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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:
Professional Medical Education
Job Category:
Professional
All Job Posting Locations:
Madrid, Spain
Job Description:
Nuestra experiencia en medicina innovadora se basa en la información y la inspiración de los pacientes, cuyos conocimientos impulsan nuestros avances basados en la ciencia.
Visionarios como usted trabajan en equipos que salvan vidas desarrollando los medicamentos del mañana.
Únase a nosotros para desarrollar tratamientos, encontrar curas y ser pioneros en el camino del laboratorio a la vida, mientras apoyamos a los pacientes en cada paso del camino.
Obtenga más información en https://www.jnj.com/innovative-medicine
To maximize company product value through high scientific quality communication with Leading Specialists on a peer-to-peer basis.
Accordingly, to strategic lines of Medical Affairs Plan, the MSL is jointly responsible for achieving short-term and long-term company goals at local level.
To be a therapeutic area scientific expert, responsible for discussing our products, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered an internal and external trusted scientific counterpart.
MSLs should have their own Activity Plan and personal objectives.
The Individual Activity Plans must be based on the MSLs Country Activity Plan, which is aligned with the Medical Affairs Component of the relevant Brand Plans
* To keep abreast of medical and scientific knowledge.
+ Continuous update on products, patient’s treatment trends, clinical activities and studies conducted within the therapeutic area in their region.
* Development and maintenance of a contact network with Leading Specialists.
+ Understand their needs, key value drivers, practical treatment patterns and scientific activities within therapeutic area
+ Communicate value of company products, incl.
clinical questionnaire discussions
+ Through scientific interactions, communicate medical benefits of products and contribute to foster innovative approaches
+ Represent the company within professional associations in the therapeutic area in cooperation with Medical Affairs/ Medical...
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Type: Permanent Location: Madrid, ES-M
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:55
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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:
R&D Operations
Job Sub Function:
Product Development Testing
Job Category:
Business Enablement/Support
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Sr.
R&D Technician to join our team located in Santa Clara, CA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
The Sr.
R&D Technician will use technical skills in the development of innovative products to treat peripheral, coronary, and heart valve diseases.
The Sr.
R&D Technician will participate on multiple cross-functional development teams that manage projects from concept through commercialization.
Perform and support a variety of development and engineering activities, which mainly focus on disposable devices prototyping, fabrication and testing.
Will work directly with other R&D technicians and R&D engineers to complete duties described below.
Essential Job Functions
* Effectively works on multiple project tasks with minimal supervision for timely completion
* Partners with engineers and other technicians to assemble functional prototypes and provide feedback on assembly process and design
* Assist engineers with product and process design, development, and optimization
* Perform equipment installation and qualification
* Assist in product and process characterization and design...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-06-02 08:03:36
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En tant qu’analyste QA pour JurisÉvolution — notre logiciel phare destiné aux cabinets juridiques — tu seras au cœur du développement qualité.
Ton travail sera essentiel pour garantir la fiabilité, la performance et la convivialité de notre produit.
Tu collaboreras étroitement avec les développeurs, analystes et chefs de produit pour t’assurer que chaque nouvelle fonctionnalité respecte nos standards de qualité… et ceux de nos clients !
Ce que tu feras au quotidien:
* Participer à l’analyse des spécifications fonctionnelles pour comprendre les besoins à tester
* Concevoir, documenter et exécuter des plans de tests (fonctionnels, régressions, exploratoires, etc.)
* Identifier, documenter et suivre les anomalies jusqu’à leur résolution
* Collaborer avec les développeurs pour comprendre les enjeux techniques et assurer une couverture optimale des tests
* Participer à l’amélioration continue des processus QA (automatisation, outils, documentation)
* Contribuer activement aux revues d’exigences et aux démos d’équipe
* Tester sur différentes plateformes (web, desktop) et navigateurs
Ce qu’on cherche chez toi:
* Expérience pertinente en assurance qualité logicielle (minimum 2 ans)
* Bonne connaissance des méthodologies Agile/Scrum
* Connaissance des outils de gestion de tests (ex.
: TestRail, Xray, Zephyr) et/ou de tickets (ex.
: Azure Devops)
* Expérience avec les tests manuels et automatisés
* Esprit analytique, rigueur et souci du détail
* Excellente capacité à communiquer (écrit/oral), autant avec les développeurs qu’avec le reste de l’équipe
* Capacité à apprendre rapidement et à s’adapter à un environnement en constante évolution
Atouts supplémentaires (mais pas obligatoires):
* Expérience dans un environnement SaaS ou logiciel B2B
* Expérience avec un logiciel ERP et/ou un logiciel de comptabilité
* Connaissance du domaine juridique ou intérêt marqué pour celui-ci
* Expérience avec des outils d’automatisation comme Cypress, Selenium ou Playwright
* Connaissances en SQL ou en lecture de logs pour diagnostiquer des erreurs
Nous pouvons vous offrir:
* Un salaire et des avantages très compétitifs
* Une organisation multinationale avec la possibilité de travailler à l'étranger
* Un ordinateur portable et tous les accessoires pour être bien installé chez soi
* 5 jours de congé personnel par année, en plus des vacances
* Des plans d'épargne-retraite et un programme de bonification d’achat d’actions (CSU.TO)
* Un plan d'assurance complet incluant : médical, dentaire, vision, assurance-vie et invalidité à long terme
* De nombreuses opportunités de formation, axées sur les compétences, le savoir-faire et le développement personnel
Prêt(e) à faire une vraie différence dans le monde juridique?
Fais-nous parvenir ton CV (...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-06-01 08:10:48
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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:
We are seeking a highly motivated and intellectually curious Data & Analytics Advisor to join our Global Commercial Analytics team.
This role offers the opportunity to drive impactful insights from data, solve complex business challenges, and collaborate with a team of similarly driven individuals.
The ideal candidate is a natural problem-solver with a passion for data, a people-first approach, and a proven ability to work independently and collaboratively across functions.
The role will develop Tableau reports and use Tableau heavily to extract data and insights.
Your Responsibilities:
* Report Development & Insight Generation: Create insightful Tableau reports using commercial data to answer key business questions, extracting and presenting information in a clear and compelling manner to drive data-informed decision-making.
* Data-Driven Insights: Analyze data to uncover actionable insights, effectively communicating complex information through compelling data stories and visualizations.
* Problem-Solving & Solution Design: Proactively identify business challenges and develop innovative, data-driven solutions.
* Root Cause Analysis: Tenaciously pursue answers and solutions, asking questions until the root cause of issues is identified and addressed.
* Stakeholder Management: Build strong relationships with stakeholders across different functions and levels, effectively managing expectations and ensuring alignment.
* Cross-Functional Collaboration: Collaborate seamlessly with teams and leaders across the organization to drive projects forward and achieve shared goals.
* Project Ownership: Take ownership of assigned projects, demonstrating accountability and driving them to successful completion.
* Prioritization & Time Management: Effectively prioritize tasks and manage time to deliver high-quality results in a fast-paced environment.
* Technical Expertise: Leverage advanced knowledge of Tableau (required) and preferably Power BI for reporting and visualization.
Knowledge and preferably expertis...
....Read more...
Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 140000
Posted: 2025-06-01 08:10:47
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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: Animal Health Clinical Research Associate
Operationally manage the logistics of ongoing animal clinical trials performed at the Fort Dodge, IA site including, but not limited to: animal socialization, the collection of clinical samples and/or observations, clinical operations, and the execution of other study events.
Your Responsibilities:
* Animal Care and Procedures: Independently performs and completes animal procedures in compliance with regulations, working instructions, and SOPs, including administering test articles, collecting samples, and conducting health observations.
* Study Execution and Management: Leads and manages multiple assignments related to R&D animal product development, executes in-life study events, coordinates scheduling and resource management, and supports business-facing functions like study scheduling and sourcing.
* Protocol Development and Review: Reviews and provides recommendations for study protocols and SOPs, collaborating with stakeholders to identify potential impacts on study execution, animal welfare, and regulatory compliance.
* Data Management and Quality Assurance: Performs concurrent documentation of study activities, reviews raw data for accuracy, and ensures high-quality results.
* Collaboration and Communication: Establishes and maintains relationships with key stakeholders (Study Directors, Laboratory Staff, Animal Care Staff) and communicates effectively within the team and across functions.
Troubleshoots problems and implements corrective actions as needed.
What You Need to Succeed (Minimum Qualifications):
* Veterinarian Technician Certificate or Associate Degree in relevant field (examples: biology, animal science, etc.) with relevant animal experience.
* Required to achieve AALAS (American Association of Laboratory Animal Science) described LAT (Laboratory Animal Technician) within one year of employment.
What Will Give You the Competitive Edge (Preferred Qualifications):
* Bachelor of Science in relevant field (examples: biology, animal scienc...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 77000
Posted: 2025-06-01 08:10:44
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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: Sr.
Specialist - Packaging Mechanic
The Packaging Mechanic is technical process leader on the Fill Finish operations team responsible for manufacturing setup, process efficiency, and production quality.
The role is responsible for execution and oversight of the primary, secondary, and tertiary packaging operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, mechanical setup, troubleshooting, change over, and line testing.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in vial filling and/or cartoning operations
* Strong knowledge of mechanical systems and instrumentation with packaging and vision system experience.
What will give you a competitive edge (preferred qualifications):
* Maintenance or instrumentation experience
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employe...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2025-06-01 08:10:40
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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: Sr.
Specialist - Downstream Operations Technician
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights incl...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 40
Posted: 2025-06-01 08:10:39
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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 Environmental, Health & Safety Manager has the responsibility for managing the Environmental, Health & Safety programs.
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.
* 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 workplace injury.
* Monitor return to work instructions given by health care provider and advise area man...
....Read more...
Type: Permanent Location: Sparta, US-WI
Salary / Rate: Not Specified
Posted: 2025-06-01 08:06:15
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En tant que gestionnaire de produits, ce professionnel sera chargé de guider la découverte et le développement de solutions innovantes qui répondent aux besoins futurs du marché.
Il collaborera avec les ingénieurs, les chercheurs et les dirigeants pour définir la vision du produit, hiérarchiser les initiatives et piloter le développement du produit.
Responsabilités et tâches:
* Définir et gérer la feuille de route des produits de R&D, en veillant à l'alignement sur les objectifs et les stratégies à long terme de l'entreprise;
* Diriger la découverte et l'exploration des technologies et tendances émergentes afin d'identifier de nouvelles opportunités de produits;
* Collaborer avec les parties prenantes au sein de l'organisation;
Exigences:
* Baccalauréat en informatique, en ingénierie, en gestion de produits ou dans un domaine connexe, ou expérience pertinente;
* Plus de 4 ans d'expérience dans la gestion de produits, avec un accent sur les produits logiciels;
* Expérience technique et compréhension des processus de développement de logiciels;
* Expérience de la gestion du cycle de vie des produits, de la conception au lancement;
* Une connaissance de base de l’anglais est requise, car nous avons des clients, des partenaires et fournisseurs anglophones, et le titulaire du poste peut avoir à l’occasion à communiquer dans cette langue.
Expérience appréciée:
* Expérience préalable dans le domaine des logiciels de gestion et d'application des règles de stationnement;
* Expérience préalable avec la reconnaissance automatique des plaques d'immatriculation (ALPR/ANPR);
* Expérience préalable avec un logiciel d'application des règles de stationnement, de circulation, d'arrêté municipal ou de code.
*Seuls les candidats retenus seront contactés.
Harris est un employeur souscrivant au principe de l'égalité des chances et les membres des groupes cibles suivants sont encouragés à postuler : les femmes, les personnes handicapées, les autochtones et les minorités visibles.
Si vous êtes une personne handicapée, une assistance au processus de sélection est disponible sur demande.
L'équipe de Harris Talent Acquisition n'utilise pas de SMS pour contacter les candidats ou solliciter des informations confidentielles.
Nous encourageons tous les candidats à postuler aux postes annoncés.
Ils seront contactés soit par un responsable de Harris, soit par un membre de l'équipe d'acquisition de talents pour un entretien, une fois que les critères requis auront été remplis.
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As a Product Owner, this professional will be responsible for guiding the discovery and development of innovative solutions that address future market needs.
They will collaborate with engineers, researchers, and leadership to define product vision, prio...
....Read more...
Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 85000
Posted: 2025-05-31 09:00:39
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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.
About the Role
Seeking an opportunity where you can create meaningful change, contribute to heritage preservation, and support responsible business practices? We have an exciting and rewarding opportunity for a Cultural Heritage Advisor to join our External Relations and Sustainability team and play a vital role in protecting and managing heritage values across our Western Australian operations.
As a Cultural Heritage Advisor, you will be instrumental in strengthening our organisation’s social performance by delivering cultural heritage survey programs, managing cultural heritage values identified as a result, and fostering positive relationships with internal stakeholders and Traditional Owners.
In this role, your key contributions will be:
* Enhancing cultural heritage management by identifying survey and monitoring needs and developing effective scopes of work.
* Coordinating field-based programs, ensuring the successful scheduling and execution of cultural heritage surveys and monitoring activities in collaboration with Traditional Owners.
* Implementing cultural heritage management actions in consultation with Traditional Owners.
* Supporting the development of applications for statutory approvals under the Aboriginal Heritage Act 1972, Aboriginal Heritage Regulations 1974 and Heritage Act 2018 where impacts to cultural heritage places cannot be avoided.
* Working safely in the field and confidently supporting Traditional Owners, consultants and field support teams to adhere to Alcoa’s safety systems and processes.
* Providing technical advice on heritage matters, reviewing survey deliverables, and contributing to process improvements in cultural heritage management.
What’s on offer
* Attractive remuneration and variable bonus plan.
* Employee growth and development opportunities.
* Parental leave support for all caregivers.
* Employee assistance program for personal support services.
* Alcoa Live Well program offering travel, lifestyle, health and wellbeing discounts.
* Generous leave entitlements including a leisure a day off every 4-week period.
What you can bring to the role
* Tertiary qualifications in either archaeology, anthropology, or cultural heritage management with previous experience in a related field.
* Demonstrated ability to work with Aboriginal people in a sensitive, respectful, and culturally appropriate manner.
* Knowledge and understanding of cultural heritage legislation in Western Australia and relevant industry standards and best practices.
* Strong analytical skills with the ability to interpret and communicate complex data.
* Sound working knowledge of Geographic Information Systems (GIS) skilled in creating maps...
....Read more...
Type: Permanent Location: BOORAGOON, AU-WA
Salary / Rate: Not Specified
Posted: 2025-05-31 08:56:23
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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:
Alcoa is seeking a highly motivated and experienced Environmental Advisor to join our team and play a crucial role in shaping the future of sustainability.
This exciting opportunity will involve developing and implementing ground disturbance assessment programs across Alcoa’s Mining Operations in Western Australia.
Reporting into the Environmental Compliance Specialist, this position will be offered on a family friendly Monday to Friday roster, based at the WA Mining Hub, located onsite at the Pinjarra refinery, and will require ad hoc site travel to all our WA Mining locations.
Key Responsibilities:
* Prioritising and managing permit assessments to ensure they align with the established mine plan schedules.
* The role requires a strong understanding of WA Mining compliance commitments to ensure that all activities adhere to relevant regulations.
* The incumbent will be responsible for training personnel in the ground disturbance permit process requirements, ensuring consistent understanding and adherence.
* Utilising geographical information systems, the role will assess permit activity areas against compliance requirements to identify any potential issues or discrepancies.
* The role will also involve supporting projects to implement new ground disturbance permit software, contributing to the efficiency and effectiveness of the permit assessment process.
The Environmental Advisor will provide expert advice on activities identified as part of permit assessments, drawing on their knowledge and experience in the field.
What’s on offer:
* Career development opportunities to pursue your passion
* Monthly Leisure Day
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
* Ideally you will hold a bachelor’s degree in environmental science, environmental engineering, or similar – or have equivalent hands-on experience in a similar role.
* Strong analytical expertise in assessing ground disturbance activities against compliance criteria.
* A solid understanding of the mining process and its operations.
* Proven experience in working collaboratively with mine planning and mining operations teams.
* A strong background in GIS and its applications.
* Excellent communication and interpersonal skills, and ideally the successful candidate will have a passion for ...
....Read more...
Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-05-31 08:56:16
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Accounts Payable Analyst I - (Korean Speaker) - (Global Business Services)
Job Description
Accounts Payable Analyst I - (Korean Speaker) (Global Business Services)
Your Job
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Role Overview & Primary Accountabilities:
* Execute payment for vendor and expense claims. Ensure expenditures are duly paid.
* Attend queries from Query Management Team
* To perform First Strike Report to prevent duplicate payment
* Review and coordinate vendor master maintenance, vendors payment, blocked payment, aging reports and supporting documents.
* Payment Forecast to Treasury Team
* Support back up plan & ad-hoc tasks.
* Ensuring appropriate internal controls in place.
* Support and execute continuous improvement (CI) initiatives to streamline existing accounts payable processes.
* Perform analysis & trouble shoot exceptions to drive KPI results.
* Support internal & external audit query to Team Leader.
* Support in operation meeting.
* Support SME for APAC (within team's portfolio)
* Responsibilities include issue resolution and engage in process improvement AP projects.
* AP Project sustainability with improvement idea.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact.
We’re founded on 151 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity.
It’s all here for you at Kimberly-Clark.
Led by Purpose.
Driven by You.
About You
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
You love what you do, especially when the work you do makes a difference.
At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.
When you join our team, you’ll experience Flex That Works: flexible (hybrid) work arrangements that empower you to have purposeful time in the office and partner with your leader to make ...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2025-05-31 08:54:44
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Health and Safety Team Leader
Job Description
As a person, you’re a learner – a natural leader – someone who is always taking initiative to make things better and bring others along with you.
You live your life in alignment with the highest values of integrity and quality, always ensuring your responsibilities become a long-term success story.
In this role, you’ll help us deliver better care for billions of people around the world.
Position Summary:
The incumbent reports to the EHS Site Manager and has the responsibility to implement the site safety and sustainability strategies in the Beech Island CTEC process system.
The incumbent must work collaboratively with the site EHS team, Global EHS leaders, and all mill leaders to identify and lead appropriate initiatives that deliver continuous improvement in environmental, health and safety results.
It starts with YOU.
In this role, you will:
* Provide organizational and functional leadership to ensure that EHS systems meet Kimberly-Clark Standards, Best Practices and federal and state regulatory requirements.
The incumbent will provide leadership for continuous improvement in all EHS activities in support of achieving an injury-free work environment.
Lead crisis response to events as appropriate, ensuring effective investigation and follow-up.
* Provide personal and organizational sensitivity, vision, inspiration, innovation, talent building, decisive, strong communication, collaborating and influencing skills. Knowledge of regulatory requirements of OSHA, NFPA, and other federal, state and local agencies.
* Analyze EHS data, providing insights regarding results and trends through investigation and thorough problem solving, making recommendations for improvements that address substandard acts or conditions.
* Catalyst for site safety culture initiatives (People-Based Safety) and programs focused on the positive impact of Mindsets and Behaviors required to deliver a zero-injury work environment.
* Support of Contractor Safety ensuring adherence to KC safety requirements of contractors, vendors and visitors.
* Contribute to an environment in which all team members are respected regardless of their individual differences and are motivated to improve their individual/team contributions so as to achieve desired business results.
About Us
Huggies®.
Kleenex®.
Cottonelle®.
Scott®.
Kotex®.
Poise®.
Depend®.
Kimberly-Clark Professional®.
You already know our legendary brands—and so does the rest of the world.
In fact, millions of people use Kimberly-Clark products every day.
We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.
At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth and impact.
We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opport...
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Type: Permanent Location: Beech Island, US-SC
Salary / Rate: Not Specified
Posted: 2025-05-31 08:54:27
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SUMMARY
The California Department of Public Health’s Microbial Diseases Laboratory Program is responsible for diagnostic and surveillance testing, applied research projects, and education and training for the identification and characterization of bacterial, mycobacterial, fungal, and parasitic pathogens of public health importance.
Under the direction of the Supervisor of the Quality, Safety & Support Unit, within the Microbial Diseases Laboratory (MDL) Branch, the Microbiologist II performs duties associated with method validation and routine testing of microbial pathogens using advanced molecular detection (AMD) methods, primarily including methods utilizing next generation sequencing (NGS). This position will provide programmatic support for a variety of priority AMD validation projects and assists with surge testing for AMD methods across MDL laboratories, as qualified and assigned.
The position is Monday-Friday, 40 hours per week; weekend, holiday, and overtime coverage may be required during a public health emergency.
The salary range is $36.53 - $49.15 per hour depending on experience and qualifications
If hired for this position, you will be required to provide proof that you are fully vaccinated for COVID-19 prior to your start date or have a valid religious or medical reason qualifying you for an exemption (that may or may not require an accommodation).
ESSENTIAL FUNCTIONS
* Specimen receipt and data entry into Laboratory Information Management System (LIMS).
* Cultivates bacterial or fungal pathogens and quality control strains.
* Develops and optimizes standard operating procedures (SOPs) for next generation sequencing using various sequencing platforms, including but not limited to the Illumina and Nanopore platforms.
* Performs DNA extraction, library preparation, and sequencing of microbial pathogens using various sequencing platforms.
* Implement protocols and workflows on liquid handlers as needed
* Analyzes genomic sequences using validated pipelines and software.
* Participates in proficiency testing and adheres to Branch QC/QA policies for laboratory operations including biosafety, chemical hygiene, and other applicable standards.
* Complies with MDL’s Quality Management system, including complete, timely and accurate recording of results and quality documentation.
* Reviews test results for completeness and accuracy.
* Maintains inventory of essential chemicals, reagents, and disposables.
* Prepares technical reports and compiles data related to applicable grants and projects.
* Communicate effectively with internal and external partners.
* Assists with planning for educational events and in training of public health microbiologist trainees and other partners
* Provides technical consultation to laboratory staff and other local, state, and federal partners
* Attends to training and informational meetings/webinars/conference.
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Type: Permanent Location: Richmond, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-31 08:53:40
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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:
Guatemala City, Guatemala, Guatemala, Panama, Panamá, Panama, San José, San Jose, Costa Rica
Job Description:
Essential Job Duties and Responsibilities
The MSL Mission is to, through customized interactions, discuss our treatments with physicians and other customers to shape behaviors and support informed decision making whilst identifying and bringing medical insights into the organization as inputs to medical strategy.
The main activities are:
• Build relationships with community and academic HCPs focusing on changing medical behavior through the exchange of scientific knowledge
• Convey the value of the attributes related to the innovation (ie, efficacy, safety, effectiveness, adherence, QoL) to gain attribute endorsement with stakeholders
• Shaping medical practice by changing behaviors within the HCP Community during product pre
launching phases - prepare the health care environment and medical community, accelerate adoption (PIs engagement and pre-approval access programs)
• Follow up on education, adoption of new knowledge, identifying barriers for medical practice change for innovative products
• Respond to scientific inquiries of HCPs/investigators/health care systems and population health decision makers
• Integrates scientific data into real life practice to meet customer/audience needs
• Identify potential sites and support sites recruitment when needed in alignment with the TA
Head/Senior medical manager
• Execute Medical Field Educational Events focused on pipeline close to launch and key in line products
• Gather insights from Field interactions regarding scientific knowledge, treatments paradigms, Competitors, medical needs and opportunities
• Draw and execute the territory and KOL engagement plan according to the strategy and validated by the other MAF stakeholders
• Deep scientific knowledge according to business/regulatory needs
Requirements:
* Any health care/biomedicine career, desirable post-graduation or MSc/PhD.
* It is required that the candidates have Intermediate / advanced English reading, writing and speaking skills.
* No experience of MSL is required.
* Skills Ability to learn and effectively convey clinical and non-clinical technical information; fast Learner; ability to network and matrix, a...
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Type: Permanent Location: Panama, PA-8
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:35
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
MedTech Sales
Job Sub Function:
Technical Sales - MedTech (Commission)
Job Category:
Professional
All Job Posting Locations:
Cleveland, Ohio, United States, Columbus, Ohio, United States
Job Description:
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke.
You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
We are searching for the best talent for the Associate Clinical Account Specialist position to be in Cleveland and Columbus, OH.
.
Purpose:
The Associate Clinical Account Specialist (ACAS) position is a 6-9 month training position for those with little to no electrophysiology (EP) experience.
Upon successful graduation from the program, the ACAS will be promoted to a Clinical Account Specialist (CAS).
As a CAS the candidate will provide expert clinical product and technical assistance and training to physicians and EP lab staff on the effective use of the Electrophysiology’s systems and catheter equipment (e.g., The CARTO® System, associated software modules and RF generator) during case procedures within an assigned geography.
The expectation that is that this work leads to meeting and/or exceeding business goals.
You will be responsible for:
Under (e.g.
limited supervision, general direction, etc.) and in accordance with all applicable federal, state and local laws/regulations and corporate Johnson & Johnson, procedures and guidelines, the ACAS will:
* Attend all portions of the ACAS fellowship training program without exception.
* Engage in dialogue with multiple internal and external business partners and stakeholders, and formulate solutions based on dialogue and input gained during training.
* Understand the dynamics of an EP lab, including, but not limited to physicians, nurses and technicians, clinical and hospital administrators and staff.
* Prioritize and appropriately respond to re...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:09
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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:
Marketing
Job Sub Function:
Marketing Insights & Analytics
Job Category:
Professional
All Job Posting Locations:
Titusville, New Jersey, United States of America
Job Description:
We are searching for the best talent for an Associate Director, Integrated Analytics – Pulmonary Arterial Hypertension, to be based in Titusville, NJ.
About Pulmonary Hypertension
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 Pulmonary Hypertension team is focused on transforming the disease into a long-term manageable condition.
Bringing your passion for health to this team will help discover and develop effective treatments that help patients live their best possible life.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Purpose: The Associate Director, Integrated Analytics – Pulmonary Arterial Hypertension (PAH) position is responsible for generating, integrating, and translating insights into growth opportunities that shape decisions and drive organizational action for the PAH portfolio (OPSUMIT®, OPSYNVI® and UPTRAVI®). This position will partner closely with cross functional brand partners and serves as an internal consultant to the Sales & Marketing team and senior leaders.
This position plays a leading role in advising and counseling management in the development and evaluation of new and existing business strategies and tactics and as a result, shares accountability for business results.
Key Responsibilities:
* Develop insights and actionable recommendations influencing business partners at all levels to incorporate in decision making
* Leverage disparate data sources to address key business questions and uncover business opportunities
* Serve as a leader in integrating data and analytics (national, subnational, payer) with cross functional findings and insights developed by peers across the organization
* Integrate payer data and insights into ongoing business analytics to drive a holistic view of the customer and market
* Serve as a champion for the implementation of cross-functional capabilities to drive impact for brand or franchise and drive organiza...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-05-31 08:35:06
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Biostatistics
Job Category:
Scientific/Technology
All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom
Job Description:
The Principal Statistical Programming Lead is a highly experienced Statistical Programmer with expert knowledge of Statistical Programming languages, tools and data structures, proven technical and analytic abilities and strong capabilities in leading Statistical Programming activities and programming teams in accordance to departmental processes and procedures.
This position is accountable for the planning, oversight and delivery of statistical programming activities in support of one or more clinical projects, compounds and/or submissions generally of high complexity/criticality.
In addition, this position leads and/or contributes expert knowledge and technical skills to Therapeutic area and/or departmental innovation and process improvement projects.
In this role, the Principal Statistical Programming Lead is responsible for making decisions and recommendations that impact the efficiency, timeliness and quality of deliverables with a high degree of autonomy and provide leadership, direction and technical and project specific guidance to programming teams.
Accountable for Statistical Programming team delivery for 1 or more clinical projects of high complexity, scope and/or criticality.
Provides matrix leadership to 1 or more programming teams, coordinating and overseeing programming team activities.
May act as a section lead of programming activities supporting a clinical development program, compound or submission.
Contributes to and applies strategic decisions and recommendations, developing and maintaining detailed programming strategy and plans.
Provides technical and project specific guidance to programming team members to ensure high quality and on-time deliverables in compliance with departmental processes.
Coaches and trains junior colleagues in techniques, processes and responsibilities.
Integrates Johnson & Johnson’s Credo and Leadership Imperatives into team goals and decision making.
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Type: Permanent Location: High Wycombe, GB-BKM
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:38
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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:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development & Research – MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Lisbon, Portugal
Job Description:
Johnson & Johnson is recruiting for a Global Medical Safety Physician Fellow. This position will be located in Lisbon, Portugal.
The Global Medical Safety Physician Fellowship is an 18 month program designed to provide qualified physicians the opportunity to gain specialized and in-depth training in key areas of pharmacovigilance within the pharmaceutical industry.
This Fellowship does not provide certifications of any kind.
Principal Responsibilities:
* Participate and complete training in several areas of pharmacovigilance, which include the following: safety surveillance and signal evaluation; identification of new potential safety concerns; characterization of emerging and known product safety profiles; the design and implementation of risk minimization strategies.
* Provide medical expertise in the evaluation of safety data from a variety of sources (interventional and noninterventional clinical studies, post-marketing data, literature reports, and other sources of safety data) as part of the overall pharmacovigilance surveillance process; this includes medical review of individual case safety reports (ICSRs) and evaluation of aggregate safety data.
* Ensure communication of potential new safety concerns and trends to the Medical Safety Officer (MSO) and the Safety Management Team (SMT).
* Support SMT activities such as the evaluation of safety issues to characterize any emerging or known product safety profiles, preparation of aggregate safety reports, such as Periodic Benefit Risk Evaluation Reports (PBRERs), ad-hoc regulatory reports, and interpretation of surveillance and product quality data.
* Work in a cross functional, matrix team environment.
* Contribute to, when appropriate, the design and implementation of risk mitigation strategies to ensure the safe and appropriate use of Janssen Research & Development, LLC products.
* Provide (2) presentations concerning Pharmacovigilance and/or pertinent medical topics to your team.
* Provide assistance in the Medical Affairs team's activities concerning pharmacovigilance, quality, and regulatory affairs.
* Assist in the planning and execution of Medical Affairs activities, both in-office and ...
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Type: Permanent Location: Lisbon, PT-11
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:37
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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:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Business Enablement/Support
All Job Posting Locations:
Shanghai, China
Job Description:
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:31
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Support
Job Category:
Business Enablement/Support
All Job Posting Locations:
Beijing, China
Job Description:
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-05-31 08:34:31
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As Global Director of Product Management you will be responsible for steering the product roadmap, achieving market growth and participation gains, orchestrating campaigns that drive specific product growth, deploying high quality standards and embedding a getting things done culture.
In this role, your responsibilities will be:
Participation on the Leadership Team
* Working collaboratively to craft and develop the business strategy.
* Drives business growth consistent with that of an innovative technology / business model aligning with the MSOL vision.
* Works to integrate the Corrosion and Erosion business and products into the broader Emerson organizations where appropriate in an expeditious manner.
Strategic
* Develop the vision, mission, and goals for delivering value to customers via data and analytics as well as through the entire system – both hardware and software
* Steer the product management and marketing team to influence end users and to understand future industry requirements.
* Maintain and strengthen collaborative capacity with key universities and research facilities.
* Coordinate and seek alignments within Measurement Solutions and Emerson through global forums, Emerson centres of excellence and through peer contacts.
* Collaborate with Engineering Managers to establish the Product Development strategy, objectives, and metrics aligned with overall CE strategic goals.
Functional Management and Technical Leadership
* Collaborate with sales leadership, world area marketing and business development and marketing/promotional teams to achieve growth goals.
* Direct pricing and discount structure strategy and execution.
Navigate competitive and market forces to understand and respond to changing market conditions.
* Defining and achieving product line financial targets of revenue, unit growth, profitability, and market participation (P&L).
* Ensure delivery of product releases to time and budget and engage with and steer the group NPD pipeline management processes.
Who you are:
Pushes self and helps others achieve results.
Encourages the open expression of diverse ideas and opinions.
For this role, you will need:
* Considerable experience at a senior level leading large multi-disciplinary engineering teams, new product development, research, and production support
* Proven strong people, leadership skills and track record to perform strategic analysis.
* Successful track record of product development projects and experience in sales management and leadership.
* Strong interpersonal, communication and collaboration skills with ability to work with all levels of the business, from diverse technical and functional subject areas.
* Degree in Engineering, Marketing or Business, coupled with a strong technical orientation acquired either through an Engineering degree or years of experience.
* Travel is required.
Preferred Qualifications...
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Type: Permanent Location: CRAWLEY, GB-WSX
Salary / Rate: Not Specified
Posted: 2025-05-31 08:32:25
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Ardurra is seeking a full-time Senior Ecologist to join our team in Orlando, FL.
This role focuses on environmental permitting, regulatory compliance, and database management for transportation-related projects.
The ideal candidate will possess strong ecological assessment skills and a solid understanding of permitting requirements for both state and federal agencies.
Primary Function:
We are seeking a motivated and knowledgeable Sr Ecologist to play a key role in the planning, execution, and management of wetland and natural resource projects throughout our Orlando Projects.
This is an exciting opportunity to work on diverse watershed projects in a collaborative and supportive work environment.
Primary Duties:
* Review roadway plans to determine permitting requirements for minor and major transportation projects, including identification and assessment of wetlands and protected species affected, and assessment of stormwater impacts
* Prepare state and federal permit application packages that describe the site assessments, stormwater data, agency jurisdiction, the measures necessary to satisfy permit requirements, and summaries of meetings with the regulatory agencies
* Conduct wetland inventories and Environmental Assessments, including a focus on protected species
* Assist in preparing and reviewing reports in support of projects, including protected species, natural habitat, environmental impacts, biological evaluations, minor NEPA/NMSA, and related regulatory requirements and compliance guidelines
* Review documents for projects prepared by others, including pre-design environmental documents, permit application packages, exemption verifications, or need for additional wildlife surveys
* Perform QA/QC reviews to ensure completeness, accuracy, and conformity to established industry standards and local, state, or federal criteria
* Provide practical solutions to project challenges by applying accepted procedures and methodologies and collaborating with others
* Support the preparation of draft environmental scope, units, and staff hours for projects based on existing transportation permitting policies and guidelines
* Monitor project budgets and schedules to ensure profitability and timeliness of deliverables
* Mentor junior-level team members while being a positive leader for the team
* Contribute to business development efforts by supporting proposals and identifying new opportunities
Education and Experience Requirements:
* Bachelor’s degree in physical or natural sciences or a related field such as Environmental Science, Biology, or Ecology
* 10+ years of prior practical experience (or 7+ with a relevant Master’s degree)
* Familiarity or established relationships with FDOT, regulatory agencies, and other municipal clients is strongly preferred
* In-depth knowledge of FDOT and regulatory agency criteria, standards, and plans preparation requirements
*...
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Type: Permanent Location: Orlando, US-FL
Salary / Rate: Not Specified
Posted: 2025-05-31 08:30:09
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Strategic Healthcare Programs (SHP) is a leader in analytics and performance management solutions serving the post-acute market. We are an industry leader in helping Home Health, Hospice, and Skilled Nursing providers improve their financial and quality performance while complying with many regulatory requirements Additionally, we connect the post-acute world to the broader provider markets to allow for optimal management across the continuum of care.
The Survey Processor plays an integral role in the timely and accurate processing of survey data.
Duties and Responsibilities:
* Receive inbound mail delivery
* Sort and cut received mail
* Set up the mail cart of the day
* Handling mail accurately by opening, extracting and classifying the content of each envelope
* Scanning of surveys along with documentation
* Operation of a PC and a scanner for data input and review
* Archive completed survey trays
* Move shred bins to shredding area when scheduled
Knowledge, Skills and Abilities
* Able to follow specific instructions and procedures without deviation
* Excellent attention to detail
* Excellent communication is a must
* Proficient in core computer skills (Excel, Word, etc.)
* Be able to lift up to 40 lbs.
and push a 65-gallon shred container on wheels.
* Maintain an acceptable level of work quality
Pay:
$19.00 per hour.
Benefits
We value work/life balance.
Temporary part-time employees are not eligible for health benefits, but are eligible for paid vacation, sick time, and holidays.
This is an on-site temporary part-time position this Summer, working approximately 5 days in June, 10 days in July, and 10 days in August.
The hours are 8am – 1pm, on the days of scheduled work.
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 information, please review the Know Your Rights notice from the Department of Labor.
Administration
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Type: Permanent Location: Goleta, US-CA
Salary / Rate: Not Specified
Posted: 2025-05-30 09:31:32
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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
As a Technical Consultant within Elanco’s SBU team, you will be a trusted technical partner to customers and internal teams across the food animal health space.
You will position Elanco as the partner of choice by delivering exceptional technical expertise, market-leading product solutions, scientifically sound research, and value beyond product - including consulting, diagnostics, analytics, and market access support.
This role is field-based and requires travel up to 50%.
You will work cross-functionally within account teams, train Elanco colleagues, engage with industry stakeholders, and influence the long-term direction of our food animal portfolio through research, innovation, and customer-centric solutions.
Your Responsibilities:
Sales and Marketing Support
* Collaborate directly with customers and account teams to support Elanco’s commercial goals
* Identify opportunities and position Elanco products as solutions for customer challenges
* Participate in account planning and help implement Elanco’s value strategy at the customer level
* Support training efforts and contribute to product launch readiness
* Develop and deliver educational events and technical materials for internal and external stakeholders
Customer and Technical Leadership
* Train and coach Elanco teams on disease, product knowledge, and industry practices
* Build strong relationships with external veterinarians, consultants, and academic partners
* Serve as a technical authority to influence decisions at customer and industry levels
* Represent Elanco in key industry organizations and maintain thought leadership presence
Research and Innovation
* Conduct applied research with Elanco-approved products to generate field-relevant data
* Align technical research with business priorities and lifecycle planning for key brands
* Contribute to peer-reviewed publications and present at scientific meetings
* Support R&D efforts, including product line extensions and innovation ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-05-30 09:20:53
