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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: Lab Technician - Quality Control
As a Quality Control Technician, you will play a crucial role in ensuring the accuracy and integrity of laboratory testing within our Quality Control and Environmental Control Laboratories.
In this position, you will be responsible for executing precise testing, participating in laboratory investigations, and maintaining equipment in compliance with GMP and safety guidelines.
This position will offer a one-time sign-on bonus of $2,500!
Your Responsibilities:
* Perform timely and accurate testing of laboratory samples according to approved methods.
* Adhere to safety protocols and serve as a role model for safety practices on your shift.
* Conduct data entry and verification reviews with high attention to detail.
* Troubleshoot equipment and methodologies as needed.
* Engage in continuous improvement activities and self-inspections.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience in a laboratory environment with a focus on quality control.
* Top 2 skills: Strong attention to detail and ability to work in a highly regulated environment.
What will give you a competitive edge (preferred qualifications):
* Familiarity with GMP and safety guidelines.
* Experience with laboratory investigations and equipment maintenance.
* Ability to work flexible shifts, including 12-hour and 8-hour schedules.
* Previous involvement in safety and ergonomic initiatives.
* Strong problem-solving skills related to laboratory operations.
Additional Information:
* Location: Clinton, IN Manufacturing Site
* Required to work in a laboratory environment (wearing safety glasses and laboratory clothing/PPE required). Some exposure to allergens is possible in the laboratory environment.
* Shifts may vary to include: 12-hour rotating (5:45-6:00), 12-hour day (5:45-6:00), 12-hour night (5:45 – 6:00), and/or 8-hour shifts.
* Unscheduled overtime may be required.
This ...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: Not Specified
Posted: 2025-02-14 07:32:42
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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: Global Business Development Leader
As the Global Business Development Leader you’ll play a pivotal role in shaping Elanco’s future.
This high-impact position focuses on driving strategic deals, including licenses, partnerships, M&A, and collaborations, to strengthen Elanco's innovative portfolio in animal health.
You’ll build relationships with key players across the industry, identify opportunities to enhance our offerings, and deliver value by acquiring transformative technologies and products.
In this role, you’ll partner closely with cross-functional teams (including R&D, legal, and finance) to align innovation strategies with business objectives.
From leading deal negotiations to influencing the external partnering environment through venture capital and funding strategies, you’ll be at the forefront of advancing Elanco’s long-term vision.
If you’re passionate about driving impactful change and shaping the future of animal health, this is your opportunity to make a difference.
Your Responsibilities:
* Develop and execute a strategy-driven business development agenda, including licenses, collaborations, divestitures, distribution agreements, and M&A opportunities to expand Elanco’s portfolio.
* Establish and nurture relationships with Animal Health companies and technologies/products in development or revenue-generating stages to drive growth and innovation.
* Lead cross-functional transaction teams through deal negotiations, ensuring successful execution and alignment with strategic objectives.
* Partner with internal stakeholders, including R&D, legal, IP, tax, and corporate finance, to ensure seamless integration and progression of external innovation strategies.
* Identify, evaluate, and qualify potential targets that align with Elanco’s pipeline, technology needs, and long-term business goals.
* Shape the external partnering environment through participation in venture capital, external funding strategies, and positioning Elanco as a preferred partner.
* Support leadership by ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-02-14 07:32:36
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Diese Stelle ist auf 3 Jahrebefristet.
Wir brauchen DICH als neuen Pharmawerker (m/w/d) Abfüllung!
Deine neue Abteilung:
Die Hauptabteilung „Diagnostics Operations Mannheim“ (DOM) am Standort Penzberg sieht sich in der Verantwortung, dass Patienten präzise medizinisch-diagnostische Resultate erhalten.
Hierfür beliefern wir Patienten, Labore und Krankenhäuser mit diagnostischen Tests und agieren dabei mit größter Sorgfalt und Leidenschaft.
Für uns steht „DOM“ für Zuverlässigkeit, Qualität und Wachstum.
Mit unserer zupackenden, optimistischen Einstellung gestalten wir unsere Zukunft zum Wohle der Patienten, unserer Mitarbeitenden, für uns als Organisation, Global Operations und für Roche.
Dein neues Aufgabengebiet:
Wir suchen einen Pharmawerker (m/w/d), der gemeinsam mit uns Produkte für die In-Vitro-Diagnostik abfüllt und dabei die gute Laune im Team nicht zu kurz kommen lässt.
In Deiner neuen Funktion erwarten Dich verschiedene spannende Aufgaben, die wir vertrauensvoll in Deine Hände legen:
* Abfüllung von Produktionschargen, Servicechargen und Reagenzien in unterschiedlichen Räumlichkeiten und Gebäuden
* Bedienung und Umrüstung von kleinen Abfüllgeräten und großen Abfüllanlagen
* Manuelle Tätigkeiten, wie z.B.
das Etikettieren von Flaschen, oder Handabfüllungen mit Pipetten
* Vorbereitung, Reinigung und Desinfektion der Abfüllmaschinen und Anlagen sowie von Geräten und Räumlichkeiten laut Arbeitsanweisung und Hygieneplan
* Durchführung von Füllmengenkontrollen
* Nachvollziehbare und exakte Dokumentation in Herstellprotokollen oder anderen Dokumenten, z.B.
Durchführungsprotokollen zum Hygieneplan, Belegungsblättern und Logbüchern von Geräten und Anlagen
* Ablieferung fertig abgefüllter Reagenzien
* Umgang mit potentiell infektiösem Material der Klasse S2 (Humanmaterial)
* Sachgerechte Entsorgung von kontaminierten und sonstigen Materialien
Diese Position erfordert die Bereitschaft zum Umgang mit Humanmaterial, sowie das Heben und Bewegen von Lasten bis zu 15 kg mehrmals wöchentlich und einen wechselnden Einsatz in unterschiedlichen Gebäuden.
Wer du bist:
Wenn Du die folgenden Voraussetzungen mitbringst, bist Du genau die richtige Person für uns und kannst in der Abteilung „Diagnostic Operations Mannheim“ am Standort Penzberg durchstarten, Dein Wissen an uns weitergeben und Deine Kompetenzen in einem der größten Pharmaunternehmen der Welt noch weiter ausbauen:
* Du hast eine erfolgreich abgeschlossene Berufsausbildung; vorzugsweise als Chemi...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-02-14 07:18:40
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L’hôtel Carlton Cannes, a Regent Hotel, a rouvert le 13 mars 2023, suite à son magnifique projet de rénovation et d’extension.
Depuis son inauguration en 1913, l’établissement n’a jamais connu pareille transformation.
110 ans après son ouverture, la « Grande Dame » entre dans un nouveau siècle et c'est avec bonheur que nous écrivons le prochain chapitre de son histoire.
L’hôtel est entièrement rénové et dispose de deux ailes prolongées dévoilant de nouvelles suites, d’un jardin intérieur de 2000m² agrémenté d’un bar et d’une piscine à débordement, d’un fitness & spa et d’un centre de conférence de 1800m².
Notre Maison est à la recherche de notre Assistant(e) Gouvernante Générale pour rejoindre notre équipe dans le cadre d’un contrat à durée indéterminée.
PRINCIPAUX OBJECTIFS DU POSTE
Vous assisterez la Gouvernante Générale dans l’ensemble de ses missions et plus particulièrement :
* Vous dirigerez et contrôlerez la qualité des services et prestations délivrée par le service Housekeeping et la Lingerie
* Vous serez responsable de la coordination journalière des activités et du respect des standards d’excellence, des procédures et des normes d’hygiène en vigueur au sein de l’hôtel.
* Vous participerez activement au recrutement et à la gestion quotidienne des équipes Gouvernant(e)s, Valets et Femmes de Chambre, Valets d’étages, Lingères, Agents d’entretien.
* Vous participerez à l’élaboration du budget annuel pour le service et vous suivrez et analyserez les ratios afin de mettre en place toute action corrective.
* Vous contribuerez à la satisfaction de notre Clientèle par votre attitude, votre disponibilité et votre présence sur le terrain.
QUALIFICATIONS ET AUTRES EXIGENCES
Pour remplir ce rôle avec succès, vous devez posséder idéalement les compétences, l'attitude, les comportements et les valeurs suivantes :
* Issu(e) d’une formation supérieure en Hôtellerie, vous justifiez d’une expérience réussie de cinq années au minimum en qualité de Gouvernant(e) ou Assistant(e) Gouvernante Générale au sein d’Etablissements de luxe de grande capacité.
* Vous maîtrisez parfaitement le français et l’anglais tant à l’oral qu’à l’écrit.
* Doté(e) d’une excellente présentation, vous êtes dynamique, flexible et êtes animé(e) d’un sens développé du service client de très haute qualité.
* Vous alliez fermeté et diplomatie avec habileté, afin de vous adapter à tout type de demandes clients et d’entretenir de bonnes relations avec vos équipes.
* Vous avez une pratique aisée de l’environnement Windows et des logiciels hôteliers (Opera Cloud, Hopr,..)
* Vous êtes reconnu(e) pour vos qualités de leader.
* Vous faites preuve d'une grande capacité d’adaptation pour mener plusieurs projets de front.
* Vous êtes reconnu(e) pour être une personne pr...
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Type: Permanent Location: Cannes, FR-06
Salary / Rate: Not Specified
Posted: 2025-02-13 07:41:00
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L’hôtel Carlton Cannes, a Regent Hotel, a rouvert le 13 mars 2023, suite à son magnifique projet de rénovation et d’extension.
Depuis son inauguration en 1913, l’établissement n’a jamais connu pareille transformation.
110 ans après son ouverture, la « Grande Dame » entre dans un nouveau siècle et c'est avec bonheur que nous écrivons le prochain chapitre de son histoire.
L’hôtel est entièrement rénové et dispose de deux ailes prolongées dévoilant de nouvelles suites, d’un jardin intérieur de 2000m² agrémenté d’un bar et d’une piscine à débordement, d’un fitness & spa et d’un centre de conférence de 1800m².
Notre Maison est à la recherche de sa/son Responsable Majordome – Head Butler en CDI afin d’offrir une expérience inégalée à nos Clients.
PRINCIPAUX OBJECTIFS DU POSTE
* Vous êtes responsable de la bonne organisation du service Butler
* Vous êtes garant du respect de nos standards d’excellence en matière d’hospitalité.
* Vous transmettez votre savoir-faire aux équipes dans le cadre de formations terrain.
RESPONSABILITES
* Manager et coordonner l’équipe des Butlers pour garantir un service personnalisé et haut de gamme.
* Former les nouveaux Butlers sur les standards d’accueil, protocoles de service et bonnes pratiques.
* Participer à l’organisation de services spéciaux en chambre.
* Collaborer avec les équipes de gouvernance et d’entretien pour garantir la disponibilité et la qualité des chambres.
* Soutenir les équipes opérationnelles lors de périodes de forte activité ou d’événements spéciaux.
QUALIFICATIONS ET AUTRES EXIGENCES
Pour remplir ce rôle avec succès, vous devez posséder idéalement les qualifications, l'attitude, les comportements, les compétences et les valeurs suivantes :
* Vous justifiez d’une expérience réussie de 10 années minimum dans le même rôle ou rôle similaire en France et à l’étranger dans des établissements hauts de gamme.
* Vous maîtrisez parfaitement le français et l’anglais; une troisième langue est un atout.
* Vous détenez une certification d’une école de majordome reconnue mondialement.
* Vous êtes reconnu(e) pour vos qualités managériales : capacité à former, encadrer et motiver une équipe de majordomes pour atteindre des objectifs de service.
* Vous êtes à l’aise avec les outils de gestion hôtelière et des tendances en matière de digitalisation des services.
* Vous maîtrisez les standards de service ultra-luxe et palace, les bonnes pratiques en termes de protocole et étiquette internationale.
* Vous détenez une connaissance approfondie des accords mets et vins ainsi que les tendances culinaires et les arts de la table.
* Vous maîtrisez les tâches associées aux services de gouvernante, telles que le packing, unpacking, repassage, et prise en charge des effets personnels des clients de manière minut...
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Type: Permanent Location: Cannes, FR-06
Salary / Rate: Not Specified
Posted: 2025-02-13 07:37:09
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Ardurra is currently hiring a Hydrologist/Hydraulic Engineer/Civil Engineer to join our office in Phoenix, Arizona.
Summary
In this role, you will have the opportunity to be a part of the growing Ardurra family in the Drainage Engineering Group.
You will help to evaluate drainage and design a wide variety of exciting drainage projects throughout the Southwest region.
This includes projects supporting drainage for roadway, land development, commercial/industrial developments, parks, and municipal facilities as well as drainage studies/design for public agencies.
Work/life balance is important at Ardurra, once you have been established in this role, there is a potential for a hybrid work schedule mutually agreed upon by your supervisor.
Primary Function
* Provide design and help evaluate a variety of civil engineering projects (both public and private) to support our Drainage Engineering Group.
* Perform drainage calculations using various softwares, and/or equations.
* Frequent collaboration with other engineering departments (transportation, public works, water/wastewater, site civil and surveying).
* Assist with client interface, budgets, and schedules, and executes on time/on budget project delivery.
* Assist with preparing project proposals, scope/fees, and RFP responses.
* Help plan, organize, and supervise design activities for a variety of complex civil engineering projects (e.g., a multi-structure facility requiring frequent interface and collaboration with various consultants and disciplines).
* Prepare drainage design plans, base files, and reference files using Auto CAD software.
* Coordinate with project design team members, clients, contractors, subconsultants, and permit agency representatives regularly.
* Prepare and review technical engineering reports and calculations.
* Facilitate and collaborate during project construction administration by interacting with the construction team/GC, reviewing Shop Drawings/submittals, and addressing RFIs.
Education and Experience Requirements
* 0 to 5 years of related professional experience in Civil Engineering, Water Resources and/or Drainage field.
* Drainage design experience is desired and preferred, including drainage softwares.
* Engineer-in-Train (EIT) certification preferred but not required.
* Professional Engineer (PE) license in AZ will be a plus.
* Education: bachelor’s degree in civil engineering, or related field, from an accredited university or college.
* Proficient working knowledge of applicable software, such as, Microsoft Office, AutoCAD Civil 3D, and Bluebeam.
* Strong communication skills both written and verbal.
* Strong organizational, analytical, and problem-solving skills.
* Highly self-motivated, able to work both independently and in a collaborative environment.
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our...
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Type: Permanent Location: Phoenix, US-AZ
Salary / Rate: Not Specified
Posted: 2025-02-13 07:19:34
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About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Overview
The Upstream Marketing Devices, Senior Manager, is responsible for supporting the development of global pipeline innovations, global upstream marketing strategies incl.
positioning, messaging, branding, and overall strategic planning and product launches, all in collaboration with internal and external stakeholders to drive growth for the Global Aesthetics Devices business.
This candidate will be accountable for collecting, organizing, interpreting, and maximizing external marketing efforts including:
* Early-Stage Upstream Developments
* Consumer & HCP Market Research
* Customer Feedback, Market Insights, & Commercial Strategies
* Scientific Publications & Opportunities
What you will do
* Global Marketing:
+ Drive select pipeline projects by providing customer feedback, market insights, and work cross-functionally to drive product development programs.
Upstream Marketing Devices, Senior Manager will be responsible for defining marketing requirements and validating product inputs in collaboration with HF engineers and training lead, supporting financial forecasts and business cases, development of launch plans, and collecting research and data to support commercial strategy.
* Global Market Research:
+ Partner with Market Analytics and external partners to execute market research initiatives around customer needs and product validation.
Provide technical expertise to assist in their execution.
Stay connected with market needs through frequent interaction with regional marketing partners, customers (In-region visits, attendance at industry meetings, review medical journals, etc.).
* Global Scientific Strategy:
+ Responsible for supporting the development of the scientific publication strategy for responsible products in close partnership with Clinical Affairs, Medical Affairs, Regulatory Affairs and Marketing teams.
* Global Launch Strategy:
+ Responsible for supporting and executing new product launches in close partnership with regional teams and other key stakeholders.
+ Specific responsibilities include leading the development of select marketing strategy, branding, positioning, messaging, and key asset creation, in collaboration with Training Lead and Downstream Team when needed.
Additional responsibilities include close collaboration with Technical Operations and Global Digital Technology Teams to ensur...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-02-12 08:21:37
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About the Company: Merz is a family-owned medical device and pharmaceutical company headquartered in Germany.
Our Global Technical Operations based in WI manufactures, packages and ships several innovative products so that people all over the world can live better, feel better, and look better.
This position is responsible for providing Quality Engineering and Technical Support for operations, sustaining engineering, R&D, and New Product Introduction.
This position would include supporting NCR and CAPA activities.
This position would evaluate the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards and Regulations and recommend where corrections or improvements are needed.
Provide direct support to Quality personnel regarding operation of the department and Quality System.
Provide support to other departmental activities as directed.
Key Responsibilities:
Quality initiatives
• Identify new quality improvement initiatives / projects in accordance with cGMP expectations to improve compliance, quality levels (reducing defects), and improve operational efficiencies.
• Works with manufacturing and other functional groups on manufacturing regulatory compliance issue.
• Support training program by delivering assigned training tasks.
NCR and CAPA
• Support / lead corrective/preventive actions and product non-conformance including capturing data and investigations associated with product deviations, product non-conformances (NCR), CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement and reporting.
• Conduct CAPA and NCR review and approvals.
• Run the Material Review Board (MRB).
Adherence to regulations
• Assist with adherence to all Federal, State and Local Regulations controlling the manufacture medical devices, cosmetics, and pharmaceuticals.
Inspections
• Support with federal, state, and local regulatory officials during regulatory inspections.
Other duties as assigned
• Provides support to Quality Management personnel and perform other duties as assigned.
Education:
• BS in Engineering or equivalent experience.
Required
Experience:
• 2 years in Medical Device or similar experience.
Required
• 2 years in a quality role.
Preferred
• ASQ Certification as a Quality Engineer or equivalent.
Preferred
Knowledge Skills and Abilities:
• Knowledge of regulatory requirements for medical device / pharmaceutical organization.
• Strong technical and general problem-solving skills required; experience with NCR/CAPA processes.
• Computer skills in Microsoft Word, Excel, PowerPoint, Visio and Access; Adobe; and Quality System Management Software.
• Familiar with ISO 13485 Quality System Standards, ISO 14971, FDA Quality System Regulations, GMPs, and/or other international medical device regulations
Benefits:
• Comprehensive Medical, Dental, and Vision plans
• 20 days of Paid Time Off
• 15 paid holidays
• Paid Sick Leave
• Paid Pa...
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Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2025-02-12 08:21:33
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About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Overview
This is a 10-week working assignment with the Global Finance team in Raleigh. There will be real-world working experience in all corporate aspects; from Financial Planning & Analysis (FP&A) to Accounting.
There will be a mix of both project-based and cadence-based activities but regardless, the person can expect to have a direct impact on the business.
The minimum expectations are that this person should have a basic understanding of financial concepts (i.e., Income Statement, Balance Sheet, NPV, IRR) and be comfortable working in a dynamic environment with limited information.
The person must also be detailed-oriented and be able to self-manage competing priorities.
The end goal is that the person will have a comprehensive understanding of how a best-in-class financial organization performs and whether this is a future career for them.
Essential Duties and Responsibilities
* Advise management on the financial implications of business activities.
* Analyze current and past trends for key performance indicators (KPIs) and recommend courses of action to improve performance if necessary.
* Compile monthly reporting packages for Global leadership, including actual vs.
budget/forecast variance analysis, updates, and year-end projections.
* Assist in global presentations and provide support for the budget and forecasting process, including relevant analytics.
* Collaborate with cross-functional teams to enhance systems and processes to increase the robustness of budgeting, forecasting, financial reporting, and procurement.
* Manage special projects for Global Finance as directed by senior management
* Develop and nurture strong relationships with internal stakeholders, particularly in Forecasting and Commercial teams.
* Assist with year-end close activities and reviews, and support external audit requests, as needed
Education (Preferred Majors)
* Required:
* Rising Junior & Rising Senior in a Bachelor’s Degree (in Business Relevant Majors)
Preferred:
* Currently e...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-02-12 08:21:33
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Hybrid
Employee Value Proposition:
At Taiho, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most. This is an exciting opportunity to work for early to late-stage global clinical trials and post-marketing products.
You will contribute to the growth and exciting change happening at Taiho Pharmacovigilance and have greater opportunity to expose/contribute to the company’s portfolio.
With competitive compensation, comprehensive benefits, and a commitment to professional development, Taiho empowers you to thrive personally and professionally.
Join us in our mission to and be a part of the Taiho evolution to have your imprint based on your experience in our rapidly evolving organization.
Position Summary:
* The incumbent will be responsible for global medical surveillance for Taiho, marketed and/or investigational products assigned, including review and analysis of safety data from clinical trials and from post-marketing sources, providing medical expertise to assigned project teams, the identification and investigation of safety signals, management of benefit-risk profile for assigned products and review of aggregate reports.
Responsible for keeping upper management informed of safety issues.
This is a critical role to ensure safety of patients taking Taiho investigational and marketed products.
Performance Objectives:
* Demonstrates knowledge of safety, including any emerging safety concerns and risk/benefit profile for responsible compounds, as well as regulatory guidelines as they pertain to drug safety/pharmacovigilance.
* Responsible for Individual Case Safety Report (ICSR) review.
Ensures completeness and accuracy of safety information in individual case reports through assessment of seriousness, expectedness, and causality, coding, review of narrative summary and providing case comments; provide medical inq...
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Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2025-02-12 07:38:03
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ERM is hiring an Archaeological Field Crew Lead to support survey efforts for projects located in La Paz and Maricopa Counties, AZ.
The Archaeological Field Crew Lead will supervise up to three field archaeologists and be responsible for the day-to-day tracking of field results, safety, and hours worked.
The crew lead communicates daily with the Field Director who consolidates the survey results each day.
This is a full-time (40+ hours a week), fixed-term, field-based role with a duration of 8 weeks, extendable.
RESPONSIBILITIES:
* Safely and effectively lead field teams conducting pedestrian cultural resource inventories.
* Supervise the recording of artifacts, features, and sites using a tablet and GPS
* Identify and record historic built environment, including in-use structures
* Maintain field notes.
* Complete Arizona site forms and Historic in-use Structure forms
* Evaluate project impacts to sites
* Compliance with corporate Health and Safety requirements
* Performing other duties as assigned or required
REQUIRED:
* Bachelor’s degree in Anthropology or related field.
* At least 2 years of experience conducting cultural resource inventories with increasing responsibility
* Ability to work outdoors in variable weather conditions and on varied terrain.
* Working knowledge of archaeological survey protocols.
* Ability to work in the field for extended periods of time.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solutions for our clients.
Our diverse team of world-class experts supports clients across the breadth of their organizations to operationalize sustainability, underpinned by our deep technical expertise in addressing their environmental, health, safety, risk and social issues.
We call this capability our “boots to boardroom” approach for its comprehensive service model that allows ERM to develop strategic and technical solutions that advance objectives on the ground or at the executive level.
Please submit your resume and brief cover letter.
Based on review of these responses, shortlisted candidates will be invited for interviews.
ERM does not accept recruiting agency resumes.
Please do not forward resumes to our jobs alias, ERM employees or any other company location.
ERM is not responsible for any fees related to unsolicited resumes.
ERM is proud to be an Equal Employment Opportunity employer.
We do not discriminate based upon race, religion, color, national origin, gender...
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Type: Permanent Location: Scottsdale, US-AZ
Salary / Rate: Not Specified
Posted: 2025-02-12 07:21:16
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About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Overview
The Research Assistant is utilized in preclinical laboratory work activities related to the preparation of tissue samples, applying ultrasound treatment to tissue samples, and cutting of ex vivo tissue samples for the assessment of the output efficacy of medical devices.
This individual will be involved in planning and executing statistically driven experiments to determine biological effects of ultrasound through bench top synthetic materials and ex vivo tissue studies.
This position requires mechanical aptitude, visual inspection, use of microscopes, documentation and recording of data as well as some quality assurance sampling, testing, and measuring skills using various precise measuring equipment.
What you will do
* Pre-clinical Laboratory Science:
* Collection, tabulation, and analysis of pre-clinical testing data of Ulthera's current and future product lines.
* Utilizes Cryostat or other cutting equipment for tissue evaluation.
* Follows standard operating procedures for the grossing of small specimens, quality control, and quality assurance.
* Creating, expanding, or implementing histological techniques and experimental setups to match the technical needs of Ultherapy-based projects & experiments.
* Develop benchtop metrics for therapy and imaging system performance
Laboratory organization:
* Maintains all pathology laboratory equipment including preventative maintenance (PM) and inform Lab Manager of any equipment problems.
Coordinate with Lab Manager to schedule service.
* Document all PM, repairs, on-site service, and off-site technical support and maintain service records with strong attention to detail in all written communications
Design Controls documentation:
* Writing and revising laboratory work instructions and SOPs
Other duties as assigned:
* Must be safety minded, prepared to read, understand, and follow safety requirements
Minimum Requirements
* Bachelor of Science (B.S.) In Biological Sciences in related field "or"
* 1-2 years Of laboratory experience
* Experience in tissue preparation, cryosectioning, or histological techniques
* Must be action-oriented with demonstrated customer focus and problem-solving skills and a focus on technical excellence, customer responsiveness and creative thinking
Preferred Qualifications:
* Capable of performing various staining methods, including b...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-02-11 07:34:55
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Notre Maison est à la recherche de son/sa Gouvernant(e) des Lieux Publics pour rejoindre notre équipe Housekeeping en CDI.
Vous serez garant(e) de l’entretien, de la propreté et de la bonne tenue des espaces publics.
Nous souhaitons que nos clients bénéficient d’attentions particulières et à ce titre nous avons besoin que vous soyez attentif(ive), prévenant(e) et que vous fassiez en sorte de créer des moments mémorables et individualisés.
MISSIONS
Vos missions seront les suivantes, sans qu’elles soient totalement exhaustives :
* Gestion des Espaces Publics
Superviser le nettoyage et l'entretien des halls, couloirs, salles de réunion, restaurants, bars, et autres espaces communs.
S'assurer que l’ensemble des lieux sont toujours en parfait état de propreté et d'esthétique
* Coordination des Équipes
Encadrer et organiser le travail des équipes en charge du nettoyage des lieux publics.
Élaborer les plannings de travail et répartir les tâches en fonction des besoins de l'hôtel.
* Contrôle de Qualité
Réaliser des inspections régulières et des audits des lieux publics pour s'assurer de la conformité avec les standards de l'hôtel.
Prendre des mesures correctives en cas de non-conformité et former le personnel sur les bonnes pratiques.
* Gestion des Fournitures
Gérer l'approvisionnement des produits de nettoyage et des équipements nécessaires à l'entretien des lieux publics.
Établir des relations avec les fournisseurs et contrôler leur travail.
* Interaction avec les Clients
Être à l’écoute des retours et des demandes des clients concernant la propreté des lieux publics.
Collaborer avec d'autres départements pour garantir une expérience client fluide.
* Rapport et Suivi
Établir des rapports et planning de nettoyage sur l'état des lieux publics et les actions menées.
Proposer des améliorations et des innovations pour optimiser l'entretien des espaces.
QUALIFICATIONS
Pour remplir ce rôle avec succès, vous devez posséder les qualifications, l'attitude, les comportements, les compétences et les valeurs suivantes :
· Une expérience significative réussie en qualité de Gouvernante idéalement au sein d’établissements hôteliers de gamme luxe supérieur et de grande capacité
· La maîtrise du français et de l’anglais
· Sens de l’organisation, rigueur et souci du détail du détail
· Des compétences en leadership pour gérer et motiver efficacement les équipes
· Sens des responsabilités, autonomie et dynamisme
Vous devez répondre aux exigences légales pour travailler en France.
AVANTAGES
En retour, nous vous offrirons un salaire et des avantages sociaux compétitifs et des opportunités d'acquérir de nouvelles compétences et de faire progresser votre carrière.
Vous rejoindrez une équipe passionnée par la création d’expériences mémorables qui font que nos clients se sentent spéciaux, faisant du Carlton Cannes, a ...
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Type: Permanent Location: CANNES, FR-06
Salary / Rate: Not Specified
Posted: 2025-02-11 07:18:31
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SRI Healthcare, LLC, a Subsidiary of NOVO Health Services offers a healthcare service that provides a total and unique opportunity for hospitals to source their Sustainable Reusable Sterile Packs as well as other sustainable healthcare linens such as DermaTherapy®, Isolation Gowns, Sterilization Wrap, and cubicle/privacy curtains.
SRI's products and services help Healthcare providers attain their sustainability goals, improve surgeon and staff satisfaction while ensuring continuity of supply.
SRI operates three regional processing facilities located in Raleigh, NC, Chattanooga, TN, and Mason, OH.
Our state-of-the-art, FDA-regulated service centers provide daily processing, assembly, and delivery of reusable products required for surgery.
SRI is the only “one stop shop” service provider in U.S.
currently serving all healthcare-related end markets with Sterilized Reusable Surgical Solutions.
Job Summary:
We are currently looking for a Soil Sorter, at our Mason Healthcare Laundry facility. We are looking for someone who is confident in decision making, can act quickly, and has excellent communication skills. If you are ready to make a commitment to measurable performance and continuous improvements, then we want to hear from you!
The successful candidate will:
* Able to understand and follow Standard Operating Procedures (SOP’s).
* Open laundry carts and empty hamper bags onto sorting table.
* Sort linen by fabric type.
* Accurately weigh sorted loads and send linen to washers via negative air system as well as operate laundry equipment in either automatic or manual mode.
* Identify instruments, sharp items, hospital-owned linen, and other foreign objects and place them in appropriate receptacles.
* Place empty laundry carts in cart wash and operate washing machinery.
* Deposit all instruments and other washable, returnable objects in wash rack and process through dishwasher or commercial washer, as well as wash all stainless basins.
* Completely clean and disinfect soil sort area at end of shift.
* Mentor / train fellow associates.
* Other duties as assigned.
Job Requirements:
* Able to follow directions and procedures accurately.
* Detail-oriented, organized, and efficient.
* Able to keep accurate records of laundry poundage by hospital.
* Good mechanical aptitude.
* Able to meet productivity standards and work quickly.
* Able to multitask.
* Self-motivated / Self-starter.
* Ability to communicate effectively with supervisors and coworkers.
* Ability to read and understand applicable Standard Operating Procedures
Education:
* High school diploma or GED preferred.
Why work for SRI Healthcare?
SRI Healthcare strives to be the employer of choice in the hospital sterilization industry.
To do that, we provide a safe, positive work environment where our associates experience tremendous growth and related opportunities for ...
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Type: Permanent Location: Mason, US-OH
Salary / Rate: Not Specified
Posted: 2025-02-11 07:16:19
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Position Summary:
Reporting to the Chief People Officer, the Director of Organizational Change Management (OCM) will be responsible for designing, leading, and executing change initiatives that align with the company’s strategic goals.
This role will be instrumental in ensuring associates at all levels embrace and adopt changes to processes, systems, and culture.
The ideal candidate combines strategic vision with a hands-on approach to effectively manage change in a fast-paced manufacturing environment.
Key Responsibilities:
1.
Change Strategy Development:
+ Develop and implement a comprehensive organizational change management framework to support business transformation initiatives.
+ Collaborate with senior leadership to align change management strategies with business goals.
2.
Project Leadership:
+ Lead OCM efforts for high-impact projects, including process optimization, technology implementation, and cultural transformation.
+ Oversee the planning, execution, and measurement of change initiatives.
3.
Stakeholder Engagement:
+ Build strong relationships with key stakeholders across the organization to ensure alignment and support for change efforts.
+ Act as a trusted advisor to senior leaders on change management best practices.
4.
Training and Communication:
+ Design and deliver targeted communication plans to enhance associate awareness and understanding of change initiatives.
+ Collaborate on the development of training programs to equip associates with the skills and knowledge to succeed in a changing environment.
5.
Measurement and Evaluation:
+ Establish metrics to track the effectiveness of change initiatives and associate adoption rates.
+ Use data-driven insights to adjust strategies and drive continuous improvement.
6.
Team Leadership:
+ Work across functional operational teams to develop a network of change “champions” and resources to focus on change.
Mentor and coach leaders to foster professional growth and expertise in OCM methodologies.
Qualifications:
* Education:
+ Bachelor’s degree in Organizational Development, Human Resources, Business Administration, or a related field; Master’s degree preferred.
* Experience:
+ 10+ years of experience in change management, organizational development, or HR leadership roles.
+ Proven track record of implementing successful change initiatives in a manufacturing environment.
+ Hands-on experience with change management tools and methodologies (e.g., Prosci, ADKAR, or similar).
+ Experience working in a global environment with a highly matrixed leadership structure.
* Skills:
+ Strong strategic thinking and problem-solving abilities.
+ Excellent interpersonal and communication skills, with the ability to influence and engage stakeholders at all levels.
...
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Type: Permanent Location: SCOTTSDALE, US-AZ
Salary / Rate: Not Specified
Posted: 2025-02-11 07:10:50
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda. Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci !
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei/delle dipendenti
Siamo alla ricerca di un un/una Analytical Method Validation Senior Analyst che si unisca al nostro Team di Quality Control Compliance.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE:
Il/la Analytical Method Validation Senior Analyst svolge le attività di convalida di metodi analitici su API, intermedi e prodotti finiti all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP, dalle normative ICH e dalle Procedure Operative Standard, riportando direttamente al/alla Quality Control Compliance Lead.
COMPITI E RESPONSABILITA’:
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Supporta il QC Compliance Lead nella ricezione, revisione e organizzazione delle richieste dei clienti per il transfer, la convalida e la verifica di nuovi metodi o adeguamento a nuove metodiche
* Partecipa e fornisce supporto, per quanto di competenza, al Transfer di nuovi Progetti, elaborando una valutazione di fattibilità e successivamente Protocolli e Report della convalida.
* Convalida metodi analitici per API, intermedi di produzione e prodotti finiti in bulk o in confezionamento di mercato.
* Consulta in autonomia linee guida, quali ICH, EurPh e documentazione inerente alla convalida di metodi analitici, ne assicura la corretta applicazione individuando eventuali disallineamenti tra i metodi esistenti e le richieste regolatorie o linee guida.
* Revisiona i dossier nella parte che compete le attività analitiche e del Controllo Quali...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-02-11 07:09:35
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i360 is seeking a Survey Research Analyst to join our small and dynamic Survey Research Team.
We interview over half a million US adults each year across a range of political, consumer behavior, macroeconomic, and societal topics.
Frequently collaborating with a variety of i360 capabilities (data science, analytics, digital, sales), the Survey Research Team deploys rigorous research methodologies and technologies - paired with i360's proprietary nationwide database - to form he basis of data-driven decision making across political and commercial verticals.
i360, where The Data is the Difference, is the leading data and technology provider for those advancing a free and prosperous society through the campaign, nonprofit, and advocacy communities.
i360 is a dynamic workplace sitting at the intersection of public policy, technology, and business, and is seeking team members who are excited about building the next generation of political technology.
What You Will Do
As a Survey Research Analyst, you'll combine strong statistical programming skills, a deep knowledge of survey methodologies, and domain expertise in public opinion research to drive our team's data collection, reporting, analytics, and consultative offerings.
• Utilize proprietary R packages to ingest, transform, and weight survey data
• Utilize internal tools and write SQL code to retrieve sample frames, mode-specific fielding quotas, and survey metadata
• Generate and adapt R code to ingest, transform, and load survey response data into SQL databases and reporting tools
• Generate and adapt R code to weight survey response data
• Run exploratory statistical tests, regressions, and segmentation/clustering analysis on survey data using R
• Analyze survey research data into digestible key findings and client consultative reports
• Write functions and packages in R to automate routine data pipelines and processes
• Collaborate with team members to improve research methodologies and weighting procedures
• Collaborate with team members to improve internal processes and approaches
Who You Are (Basic Qualifications)
• 2+ years of survey research experience
• Proficiency in R, with a record of experience utilizing R to conduct survey research analysis and weighting
• SQL proficiency, with experience writing performant queries to access databases with millions of records
What Will Put You Ahead
• Bachelor's degree in statistics, survey research science, political science, or another related field
• Experience communicating survey research intricacies to lay audiences, internal and external
• Political campaign / public policy experience or demonstrated interest / expertise
• History of using git to maintain and track code
• Previous experience working with the AWS suite, specifically S3, Batch, and Lambda
• Previous experience developing apps in R Shin
At Koch companies, we are entrepreneurs.
This means we openly challenge the status...
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Type: Permanent Location: Arlington, US-VA
Salary / Rate: Not Specified
Posted: 2025-02-11 07:07:15
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Introduction
Chez MédiSolution, nous sommes spécialisés dans le développement de logiciels novateurs destinés à optimiser les opérations et les processus de prise de décision dans le domaine médical.
Notre culture d'entreprise est solidement ancrée dans des valeurs qui stimulent le développement tant sur le plan professionnel que personnel.
Description de poste
Relevant du Vice-Président, Recherche et Développement, le Directeur, Recherche et Développement joue un rôle clé dans la gestion et la coordination des projets stratégiques de l’organisation.
Ce poste hybride combine des compétences techniques et de gestion, requérant un mélange équilibré de vision produit, expertise en gestion de projet, connaissance des processus agiles et sens des affaires.
Le titulaire du poste sera responsable de l'innovation continue, de l'amélioration et de la qualité des produits des solutions existantes ainsi que de l'intégration de nouvelles acquisitions et de solutions tierces dans l'écosystème actuel de l'entreprise.
Il supervisera également le soutien, la coordination et le développements des équipes associées.
En tant que leader autonome et hautement motivé, le Directeur R&D valorise le travail d'équipe et accorde une priorité au succès collectif, à la satisfaction des clients et à l’optimisation des opérations.
Il sera responsable de la gestion de 20 employés répartis dans trois équipes distinctes, opérant dans un environnement bilingue, francophone et anglophone.
Ce poste offre une opportunité unique de contribuer à la stratégie globale de l’entreprise tout en ayant un impact direct sur l’innovation et la performance organisationnelle.
Responsabilités principales
* Leadership stratégique :
+ Inspirer et diriger une équipe diversifiée composée de développeurs et de personnel de soutien dans un environnement de télétravail.
* Gestion de projets :
+ Assurer la planification, l'exécution et la livraison des projets, tout en veillant à respecter les délais, les budgets et les objectifs stratégiques.
* Amélioration continue :
+ Identifier des opportunités d'innovation et de développement pour améliorer les produits et intégrer de nouvelles solutions technologiques.
* Gestion du capital humain:
+ Optimiser le déploiement des ressources humaines au sein des équipes R&D en veillant à aligner les compétences et les talents sur les priorités stratégiques.
+ Assurer une gestion proactive des effectifs, incluant la planification des besoins, le développement des compétences et la mobilisation des collaborateurs pour maximiser leur contribution.
* Collaboration :
+ Travailler efficacement avec des parties prenantes internes et externes pour aligner les objectifs et assurer une communication fluide et transparente.
* Développement de talents :
+ Créer un environnement de travail moti...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: 115000
Posted: 2025-02-09 07:02:18
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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.
Sous la supervision du Directeur Régional Amérique du Nord, soutien opérationnel ITAS, vous serez responsable de fournir un leadership aux opérations IT/OT et d'automatisations courantes du site et de nos installations au port de Trois-Rivières, incluant la gestion du personnel, la stratégie ITAS, la supervision des applications manufacturières, les solutions de contrôle de procédés, l'infrastructure, la gestion des coûts et de la conformité.
Les responsabilités clés comprennent:
* Assurer la gestion du personnel ITAS local de l'usine, incluant la gestion du rendement d'une équipe de 10 professionnels permanents et environ 18-20 ressources contractuelles;
* Garantir la satisfaction de la clientèle grâce à des solutions informatiques, manufacturières et de contrôle de procédé efficaces et économiques;
* Utiliser et promouvoir efficacement les solutions corporatives Alcoa et les services régionaux/globaux pour offrir des solutions harmonisées;
* Représenter les clients de l'usine et leurs besoins auprès de l'organisation ITAS du groupe Alcoa;
* Participer à l'élaboration et à la mise en œuvre de la stratégie ITAS au niveau de l'usine.
Superviser les activités ITAS de l'établissement, y compris la livraison d'applications des équipes corporatives.
Ce que vous apportez au rôle:
* Un baccalauréat en informatique, en génie informatique, en génie de production automatisée ou en génie électrique, avec 6 à 8 ans d'expérience pertinente, de préférence dans un environnement industriel;
* Une expérience pertinente en gestion ou gestion de personnel;
* Maîtrise du français et de l'anglais avancés à des fins de communication avec les équipes corporatives Alcoa et les fournisseurs externes;
* Une connaissance des technologies utilisées dans l'informatique industrielle, l'automation et le contrôle de procédé;
* Des connaissances générales des alumineries ou du domaine manufacturier impliquant des opérations en continu;
* La capacité à répondre aux besoins critiques des clients sur une base de 24/7.
Ce qui est offert:
Pour vous soutenir, vous et votre famille, Alcoa offre un ensemble d'avantages sociaux exceptionnels dès le premier jour d'emploi.
En plus des avantages médicaux, nous proposons des groupes de ressources, des options de plans de retraite et un plan de vacances de premier ordre pour un meilleur équilibre travail-vie personnelle.
Vous bénéficierez également de :
* Une rémunération globale attirante
* Un régime de retraite à cotisation déterminée
* Un programme de reconnaissances (vacances)
* Un programme de rémunération incitative (bonis)
* Une cafétéria, un gym et un service santé...
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Type: Permanent Location: Deschambault, CA-QC
Salary / Rate: Not Specified
Posted: 2025-02-09 07:00:32
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At MTM Transit, it is never just a ride, it's personal.
We understand that our passengers deserve personalized attention and exceptional care and to us, every trip is important.
We have exciting opportunities to join our growing team where your work has a direct impact on the communities we serve.
Our company culture is one of innovation, collaboration, and growth.
If you are passionate, driven, and ready to join a team where your work will directly transform and shape our industry, then we want to talk to you!
What Will Your Job Look Like?
The Manager, Safety and Training is responsible for implementing safety and training programs as defined by the Leadership of Safety Administration and will ensure compliance with State and Federal regulations, as well as corporate, client guidelines and policies.
This position is contingent upon the award of RFP for Montgomery County Access/Paratransit Services.
Location: Montgomery County, PA
What you’ll do:
* Manage a consistent safety culture that incorporates various departments, such as operations, safety and maintenance
* Oversee Corporate Safety Incentives and programs effectively and consistently, including assignment of Safety Points
* Implement and support the company and client’s safety management system (SMS) safety plan and initiatives Manage and monitor the FTA’s drug and alcohol DAMIS reporting requirements
* Monitor and support all location insurance claims activities to ensure effective communication with claimants, to help control claims costs and support claims closure
* Lead and support the local safety committee and SMS Ambassador group
* Oversees the locations worker compensation program to ensure compliance and effectively reduce/eliminate claims
* Deliver proper classroom, behind the wheel and mobility management training in accordance with contractual and company requirements
* Promote employee self-responsibility to achieve all safety goals and training requirements
* Ensures all new hires meet minimum qualifications for each division including, background and DMV checks
* Ensure all safety manuals, programs and policies and practices are current and meet the needs of the operating divisions; updating as appropriate
* Successfully complete all related audits including those conducted by the Company, the Client, internal staff members, and state and federal regulatory agencies
* Review, determine and respond to all vehicular, passenger and employee accidents/incidents, indicating the cause and preventability, identifying potential trends to be addressed in future training efforts
* Provide functional expertise in safety regarding hiring of safety department employees
* Collaborate with local Leadership to deliver comprehensive safety meetings and plans
* Act as the location drug program manager, ensuring compliance of FTA/DOT regulations
What you’ll need:
Experience, Education & Certificat...
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Type: Permanent Location: Philadelphia, US-PA
Salary / Rate: Not Specified
Posted: 2025-02-09 06:56:06
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ERM is hiring a Site Safety Manager to support our client’s solar construction projects in Hinesville and Southeast Georgia.
In this critical role, you will be responsible for communicating with stakeholders, ensuring project timeline, and providing leadership to contractors and vendors associated with the delivery of company projects.
The Site Safety Manager will have broad knowledge of construction safety. This is a full-time (50 hours/week), limited-term role for the duration of 12 months, renewable.
RESPONSIBILITIES:
* Ensure the seamless execution of this project and maximizing impact on the sustainable energy landscape.
* Serve as the liaison between the developer and project stakeholders, ensuring effective communication and project progress.
* Collaborate with cross-functional teams to ensure project milestones are achieved on schedule.
* Address stakeholder inquiries, concerns, and provide regular updates on project status.
* Monitor project performance, budget adherence, and timelines.
* Facilitate transparent communication between the developer and key stakeholders.
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide daily observations of on-site safety practices.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
* Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* Proven experience in renewable energy project management, particularly in solar energy and battery storage.
* 10+ years’ experience in construction safety on power, utility, civil projects; experience in solar or renewable construction projects.
* High School Diploma or equivalent is a must; bachelor’s degree preferred.
* CHST, CIH, OSHT, CSP or CUSP certification is preferred.
* 30 hour OSHA construction safety class or equivalent.
* Comprehensive understanding of the design & construction process.
* Strong leadership and communication skills; can independently project manage with little to no oversight.
* Strong interpersonal skills for building lasting relationships with project stakeholders.
* Exceptional organizational abilities and meticulous attention to detail.
* Ability to excel in a dynamic, fast-paced work environment.
* Familiarity with solar energy and battery storage technologies, industry trends, ...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-02-08 07:55:25
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ERM is hiring a Site Safety Manager to support our client’s solar construction projects in Petersburg, Virginia.
In this critical role, you will be responsible for communicating with stakeholders, ensuring project timeline, and providing leadership to contractors and vendors associated with the delivery of company projects.
The Site Safety Manager will have broad knowledge of construction safety. This is a full-time (50 hours/week), limited-term role for the duration of 10 months, renewable.
RESPONSIBILITIES:
* Ensure the seamless execution of this project and maximizing impact on the sustainable energy landscape.
* Serve as the liaison between the developer and project stakeholders, ensuring effective communication and project progress.
* Collaborate with cross-functional teams to ensure project milestones are achieved on schedule.
* Address stakeholder inquiries, concerns, and provide regular updates on project status.
* Monitor project performance, budget adherence, and timelines.
* Facilitate transparent communication between the developer and key stakeholders.
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Provide daily observations of on-site safety practices.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
* Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* Proven experience in renewable energy project management, particularly in solar energy and battery storage.
* 10+ years’ experience in construction safety on power, utility, civil projects; experience in solar or renewable construction projects.
* High School Diploma or equivalent is a must; bachelor’s degree preferred.
* CHST, CIH, OSHT, CSP or CUSP certification is preferred.
* 30 hour OSHA construction safety class or equivalent.
* Comprehensive understanding of the design & construction process.
* Strong leadership and communication skills; can independently project manage with little to no oversight.
* Strong interpersonal skills for building lasting relationships with project stakeholders.
* Exceptional organizational abilities and meticulous attention to detail.
* Ability to excel in a dynamic, fast-paced work environment.
* Familiarity with solar energy and battery storage technologies, industry trends, and sustaina...
....Read more...
Type: Permanent Location: Richmond, US-VA
Salary / Rate: Not Specified
Posted: 2025-02-08 07:55:24
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Company
Federal Reserve Bank of New York
Federal Reserve Bank of New York
Working at the Federal Reserve Bank of New York positions you at the center of the financial world with a unique perspective on national and international markets and economies.
You will work in an environment with a diverse group of experienced professionals to foster and support the safety, soundness, and vitality of our economic and financial systems.
The Bank believes in work flexibility to balance the demands of work and life while also connecting and collaborating with our colleagues in person.
Employees can expect to be in the office a couple of days per week as needed for meetings and team collaboration and should live within a commutable distance.
What we do:
Economists provide analytic support for the New York Fed's core missions and engage in scholarly research on a broad range of topics.
They contribute to the formulation and implementation of monetary policy, the supervision of financial institutions, the smooth operations of the payments system, the analysis of the impact of policies on consumers and communities and the way in which the financial system supports economic growth using insights from macroeconomics, microeconomics asset pricing and corporate finance.
Areas of research include financial intermediation, monetary policy, household and public policy and financial stability.
As an Economist, you will:
* Conduct scholarly research for publication in high-quality, peer-reviewed academic journals.
* Provide rigorous analysis of policy issues related to the Bank’s mandate using advanced modeling and econometric techniques.
* Contribute analytical work and prepare technical memoranda and briefings for senior bank leaders in support of policy decisions.
* Collaborate with subject matter experts on model development, forecasts, and analysis.
* Engage in outreach to the academic and official sector research communities through participation in seminars and conferences, as well as technical working groups.
* Perform in accord with the Bank’s touchstone behaviors, as described below.
What we are looking for:
* PhD in Economics, Finance, or a related field preferred
Please visit our website to learn more and review the FAQs prior to submitting your application.
Please indicate your area of interest in your cover letter and/or application: Fields of interest:
C – Mathematical and Quantitative Methods
D – Microeconomics
E – Macroeconomics and Monetary Economics
F – International Economics
G – Financial Economics
H – Public Economics
J – Labor and Demographic Economics
L – Industrial Organization
R – Regional, Real Estate, and Transportation Economics
Salary Range: 160,000-217,600-275,200 / year
Touchstone Behaviors set clear expectations for leading with impact at every stage of our careers and aspire to achieve in our continued growth and development.
* Communicate Authentically...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-02-08 07:48:35
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Was macht unseren Bereich aus:
Diagnostics Operations Penzberg ist als Teil der Diagnostics Global Operations der wichtigste Produzent von qualitativ hochwertigen Einsatzstoffen bis hin zu speziellen Kits für die Diagnostik-Division von Roche.
Es erwartet Sie eine vielseitige, interessante und verantwortungsvolle Aufgabe im Bereich Manufacturing.
Hier werden biochemische und chemische Reagenzien und Einsatzstoffe für alle Geschäftsbereiche und vor allem die In-vitro-Diagnostik mehrerer Roche Geschäftseinheiten hergestellt.
Das Team:
Unser Team ist Teil des Themenclusters Festphasenchemie und stellt modifizierte Oligonucleotide, Peptide sowie Konjugate in kleinem Scale unter GMP Bedingungen her.
Mit diesen Produkten unterstützen wir eine Vielzahl diagnostischer Assays im Bereich der PCR, Immundiagnostik und im Sequencing-Umfeld.
Unser Antrieb gilt der Produktion dieser qualitativ hochwertigen Produkte, der Einführung neuer Produkte und der ständigen Verbesserung unserer Produktionsprozesse in einem stark wachsenden Umfeld.
Gestalten Sie unseren Bereich für die Zukunft mit und unterstützen Sie uns mit Ihrem Know-how:
* Als Chemikant oder Chemielaborant in der Peptid- und Oligonucleotidproduktion stellen Sie Peptide und Oligonucleotide in kleinem Scale her.
Die Tätigkeiten finden in einem GMP Bereich statt.
* Neben der Abarbeitung von Produktionsaufträgen unterstützen Sie unsere Gruppe bei folgenden Themen:
* Übernahme neuer Verfahren und Implementierung neuer Produkte
* Mitarbeit bei Erstellung und Überarbeitung von Vorgabedokumenten
* Mitarbeit bei Validierungen und Qualifizierungen
* Geräteverantwortlicher
Für diese verantwortungsvolle und spannende Position suchen wir genau SIE:
* Sie haben eine Ausbildung als Chemikant, Chemielaborant (oder Ähnliches) erfolgreich abgeschlossen oder stehen kurz davor.
* Idealerweise haben Sie bereits theoretische und praktische Erfahrung im Bereich der organischen Chemie und/oder der HPLC Chromatographie.
* Auf Ihre guten Englisch- und sehr guten Deutschkenntnisse sowie guten Kenntnisse gängiger EDV-Anwendungen können wir uns jederzeit verlassen.
* Eine strukturierte, gewissenhafte und selbstständige Arbeitsweise zeichnen Sie aus.
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-02-08 07:15:14
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Die Abteilung
Im Bereich der Abfüllung Elecsys werden mit 46 Mitarbeitern mehr als 65 Millionen Reagenzienflaschen pro Jahr abgefüllt.
Mit diesen immunologischen Testreagenzien werden weltweit von unseren Kunden jährlich über zwei Milliarden Blutuntersuchungen durchgeführt.
Um den hohen Qualitätsstandard unserer GMP-Produktion zu erhalten, benötigen wir Verstärkung!
Wie sieht Ihr Arbeitsalltag als Facharbeiter mit Sonderfunktion (m/w/d) in unserem Team aus?
* Sie unterstützen die termingerechte Bearbeitung der Produktionsaufträge und erkennen, dokumentieren und melden Auffälligkeiten darin
* Sie fungieren als erster Ansprechpartner für das Team bei fachlichen Problemstellungen und übernehmen eine fachliche Personalführung wie z.B.
bei der Einarbeitung von neuen Kollegen/Kolleginnen
* Die Übernahme der Planung, Überwachung und Koordination interner Abläufe gehört zu Ihrem Aufgabengebiet
* Die Abstimmung von Terminplänen mit beteiligen Schnittstellen sowie die Koordination von Reparatur- und Wartungsarbeiten sowie Validierungen bzw.
Qualifizierungen legen wir vertrauensvoll in Ihren Hände
* Sie stellen sicher, dass der Fertigungsprozess zeitnah und GxP-gerecht dokumentiert wird und führen Inventuren des Betriebslagerortes durch
* Sie übernehmen Fertigungskontrollen wie z.B.
der Rohstoffbestände und Verbrauchsmaterialien und führen Analysen wie Füllmengenkontrollen, visuelle Prüfungen von Einsatzstoffen, Zwischen- und/oder Endprodukten durch
Für die tägliche Arbeit bringen Sie die folgenden Voraussetzungen mit:
* Sie haben eine naturwissenschaftliche oder technische Ausbildung abgeschlossen
* Alternativ konnten Sie nach Ihrer Ausbildung mehr als fünf Jahre Berufserfahrung in einem ähnlichen Aufgabengebiet sammeln.
* Sie legen Wert auf eine gute Zusammenarbeit im Team, Feedback und Coaching
* Sie zeichnen sich durch eine selbständige, lösungsorientierte und proaktive Arbeitsweise und einem hohen Maß an Einsatzbereitschaft aus
* In der Zusammenarbeit mit unterschiedlichsten Ansprechpartnern auf verschiedensten Hierarchieebenen setzen Sie Ihre sehr gute Kommunikationsfähigkeit und Ihr sicheres Auftreten ein
Diese Tätigkeiten erfordern di...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-02-08 07:14:03
