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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:
People Leader
All Job Posting Locations:
Kibbutz Shefayim, Center District, Israel
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 an accomplished Business Intelligence (BI) Manager who will play a pivotal role in driving data initiatives at J&J IM.
This role will focus on four key pillars: Forecasting, Data Engineering, Data Science, and Insights & Reporting.
The ideal candidate will leverage their expertise to enhance decision-making processes and contribute to the strategic growth of the organization.
Key Responsibilities
Financial and Forecasting
* Financial Simulations (Crescendo): Conduct Integrated Business Planning (IBP), Financial Business Planning (FBP), and Long-Range Forecasting Plan (LRFP) simulations to support strategic planning and resource allocation
* Integration with Senior Management: Collaborate with senior management to translate data insights into actionable business knowledge, addressing specific requests and providing clarity in decision-making
* Customized Analytics Solutions: Create tailored functional dashboards, detailed weekly sales reports to meet the unique needs of various business units
Data Science / Data Engineering
* Building Data Pipelines: Design and implement data pipelines that efficiently transfer raw data from various sources into our data warehouse or lake, ensuring high-quality data flow
* Data Quality Management: Ensure that data is cleaned, transformed, and made readily available for analysis.
This includes verifying integrity and accuracy to maintain a reliable resource for stakeholders
* Predictive Modeling: Develop and implement predictive models aimed at forecasting sales volumes, thus enabling proactive decision-making and strategy formulation based on insights derived from data
* Statistical Analysis: Utilize statistical methodologies and Machine Learning models/algorithms to ex...
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Type: Permanent Location: Kibbutz Shefayim, IL-M
Salary / Rate: Not Specified
Posted: 2025-09-13 08:29:04
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
Poszukujemy magistra farmacji z minimum 2-letnim doświadczeniem w aptece lub hurtowni farmaceutycznej, który dołączy do naszego zespołu na stanowisko Commercial Quality Specialist.
Oferta jest idealna zarówno dla osób na początku swojej kariery zawodowej, jak i tych, które chcą rozwijać się w zakresie jakości i dystrybucji produktów leczniczych.
Rodzaj umowy:
Umowa na zastępstwo na okres urlopu macierzyńskiego do kwietnia 2026.
Główne obowiązki i odpowiedzialności:
Wykonywanie zadań zgodnie ze standardami i procedurami systemu jakości dotyczącymi dystrybucji, przechowywania i transportu produktów leczniczych (GDP).
Udział w procesach Systemu Zarządzania Jakością, w tym:
* Kontrola Zmian,
* Działania Korygujące i Zapobiegawcze (CAPA),
* zarządzanie odchyleniami, reklamacjami oraz dokumentacją.
Nadzór nad dokumentacją GxP, w tym aktualizacje, dystrybucja, archiwizacja i analiza zgodności.
Udział w audytach i kontrolach wewnętrznych.
Badanie problemów jakościowych, przeprowadzanie analiz ryzyka i przyczyn źródłowych.
Udział w procesach kwalifikacji dostawców.
Przeprowadzanie szkoleń dla pracowników dotyczących Systemu Zarządzania Jakością i wymogów GxP.
Angażowanie się w projekty rozwoju jakości oraz przegląd procedur i instrukcji dotyczących jakości.
Współpraca z partnerami wewnętrznymi i zewnętrznymi.
W przypadku nieobecności Osoby Odpowiedzialnej za Obrót Środkami Kontrolowanymi:
* Zarządzanie licencjami importowymi,
* Nadzór jakościowy nad produktami zawierającymi substancje kontrolowane,
* Zapewnienie wdrożenia i aktualizacji dokumentacji związanej z dystrybucją takich produktów.
Działania wymagające fizycznej obecności w hurtowni farmaceutycznej:
* Działanie zgodnie z delegowanymi obowiązkami Osoby Odpowiedzialnej lub Osoby Odpowiedzialnej za Obrót Środkami Kontrolowanymi.
* Zwalnianie produktów do dystrybucji na podstawie dokumentacji przychodzącej.
* Obsługa reklamacji i zwrotów we współpracy z Działem Obsługi Klienta.
* Codzienna współpraca z Operatorem Logistyki.
Wymagania:
* Wykształcenie: magister farmacji.
* Doświadczenie: minimum 2 lata w aptece lub hurtowni farmace...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-09-13 08:28:54
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A division of Harris, Cayenta is seeking an Application Consultant.
Our Client Services team has an exciting opportunity for driven individuals with Utility experience.
We are looking for an Application Consultant who is passionate about providing segregated IT transformation for our clients.
It is important for this individual to evolve into a conduit between Operations, R&D, and our clients, working cross-functionally to become a product expert and a client process advisor.
The Application Consultant role is project driven and will support a wide array of services for our Install Base customers.
This role is available remotely within Canada and the US.
All time zones are welcome.
This position requires up to 25 percent travel within North America, and applicants must possess a valid passport or visa.
What your impact will be:
* Work with colleagues and managers to proactively manage a superior technology solution for our clients.
* Provide support to existing and new clients by leading customers through our processes, communicating with those involved to ensure that solution is completed and any issues are resolved so the client can be successfully utilizing the product.
Train users in the system set up, administration and maintenance.
* Provide Business analysis, through gap analysis, root cause analysis, facilitation of business process reviews & documentation, requirements elicitation, allowing the project team to gain a comprehensive understanding of the client's needs in order to overcome barriers and achieve the organizational goals of the client.
Understand clients' business processes and configure applications based on business needs and accepted best practices.
* Own the user acceptance testing and change management process by ensuring stakeholder satisfaction with the outcome of the project through client testing and training.
* Create user documentation when required and the complete handover documentation to assist support staff in providing quality customer care.
* Build our clients’ capabilities; encouraging them to achieve success beyond their expectations by identifying opportunities for recommending additional products and services that fit the needs of our clients.
* Support Project Managers in managing engagement contracts, identifying & escalating bottlenecks, and project progress updates.
* Efficient delivery of services that ensure key project milestones are met on a timely manner, in addition to exceptional utilization of assigned resources.
* Be a leader in providing subject matter expertise to R&D and other operational groups, by understanding market trends of client needs and business practices to ensure the success of our product, incorporating industry best practices in order to maintain strengthen our position within the market.
What we are looking for:
* Knowledge of utility customer (meter to cash) life cycle.
* Knowledge of a utility Customer Infor...
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Type: Permanent Location: Camrose, CA-AB
Salary / Rate: 94000
Posted: 2025-09-12 08:32:13
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role:
Marketing Manager Poultry & Swine category CEE (CEE - Central & Eastern Europe: Poland, Ukraine Hungary, Czech Republic., Slovak Republic., Romania, Bulgaria, Greece, Slovenia, Croatia, Israel).
The purpose of this role is to deliver and execute marketing programs, supporting the CEE Poultry & Swine business category.
The Poultry category includes anticoccidial products, therapeutics & nutritional health (NH) brands.
The Swine Category includes vaccines, therapeutics and feed additives.
Your Responsibilities:
* Lead Marketing Campaigns: Execute marketing campaigns aligned with annual category plans to achieve sales targets, developing supportive programs and projects, and tracking success metrics.
This includes preparing marketing communication materials (leaflets, posters, detailers, merchandise) aligned with global and regional platforms, and partnering with regulatory to ensure compliance.
* Manage A&P Budget: Effectively manage the advertising and promotions (A&P) budget to support brand campaigns and promotions, ensuring optimal resource allocation and maximizing ROI.
* Collaborate with Internal/External Partners: Work closely with internal teams and external agencies (e.g., advertising agencies, KOLs, key vendors) on the production and approval of all artwork, ensuring compliance with industry and internal regulations.
Engage with Elanco's strategic account teams and represent swine and poultry brands.
* Drive Customer Centricity: Analyze customer needs and requirements by interacting with customers and sales teams, conducting market research, and gathering firsthand feedback through field visits.
Develop a deep understanding of customer needs and observe brand/product pricing and exposure.
* Lead Product Launches: Own the marketing component of new product launches and geo-expansion activities, including launch readiness planning, market analysis, and coordinating the production of promotional materials.
This involves working closely with the technical consultants.
What You Need to Succeed (minimum qua...
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Type: Permanent Location: Warszawa, PL-MZ
Salary / Rate: 170000
Posted: 2025-09-12 08:32:00
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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: Technical Consultant- Swine
To increase penetration of swine products by guiding KA (Key Account), key farm, specialized dealer and KOL (Key Opinion Leader) through executing educational/promotional seminars, providing professional knowledge, service & product knowledge and sharing information
Your Responsibilities:
* Provide consultation on swine farming and health care to customers.
* Hold educational/promotional seminars and deliver professional knowledge for internal/external customers.
* Update technical information for swine and work with AHP in the field.
* Make projects such as full value experience and trial.
* Collect industry information, competitor’s activities and customer needs to be reflected on country species business strategy.
* Work closely with PM, RA and sales representatives to align with marketing & technical strategies for each product.
* Be a company representative for professional communities such as swine vet society, swine disease research institute and swine integrated companies.
* Report to FA Technical & Vaccine Marketing Lead
What You Need to Succeed (minimum qualifications):
* Education: Doctor of Veterinary Medicine
* Experience: at least 3 years’ experience in animal health industry or animal production
* Should have good communication skills including presentation and managing interpersonal relationships.
* Should be results-oriented, positive, enthusiastic, self-motivated, challenging against changes and difficulties.
What will give you a competitive edge (preferred qualifications):
* Good communication on products and business with external variety of customers.
* Providing quality technical services to customer to convince company and product quality
* Can extend and communicate with other species like poultry and cattle
Additional Information:
* Travel: 60-70% domestic travel
* Location: Yeouido, South Korea
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely t...
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Type: Permanent Location: Seoul, KR-11
Salary / Rate: 63000000
Posted: 2025-09-12 08:31:52
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Essential Functions
* Performs all required testing on raw materials, in-process, and finished goods
* Performs first piece inspection on all product lines to ensure proper setup of filling and ink-jet coding equipment
* Audits manufacturing process daily for compliance with all product quality parameters
* Records all test data, properly completing all necessary reports, filling, and maintaining test data
* Test and assist in the investigation of product complaints
* Assists in the evaluation of obsolete, rejected and returned products for reprocessing
* Maintains neatness and orderliness of the Quality Control test lab
* Reports all spills and leaks, equipment malfunctions, safety hazards, accidents, near-miss accidents and material shortages immediately to the Production Supervisor
Minimum Requirements
* High school diplomas and/or 5 years QC experience in a manufacturing environment
Physical Requirements
* While performing the duties of this position, the employee is regularly required to use hands to finger, handle, or feel and talk or hear.
* Must be capable of wearing Company standard respirators as qualified by a fit test performed by an authorized agency.
* Must pass standard eye exam (corrected or uncorrected) and must pass standard color-tone.
* This position requires consistent wearing of a lab coat, safety glasses, gloves, long pants, and closed-toe shoes; with additional specific PPE depending on the chemicals or materials handled, which could include respirators, hearing protection, or specialized gloves for hazardous substances.
Benefits and Compensation
The pay range for applicants in this position generally ranges between $18.00/hour and $25.00/hour.
The range is an estimate based on potential employee qualification operations, needs, and other considerations permitted by law.
In addition to career advancement and growth, continuous training, and mentoring opportunities, Stonhard offers an excellent comprehensive health plan and financial benefits program including but not limited to, paid holidays, paid time off, 401(k) with company match, Company Pension Plan and Stock Purchase Plans.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.
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Type: Permanent Location: Fort Wayne, US-IN
Salary / Rate: Not Specified
Posted: 2025-09-12 08:27:57
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Essential Functions
* Responsible for producing (making, cutting, labeling) high-quality floors, walls, lining and specialty samples for use as field sales tools.
* Mix liquid amines and resins with silica sand in buckets or a blender and then trowel the material onto a sample board to a precise thickness.
* Once the sample cures or solidifies, coating material is applied. Once the sample passes the final curing process, the technician will cut the sample with a wet saw, sand it on a belt sander, and then lay out for final drying process.
* Once dry, the technician will label the sample and package for shipment.
* Arranges for the prompt and efficient distribution of samples
* Responsible for policing and cleaning work area, lab, storage room and saw room.
Minimum Requirements
* High School Diploma or equivalent, required
Preferred Requirements
* Prior experience in a chemical manufacturing environment.
Physical Requirements
* Bending, squatting, kneeling, lifting – frequent, up to 50 lb bags
* Utilizing forklift – 25%
* Standing and walking up to 90% of the time
* Must be capable of wearing Company standard respirators as qualified by a fit test performed by an authorized agency.
* This position requires consistent wearing of safety glasses, gloves, and steel-toed boots while on the worksite.
* Must pass standard eye exam (corrected or uncorrected) and must pass standard color-tone testing.
Benefits and Compensation
The pay for applicants in this position is generally $19.00/hour.
This is an estimate based on potential employee qualification operations, needs, and other considerations permitted by law.
In addition to career advancement and growth, continuous training, and mentoring opportunities, Stonhard offers an excellent comprehensive health plan and financial benefits program including but not limited to, paid holidays, paid time off, 401(k) with company match, Company Pension Plan and Stock Purchase Plans.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.
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Type: Permanent Location: Cherry Hill, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-12 08:27:55
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DESCRIPTION
This Environmental Permitting Specialist will lead and coordinate environmental studies and permitting efforts, including wetland delineation, habitat assessments, preparation of Local, State, and Federal permit applications.
Support technical engineering projects in the Great Lakes Region, with a focus on Pennsylvania by leading environmental document preparation and applications such as Erosion and Sediment Control Permits, General Permits, USACE Joint Permit Applications, and Nationwide permits (NPDES).
RESPONSIBILITIES
Coordinate and prepare applications for local, state and federal agencies for a variety of project types, including bridges, highways, dams, public utilities, energy utilities, and other civil/environmental projects, as needed.
This position will leverage experience with agency coordination and agency knowledge/experience to facilitate positive outcomes.
Priorities will include quality control, peer reviews, and coordination among multiple project disciplines.
A knowledge of applicable environmental laws, rules, and regulations to prepare technical reports is required.
Environmental Specialists are an integral part of the team and work closely with planners and engineers through project scoping, design, construction and beyond.
They provide technical guidance to junior environmental staff and assist and/or lead in proposal development, which includes developing environmental scopes, schedules and budgets.
ROLE ACCOUNTABILITIES
* Identify potential permitting requirements and develop permitting strategies to provide guidance to internal and external teams and clients.
* Use strong technical writing and communications skills to support the development of technical reports, work plans, memoranda, and other environmental documents necessary to develop permit applications and supporting materials for various regulatory agencies.
* Support the preparation of permit applications and supporting materials in accordance with specific local, state, and federal regulatory requirements.
* Assist with the coordination of wetlands and waterbodies delineations, flora/fauna surveys, and/or threatened and endangered species field surveys in accordance with applicable regulatory requirements.
* Support task management to assist with the growth of new and existing client relationships through delivery of quality work and data.
* Hybrid work structure allowing remote and office work as needed.
* Coordination of field assessments related to ecological aspects of projects, requiring knowledge of GPS systems and the ability to conduct fieldwork for long hours and in difficult terrain.
* Travel requirements for field assessments.
PROFESSIONAL REQUIREMENTS
* Bachelor’s degree in Environmental Science, Biology, Ecology, or a related field
* 10+ years of related experience
* Relevant regional working knowledge and experience in supporting the preparation of ...
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Type: Permanent Location: Moon Township, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-12 08:25:31
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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
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
The position is located in the Immune and Cell Biology Department, within the Discovery unit of pRED’s Large Molecules Research, where the discovery and development of next generation biotherapeutics is the primary focus.
We closely collaborate with disease therapeutic areas and other functions to convert therapeutic hypotheses into innovative therapeutics.
In this environment, we are seeking an experienced Science and Matrix Leader (m/f/d) with a strong scientific background in immune and cell biology, and a specific focus on immunology, neuroscience and/or ophthalmology.
The role requires significant industrial experience in drug discovery and development, encompassing the entire journey from target assessment to Entry into Human. You will expertly lead cross-functional teams, contribute to portfolio projects, and drive the implementation of cutting-edge cell-based functional assays to discover and characterize large molecule-based therapeutics.
The opportunity
* You will lead and inspire highly engaged cross-functional matrix teams, foster effective collaboration, and cultivate trusting relationships with internal and external partners
* You will be responsible for defining the cellular assay strategy and oversee data analysis for mode-of-action elucidations and in vitro lead selection in portfolio projects, with a particular focus on advanced, physiologically relevant human model systems
* You will conceptually develop and set up novel functional cellular assays in the fields of Immunology, Oncology, Neuroscience and Ophthalmology, employing cutting-edge assay read-out technologies including flow cytometry and advanced fluorescence microscopy
Your Profile
* Extensive industrial experience in large-molecule drug discovery, in particular leading cell-based assay development for therapeutic candidate selection in physiologically relevant model systems, including primary cells, iPSCs, organs-on-a-chip, and organoids
* Solid experience in assay readout technolog...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-09-12 08:19:18
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Supply Chain Engineering
Job Sub Function:
Manufacturing Engineering
Job Category:
People Leader
All Job Posting Locations:
Mechelen, Antwerp, Belgium, Raritan, New Jersey, United States of America
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
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-031792
Belgium: Requisition Number: R-032748
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
All Job Posting Locations:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America or Beerse, Belgium.
Job Description:
Johnson and Johnson Innovative Medicines is recruiting for the Advanced Therapies Manufacturing Science and Technology (MSAT) organization! 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.
Are you interested in joining a team that is positively impacting patients' lives by growing and scaling our high quality cell and gene therapy products? Apply today for this exciting opportunity to be part of the team!
RESPONSIBILITIES:
This is a hybrid/remote role available in multiple cities within the United States or Beerse, Belgium.
While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application.
We invite candidates from any location to apply.
The Head, Lifecycle Management is accountable for the lifecycle of produc...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:49
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
R&D/Scientific Quality
Job Category:
Professional
All Job Posting Locations:
Ciudad de Mexico, Mexico, Ciudad Juarez, Chihuahua, Mexico
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
About Cardiovascular
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for Scientist II to be in Ciudad Juárez, Chih, MX.
Purpose:
Assists with the documentation of business critical issues in R&D/Scientific Quality.
Applies functional knowledge of R&D/Scientific Quality and surfaces policies that may impact organizational objectives.
Assists with routine collection and dissemination of feedback to ensure continuous improvement of the quality management system.
Carries out processes to ensure the internal organization's alignment with overall quality priorities under direct supervision.
Follows formal escalation processes to surface issues of product quality, regulatory compliance, and quality systems.
Analyzes basic research and data related to regulatory changes, external trends, and strategy.
Understands and applies Johnson & Johnson’s Credo and Leadership Imperatives in day-to-day interactions with team.
This job is salaried.
You will be responsible for:
Under supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
* Performs complex, routine tests in...
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Type: Permanent Location: Ciudad Juarez, MX-CHH
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:38
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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:
Sales Enablement
Job Sub Function:
Sales Training
Job Category:
Professional
All Job Posting Locations:
Issy-les-Moulineaux, France
Job Description:
MISSIONS
Contribuer à la formation des collaborateurs Janssen (en intégration et en formation continue) sur les aires thérapeutiques (AT) et médicaments pour garantir un niveau d’expertise scientifique et médical dans le respect de la stratégie globale de l’entreprise et des exigences de la charte de l’information promotionnelle et de son référentiel.
A partir des enjeux de communication dans l'AT dont il a la responsabilité, mettre en place des formations de communication, proposer des sessions de training en région, et être ressource dans l'animation de trainings, en présentiel et distanciel.
ACTIVITES PRINCIPALES
Formateur Médicaments
* Recueillir annuellement les besoins de formation et de developpement des compétences sur les AT et les médicaments en responsabilité et valider les objectifs des formations avec les clients internes (principalement pour les délégués médicaux et directeurs régionaux).
* Elaborer pour chaque projet formatif un cahier des charges reprenant les objectifs généraux et pédagogiques et/ou un programme de formation en intégrant les ressources internes et externes, dans le respect des procédures.
* Identifier et coordonner des prestataires externes ou les intervenants internes pour répondre aux demandes de formation quand necessaire
* Concevoir et mettre à jour le matériel de formation et d’évaluation en fonction des besoins et des actualités (formation d’intégration, fomation continue).
* Animer les sessions presentielles et les sessions distancielles.
* S’assurer de l’intégration des connaissances et compétences des apprenants par le biais d’évaluation formative (reactivation mémoire, exercices d’appropriation lors de formation en blended learning) ou sommative (évaluation des connaissances, validation de la présentation orale)
* Recueillir les feed-backs et suggestions sur la formation dans l’objectif d’amélioration continue en mettant en place des enquêtes de satisfaction.
* Assurer la traçabilité des sessions de formations (émargement, synthèse de la formation, résultats des évaluations, gestion des absences) dans le respect des procédures internes.
* S’assurer du respect des règles intern...
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Type: Permanent Location: Issy-les-Moulineaux, FR-92
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:36
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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:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Aachen, North Rhine-Westphalia, Germany
Job Description:
Über MedTech
Wir arbeiten seit einem Jahrhundert an der Seite von Ärzten und Patienten, um das Gesundheitswesen immer wieder aufs Neue zu verbessern und zu optimieren sowie neu zu denken. Unser J&J-MedTech-Portfolio wird von Innovationen geprägt, die Barrieren an der Schnittstelle zwischen Biologie und Technologie aus dem Weg räumen.
Gemeinsam entwickeln wir die nächste Generation intelligenter, weniger invasiver und personalisierter Lösungen, um die größten und komplexesten gesundheitlichen Herausforderungen für Menschen auf der ganzen Welt zu bekämpfen.
Begleiten Sie uns auf unserem Weg, während wir Medizinprodukte weiterentwickeln und den Übergang von der Forschung ins echte Leben ermöglichen – immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/medtech
Über Kardiovaskulär
Angetrieben von Innovationen an der Schnittstelle von Biologie und Technologie entwickeln wir die nächste Generation intelligenter, weniger invasiver und personalisierter Behandlungen.
Sind Sie begeistert von der Verbesserung und Erweiterung der Behandlungsmöglichkeiten von Herz- und Gefäßerkrankungen? Sind Sie bereit, in einem Team mitzuarbeiten, das die Art und Weise, wie wir Menschen heilen, neu erfindet?
Unser Team entwickelt führende Lösungen für die Wiederherstellung des Herzens, die Elektrophysiologie und den Schlaganfall.
Werden Sie ein Teil einer stolzen Tradition der kontinuierlichen Verbesserung der Standards für die Versorgung von Schlaganfall-, Herzinsuffizienz- und Vorhofflimmern (AFib)-Patienten.
Begleiten Sie uns auf unserem Weg, während wir Medizinprodukte weiterentwickeln und den Übergang von der Forschung ins echte Leben ermöglichen – immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.
Weitere Informationen finden Sie unter https://www.jnj.com/medtech
Abiomed ist ein innovatives Medizintechnik-Unternehmen mit einer inspirierenden Mission „Patients First.“ und einem einzigartigen Firmenmotto „Herzen regenerieren.
Leben retten“.
Mit mehr als 3.000 Mitarbeitern ist Abiomed eines der am schnellsten wachsenden Medizintechnik-Unternehmen weltweit m...
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Type: Permanent Location: Aachen, DE-NW
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:29
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Shepherdsville, Kentucky, 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 Quality Analyst to be located in Shepherdsville, Kentucky.
The Quality Analyst is responsible for the oversight and execution of Quality Management Systems and compliance at the Distribution Center.
The Quality Analyst serves as a single point of contact to the Sr.
Manager, Janssen Commercial Quality and Supply Chain partners on compliance related matters and is the liaison with multiple Quality and Compliance organizations to drive timely resolution of quality and compliance related issues.
The Quality Analyst identifies business issues, identifies opportunities to continuously improve quality and compliance and leads improvement opportunities and problem solutions.
The Quality Analyst implements and executes quality and compliance programs to ensure effective and consistent processes with established standards.
You will be responsible for:
* Quality and compliance product receiving process, including, but not limited to receiving inspection activities such as review of temperature monitoring devices and systematic transactions in Warehouse Management System and/or SAP
* Monitoring and following Quarantine/Hold/Stop-Ship/Recall processes and notices
* Product refusals process activities, including, but not limited to inspection and disposition
* Serve as single point of contact to internal and external partners on Distribution Quality related matters and liaise with multiple Quality organizations to drive timely resolution of Quality related issues
* Responsible for adherence to the Deviation, Corrective and Preventative Action (CAPA), and Change Controls processes and Quality Management Systems
* Responsible for adherence to the Records Management and Retention processes
* Responsible for adhering to the Training proc...
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Type: Permanent Location: Shepherdsville, US-KY
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:25
-
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:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-09-12 08:18:08
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Global Compliance Specialist
Location: Houston, Texas (Onsite, 5 days a week)
Position Summary:
The Global Compliance Specialist will report directly to the BII Director of Risk and Compliance.
This key role in the Risk Management and Compliance department focuses on ensuring compliance with regulations (both for legal and trade compliance), completing organizational filings and questionnaires, and supporting compliance research and policy writing.
The position is vital for maintaining operational efficiency while adhering to global laws and regulations.
Essential Job Functions and Responsibilities:
Global Compliance:
* Coordinate import and export activities, including audits, record-keeping, and ensuring compliance with U.S.
Customs Regulations, Export Administration Regulations, Foreign Asset Control Regulations, and Anti-boycott Regulations.
* Assign, document, and maintain Harmonized Tariff Codes (HTSUS) and Export Classification Numbers (ECCN) for all products.
* Conduct interviews and compile information for compliance with anti-corruption and other laws and regulations pertinent to the organization’s business activities.
* Develop, implement, and improve internal processes and written work instructions to maintain compliance with regulations.
* Provide training to internal users and gatekeepers on import/export requirements.
* Serve as the primary liaison with Shared Services, customs brokers, and freight forwarders for import/export documentation, licensing, and transaction screenings.
* Stay updated on regulatory changes and update internal policies as needed.
* Coordinate the valuation of imported merchandise, ensuring proper reporting of payments and customs valuation requirements.
* Work with IT to ensure system compatibility with trade compliance requirements.
Patent Administration:
* Maintain a database of patents and trademarks and their respective locations.
* Coordinate communications with intellectual property counsel and advisors.
* Log and track intellectual property registration activity as required.
Compliance Regulations & Research:
* Conduct legal and policy research, interpreting legislation and compliance standards.
* Investigate regulatory requirements, jurisdictional regulations, and government agency guidelines.
* Provide consultation on compliance matters.
* Develop and maintain a global research network.
* Prepare research findings and assist with action planning.
Compliance Policy Writing:
* Develop and draft compliance policies and procedures to support regulatory requirements.
* Assist with the distribution and implementation of compliance policies as directed by the RM&C department.
RM&C Department Support:
* Provide research or project support as assigned by the RM&C Manager.
Position Requirements:
* Highly organized, detail-oriented, and able to manage multiple competing priorities.
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-09-12 08:16:06
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Position Focus: The Delegating RN will primarily drive between and support the senior living communities of White River Assisted Living & Memory Care (Enumclaw, WA), Hazel Dell Assisted Living (Vancouver, WA), Homewood Assisted Living
(Portland, OR)
Location Preference: Candidates who reside in Oregon are strongly preferred.
Licensure Requirement: Must have the ability to be licensed in Washington and Oregon.
General Purpose
The Delegating RN for Assisted Living or "Nurse Delegator" plays a pivotal role in ensuring residents receive exceptional care by expertly delegating nursing tasks, providing comprehensive staff training, and meticulously overseeing medication management services.
This position also assists in coordinating and completing resident assessments to ensure all individualized service plans are accurate and up-to-date.
ESSENTIAL DUTIES AND RESPONSIBILITIES
* Delegates Nursing Tasks: Delegates nursing tasks in accordance with applicable state nursing laws and practice acts, maintaining consistent communication with residents, their families, and their healthcare practitioners.
* Provides Staff Training: Develops and delivers training to staff on health-related services, including but not limited to personal care and medication administration best practices.
* Conducts Resident Assessments & Planning: Assesses the health, functional, and psychosocial status of residents.
Actively participates in the development of individualized service plans, assisting in the comprehensive management of care and services to maximize residents' ability to remain in the assisted living environment.
* Oversees Documentation & Communication: Monitors and ensures accurate documentation and clear communication of resident care and services.
Collaborates with the leadership team to ensure resident records are completed promptly and maintained in strict adherence to company policies and state regulations.
* Manages Medication Services: Maintains and oversees all aspects of medication services, including staff training, direct staff oversight, pharmacy coordination, medication room organization, and medication system integrity.
* Assists with Infection Control: Supports the management of Infection Control protocols.
Provides essential training to staff on infection control practices, investigates and reports incidents of infection, and meticulously tracks infection data.
* Ensures Regulatory Compliance & Continuous Learning: Maintains current, in-depth knowledge of all rules, regulations, and policies pertaining to resident care.
Stays informed of industry and healthcare trends and standards, applying new knowledge to meet the evolving needs of residents.
Seeks additional expertise and advice when necessary to ensure resident needs are met and proper practices are consistently followed.
* Other Duties: Performs other duties as assigned to support resident care and facility operations.
QUALIFICATIONS AND EXPERIEN...
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Type: Permanent Location: Farmington, US-UT
Salary / Rate: Not Specified
Posted: 2025-09-11 08:42:03
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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!
Um unser Team zu verstärken, suchen wir zum 01.
August 2026 motivierte und engagierte Auszubildende für den Ausbildungsberuf zum Biologielaboranten (m/w/d).
WAS DICH ERWARTET
* Praktische Arbeit im Labor: Du führst Experimente durch, arbeitest mit modernen Geräten und lernst verschiedene Labormethoden kennen.
* Untersuchung und Analyse: Du prüfst Proben, wertest Ergebnisse aus und dokumentierst sie sorgfältig.
* Vielfalt erleben: Du lernst unterschiedliche Anwendungsbereiche kennen.
* Sicherheit und Verantwortung: Du lernst Laborvorschriften, Qualitätsmanagement und Arbeitssicherheit kennen und umzusetzen.
WAS DU MITBRINGEN SOLLTEST
* Interesse und Leidenschaft für Naturwissenschaften, speziell Biologie und Chemie
* Spaß an sorgfältiger, praktischer Arbeit und genauem Dokumentieren
* Teamgeist, Zuverlässigkeit und Motivation
* Du bist mobil und besitzt einen Führerschein Klasse B
WAS WIR DIR BIETEN
* Du bekommst eine Ausbildungsbetreuung auf hohem Niveau
* Du arbeitest in einem interessanten und abwechslungsreichen Arbeitsumfeld in einem modernen und wachsenden globalen Unternehmen der Pharmaindustrie
* Attraktive und branchengerechte Vergütung
(1.
Ausbildungsjahr = 1.207 Euro, 2.
Ausbildungsjahr = 1.301 Euro,
3.
Ausbildungsjahr = 1.425 Euro, 4.
Ausbildungsjahr = 1.551 Euro)
* Du erhältst zusätzlich Weihnachtsgeld und Urlaubsgeld
* Zur Vorbereitung auf die Abschlussprüfung wirst du bezahlt freigestellt
* Wir übernehmen die Bücherkosten
* Du kannst unsere vielfältigen Benefits wie z.B.
Corporate Benefits, Betriebliche Altersversorgung, EGYM-Wellpass, Essensgeldzuschuss nutzen
* Freu dich auf spannende Teamevents
Interesse?
Bewirb dich jetzt!
Schick uns deine Bewerbung mit Lebenslauf und letztem Zeugnis über unser Online-Portal.
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 vet...
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Type: Permanent Location: Cuxhaven, DE-NI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:33:51
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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 Associate, Biochemistry
This role will be a laboratory-based position with the QC Biochemistry group responsible for a wide variety of biochemical assays.
This role will rely heavily on an ability to perform regular functions within a GMP environment and perform flawless lab work on high value projects.
Regular projects include release and stability testing, assay development, validation, training, technical writing, and regular use of specialized equipment/software.
Your Responsibilities
* Conducts a range of biochemical assays, encompassing both routine and non-routine testing, on various sample types including raw materials, in-process materials, finished goods, environmental monitoring samples, and stability samples.
This includes method development, execution, and troubleshooting.
* Prepares, reviews, and approves a variety of essential QC documentation, including test protocols, validation protocols, special outlines, reports, Certificates of Analysis (CoAs), out-of-specification/out-of-trend (OOS/OOT) investigation reports, and deviation reports.
* Ensures the QC laboratory operates in full compliance with current Good Manufacturing Practices (cGxP) guidelines, encompassing laboratory safety, performance standards, meticulous documentation practices, regular equipment maintenance, and adherence to environmental regulations.
* Generates, reviews, and approves analytical data to ensure accuracy, completeness, and regulatory compliance.
Investigates and documents any OOS/OOT results and deviations encountered during testing.
Validates new and revised testing methods and qualifies existing methodologies as needed.
* Serves as a subject matter expert (SME) and liaison between the QC department and other internal departments, external vendors, and contractors.
Provides training to other analysts on laboratory procedures and assays, and stays current with the latest analytical techniques and best practices through continuing education and software proficiency.
Participates in internal assessments and ...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 31.93
Posted: 2025-09-11 08:33:42
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Job Category:
Intern
Job Family:
Student Intern
Job Description:
As a Quality Assurance Intern, you will have the opportunity to work the Summer 2026 with Schreiber Foods at one of our plant locations. This internship will be focused on supporting food safety and quality initiatives, company objectives and plant-specific assignments.
It is designed to prepare successful interns for a possible future career with Schreiber Foods.
This Quality Assurance summer internship is located at our plant in Shippensburg, Pennsylvania.
Interns relocating more than 50 miles for the internship will receive a lump sum of $1,500.
This position offers a set rate of pay of $20.75 an hour.
What you’ll do:
* Lead small quality improvement projects within the team, working with plants and other areas of Schreiber Foods
* Creating and updating documentation for food safety and quality and lab processes
* Gaining knowledge about our products and applying that knowledge to improve processes and practices
* Inputting and analyzing data
* Completing projects related to testing, quality systems, sanitation, auditing, HACCP, training, SQF, suppliers, and other related topics
* Assisting the quality teams on ongoing projects
* Together with the leadership team, ensures compliance with Food Safety and Food Quality Plans, in addition to customer requirements.
Interprets and communicates customer requirements to plant production and/or support groups.
Establishes and Audits PCPs, CCPs and Standard Operating Procedures to define and monitor processes, to ensure customer requirements are met.
Reviews incidents during which the procedures are not met and determines appropriate corrective action for partners failing to follow standard procedures.
What you will need to succeed:
* Currently pursuing a Bachelor’s or Master’s degree in Food Science, Dairy Science, Microbiology, Bacteriology, Food Microbiology or closely related field.
* Ability to work 40 hours per week during the summer of 2026
* Ability to work at least 10 weeks of the summer, 12 weeks is preferred, with flexible start and end dates
* Effective oral and written communication skills
* Ability to work independently as well as in a team environment
* Ability to take ownership of assignments and complete them
* Desire to grow and take on new challenges and opportunities
* Ability and desire to work within a plant manufacturing setting
* Ability to multi-task
* Possess a strong technical foundation in the sciences; dairy knowledge desired but not required
* Reliable transportation
Internship benefits:
* Opportunity to complete real-world projects, participate in team meetings and contribute your ideas
* Exposure to different areas of the business around the world
* Internship program that includes engaging events and opportunities to build relationships at all levels
* Relocation as...
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Type: Permanent Location: Shippensburg, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:32:45
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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 an opportunity for you to bring your wealth of experience to the team and help shape the future of sustainability with world-changing innovations and low carbon technologies.
You have the power to shape things to make them better.
About the Role
Are you a meticulous and safety-conscious professional with a passion for precision? We're seeking a skilled Laboratory Analyst to join our team in a dynamic mining and refinery environment in Western Australia, based at our WA Mining Lab at Kwinana.
In this role, you'll be at the heart of our operations, ensuring the accuracy and integrity of our analytical data.
Your work will directly impact our mining and refinery processes, making you a vital link in our success.
Reporting to the Laboratory Supervisors, this role will be offered on an even time roster working onsite at our state-of-the-art facilities in Kwinana.
* Perform routine and non-routine laboratory analyses on process streams, troubleshooting any unusual results.
* Calibrate and maintain a range of laboratory and automation equipment to ensure it is always ready for use.
* Sample laboratory process streams safely and accurately, identifying any potential issues with sample integrity.
* Manage and verify data, entering results into our information systems and communicating out-of-specification results to operations personnel.
* Contribute to a culture of safety, reporting incidents, and complying with all safety and environmental regulations.
* Participate in our quality systems, tracking control data and helping to maintain our ISO accreditation.
* Advance your skills through our learning management system and help train other laboratory staff.
What’s on offer
* Attractive remuneration and variable bonus plan.
* Family friendly rosters that allow you to be home after each shift.
* Employee growth and development opportunities.
* Parental leave support for all caregivers,
* Paid employee volunteering hours within our community.
* Alcoa Live Well program offering travel, lifestyle, health and wellbeing discounts.
* Salary packaging for a novated car lease, employee share plan and superannuation options.
* Connect and be part of a community that celebrates diversity through our employee inclusion groups.
What you can bring to the role
* Laboratory Practices Certificate – TAFE Qualification
* Proven prior experience with process laboratory experience and demonstrated Automation Laboratory operations knowledge
* Knowledge & Training Develops Bayer Process would be highly regarded
* Experience in communication with technical and operating personnel.
* A proven understanding of the impact of the laboratory analysis results ...
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Type: Permanent Location: KWINANA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:31:55
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Job Summary
Responsible to the Continuous Improvement Manager for working closely with Engineering and Operation teams leveraging data-driven insights to enhance performance, drive procedural efficiencies, and support strategic initiatives. This department’s duties include standards, quality assurance and field inspections.
Duties require considerable knowledge of engineering and operation procedures, standards, and company policies. Expected to collaborate with other departments to collect and analyze data as needed to make recommendations and implement procedural changes, as well as control tools to monitor performance to meet company KPIs as directed by management.
Receives general direction from the Continuous Improvement Manager and Engineering Director; however, arranges their own work.
Regular contact with other departments is required to furnish or obtain information.
Regularly works with confidential data.
Essential Duties and Responsibilities
* Collects, cleans, and analyzes data from various sources to identify trends, patterns, and anomalies.
* Generates reports and dashboards to communicate findings effectively to stakeholders.
* Collaborates with Engineering and Operations teams to identify areas for improvement and develop data-driven solutions to enhance operational efficiency and effectiveness.
* Develops and implements metrics to monitor the performance of engineering and operational processes.
Tracks key performance indicators (KPIs) and provides actionable insights to drive continuous improvements.
* Provides data-driven recommendations to support strategic planning and decision-making processes within the utility.
* Ensures compliance with data governance policies and practices.
Maintains data documentation and supports efforts to improve data quality and accessibility.
* Works closely with cross-functional teams, including Engineering, Operations, and IT, to ensure data accuracy and integrity.
Facilitates data-driven discussions and supports collaborative problem-solving.
* Performs other duties as needed and/or as directed.
Minimum Qualifications of Position
* A Bachelor's degree in Data Analytics, Computer Science, Engineering, Statistics, or a related field.
* 3-5 years of experience in data analytics.
* Proficiency in data analytics tools such as SQL and advanced Excel.
Experience with data visualization tools like Tableau or Power BI.
* Strong ability to analyze complex data sets and translate findings into actionable insights.
Experience in statistical analysis and predictive modeling.
* Excellent verbal and written communication skills, with the ability to present data insights to non-technical stakeholders.
* Proven track record of identifying problems, developing solutions, and driving continuous improvements.
* Ability to work collaboratively in a team environment and manage multiple project...
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Type: Permanent Location: Sedalia, US-CO
Salary / Rate: Not Specified
Posted: 2025-09-11 08:26:22
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WTP
Environmental Laboratory Analyst III
Starting pay is $27.82/hour (This rate is non-negotiable and there is a 6-month probationary period).
After hire, pay increases are dependent on length of service, advancement in the position, and other contractual factors.
This position is represented by the AFSCME union.
For more information reference the AFSCME collective bargaining agreement: AFSCME Union Contract
Benefits offered with this position: AFSCME Benefits Summary
Role Summary
To perform routine analytical work for the Public Services Laboratory using standardized laboratory techniques and well established, prescribed laboratory procedures to collect, prepare, process and analyze public water supply, wastewater, watershed, industrial samples and other materials. Provide laboratory consultative services; conduct and/or manage projects and other laboratory related activities for the public services area, other public agencies and customers.
Work Schedule: Monday to Friday from 7:00 am to 3:30 pm.
Please note: This position requires a rotating weekend shift from 7:00 AM to 3:30 PM.
The ideal candidate will be comfortable committing to working 1-2 weekends per month.
Training and Experience Required:
* Bachelor’s degree from an accredited college or university with major work in analytical chemistry, organic chemistry, biology, environmental science or a closely related academic major, plus a minimum of two years of experience in a related field, or
* Three years of college work (90 semester credit hours), with a concentration in chemistry, microbiology or environmental science, plus a minimum of three years experience in a related field.
Minimal Licensing Requirements (position requirements at entry)
* Valid MI Driver’s License
View Additional Requirements and Information at: Environmental Laboratory Analyst Job Description
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: Ann Arbor, US-MI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:22:33
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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:
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-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
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 a Director, Global Regulatory Leader.
This position is a hybrid role and will be located in Toronto, Canada.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Profile (for global programs as assigned).
* In interacting with the Health Authorities, lead and/or participate in meetings with FDA, Health Canada, EMEA...
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Type: Permanent Location: Toronto, CA-ON
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:09
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Affairs
Job Category:
Professional
All Job Posting Locations:
Allschwil, Basel-Country, Switzerland
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
* United States - Requisition Number: R-027513
* Canada - Requisition Number: R-032876
* United Kingdom - Requisition Number: R-032879
* Belgium, Netherlands - Requisition Number: R-032880
* Switzerland - Requisition Number: R-032883
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 a Director, Global Regulatory Leader.
This position is a hybrid role and will be located in Allschwil, Switzerland.
The Director, Global Regulatory Leader will be responsible for the development, implementation and maintenance of robust global regulatory strategies for select projects spanning the same target disease areas.
Principal Responsibilities:
* Be a key contributor/leader on the Global Regulatory Team and on multiple cross-functional teams.
* Provide strategic direction to the teams and critical review of key Health Authority submissions such as IND/CTAs, meeting requests, briefing documents, response documents and marketing and supplemental applications.
* Ensure that regulatory strategies are aligned with product portfolio, regional strategies, CMC (Chemistry, Manufacturing, and Controls)-Regulatory Affairs strategy, commercial and market access strategy, and the Target Product Profile (for global programs as assigned).
* In interacting with the Health Authorities, lead and/or participate in meetings with FDA,...
....Read more...
Type: Permanent Location: Allschwil, CH-BL
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:09
