chemical Research
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
The department of Chemical Process Research & Development (CPRD) focuses on the development of synthetic methodologies and processes for small molecules, oligonucleotides, peptides and other emerging modalities.
In the group PRD (Process R&D) we currently have open positions for synthetic chemists with a passion for designing the best possible chemistry and processes.
Job description:
The API Process Research and Development (PRD) team generates creative and innovative ideas towards new synthetic routes and solutions that enable large scale manufacturing of target Active Pharmaceutical Ingredients.
Our process chemists team up with engineers, analysts, crystallization-, and safety experts to design the best manufacturing process.
These teams work closely together with the pilot plants and bridge with commercial production.
New chemical processes are developed meeting stringent requirements concerning safety, environment, technology, economy, and quality.
As a result of these endeavours, drug candidates are accelerated through the development pipeline by enabling sufficient supplies of active ingredient in support of clinical trials, registration and finally commercialization.
As a PRD scientist you will be responsible to develop the best possible process and to support the project during the different stages of development.
You will be focusing on inventing new chemistry towards new Active Pharmaceutical Ingredients and translating this chemistry into a process that can be performed in a robust, sustainable and safe way in a large-scale manufacturing plant.
Experience and skills
* PhD in Organic chemistry; post-doc experience is a plus.
* Consistent track record of scientific excellence and successful research in organic chemistry supported by peer-reviewed publications.
* Passionate t...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:10
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Pharmaceutical Sales
Job Sub Function:
Sales – Rare Diseases (Commission)
Job Category:
Professional
All Job Posting Locations:
Minneapolis, Minnesota, United States of America, Sioux Falls, South Dakota, United States
Job Description:
Johnson & Johnson Innovative Medicine is searching for the best talent for a Rare Disease Account Manager (RAM) for Immunology Autoantibody Diseases to cover the Minneapolis South Territory.
This position is field based that covers the territory of Southern Minnesota, South Dakota, and La Crosse Wisconsin area.
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
The Rare Disease Account Manager will consistently achieve or exceed sales objectives within their Local Healthcare Market (LHM).
The Rare Disease Account Manager will report to a Senior District Sales Manager.
The RAM owns the total market, developing and executing a strategy to identify patient opportunity, drive demand, and remove fulfillment barriers.
To achieve the business goals and meet customer needs, you will also ensure alignment with internal field partners, including Thought Leader Liaisons (TLLs), Area Business Specialists (ABSs), Field Reimbursement Managers (FRMs), Key Account Managers (KAMs) and Medical Science Liaisons (MSLs).
The RAM will be responsible for:
* Drive outstanding territory sales performance and product demand to ensure sales forecasts are met or exceeded within the LHM by building and sustaining strong, trusting relationships with customers and influencing key stakeholders.
* Leverage company approved marketing resources to effectively demonstrate clinical value as a solution to address identified customer and patient needs.
Leverage payer acumen to educate patients on access and affordability options.
* Analyze qualitative and quantitative market ...
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Type: Permanent Location: Minneapolis, US-MN
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:04
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product Safety
Job Sub Function:
Product Safety Risk Management MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Lisbon, Portugal
Job Description:
Johnson & Johnson is recruiting for a Medical Review Safety Physician Manager to be located in Lisbon, Portugal.
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
The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall Pharmacovigilance process; this includes single case signal detection activities for selected products as well as operational aspects of individual case medical review.
The Medical Review Safety Physician (MRSP) Manager has responsibility for determining the medical and scientific relevance of adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area.
These responsibilities include spontaneous reports, clinical and non-clinical studies, literature reports and other sources of safety data.
Additionally, MRSPs participate in matrix management activities (e.g.
Safety Management Team (SMT) and provide pharmacovigilance expertise on individual case reports.
MRSPs support activities such as evaluating safety issues from various sources including Designated Medical Events (DME) and Events of Interest (EVOI), preparation of aggregate safety reports such as PBRERs/PADERs, ad-hoc regulatory reports, Risk Management Plans, and interpretation of surveillance and product quality data.
Responsibilities include, but are not limited to the following:
* Active participation in MRSP activities which include, but are not limited to:
* Analysis and assessment of Critical Cases, including SUSARs
* Detection of single case potential safety signals/ through validation
* Identification and analysis of new safety signals and trends by conducting systematic reviews of aggregate data.
* Review local literature for potential signals assessed by vendors and Local Management Safety (LMS)
* Acti...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-10-08 08:19:01
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Control
Job Category:
Professional
All Job Posting Locations:
Jacksonville, Florida, United States of America
Job Description:
About Vision
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges.
Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life.
Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for Scientist III Microbiology to be located in Jacksonville, FL.
Purpose:
Provide expert support and guidance for Bioburden and Environmental monitoring, DI water system, and Sterilization programs to ensure compliance and optimal microbiological control.
Leads Microbiology investigations for Out of Specification (OOS) and Out of Trend (OOT) results and recommends corrective actions.
Provides technical support for the evaluation and implementation of new products and packaging materials.
Works with Regulatory Affairs, Quality Assurance, New Product Development, Engineering, Customer Relations, Operations, and Materials Management.
Provides technical leadership regarding equipment qualifications, test method validations and leads quality program / test method improvements where needed.
You will be responsible for:
* Executes sterilizers qualification and microbiological testing (i.e.
Bioburden, Air testing, growth promotion, etc.).
* Leads validation projects and recommends new methods to support laboratory compliance and efficiency.
* Participates in department company safety objectives.
* Prepares and/or approves protocols, final reports, laboratory investigations, etc.
* Reviews, trends, analyzes and reports data recommending appropriate actions.
* Develops, writes, and revises internal department procedures.
* Learns and introduces new laboratory technologies.
* Quali...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-08 08:18:55
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Technology Product & Platform Management
Job Sub Function:
Technology Operations Support
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium, Latina, Italy
Job Description:
Job Description:
J&J Innovative Medicines is recruiting a Formulation Scientist.
MSAT Small Molecule Drug Product is accountable for capturing and intensifying the scientific cornerstones for our innovative formulations and leading productivity, compliance, and sustainability throughout their commercial lifecycle.
You will be responsible for scientific assessment and optimization of formulation & process robustness, enhance product quality, and ensure regulatory compliance in the domain of liquid and/or solid dosage forms.
The ideal candidate will have a strong background in pharmaceutical development and tech transfer with a passion for innovation and problem-solving.
Responsibilities
* Provide technical support for technical transfer, PPQ, and commercial manufacturing operations, including sensitivity analysis, root cause analysis, and impact assessments.
* Plan, design, execute, and document lab and plant studies related to formulation, and process optimization in support of commercialization and lifecycle management.
* Write, review, and approve protocols, reports, and regulatory submissions, and monitor market trends, competitive landscapes, and emerging regulations to inform strategic decision-making.
* Provide subject matter expertise (SME) to prepare and support technical project reviews and operational excellence initiatives, and support or lead initiatives for compliance, resilience, formulation and process robustness optimization.
* Collaborate with expert communities in development and supply chain to establish, maintain, and deploy best practices for formulation and process development and intensification, advancing the scientific foundations in Supply Chain.
* Leverage networking and influencing skills to ensure effective collaboration with partners in R&D and Supply Chain, and prepare and review relevant technical documents, such as risk assessments, change controls, regulatory submissions, deviations, validations, protocols, procedures, ...
Requirements
* Advanced degree in Pharmaceutics, Biotechnology, Engineering, Physics, or related area
* Min 3 years of experience in development and tech transfer of solid dosage forms
...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-08 08:18:43
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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:
Product Safety
Job Sub Function:
Pharmacovigilance
Job Category:
People Leader
All Job Posting Locations:
Mexico City, Mexico
Job Description:
REGULATORY COMPLIANCE
▪ Ensure implementation and compliance with global, regional and local procedural documents applicable to Pharmacovigilance.
Accountable internally for ensuring that the LOC meets procedure defined timelines for management of safety information and any local regulatory agency defined timeline for submission of individual reports.
▪ Oversight responsibilities of case processing operational activities delegated to the Center of Excellence Case Processing hub for Latin America or external vendor as appropriate.
Case processing activities include but not limited to Inbound reporting, outbound reporting, translation of AEs/Special Reporting Situations/PQCs, literature search, due diligence.
▪ Accountable for compliance monitoring for submissions to Competent Authorities (HAs).
Reconcile compliance data provided and take appropriate corrective actions as defined by company policies and procedures.
▪ Ensure awareness of changes in regulations which may have an impact on PV activities and responsibilities.
Inform the appropriate global and regional groups (i.e.
QPPV office and regional heads) of any changes to local laws and regulations regarding Pharmacovigilance
▪ Oversight of timely elaboration and submission of all documents required by local PV legislation.
PV SYSTEMS COMPLIANCE
▪ Oversight of timely and appropriate communication & follow up of the activities related with Global Clinical Operations (GCO & GCO MAO) to comply with PV local regulations regarding clinical trials conducted in the territory as applicable, including those carried out by third parties, as per the contracts & agreements.
▪ Oversight of timely and appropriate Development of Local Implementation Memos (LIM) for Regional / PV Standard Operating Procedures/Working Practices and verify adherence.
▪ Managing and scheduling of the preparation of necessary outlines, status reports, graphs, charts, tables, and slides for periodic reviews for the Pharmacovigilance specialists.
▪ Monitor data generating activities to ensure any solicitation for information includes an appropriate review and reporting process for reporting potential AEs (e.g.
patient support programs, market research studies, marketing activities, internet sites, surveys, etc.), as applic...
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Type: Permanent Location: Mexico City, MX-CMX
Salary / Rate: Not Specified
Posted: 2025-10-08 08:18:43
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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:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Technical Fellow (Director), Advanced Therapies - MSAT to be in Raritan, NJ, Titusville, NJ, Malvern, PA, or Spring House, PA.
Purpose:
The Technical Fellow serves as a subject matter expert (SME) in CAR-T manufacturing and Quality Control analysis, playing a pivotal role in ensuring the quality and safety of cellular therapies.
This position is critical in addressing challenges that arise when non-conforming products or deviations are generated during the manufacturing process, which can impact patient treatment.
The Technical Fellow actively engages with healthcare providers to navigate these challenges, facilitating clear communication and collaborative problem-solving.
In addition to direct interaction with healthcare providers, the Technical Fellow curates and analyzes manufacturing case studies to expedite the release of drug products.
This role requires deep expertise in key areas, including apheresis collection, cryopreservation, cell processing, quality control testing, and quality release processes.
The Technical Fellow provides insights to both internal manufacturing teams and external partners, ensuring adherence to the highest standards of quality.
The Technical Fellow is also an integral member of various site/network operational teams, including planning, release, clinical/commercial rapid response teams, safety management, and site escalations.
In this capacity, they contribute to the development of robust strategies that maintain the validated state of cell therapy processes while supporting lifecycle management initiatives involving new technologies, automation, and technology transfer.
Finally, this role serves as a key thought leader and scientific expert driving manufacturing trend investigation teams towards root c...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-08 08:18:32
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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:
Non-Employee
Job Category:
Non-Standard
All Job Posting Locations:
Suzhou, Jiangsu, China
Job Description:
Contributes to assigned team at J&J.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-10-08 08:18:25
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ERM is seeking an experienced Managing Consultant, Environmental Permitting Project Manager with demonstrated experience permitting capital projects in New England and New York.
The ideal candidate will have experience with the Massachusetts Wetlands Protection Act, New England General Permits, and local land development regulations across the Northeast.
A strong candidate will have technical expertise leading multi-media environmental permitting efforts under the purview of state agencies and providing support for the development of large-scale capital expansion projects in the energy sector.
Renewable energy permitting experience is a plus.
As a senior leader, you will be fully accountable for successfully consulting on permitting-related project work to support and build ERM’s team in the Northeast, while networking with ERM's global technical team to share best practices across the industry.
RESPONSIBILITIES:
* As a “seller/doer,” contribute to business development of ERM’s full range of Impact Assessment and Permitting (IAP) services.
Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients.
Develop and expand client relationships that generate repeat business.
* Serve as Senior Technical Advisor for permitting-related activities in support of ERM clients’ capital projects (i.e., renewable energy projects, electric and gas utilities,). Lead the strategic planning and preparation of permit packages, serving in roles ranging from subject matter expert to QA/QC.
* Manage large, complex capital development projects to achieve client’s expectations for scope, budget, schedule, and quality.
* Lead, manage performance, hire and retain, inspire and mentor personnel for overall growth and success of technical team.
* Work with ERM’s existing IAP service line to deepen relationships with ERM’s key clients and establish new client relationships that result in growth.
* Support the general growth and development of ERM’s IAP technical community.
Collaborate with other ERM global practitioners to execute impact assessment projects.
Participate on teams comprised of impact assessment professionals from multiple offices around the global ERM organization.
REQUIREMENTS:
* BS/MS in environmental studies, natural resources-related science, planning, geography, civil or environmental engineering or related field; PWS, PE, CEP, AICP or similar registration desired.
* 4-6+ years of consulting experience with state/local agencies and multi-media permitting.
* Demonstrated ability to develop and maintain long-term relationships with clients, and book personal sales in new permitting consulting services.
* Solid grasp of the key impact assessment and management issues within the power and oil/gas sectors, as well as a high degree of technical competence and broad knowledge of env...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2025-10-08 08:16:27
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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
Praktikum (m/w/d) im Bereich Events & Congresses
Wer wir sind:
Die Roche Pharma AG an ihrem Standort in Grenzach-Wyhlen steuert unter anderem die medizinischen Aktivitäten, das Marketing und die Vertriebsaktivitäten für den deutschen Markt.
Der Bereich Events & Congresses verantwortet die konzeptionelle und organisatorische Planung sowie Durchführung von
Roche-eigenen Veranstaltungen, von Roche Kongress-Auftritten und von Kogressteilnahmen.
Was dich erwartet:
Während Deines Praktikums übernimmst Du folgende vielfältige Tätigkeiten:
● Unterstützung der Events & Congresses Specialists bei der Planung und Durchführung von Präsenz-, virtuellen und hybriden Veranstaltungen sowie bei der Teilnahme an deutschen und internationalen Kongressen.
● Unterstützung und Übernahme von Teil-Aufgaben in den Bereichen:
* Projektmanagement von Veranstaltungen und Kongressen
* Recherche und Buchung von Hotels, Restaurants und anderen Locations
* Einbindung digitaler Kanäle wie z.B.
des Roche Fachportals
* Teilnehmer-Management inklusive Vertragsmanagement
* Technische Betreuung virtueller Veranstaltungen
* Vor-Ort Betreuung großer Veranstaltungen
* Administrative Abwicklung der Veranstaltungen in den Roche-Systemen
Wer Du bist:
Du hast Interesse am Event & Kongress-Management im Pharmabereich und bringst idealerweise bereits erste Erfahrungen im Event & Kongress-Management sowie Projektmanagement mit.
Darüber hinaus bist Du kundenorientiert und kommunikativ, arbeitest strukturiert, selbstständig und lösungsorientiert und hast ebenso Spaß daran, Aufgaben im Team zu lösen.
Für das Praktikum im Bereich Events & Congresses bringst Du zudem folgende Voraussetzungen und Kenntnisse mit:
* Generelle Voraussetzung zur Beschäftigung als Praktikant/in ist die ordentliche Immatrikulation während des gesamten Praktikums oder aber das Praktikum wird innerhalb eines Gap Years absolviert, also nach dem Bachelorabschluss in Vorbereitung auf ein Masterstudium oder auf die Promotion.
* Du bist Student (m/w/d) mit Schwerpunkten im Bereich Event Management, der Hotellerie, Wirtschafts- oder Kommunikationswissenschaften o.ä.
* Gute Kenntnisse in MS Office (Word, Excel, Powerpoint)
* Gute Englisch- und Deutschkenntnisse in Wort und Schrift
Zeitraum: ab 01.04.2026 oder nach Vereinbarung für die Dauer von 6 Monaten
Was wir Dir bieten:
* Mobiles Arbeiten möglich
* Möglichkeit, interne Weiterentwicklungsangebote wahrz...
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Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2025-10-08 08:16:22
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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.
Alcoa, Aluminerie de Baie-Comeau
Stage en hygiène industrielle
Être stagiaire chez Alcoa, c’est travailler avec des équipes dynamiques composées de gens ouverts aux nouvelles idées.
Vous serez pleinement intégrés dans nos équipes et elles se feront un plaisir de partager leurs connaissances et expériences avec vous.
Venez vous joindre à notre équipe afin d’acquérir une expérience des plus enrichissantes en milieu industriel!
Alcoa au Canada c’est :
* Trois alumineries au Québec :
+ Aluminerie de Deschambault
+ Aluminerie de Bécancour Inc.
+ Aluminerie de Baie-Comeau
* 2 500 employés;
* 1 Centre d’excellence mondial;
* Un million de tonnes métriques de plaque, de lingot-T et de billette.
Nous visons à intéresser, développer et retenir les meilleurs talents, en plus de créer un environnement où l’accent est mis sur le respect, la santé-sécurité, la protection de l’environnement et le développement continu, afin que chaque employé puisse contribuer au succès collectif.
Session
Hiver 2026
À propos du stage :
Dans le cadre de ce mandat, le stagiaire en hygiène industrielle sera amené à effectuer les tâches suivantes :
* Mesurer le niveau d’exposition des travailleurs;
* Entrer des données dans les systèmes de gestion;
* Procéder aux essais d’ajustement d’étanchéité (fit test) pour les masques;
* Procéder aux essais pré-usage de détecteur de gaz pour l’entrée en espace clos;
* Aider dans la recherche de substituts disponibles pour des produits contenants des substances à risques;
* Tous autres tâches afin de supporter l'équipe.
À propos de vous :
* Être étudiant au DEC ou AEC en environnement, hygiène et sécurité au travail ou dans un domaine universitaire axé sur l'hygiène industrielle;
* Être axé sur le travail d'équipe;
* Autonomie.
Conditions de travail
* Vous ne demeurez pas dans la région de notre aluminerie? Vous pourriez être éligible à une prime de 600 $ pour votre logement! Nous pourrons de plus vous mettre en contact avant le début du stage avec les autres stagiaires qui seront présents à la session hiver 2026;
*
* Formations complètes à votre arrivée pour vous préparer à notre environnement industriel;
* Tous les équipements de protection individuels vous seront fournis;
* Un service médical accessible aux employés;
* La possibilité de faire plus d’un stage avec nous.
* Certaines restrictions s’appliquent.
Conditions de stage
Dates (flexible selon votre session)
Heures de travail
40 heures par semaine
Horaire de travail
Horaire de jour, du lundi au vendredi.
Dans cet affich...
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Type: Contract Location: Baie-Comeau, CA-QC
Salary / Rate: Not Specified
Posted: 2025-10-07 08:32:36
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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.
This is your opportunity to help shape the future of sustainability with world-changing innovations and low-carbon technologies.
Become a valued part of the team that’s shaping the future of aluminium, revolutionising the way the world lives, builds, moves and flies.
Be part of it and shape your world.
About the Role
Do you have a passion for people and how they interact with their work environment? If so, you’ll find a rewarding opportunity waiting for you at our Wagerup Refinery as a Health & Safety (H&S) Consultant.
You’ll work Monday through Friday, with the added bonus of a leisure day every four weeks to recharge.
As part of our H&S team, you’ll support employees across all levels of the Refinery.
Reporting to the site H&S Superintendent, you’ll become a key contributor in a dynamic team that mentors, coaches, and develops work crews to elevate their H&S performance.
You’ll also provide essential guidance to our contracting workforce.
In this role, you’ll be responsible for:
* Developing and producing reports on Health & Safety issues
* Conducting H&S audits and supporting the development, implementation, and maintenance of key H&S strategies
* Advising management on areas of concern and offering critical support during investigations and major incidents
* Designing and coordinating training programs tailored to the Refinery’s needs and H&S requirements
* Proactively reviewing performance measures and determining action plans to close any gaps
* Leading employees through a variety of H&S projects and initiatives focused on continuous improvement
What’s on offer
* Competitive remuneration and benefits packages
* Salary packaging for a novated car lease, employee share plan and superannuation options.
* Generous leave entitlements including a leisure a day off every 4-week period.
* Flexible hybrid working options available
* Parental leave support for all caregivers
* Career development opportunities to pursue your passions
What you can bring to the role
* You hold tertiary qualifications in Environment, Health & Safety or a related field, or you’ve completed a Certificate IV or Diploma in the H&S space
* You bring strong Health & Safety experience, ideally gained in a heavy industry or industrial setting
* You understand and apply legislative standards to ensure Alcoa remains compliant with H&S requirements
* You have excellent interpersonal skills that empower you to lead others in continuously improving health and safety systems and performance
Additional information
* Interviews may progress prior to the closing date, although all applications will be considered.
* You will only be contacted if you are shortliste...
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Type: Permanent Location: WAROONA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-10-07 08:32:35
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Ready to lead from the front? We’re looking for a Rooms Division Manager to oversee our front office, housekeeping, concierge and club lounge departments.
Setting the tone to deliver truly memorable guest experiences from the first moment to the last.
A little taste of your day-to-day:
Every day is different, but you’ll mostly be:
* Overseeing the daily operations of Front Office, Club InterContinental Lounge, Concierge, and Housekeeping.
* Leading, developing, and motivating department leaders to achieve service and financial goals.
* Driving guest satisfaction scores and maintaining the hotel’s reputation for excellence.
* Managing budgets, labour costs, and productivity targets.
* Collaborating closely with other hotel departments to ensure a flawless guest journey from arrival to departure.
* Maintaining strong compliance with IHG brand standards, safety, and operational policies.
What We need from you:
* Proven experience as a Front Office Manager, Rooms Division Manager or similar leadership role in a hotel environment.
* Strong leadership and communication skills with a hands-on, guest-focused approach.
* Excellent knowledge of front office systems, housekeeping operations, and service standards.
* Financial acumen and the ability to analyse data to drive performance.
* A passion for developing people and creating a culture of excellence.
What you can expect from us:
We give our people everything they need to succeed.
From a competitive salary that rewards all your hard work to a wide range of benefits designed to help you live your best work life – including a full uniform dry cleaning, impressive room discounts, gym membership, meals while on duty and some of the best training in the business.
Our mission is to welcome everyone and create inclusive teams where we celebrate difference and encourage colleagues to bring their whole selves to work.
IHG gives every member of the team the room they need to belong, grow and make a difference in a collaborative environment.
We know that to work well, we need to feel well – both inside and outside of work – and through our myWellbeing framework, we are committed to supporting wellbeing in your health, lifestyle, and workplace.
So, join us and you’ll become part of our ever-growing global family.
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Type: Permanent Location: Sydney, AU-NSW
Salary / Rate: 105000
Posted: 2025-10-07 08:30:52
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We are currently seeking School Psychologists in the following areas:
Goshen, NY; Wappinger, NY; Sugar Loaf, NY; Ulster County
Liberty POST is currently seeking a motivated and energetic School Psychologist for per diem employment to work with children who are birth-5 years old through Early Intervention and Preschool Special Education programs.
Immediate positions are available.
Liberty POST has offered its clients a range of high-quality and individualized services since 1994.
Backed by Liberty Resources Inc.
and part of a large social services circle, originally POST was a speech-language practice in Syracuse NY and has grown to provide a range of services throughout all of New York State and New Jersey.
We employ over 500 professionals in a variety of settings and offer a collaborative team approach to provide evaluation, direct therapy, and family education through child-directed play.
We are focused on the importance of a child’s natural learning environment, a family’s unique strengths and needs and the diverse population we serve.
Job Duties and Responsibilities:
* Evaluate, monitor and track child’s progress and adjust treatment plans accordingly.
* Test and evaluate child’s abilities to determine realistic goals.
* Record information on the initial evaluation, treatment, and progress in a timely manner using Electronic Medical Record system.
* Proficient at writing detailed analysis and reports.
* Effectively organize and maintain confidentially of child’s records and other documentations.
* Follow all state laws and regulations as it pertains to Early Intervention, CPSE/CSE special education.
Qualifications, Knowledge and Experience:
* Master's degree in School Psychology required
* Minimum of two years working with children in special education required
* Certification in NYS as a School Psychologist required
* Knowledge and experience administering standardized testing in the following areas: cognitive, achievement, behavioral/social-emotional and adaptive skills.
* Experience using Frontline (formerly IEP Direct) to assist in developing IEPs.
Benefits for this position:
* Health Benefits and Retirement packages available for FT positions
* Accrual of sick time based on NYS Sick time Laws
* Mentoring is offered to all providers
* Access to unlimited CEU courses offered that are accredited through ASHA, AOTA, APTA and CTLE
* Flexible scheduling
* Work with a team of professionals that care about making a difference
* Payment is biweekly with direct deposit
Job Type: Per Diem
Pay Rate:
* Evaluations - Psychological: $180
* Social History: $125
* Observation: $40
* CPSE meetings: $25
Liberty POST is an equal opportunity employer.
We offer equal employment opportunities to all persons without regard to race, color, ethnicity, religion, sex, sexual orientation, national origin,...
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Type: Permanent Location: Goshen, US-NY
Salary / Rate: Not Specified
Posted: 2025-10-07 08:24:46
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Salary Range: $35.23-$50.83 per hour
SUMMARY
Housing for Health (HFH) is a program office within Community Programs, a division under the Los Angeles County Department of Health Services (DHS).
HFH was created and put into implementation in support of the Los Angeles County Homeless Initiative recommendations in response to and in support of the County’s effort to address and combat homelessness in the communities residing within Los Angeles County.
Our organization follows a hybrid work structure where employees work both remotely and from the office, as needed.
The HFH Interim Housing (IH) program serves individuals with complex health and/or behavioral health conditions who need a higher level of support services than is available in most shelter settings.
The program offers temporary housing in a stable environment to assist clients in stabilizing, increasing independence and completing permanent housing goals.
The HFH IH program collaborates with County’s Chief Executive Office Homeless Initiative team to implement interim housing projects under the Pathway Home initiative.
Pathway Home is an encampment resolution project with the goal of reducing unsheltered homelessness in communities across the county through the provision of interim housing and supportive services.
The Assistant Staff Analyst (ASA) on the Interim Housing Pathway Home team will provide programmatic oversight of a portfolio of interim housing projects.
This oversight includes regular engagement with contracted IH providers via case conferences and other meetings, monitoring of programmatic expectations, technical assistance, and problem-solving support.
As needed or requested, the ASA will be present at IH sites to support with addressing provider and/or participant needs.
They will work collaboratively across IH team members and CEO stakeholders to ensure the needs of the program are being met.
Ideal candidates will be organized, have knowledge of mainstream services for people experiencing homelessness, and be flexible to meet the changing needs and demands of the program.
This is a full time, benefitted position (40 hours per week).
Employment is provided by Heluna Health.
ESSENTIAL FUNCTIONS
* Provides oversight of a portfolio of IH facilities and is responsible for ensuring adherence to the statement of work.
* Conduct regular case conferences with assigned portfolio of IH facilities/providers, and document notes and other action items from scheduled meetings.
* Support, as needed and/or as opportunities are available, with permanent supportive housing connections for participants and/or in collaboration with partners.
* Track and complete quality assurance of contracted provider documentation (i.e., case notes, assessments, care/housing plans, etc.) in information systems.
* Provide problem solving and intervention supports and recommendations as it pertains to participant crises and/or needs.
* ...
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Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: 35.23
Posted: 2025-10-07 08:23:12
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At Actus Nutrition, our focus is to create high-quality ingredients designed to optimize health and nutrition.
We are passionate and dedicated people.
Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.
The EHS Manager has the responsibility for managing the Environmental, Health & Safety programs at the Port Edwards and Wautoma, Wisconsin facilities.
Essential Functions:
* Monitor and assist the facility with compliance of all applicable company environmental, safety and health standards as well as all federal, state and local regulations.
* Develop compliance plans for air and water permits. Manage WPDES permits.
* Oversee and maintain compliance with PSM programs in cooperation with site managers including engineers, maintenance supervisor, plant manager and production manager. Work cooperatively with outside consultants.
* Develop and maintain company environmental, health and safety programs at the facility.
* Work with the highest ethical standard for legal compliance and demonstrate a true passion for employee safety.
* Manage plant safety, health and loss prevention programs.
* Develop policies and procedures to ensure that occupational safety and health standards are maintained throughout the facility.
* Utilize IH equipment to determine employ’s exposures to noise and air contaminants.
* Perform fit-testing for respirator users.
* Maintain all required environmental, health & safety program records and legal documents.
* Regularly inspect plant for unsafe conditions as they relate to equipment, process, and facility.
* Actively participate with the plant management team to develop corrective actions for identified risks.
* Track corrective actions to completion in accordance with the facility corrective action tracking program.
* Professionally train, counsel and advise personnel on all identified safety risks, and establish a proactive approach to providing a safe working environment for everyone at the plant.
* Conduct new employee EHS orientations.
* Lead and oversee the monthly EHS training program.
* Schedule and assist the plant with having monthly safety committee meetings.
* In cooperation with area managers and first-line supervisors investigate all injuries, environmental releases and serious near misses.
* Immediately report all injuries, environmental releases and serious near misses to the Plant Manager. Submit a written notification of all injuries, environmental releases, and serious near misses to the corporate EHS department using the RCI reporting program.
* Complete a first report of injury with Workers Compensation Carrier if required for a w...
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Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2025-10-07 08:20:37
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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:
Finance
Job Sub Function:
Accounting
Job Category:
Professional
All Job Posting Locations:
Paranaque, National Capital Region (Manila), Philippines
Job Description:
“Reimagine the possibilities” at Johnson and Johnson Global Finance! We live this motto every day by creating game-changing business solutions for the world’s largest and most broadly-based healthcare company.
As a member of our Global Finance team, you will have exclusive access to a network of financial professionals located in over 60 countries.
This new network will help you build on your current skills and explore opportunities to grow your career in J&J.
Key Responsibilities:
1.
Be compliant with applicable laws and regulations, and follow guidelines in the J&J Credo 2.
Maintain Operational Excellence
* Responsible for executing accounting and daily operations for Intercompany Accounting process area.
* Timely closing & execution of financial periods as per closing calendar and in accordance with SLA commitments, fully observing Compliance, Internal Audit & SOX requirements.
* Accountable for completeness, accuracy and validity of the actuals reported within process/entity scope.
* Deep expertise, fully knowledgeable of the Worldwide Procedures and compliance requirements for respective areas.
* Regular focus on Balance Sheet reconciliations to minimize open items.
* On the job training for new team members / BPO partners.
* Support auditors and legal authorities with the execution of required activities.
* Understand, adhere, and execute per worldwide policies and procedures.
Identify compliance risks and recommend solutions.
* Ensure strong internal controls are in place, in order to achieve “adequate” internal and external audit ratings.
3.
Talent Management
* Recruit, Onboard and Training of new joiners.
4.
Be a Trusted Business Partner
* Execute global Strategy & Solutions in line with taxonomy.
* Support Process Subject Matter Experts (SME's) and Operational Key Contacts (OKC's) to ensure cross sector, cross region, and cross process alignment, ensuring good documentation is maintained and consistency of a global approach.
5.
Create Game-Changing Innovation
* Generate ideas, fosters, and implements continuous improvement mindset, identifying and pursuing process efficiency opportunities.
* Execute process improvements, generating id...
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Type: Permanent Location: Paranaque, PH-00
Salary / Rate: Not Specified
Posted: 2025-10-07 08:16:47
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
Anaheim, California, United States, Baltimore, Maryland, United States, Cincinnati, Ohio, United States of America, Danvers, Massachusetts, United States of America, Horsham, Pennsylvania, United States of America, New York, New York, United States, Philadelphia, Pennsylvania, United States, Tampa, Florida, United States of America, Titusville, New Jersey, United States of America, Wilmington, Delaware, United States
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for a Technical Product Manager - Global Trade Compliance to be located in Titusville, NJ or Beerse, Belgium location.
This position has the potential to be located at another J&J facility within the United States for the right talent.
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/Titusville, NJ - Requisition Number: R-026664
Beerse, Belgium - Requisition Number: R-028152
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Innovative Medicine Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one “clean” ERP as a standardized platform for growth and efficiency gains.
The program will simplify the Innovative Medicine ERP landscape from 7 platforms to 1, standardizing processes to drive a cost effective, fit for purpose digital backbone that will enable us to support the Innovative Medicines business with agility.
Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.
This role will shape and deliver the Innovative Medicine global template for the Global Trade Compliance processes and enable new capabilities for emerging supply chain needs within IM E2E Supply Chain (R&D, Clinical and Commercial)
The position leads design and delivery of Global Trade Compliance capabilities in SAP S/4HANA and SAP GTS E4H and governs the J&J IM template while driving the capabilit...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-07 08:16:36
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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:
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 a Scientist, Process Development to be located in Malvern, PA.
You will be responsible for:
* Leading equipment qualification activities according to industry standards to support drug product pharmaceutical manufacturing and R&D activities.
* Leading, facilitating, and participating in technical discussions to successfully resolve problems with equipment suppliers, methods, project issues, and deviations.
* Designing, developing and deploying automation within manufacturing unit operations to ensure competitiveness and organizational excellence.
* Progressing the technical understanding of process impact on drug product, ensuring consistent scientific excellence and scientific quality standards are met.
* Leading, supporting, and contributing to internal Fill/Finish activities in support of Lead Stability Development batch manufacturing.
Responsible for ongoing production and continuous improvement initiatives.
* Potential opportunity to develop process engineering skills including the use of multiphysics software for process modeling and the statistical analysis of data.
Qualifications / Requirements:
Education:
* A minimum of a Bachelor's degree in System or Electrical Engineering with 3+ years of industry experience is required.
An advanced degree (Master's) with 2+ years of experience is preferred.
Experience and Skills:
* Experience in GxP automation equipment commissioning, qualifications, and life-cycle management are required.
* Experience and knowledge in GxP Fill/Finish applications are preferred.
* Proficiency in sensors and signal conditioning, circuit design/analysis and ...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-07 08:16:34
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PD&E Planner
Ardurra has an exciting opportunity for a Planner in our Project Development and Environment (PD&E) group in Orlando, Florida.
The position includes working with senior staff to prepare planning studies, alternative analyses, environmental impact assessments, and technical reports, including preparation of National Environmental Policy Act (NEPA) documents.
The ideal candidate will provide engineering and planning services supporting PD&E studies.
Essential Tasks
* Reviewing development plans for transportation system effects, infrastructure requirements, or compliance with applicable transportation regulations
* Documenting existing conditions and performing, analyzing, and summarizing research
* Working with our roadway design group to develop conceptual alternatives and design ideas for new or improved transportation infrastructure, such as interchanges, intersection improvements, pedestrian projects, and multi-modal facilities
* Collaborating with a team to complete feasibility studies, Efficient Transportation Decision Making documentation, PD&E studies, and other technical materials
* Performing QA/QC reviews to ensure completeness, accuracy, and conformity to engineering standards and practices
* Assisting in the pursuit of PD&E projects and other business development activities
* Assisting in the development of meeting materials, set up and break down of meetings, attendance, and facilitation
* Coordinating community review and public involvement activities for PD&E projects
* Identifying and coordinating with key stakeholders, special populations, and the general public
* Coordinating activities across multiple disciplines, both in-house and externally
Preferred Qualifications
* Bachelor’s degree in civil engineering, urban planning, economics, environmental or social science, geography, or a related field
* Ability to obtain a PE license or ACIP certification in the state of Florida once qualified.
* Three or more years of prior practical experience working on PD&E and transportation planning projects
* Familiarity with NEPA and Florida PD&E project requirements
* Proficiency with Microsoft Office
* Ability to communicate technical and complex information and to work well with others
* Possess attention to detail, organizational skills, and a positive attitude
* Ability to work independently
* Ability to multi-task and apply critical thinking skills
* Ability to work outside of regular business hours as needed (in case of public meetings or pop-up events)
* Ability to represent the client in a professional manner and maintain composure in tense environments
* Experience working in customer service is a bonus
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further informatio...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-07 08:12:27
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At Elanco (NYSE: ELAN) â 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.
Weâre driven by our vision of âFood and Companionship Enriching Lifeâ and our approach to sustainability â the Elanco Healthy Purpose⢠â 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, youâll 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 animalsâ lives better makes life better â join our team today!
Role: Principal Data Scientist
Responsibilities:
* This role supports the needs of the Global Analytics & Insights team, part of the Corporate Strategy Team, with a focus on providing Advanced Analytics (to include statistical modeling, regression analyses, market basket, churn modelling methods) to work on program/promotion design and ROI post program.
Additional project-based work around price elasticity, mixed market modelling, segmentation, game theory modelling and predictive analytics (e.g., customer lifetime value) will be in scope.
The overarching goal of all work will be to find efficiencies in current promotional spend and optimize future business activities.
* This position is responsible for managing all aspects of project-based analyses including data preparation, analysis design, implementation using appropriate methods & results presentation.
* Leading readouts and review with internal customers.
* Lead discussions with customers to uncover needs, design and deliver analytics solutions.
Enable measurement and improved effectiveness of rebates, media spend, pricing and sales force activities leveraging statistics and data science techniques.
* Collaborate with internal stakeholders, descriptive analytics team and cross-functional teams to solve business problems, propose efficiencies and innovative approaches.
* Constantly innovate in data science domain, constantly bringing new expertise to the team and adding to team knowledge
* Guide the junior members on technical and functional aspects, problem formulation, approach design, model building, model refinement and selection, reviewing and storyboarding the results.
* Consistent, constant alignment with all members of team in Greenfield, Indiana.Â
* Maintain an environment open to change and innovation, recognizing improvements in existing tools and anticipating new technologies to deliver world class analytics and maximize effectiveness
Minimum Qualification:
* Education: Bachelorâs Degree in quantitative or management field.
(Masterâ...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-10-06 08:04:40
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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: Quality Control /Environmental Monitoring Technician
Environmental Monitoring / QC Technician Microbiology will report to the QC Supervisor, Microbiology or equivalent.
This position will conduct routine and non-routine environmental monitoring of the manufacturing facilities and associated utilities, as well as microbiology analysis.
Your Responsibilities:
* Conducts Environmental Monitoring: Performs routine and non-routine sampling of manufacturing environments (air and surfaces) and utilities (WFI, USP Water, Pure Steam, Clean Compressed Air).
Maintains gowning qualifications for sterile environments.
* Ensures cGMP Compliance: Upholds cGMP, safety, and environmental standards within the QC lab, generating accurate and compliant data.
Participates in internal assessments and audits.
* Performs Microbiological Testing: Executes routine and non-routine analyses of raw materials, in-process materials, finished goods, and stability samples.
Conducts a variety of microbiology tests, including bioburden, sterility, and microbial identifications.
* Supports Investigations and Deviations: Assists in the investigation of out-of-specification/out-of-trend results, environmental monitoring excursions, and deviations.
Contributes to the preparation of Certificates of Analysis.
* Develops and Maintains QC Methods: Assists in developing, qualifying/validating, and transferring new test methods.
Contributes to the writing and revision of testing methods, specifications, SOPs, and validation protocols/reports.
Maintains lab inventory and performs routine equipment maintenance and cleaning.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma/GED with 5years experience, BA or BS degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or closely related field, or comparable experience.
* Experience: Technical skills in Environmental Monitoring to include, but not limited to, monitoring of manufacturing environment and utilities.
* Excellent c...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 36.5
Posted: 2025-10-06 08:04:40
