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This is an outstanding opportunity for a Principal Consultant, Hydrologist looking for a leadership role in our Water practice. We work throughout all parts of the mining life cycle: your work will help our clients deliver their initial and expansion-phase environmental assessments, resolve challenges in permitting applications, help refine operational decisions and guide major decisions during the closure planning.
You can work from our Boston office, choose to work remotely, or combine in-person and remote work into a hybrid model that best meets your needs. This is a senior leadership role where you will help shape our strategy and share in the accountability for how we grow our business in our region.
Why This Role Matters
ERM is a leading global provider of environmental, health, safety, risk, and social consulting services with offices in over 40 countries.
We have worked with many of the Global Fortune 500 companies delivering innovative solutions for business and selected government clients helping them understand and manage the sustainability challenges that the world is increasingly facing.
Your work will contribute directly to the success of these projects.
What Your Impact Is
As a Principal Consultant with leadership experience, you will be equipped to provide oversight and technical strength and guidance to our Integrated Water Resources team, tapping into expertise from hydrology, hydrogeology, geochemistry, and toxicology, and focusing on integrating these teams to deliver insights and value for our clients through technical analyses and the development of robust mass balance and geochemical models.
This is an opportunity to utilize your established technical expertise leading water-related environmental assessments and permitting for large-scale capital projects with a focus on the Mining Sector.
You will embrace the challenge of being a main point of contact for our clients for water management related scopes.
You will serve as a representative of our company and play a key role building our business and winning new projects.
Your big-picture understanding of our business, and ability to build strong client relationships based on trust and mutual benefit will be critical.
What You'll Bring
* Master's Degree in civil or environmental engineering or related field.
* 8+ years (15+ years preferred) of consulting experience in water resource management, impact assessment and permitting in the Mining Sector.
Specific expertise in hydrometeorology, water balance and/or geochemical modeling, hydraulic and hydrologic modelling and modeling of environmental water quality.
* Solid grasp of the key regulatory drivers within the mining and energy sector, as well as a high degree of technical competence and broad knowledge of impact assessment best practices.
* Well-developed team building and influencing skills; unquestionable integri...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: Not Specified
Posted: 2026-07-02 10:31:48
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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.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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!
Au sein d’un laboratoire de contrôle qualité basé sur site, vous contribuez au maintien du statut qualifié des équipements d’analyse et au bon fonctionnement des activités du laboratoire.
Dans ce rôle, vous intervenez sur la maintenance, la métrologie, la qualification et l’installation d’équipements, tout en garantissant la conformité technique et documentaire dans un environnement pharmaceutique exigeant.
Vos responsabilités :
* Réaliser les opérations de maintenance préventive et curative, de métrologie et de qualification des équipements de laboratoire selon les plans établis, notamment sur des équipements tels que la chromatographie liquide haute performance (HPLC), les balances et les équipements UV.
* Vérifier la conformité technique des interventions réalisées et leur conformité aux Bonnes Pratiques de Fabrication (BPF), puis mettre à jour la documentation et les systèmes associés.
* Participer à l’installation de nouveaux équipements et systèmes de laboratoire, en coordonnant les actions avec les achats, l’informatique, l’Assurance Qualité et les fournisseurs selon les plannings définis.
* Assurer le suivi des entreprises extérieures, négocier les délais d’intervention lorsque nécessaire et établir les contrats avec les prestataires.
* Contribuer à l’amélioration continue du laboratoire et à la mise en place de Corrective and Preventive Actions (CAPA).
Ce dont vous avez besoin pour réussir (qualifications minimales) :
* Bac+3 minimum en chimie analytique ou dans une discipline scientifique connexe.
* Minimum 5 ans d’expérience en laboratoire de contrôle qualité ou en laboratoire analytique.
* Expérience en maintenance préventive et curative, métrologie et qualification d’équipements de laboratoire analytique.
* Maîtrise des Bonnes Pratiques de Fabrication (BPF) et de la gestion documentaire associée.
* Maîtrise des outils bureautiques, notamment Excel et Word.
* Niveau d’anglais permettant de lire et comprendre la documentation technique de laboratoire et les pharmacopée...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 38600
Posted: 2026-07-02 10:02:42
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Cayenta, a division of Harris; is seeking a Vice President of Research & Development who brings a unique blend of business acumen and technical prowess.
This position calls for adept management and project management capabilities, a visionary approach to product development, financial insight, exceptional communication skills, and a deep understanding of the agile process.
As the VP of R&D, you'll be at the forefront of driving continuous innovation.
Your responsibilities include enhancing existing products, seamlessly integrating newly acquired products into our corporate portfolio, and ensuring the smooth incorporation of third-party solutions with Harris' product offerings.
This role is not just about managing processes; it's about leading and inspiring a diverse team of product managers, engineers, architects and more across multiple the US and Canada, working on various products.
Your role as a highly motivated self-starter and team player will be pivotal.
With a focus on both team and client success, as well as the efficiency of business operations, you will guide and motivate a team of 60-70 individuals.
Holding P&L responsibility and forecasting for your team, you'll not just lead but also empower, fostering an environment of innovation and excellence within Cayenta.
This is a chance to make a significant impact in a role that challenges and rewards in equal measure.
This remote role welcomes candidates anywhere in Canada and the US.
Travel is required as needed, approximately 25-50%.
Candidates must hold a current, valid passport and be legally eligible to travel internationally.
This includes either passport based visa exemption or possession of any required travel visas for entry into Canada, the United States, and the Caribbean.
Salary:
130K - 155K
What your impact will be:
* Translating business goals & product requirements into actionable development plans.
* Ensuring that development projects are delivered on time and within budget while prioritizing progress over perfection, particularly on two door decisions.
* Leading a multidisciplinary R&D organization spanning Product Management, Engineering, Cloud, Security & Compliance, and AI Operations.
* Evolving the R&D organization through business transformation, leveraging artificial intelligence to drive innovation, efficiency, and long-term growth.
* Strategic planning, direction and control of product development activities; as well as technical input into the overall business strategy.
* Managing both onsite & offshore development teams.
* Proactively nurturing and building channels of communication across business units to ensure collaboration and achievement of organizational goals.
* Providing technical direction and guidance for all product development needs throughout the organization.
* Communicating industry trends and emerging new technologies that can provide the organization with an advantage.
* Managing strate...
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Type: Permanent Location: Victoria, CA-BC
Salary / Rate: 155000
Posted: 2026-07-02 09:57:40
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Plant Scientist - Field Research Lead
Job Description
You were made to create Better Care for a Better World: exploring uncharted questions, engineering innovative solutions, advancing scientific understanding, and constantly pushing the boundaries of what’s possible.
You want to be part of a performance culture dedicated to solving real-world problems with purpose and precision.
You want to work in an environment that promotes sustainability, inclusion, wellbeing, and career development.
In this role, you’ll help us shape the future and improve lives for billions of people around the world.
It starts with YOU.
Please Note: Position location is within a commuting distance of West Central / Southwest Arizona. K-C Relocation Benefits available.
About You
In one of our professional roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center.
Job responsibilities include:
We are seeking a professional to be our local lead for the agronomic development towards commercialization of a new crop. The position will be responsible for working with Project Management in designing learning goals and executing field trials, managing multiple research collaborations, collecting and analyzing field data, and developing commercial-scale protocols across the agronomic spectrum. This role will collaborate regularly with lead agronomists, scientists, and other cross-functional partners in the organization; lead and perform extensive in-field trial work, field management, data collection & organization.
Principal Accountabilities:
* Lead 1-2 junior scientists to accurately collect, analyze, and document data to drive key genetic, plant architecture, phenotyping, and growth and development information.
* Conceiving, designing, conducting, and reporting research in the field and greenhouse to provide options for agricultural systems that increase production, drive yield and nutrient uptake, and deliver results that provide better understanding of a new crop and design of commercial protocols
* Understands and embodies our mission & vision
Optimistic and innovative; solution-oriented; able to function in the speed and ambiguity of new crop development and commercial protocols
Collaborates well across functions; creates an inspiring and collegial work environment
Values, communicates and interacts with others with high levels of transparency and respect
Mentors and builds talent of team members
Strong focus on workplace safety
* Support agricultural team in completion of various research projects using biology, agriculture, greenhouse, industrial technology, and laboratory skills
* Build and sustain positive relationships with research partners and manage technical aspects of those partnerships across the agronomic spectrum
* Prepare documentation of study results, as well as procedures, paying close attention...
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Type: Permanent Location: Phoenix, US-AZ
Salary / Rate: Not Specified
Posted: 2026-07-02 09:55:30
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OH&S Coordinator
Job Description
Safety Specialist (Manufacturing)
Join the team behind iconic brands like Huggies®, Kleenex®, Cottonelle®, Scott®, Kotex®, Poise®, Depend®, and Kimberly-Clark Professional® [local brands can be input here, be sure to use register sign ®]. At Kimberly-Clark, it’s all here for you—innovation, growth, and the chance to make a real impact.
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.
About You
We are seeking a hands-on Safety Specialist to join our manufacturing site in Binh Duong.
This role is site-focused and execution-driven, with a strong emphasis on contractor safety management, shopfloor risk control, and enforcement of safe work practices.
The position supports the implementation of the Occupational Health & Safety Management System in line with ISO 45001 and internal standards, working closely with Operations, Engineering, Maintenance, and contractors on a daily basis.
Key Responsibilities:
Contractor Safety Management – 35%
· Manage contractor OH&S processes including:
o Contractor pre‑qualification and safety assessment.
o Risk assessment and method statement review.
o Permit‑to‑Work (PTW) issuance and monitoring.
o Conduct safety induction and toolbox talks for contractors.
· Perform inspections and observations of contractor activities on site.
· Monitor contractor safety performance and follow up on violations or incidents.
Expected Outcome: All contractor activities are executed safely with controlled risks and with zero serious incidents and full OH&S compliance.
OH&S Management System Implementation – 30%
· Support the implementation, maintenance, and continuous improvement of the KC performance standard system and ISO 45001 Occupational Health & Safety Management System.
· Assist in:
o Hazard Identification and Risk Assessment (HIRA).
o Job Safety Analysis (JSA).
o Incident investigation and root cause analysis.
· Track OH&S actions, KPIs, audit findings, and corrective actions.
· Participate in internal and external OH&S audits and inspections.
· Support OH&S objectives, action plans, and risk‑based planning.
· Promote worker consultation and participation in OH&S activities.
· Serve as the site Performance Standard Owner for relevant Kimberly‑Clark OH&S Performance Standards, including deployment, effectiveness monitoring, gap closu...
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Type: Permanent Location: Bình Duong, VN-57
Salary / Rate: Not Specified
Posted: 2026-07-02 09:55:23
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Site Manager, Occupational Health & Safety (Neenah, WI - Cold Spring Facility)
Job Description
As an integral part of the Occupational Health & Safety (OH&S) team, the Site Occupational Health & Safety Lead assumes a leadership position, spearheading Kimberly-Clark’s (K-C) commitment to Better Care for a Better World.
This role provides strategic leadership specifically for the occupational health and safety aspects of OH&S and E&S programs and systems, focusing on the company’s moderately complex locations.
The primary objective is to ensure strategic alignment with K-C OH&S and E&S Standards and compliance with local legal requirements.
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.
In this role, you will:
* Legal Compliance Management: Interpret, understand, and continuously monitor/manage changing implications of relevant legal requirements applicable to site activities and operations.
* Complex Risk Assessment: Able to identify and understand complex occupational health and safety hazards, assess associated risks, and develop similar skills and capabilities in others.
* Subject Matter Expertise: Stay skilled in pertinent occupational health and safety subjects, particularly those covered by K-C OH&S and E&S Performance Standards and linked to operation-specific risks.
* Leadership in Incident Management: Participate in occupational health and safety incident investigations and conduct causal analyses while building similar skills and capabilities in others.
* Training Development and Delivery: Develop, deliver, and train others across a broad spectrum of OH&S and E&S topics relevant to moderately complex operations.
* Program Maturity Assessments: Conduct routine checks/self-assessments of the site's occupational health and safety program maturity and performance in moderately complex operations.
* Leadership Skills: Demonstrate relevant leadership skills related to accountability, positive role modeling, and commitment as per the Leadership Curriculum.
* Technological Acumen: Leverage data and digital systems/platforms to improve decision-making and problem-solving.
Address technological advancements, such as automation, as relevant to tasks/duties of the role.
* Project Management and Change Management: Exhibit capabilities in project management and managing change effectively.
* Lean Mindset and Collaboration: Role model a lean mindset, emphasizing continuous improvement and value to the customer.
Embrace a "go to where the work happens" attitude.
Demonst...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2026-07-02 09:54:35
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Your Job
Georgia-Pacific is currently looking for a Process & Product Development Engineer to join the Packaging Research & Development Team.
The selected candidate will support innovation initiatives focused on corrugated products.
This is a dynamic role that works with a cross functional team to develop and commercialize new processes, products and product improvements.
Our Team
The Process & Product Development Engineer will primarily work from Georgia-Pacific Packaging's Innovation Institute® in Norcross, GA (right outside of Atlanta), but should expect to travel up to 30% of the time.
We are looking for candidates who want to join our team and create long term value for the business.
We seek those who have the courage to challenge the status quo, and who want to find fulfillment in what they do.
If your passion is innovation, and you enjoy team collaboration, transformation, and continuous improvement-we'd like to learn more about you!
What You Will Do
* Act as technical lead for development and commercialization of corrugated processes, products, and product improvements.
* Serve as technical SME and project manager for cross functional projects that include commercial teams, suppliers, operations, and customers.
* Define project scope, schedules, budgets and deliverables; track milestones and drive project closure.
* Conduct literature and vendor research, design experiments, develop hypotheses, and propose high impact corrugated research and improvement projects.
* Plan, execute and coordinate corrugated plant and lab trials to validate hypotheses and generate sample products for downstream testing.
* Analyze experimental data using appropriate statistical methods and software to produce statistically sound conclusions and recommendations.
* Expand and maintain internal testing capabilities as new needs arise; document methods and transfer learnings to operations.
* Follow plant safety procedures and support safe execution of trials.
* Perform hands-on work in lab and manufacturing environments during trials; ability to lift up to 50 lbs with or without assistance.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in Mechanical Engineering, Industrial Engineering, Materials Science, Chemical Engineering, Packaging, or a related field.
* 3+ years of professional experience applying analytical thinking and problem-solving in R&D, product development, or manufacturing settings.
* 3+ years' experience working in a production environment (e.g.
converting, paper/packaging plant or R&D role)
* Demonstrated project management experience leading cross-functional projects (planning, resourcing, schedule and risk management).
* Experience with experimental design, hypothesis testing, and literature/vendor research.
* Proficiency analyzing test data and deriving statistically sound conclusions.
* Able to travel up to 30%.
What Will Put You Ahea...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2026-07-02 09:54:30
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Your Job
Georgia-Pacific is currently looking for a Process & Product Development Engineer to join the Packaging Research & Development Team.
The selected candidate will support innovation initiatives focused on corrugated products.
This is a dynamic role that works with a cross functional team to develop and commercialize new processes, products and product improvements.
Our Team
The Process & Product Development Engineer will primarily work from Georgia-Pacific Packaging's Innovation Institute® in Norcross, GA (right outside of Atlanta), but should expect to travel up to 30% of the time.
We are looking for candidates who want to join our team and create long term value for the business.
We seek those who have the courage to challenge the status quo, and who want to find fulfillment in what they do.
If your passion is innovation, and you enjoy team collaboration, transformation, and continuous improvement-we'd like to learn more about you!
What You Will Do
* Act as technical lead for development and commercialization of corrugated processes, products, and product improvements.
* Serve as technical SME and project manager for cross functional projects that include commercial teams, suppliers, operations, and customers.
* Define project scope, schedules, budgets and deliverables; track milestones and drive project closure.
* Conduct literature and vendor research, design experiments, develop hypotheses, and propose high impact corrugated research and improvement projects.
* Plan, execute and coordinate corrugated plant and lab trials to validate hypotheses and generate sample products for downstream testing.
* Analyze experimental data using appropriate statistical methods and software to produce statistically sound conclusions and recommendations.
* Expand and maintain internal testing capabilities as new needs arise; document methods and transfer learnings to operations.
* Follow plant safety procedures and support safe execution of trials.
* Perform hands-on work in lab and manufacturing environments during trials; ability to lift up to 50 lbs with or without assistance.
Who You Are (Basic Qualifications)
* Bachelor's degree or higher in Mechanical Engineering, Industrial Engineering, Materials Science, Chemical Engineering, Packaging, or a related field.
* 3+ years of professional experience applying analytical thinking and problem-solving in R&D, product development, or manufacturing settings.
* 3+ years' experience working in a production environment (e.g.
converting, paper/packaging plant or R&D role)
* Demonstrated project management experience leading cross-functional projects (planning, resourcing, schedule and risk management).
* Experience with experimental design, hypothesis testing, and literature/vendor research.
* Proficiency analyzing test data and deriving statistically sound conclusions.
* Able to travel up to 30%.
What Will Put You Ahea...
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Type: Permanent Location: Norcross, US-GA
Salary / Rate: Not Specified
Posted: 2026-07-02 09:54:29
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At MTM, we are not just colleagues; we are collaborators on a shared mission; communities without barriers.
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 Business Intelligence Developer II will define, develop and deploy complex dashboards, reports, online analytical processing (OLAP), and visualizations to enable metrics-driven decisions.
The Business Intelligence Developer II will be able to understand business activities in multiple business/functional areas and be able to capture requirements, identify required data sources, design and implement complex business intelligence solutions, and contribute to the data strategy, keeping in mind data governance and compliance guidelines.
This position does not support OPT STEM or H-1 Visa Sponsorship
Visa sponsorship is not available for this position.
What you’ll do:
* Develop and execute relational and multidimensional database queries and stored procedures
* Design and develop complex dashboards, reports, OLAP cubes, and visualizations using MTM’s Software Development Lifecycle (SDLC)
* Identify, analyze, and interpret trends or patterns in complex data sets
* Solicit and document requirements for dashboards, reports, OLAP, and visualizations
* Maintain report documentation and data dictionary
* Monitor reporting systems for issues with data and report executions
* Provide daily support for reporting systems, which includes maintenance and enhancements to reporting systems as well as responding to assigned tickets, troubleshooting and final resolution
* Ensure all reports and data transfers comply with MTM and HIPAA security guidelines
* In collaboration with others, develop and maintain databases and Business Intelligence systems necessary for projects and department functions
What you’ll need:
Experience, Education & Certifications:
* High School Diploma or GED
* Bachelor’s degree in computer science or related field from an accredited college or university, or equivalent work experience
* 3 years’ experience with Business Intelligence tools, such as SSRS, Crystal, SSAS, Power BI, Tableau or Qlik
* 3 years’ experience with MS SQL Server or other Relational database systems
* Proficient in Microsoft Office Suite
Skills:
* Skilled in SQL development and troubleshooting, including developing stored procedures
* In-depth understanding of database management systems, OLAP, and Business Intelligence concepts
* Understanding of database design and data modeling
* Ability to understand business processes in order to create solutions that enable the business to effectivel...
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Type: Permanent Location: SAINT LOUIS, US-MO
Salary / Rate: 80000
Posted: 2026-07-02 09:14:06
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
The Opportunity
As an experienced DMPK-PD Project Leader within the Translational DMPK-PD Group, you will be pivotal in ensuring the right drug is delivered at the right dose, safely and efficaciously, to patients.
You will lead nonclinical and translational strategies, collaborating across therapeutic areas to transform scientific hypotheses into groundbreaking clinical candidates.
Your Impact & Responsibilities:
* Strategy & Design: Define and lead drug design and optimisation strategies and compound profiling integrating cutting-edge Drug Metabolism and Pharmacokinetics (DMPK) principles, with a strong focus on target biology validation and translational PK/Pharmacodynamics (PD) concepts.
* Translational Expertise: Serve as the subject matter expert, guiding early discovery teams in developing sophisticated translational strategies for clinical evaluation of target modulation, leveraging deep biochemical and pharmacological knowledge.
* Modelling & Simulation (M&S): Execute fundamental M&S activities, including PKPD, Physiologically-Based Pharmacokinetics (PBPK), Drug-Drug Interaction (DDI), and human dose/regimen prediction, to provide essential support for projects spanning from Lead Optimisation (LO) through early...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 09:03:05
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
This position sits within the Clinical Pharmacology Section in the Quantitative Clinical Pharmacology Department in pRED / Pharmaceutical Sciences, but maintains a company-wide footprint.
The scope of influence transcends individual teams, regularly partnering across major organisational boundaries and cross-entities (e.g., pRED, gRED, PDR) to shape institutional knowledge.
The Opportunity
In this role, you will serve as a senior enterprise leader and expert in Clinical Pharmacology, including Model-Informed Drug Development (MIDD) and Quantitative Medicine, solving high-risk development challenges and embedding advanced computational capabilities to accelerate the R&D pipeline.
Operating on a senior strategic and scientific track, you will hold high accountability for shaping long-term scientific and development strategies and capital allocation for entire disease areas or global functions.
Additionally, you will drive high-stakes corporate due diligence for licensing opportunities, lead complex global health authority negotiations, and act as a strategic mentor across the wider organisation.
* High-Impact Strategic and Scientific Leadership: Formulate and evolve overarching Clinical Pharmacology and MIDD strategies for h...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:43:03
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients in order to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
Within the Clinical Pharmacology Section in the Quantitative Clinical Pharmacology Department, this position operates globally, is deeply embedded within cross-functional matrix project teams and can support multiple of Roche's focus disease areas (CVRM, Immunology, Neuroscience, Oncology and Ophthalmology).
The Opportunity
In this role, you will lead the scientific advancement of clinical programs by serving as the core quantitative and clinical pharmacology lead within cross-functional project teams.
You will drive all aspects of Clinical Pharmacology (CP) across all development phases and strategically apply Model-Informed Drug Development (MIDD) approaches to optimise trial designs, justify dose selections, inform development decisions and mitigate risks across both early and late-stage development.
Your scope will be modality-agnostic, giving you oversight that spans small molecules, large molecules, and novel platforms.
* Strategic & Quantitative Plan Execution: Actively contribute to the development of clinical development strategies, including the design of clinical trials and lead the development, implementation, and execution of the Clinical Pharmacology and MIDD strategies for assigned assets across all d...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:43:00
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
This position is located in Pathology and Applied Safety Science, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
As an engaged Digital Pathologist, you will play a pivotal role in the development, validation, and implementation of pathology investigations and the application of computational pathology approaches for translational safety assessment.
Your primary responsibility will be to propose, conduct, and report computational toxicologic pathology approaches to understand mechanisms of toxicity, leveraging modern tools to maximise scientific insights, drive innovation, and advance our therapeutic pipeline.
You will support the automation of pathology algorithms, workflows, and platforms, remaining accountable for the scientific delivery of pathology data to inform risk assessment across projects ranging from small molecules to complex biological products.
* Core Portfolio Toxicologic Pathology: Provide expert pathology support in preclinical development, aligning toxicity study designs with current science and regulatory guidelin...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:42:28
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
This position is located in Pathology and Applied Safety Science, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
As an engaged Junior Investigative Toxicology Scientist within our Pathology and Applied Safety Science department, you will play a pivotal role in the development, validation, and implementation of nonclinical assays for translational safety assessment.
Your primary responsibility will be to propose, conduct, and report investigative toxicology experiments to understand mechanisms of toxicity and predict toxicity liabilities of early drug series.
Leveraging modern tools to maximise scientific insights and drive innovation, you will support the development of in vitro predictive safety models and remain accountable for the scientific delivery of modern toxicology assays to inform risk assessment across projects ranging from small molecules to complex biological products.
The Junior Investigative Toxicology Scientist is primarily a wet lab-focused position with the majority of time dedicated to hands-on experimental work in the ...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:42:26
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
This position is located in Pathology and Applied Safety Science, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
As an engaged Pathology and Applied Safety Science Hematology & Safety Biomarker Expert, you will play a pivotal role in the development, validation, and implementation of assays for translational safety assessment. Your primary responsibility will be to propose, conduct and report relevant assays to understand mechanisms of toxicity, leveraging modern tools to maximise scientific insights, drive innovation, and advance our therapeutic pipeline in a highly collaborative environment.
* Strategic Biomarker Integration & Translational Safety: Collaborate with experts to develop and execute integrated in vitro and in vivo hematology and safety biomarker strategies, provide subject matter expertise for clinical candidate selection, and deliver comprehensive safety risk assessments for regulatory documentation (e.g., IND/CTA).
* Multi-Disciplinary Laboratory Expertise: Allocate approximately 50% of working time to wet-...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:41:18
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs.
At pRED, we are united by our mission to transform science into medicines.
Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines.
By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers - we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics.
This position is located in Pathology and Applied Safety Science, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity
* In Vivo - in vitro Immunosafety Integration & Mechanistic Strategy: Formulate, implement, and champion integrated immunosafety strategies for portfolio projects, ensuring the scientific validation and execution of predictive immunological biomarkers.
Interrogate and decode in vivo immunosafety findings (e.g., changes in lymphoid architecture, immunogenicity readouts, cytokine profiles, or systemic hypersensitivities) and connect them back to mechanistic context using investigative in vitro tools.
Translate complex immunological findings into unified safety position documentation, presenting definitive impact summaries for target validation, compound profiling, and IND/CTA-enabling packages.
* Advancing In Vitro Cellular Models via Immunological Elements: Proactively apply human immunology elements (e.g., primary immune cells, immune-epithelial co-cultures, inflammatory stimulus circuits) to upgrade the physiolog...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2026-07-02 08:41:16
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The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company’s unwavering commitment to its mission, Safeguarding Global Health®.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry.
With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality.
We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Job Summary
The Consulting Study Director is a trusted advisor and consultative expert for clients and serves as the initial customer contact for validation studies, large projects, and other testing requiring a high degree of consultation.
The position requires the highest level of customer service and broad technical expertise.
The Consulting Study Director assists Sales with quote generation, develops test protocols, ensures testing setup is complete, and facilitates a smooth transition of projects to Production Study Directors.
This enables production teams to focus on testing while delivering an exceptional client experience.
The primary responsibility of this role is to help clients plan and organize projects through specialized expertise, high availability, and a high-touch customer service approach.
Essential Job Functions
Study Consulting
* Demonstrate deep understanding of industry regulations, standards, and guidelines (GMP, GLP, FDA, AAMI, ISO, ASTM, USP, etc.).
* Collaboratively develop test protocols and testing strategies to meet client expectations.
* Partner with Production Study Directors to ensure seamless project handoffs.
* Assist clients and production teams with unexpected or unique testing challenges.
* Coordinate technical consulting activities including summary protocols, written justifications, sample plan justifications, risk assessments, and special projects.
Customer Focus
* Provide exceptional customer service.
* Maintain extensive client phone contact.
* Build strong relationships with clients, Sales, Service Center, and Production Study Directors.
Regulatory Compliance
* Follow applicable regulatory requirements (GMP, GLP, ISO, etc.).
* Stay current on regulatory trends.
* Follow company policies and procedures.
Professional Development
* Complete required training on time.
* Stay current on scientific literature, test methods, and best practices.
* Perform other duties as assigned.
Job Requirements
* Excellent internal and external customer service skills.
* Stron...
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Type: Permanent Location: Taylorsville, US-UT
Salary / Rate: Not Specified
Posted: 2026-07-01 10:11:36
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ERM is hiring a Certified Industrial Hygienist to support our key client’s tech operations in North Chesterfield, VA. As a Certified Industrial Hygienist, you will utilize your broad knowledge to recognize and evaluate potential hazards and recommend controls.
You will provide technical direction and advice to management, developing and using advanced techniques to evaluate work environments. This is a part-time (8-16 hours per week) limited term role with a duration of 3 months, extendable.
Key Responsibilities
* Provide subject matter expertise on how to advance site occupational health programs and ensure compliance with Industrial Hygiene best practices and regulatory requirements.
* Review and approve plans for Industrial Hygiene Monitoring samples and provide oversight and analysis on the results of this monitoring.
* Review and approve requests for new chemicals at the site.
If approved, ensure that site new chemical process is executed per procedures.
* Provide direction and guidance to the Health Services Team regarding Medical Surveillance.
* Use Cority (Safety and Occupational Health software) to update workplace segmentation data, document and complete action items.
* Conduct, review, analyze, and document qualitative and qualitative assessments focused on hazards, including chemical, physical, biological, ergonomic hazards.
* Research and review PPE change and addition requests.
* Review quarterly breathing air testing results and communicate results to manufacturing areas.
* Provide direction and guidance to the site OH team (includes ensuring that OH equipment is properly maintained and providing direction on activities related to Asbestos, Lead and Lasers).
* Assist site IH team with right-sizing processes and procedures for the site.
Required Skills & Experience
* Bachelor’s Degree in Occupational Safety, Engineering or related degree preferred.
* Must be a Certified Industrial Hygienist.
* Demonstrated expertise in industrial hygiene, exposure science, occupational health, and risk management.
* Strong analytical skills with the ability to interpret complex data and develop actionable solutions.
* Experience designing and implementing exposure controls and workplace health programs.
* Proven leadership in multi-work environments and perhaps geographical legislative requirements, with the ability to influence across functions.
* Excellent communication, negotiation, and stakeholder‑engagement capabilities.
* Knowledge of ISO 45001, corporate management systems, and regulatory frameworks.
* Ability to mentor others, lead projects, and drive continuous improvement.
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 ...
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Type: Contract Location: Richmond, US-VA
Salary / Rate: Not Specified
Posted: 2026-07-01 10:11:02
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At ERM, you’ll partner with global organizations to elevate occupational health and safety performance, reduce risk, and drive meaningful, lasting impact across complex environments.
This role is ideal for a safety professional ready to apply deep technical expertise while growing alongside one of the world’s leading sustainability consultancies.
Why This Role Matters?
Health and safety excellence is foundational to resilient, responsible organizations.
As a Consultant, Health & Safety in our Cleveland office, you’ll help clients protect people, strengthen compliance, and build proactive safety cultures across industrial, high‑tech, pharmaceutical, energy, and chemical environments.
Your work will directly support safer operations—locally and globally—while advancing ERM’s mission to create a more sustainable future.
What Your Impact Is:
* Deliver high‑quality health and safety compliance support for complex client projects across North America and beyond
* Identify, assess, and mitigate workplace health and safety risks through rigorous technical analysis
* Support innovative EHS programs that move clients beyond compliance toward best‑in‑class performance
* Collaborate with ERM’s national and global technical experts, contributing to knowledge‑sharing and continuous improvement
* Build trusted client relationships by consistently delivering projects on time, on budget, and to scope
What You’ll Bring:
Required
* Bachelor’s degree in Safety, Occupational Health, Engineering, or a related scientific discipline.
* 3+ years of EHS experience supporting day-to-day operations in a warehouse, manufacturing, production, logistics, or other operational environment.
* Strong written and verbal communication skills, with the ability to translate technical findings clearly.
* Ability to work independently while contributing effectively to multidisciplinary teams.
* Strong organization skills and ability to track actions, documentation, and follow-through.
* Ability to spend significant time on the floor in an active operations environment.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* This position is not eligible for immigration sponsorship.
Preferred
* Experience supporting warehouse operation, light industrial, new site openings, temporary labor environments and contractor safety programs.
* Familiarity with ergonomics in repetitive manual tasks, machine guarding, lockout/tagout concepts.
* OSHA 30 or similar EHS certification/training.
* Ability to thrive in fast‑paced, innovative client environments while producing high‑quality deliverables.
* Abil...
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Type: Permanent Location: Cleveland, US-OH
Salary / Rate: Not Specified
Posted: 2026-07-01 10:11:01
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Shape and Lead the Future of Health & Safety.
At ERM, you won’t just help organizations meet compliance—you’ll help them transform how they protect their people.
As part of our global team, you’ll influence safety performance across diverse industries, strengthen risk‑reduction strategies, and play a hands-on role in building safer, smarter, and more sustainable workplaces.
This role is ideal for experienced professionals ready to expand their impact, grow into senior consulting pathways, and work alongside industry-leading experts on high‑visibility projects worldwide.
Why This Role Matters
Safety is more than a program—it’s a critical driver of operational excellence and organizational resilience.
As a Consultant, Health and Safety, you’ll help clients proactively address their most significant EHS risks, enhance safety culture, and achieve regulatory compliance with confidence.
You’ll support global clients through complex technical challenges while gaining exposure to mentorship, cross-functional projects, and long-term career growth within ERM’s rapidly expanding Safety Services team.
This is a key stepping stone toward senior consultant and leadership roles across our global practice.
What Your Impact Is
* Drive the development and implementation of Safety Management Systems that set industry benchmarks.
* Lead risk assessments and incident investigations that uncover root causes and prevent future harm.
* Shape safety and industrial hygiene programs that safeguard worker health through rigorous exposure assessments.
* Partner with global ERM experts to deliver innovative, outcome-focused solutions for complex technical and regulatory challenges.
* Expand ERM’s Safety Services portfolio by building lasting client relationships and identifying new business opportunities.
What You’ll Bring
Required
* BS/MS degree in a related field or equivalent experience (6+ years in lieu of education).
* 2–3 years of relevant experience in safety, risk management, and EHS compliance. Additional experience with environmental compliance is a plus but not required.
* Hands-on experience with running safety programs.
* Strong communication skills and ability to work independently and collaboratively.
* Willingness to travel (up to 80% during peak project periods) domestically and internationally.
* This position is not eligible for immigration sponsorship.
Preferred
* Certifications such as CSP or CIH (or aspirations to obtain certification) are a plus, and ERM supports professional development to help you achieve them.
* Consulting experience with proven ability to develop client relationships and deliver high-impact solutions.
* Expertise in delivering corporate H&S strategies, including safety culture, leadership, and serious injury/fatality risk reduction.
Key Responsibilities
* Implement Safety Management Sy...
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2026-07-01 10:10:09
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labVoyant Beauty believes our people are more than just employees; they’re the driving force behind everything we achieve.
Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual’s contribution is valued and celebrated.
We invest in their growth, providing opportunities for development and advancement within our dynamic team.
Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products.
We work with various brands, retailers, antechniciand businesses to create customer formulations and products tailored to their needs.
This can include skincare, haircare, bath and body products, fragrances, and more.
Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life.
Safety is a core value at Voyant Beauty.
We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel.
If you’re seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you.
Come join us and be a part of our journey.
A Brief Overview
The R&D Technician is responsible for handling laboratory raw material supplies, including lifting materials weighing up to 45-50 pounds.
This role provides general support in the lab, maintaining accurate records, and ensuring proper transfer of information.
The ideal candidate will be detail-oriented, organized, and capable of working efficiently in a dynamic environment.
What you will do
* Responsible for laboratory raw material supply with ability to handle 45-50 pounds.
* Assist in general laboratory support functions.
* Record, maintain, and transfer technical information.
* Adhering to safety standards and regulatory guidelines in the lab or production area.
* Duties may vary slightly by location.
Education Qualifications
* High School Diploma (Required)
Experience Qualifications
* less than 1 year Prior experience in a laboratory setting preferred (Preferred)
Skills and Abilities
* Ability to work with minimum supervision (Low proficiency)
* Computer skills to include working knowledge of Microsoft Word, Excel, and Outlook (Low proficiency)
* Understanding of basic laboratory operations, including safety protocols and proper handling of chemicals and materials.
(Low proficiency)
* Knowledge of proper storage, labeling, and handling techniques for raw materials, including weight limits and material safety data sheets (MSDS).
(Low proficiency)
* Familiarity with recording, maintaining, and transferring technical information accurately in laboratory environments, using both manual and digital systems.
(Low proficiency)
* Ability to prioritize tasks effectively in a fast-paced laboratory setting while maintaining high standards of...
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Type: Permanent Location: Chatsworth, US-CA
Salary / Rate: 27.115
Posted: 2026-07-01 08:56:31
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Southwest Power Pool (SPP) is about more than power.
We’re about the power of relationships.
Our employees have the opportunity to work together to ensure electricity is delivered reliably and affordably to the millions of people living in our service territory.
We have been voted one of Arkansas’ Best Places to work by Arkansas Business and we are looking for a member of our team who is passionate about our mission to keep the lights on!
We have a core ideology here at SPP that we stand by: Do the right thing, for the right reason, in the right way.
We believe in supporting our employees through a fantastic benefits package:
* Competitive and transparent pay with bonus opportunities
* Excellent insurance package including three great medical plans to choose from, employer-paid short-term disability, long-term disability, and life insurance
* Relocation bonus (if applicable)
* Hybrid working environment for positions that are eligible
* Fantastic contributions to your retirement through a 401(k) savings plan with employer-match benefits and a pension (defined benefit plan) fully funded by SPP
PLEASE NOTE: SPP is not able to sponsor employment visas or student-work authorizations (STEM OPT) for this position.
Please ensure you are eligible to work in the U.S.
without sponsorship prior to applying.
COMPENSATION INFORMATION
The salary range(s) represents our good faith estimate for the role at this time.
While we strive to provide competitive and transparent compensation, there may be circumstances where an offer is above or outside of the listed range.
We are open to discussing salary expectations with qualified candidates considering factors such as the candidate's qualifications, skills, competencies, experience and geographic location will all be considered during the hiring process.
* Lead Market Monitor Pay Range: $109,500.00 -$142,250.00
* Senior Market Monitor & II Pay Range: $95,200.00 - $123,700.00
* Market Monitor II Pay Range: $76,000.00 - $96,900.00
Join Our Team at SPP as a Market Monitor!
The SPP Market Monitoring Unit (MMU) plays a crucial role in maintaining the integrity and reliability of SPP's wholesale electricity market across 14 states in the central and western U.S.
As part of our team, you’ll be integral in ensuring that market activities are fair, transparent, and compliant with regulatory requirements.
The MMU operates independently from SPP and its stakeholders to help ensure a high degree of objectivity in its evaluation of and reporting on market operations and potential issues. The MMU has a unique role where it provides both an independent and objective opinion on market design, operation, and related issues, as well as recommendations to improve market efficiency and equity across all participants. These opinions extend to existing and proposed rule changes and/or new policies that impact SPP’s market design or reliability. The surveillance team investig...
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Type: Permanent Location: Little Rock, US-AR
Salary / Rate: Not Specified
Posted: 2026-07-01 08:48:02
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At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Praktikum im Sustainability Bereich bei RDA Ludwigsburg
Wir sind das Sustainability Netzwerk am Roche Standort Ludwigsburg und treiben mit viel Engagement und Leidenschaft die Themen rund um Nachhaltigkeit voran.
Bestehend aus den Bereichen SHE (Safety, Health, Environment), Mobility und Energiemanagement unterstützen und beraten wir bei der Planung und Umsetzung von Nachhaltigkeitsstandards und regulatorischen Anforderungen.
Bei uns erhältst du Einblicke in das tägliche Geschäft des Sustainability Teams eines dynamischen Entwicklungs- und Produktionsstandortes.
Während dem Praktikum kannst du eigene Ideen einbringen und operative Aufgaben und Projekte im Bereich Nachhaltigkeit mitgestalten.
Dabei kannst du deine im Studium erlernten Fähigkeiten in der Praxis anwenden und wertvolle Berufserfahrung sammeln.
Nutze deine Chance und werde Teil unseres Teams!
Während deines Praktikums wirst du die Möglichkeiten haben mit deinen Beiträgen an folgenden Aufgaben mitzuwirken:
* Implementierung technischer Lösungen & KI: Eigenständige Identifikation, Evaluierung und Einführung von neuen Software- oder KI-Lösungen zur Optimierung und Automatisierung von Nachhaltigkeitsprozessen (z.
B.
KI-gestützte Datenanalysen, automatisierte Workflows oder digitale Tools zur Verbrauchsüberwachung).
* Energie- und Umweltmanagement: Datengestützte Unterstützung bei Projekten zum Energie- und Umweltmanagement (z.
B.
Ermittlung und Durchführung von Energie- und Abfalleinsparprojekten).
* Operative Unterstützung: Mithilfe bei Risk Assessments und Durchführung von Unfallanalysen sowie Unterstützung bei Compliance- und Governance-Themen.
* Kennzahlen & Analytics: Unterstützung bei der Erfassung, Berechnung und modernen, ggf.
automatisierten Darstellung von Kennzahlen und KPIs.
* Schulungen & Training: Mithilfe bei der Organisation und Durchführung von Schulungen und Unterweisungen.
* Kommunikation & Awareness: Mitgestaltung und Optimierung des Intranet-Auftritts und der standortweiten Kommunikation von Nachhaltigkeitsthemen zur Erhöhung des Bewusstseins der Mitarbeitenden.
Schwerpunkttätigkeiten des Praktikums werden im Zusammenhang mit Projektaufkommen und Interessen des/der Kandidaten/in festgelegt.
* Ausbildung: Laufendes Bachelor- oder Masterstudium eines Studienganges im Bereich Umweltinformatik, Wirtschaftsinformatik oder eines Ingenieurstudienganges (Wirtschaftsingenieurwesen, Maschinenbau, Umweltingenieurwesen etc.) mit einem Schwerpu...
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Type: Permanent Location: Ludwigsburg, DE-BW
Salary / Rate: Not Specified
Posted: 2026-07-01 08:36:36
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Your Job
Join Georgia-Pacific at the Neenah Technical Center as a Senior Research Scientist, Papermaking focused on advancing papermaking technologies for tissue-based consumer products! You will lead early-stage research and pilot trials, design experiments, evaluate results, and translate successful concepts into commercially viable solutions that improve product performance and manufacturing processes.
Our Team
You'll be part of a multidisciplinary R&D group within GP Consumer Products that collaborates closely with product development, operations, and engineering teams.
The team partners with external organizations, universities, suppliers, and OEMs, to scout and adopt breakthrough technologies and drive measurable improvements at scale.
What You Will Do
* Identify and lead research projects involving papermaking technologies for our manufacturing processes of tissue-based consumer products, leading to new or improved products or machine performance.
* Design, develop, prototype, and test cutting-edge papermaking components, equipment, and machinery while working with cross-functional teams to drive innovation.
* Act as a Subject Matter Expert in tissuemaking technology.
Participate in troubleshooting, training, and knowledge transfer to provide direction to team members.
* Effectively work with various internal capabilities, including Operations, Engineering, and Product Development to drive transformation within the company and scale experiments from pilot to commercial feasibility.
* Collaborate with external partners, including academic partnerships, industry consortiums, and supplier/OEMs to identify and screen new technologies as well as stay up-to-date on industry advancements.
* Use economic thinking to determine viability, use the scientific method to evaluate, use statistical methods to analyze data, and use written and verbal techniques to communicate and document the results and next steps.
* Support the organization through developing Intellectual Property that includes competitive intelligence, invention disclosures, patent applications and maintaining trade secrets.
* Improve current test methods or develop new test methods for characterizing and evaluating various papermaking technologies.
Be creative and think beyond the obvious.
Who You Are (Basic Qualifications)
* Bachelor's degree in papermaking, chemical engineering, or a related field.
* Five (5) or more years of relevant experience in the paper industry.
* Demonstrated experience in an R&D environment leading research projects and scaling successful concepts toward commercialization.
* Proficient with experimental design and statistical analysis methods (e.g., DOE, ANOVA, regression) and comfortable documenting and communicating technical results.
* Willing and able to travel up to 25%.
What Will Put You Ahead
* Advanced degree (Master's or PhD) in papermaking, chemical engineering, or a r...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2026-06-30 10:21:21
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Greif is a global leader in performance packaging located in 40 countries.
The company delivers trusted, innovative, and tailored solutions that support some of the world's most in demand and fastest-growing industries.
With a commitment to legendary customer service, operational excellence, and global sustainability, Greif packages life's essentials - and creates lasting value for its colleagues, customers, and other stakeholders.
Learn more about the company's Customized Polymer, Sustainable Fiber, Durable Metal, and Integrated Solutions at www.greif.com and follow Greif on Instagram and LinkedIn.
OUR VISION:
To Be the Advantage That Helps Our Customers Win.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034605 Account Manager, Outside Sales (Open)
Job Description:
The Account Manager is responsible for managing a defined portfolio of customer accounts within Greif’s Tube and Core division and serving as the primary point of contact for day-to-day account management.
This role is focused on building strong customer relationships, supporting account growth, identifying opportunities to improve value and profitability, and ensuring a high level of service through effective coordination with internal teams.
Local Presence Matters: The selected candidate must reside near Dalton, GA and surrounding area.
This ensures you can effectively manage accounts and travel within the assigned territories.
Company car provided.
Key Responsibilities
* Own a defined territory; deliver revenue, volume, and margin targets through disciplined opportunity management.
* Develop and execute account plans for top accounts; align stakeholders and set quarterly growth actions.
* Qualify, propose, and negotiate customer agreements; leverage pricing frameworks and value selling to expand margin.
* Forecast monthly and quarterly results with high accuracy; manage mix and capacity constraints proactively.
* Coordinate plant/site visits, product trials, and technical consultations to accelerate deal cycles.
* Collaborate with Inside Sales, Customer Service, and Supply Chain to drive flawless execution.
* Use CRM to manage pipeline health, risk, and coverage; ensure data completeness and timeliness.
* Monitor and address service or quality issues; escalate and drive corrective actions with cross-functional teams.
* Map buying centers and expand relationships beyond purchasing into operations and leadership.
* Champion safety and compliance in all customer engagements and internal activities.
* Performs other duties as assigned.
Education & Experience
* Typically possesses a Bachelor's degree (or equivalent)
* Typically requires 4-8 years of experience.
Knowledge & Skills
* Proficiency with CRM for pipeline, forecasting, and account management.
* Strong commercial acumen with demonstrated pricing and negotiation capa...
....Read more...
Type: Permanent Location: Delaware, US-OH
Salary / Rate: Not Specified
Posted: 2026-06-30 10:16:47
