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Analytical Chemist
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Type: Permanent Location: Ridgefield, US-NJ
Salary / Rate: 85000
Posted: 2026-06-02 07:54:08
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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
Deine Abteilung
In der Abteilung Manufacturing, Science & Technology (MSAT) stellen wir die technische und strategische Kompetenz für die Bereitstellung der klinischen Pipeline, die Einführung und die Unterstützung der kommerziellen Produktion sicher.
Unser technischer Support, Engineering, Systeme, Daten und Dokumente sind essentiell für die Herstellung, Bewertung und Freigabe hochwertiger Produkte.
MSAT Process Science ist u.a.
am Troubleshooting von pharmazeutischen Proteinwirkstoffen, bei der Bewertung von Einsatzstoffen sowie an lokalen und globalen Gremien beteiligt.
Dein Team
Wir sind ein souveränes Team aus Biotechnologie-Ingenieuren, Labortechnikern, Labormitarbeitern und Managern im Bereich Aufreinigung (Downstream-Processing).
Modernes Aufreinigungsequipment, innovative Analysemethoden und diverse Dokumentations- und Auswerte-Tools stehen uns zur Verfügung.
Selbständiges und eigenverantwortliches Arbeiten sind für unsere Aufgaben essentiell, doch der Teamzusammenhalt und der Spaß an der Arbeit sind für uns genauso wichtig.
Ein offener und ehrlicher Umgang miteinander, geprägt durch Respekt und Wertschätzung, ist uns besonders wichtig.
Deine Aufgaben
Unterstützung unserer Projektarbeiten im Bereich:
* Fehlersuche, -analyse und -behebung im Umfeld des Downstream Processings
* Planung, Bearbeitung und Auswertung von Laborversuchen zur Optimierung, Skalierung und Validierung von Aufreinigungsverfahren (Downstream Processing)
* Anwendung diverser chromatographischer (ÄKTA, HPLC) und spektroskopischer Verfahren sowie Filtration im Labormaßstab
Dein Profil
* Du aktuell für ein naturwissenschaftliches oder ingenieurwissenschaftliches Studium immatrikuliert bist
* Du das Thema Proteinaufreinigung nicht nur aus der Theorie kennst
* Dir auch die analytischen Anwendungen der Chromatographie und Spektroskopie vertraut sind
* Du sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift hast
* Selbstständiges und eigenverantwortliches Planen und Arbeiten für dich selbstverständlich sind
* Du ein wahrer Teamplayer bist, ein hohes Durchsetzungsvermögen besitzt und auch in Belastungssituationen immer den Überblick behältst und den Spaß an der Arbeit nicht vergisst
* Erfahrung mit statistischen Methoden (z.B.
DoE, multivariate Datenauswertung) und dem systematischen Umgang mit großen Datenmengen ist von Vorteil
Deine Vorteile
* Flexible Zeiteinteilung
* 2268 € Vergütung im Monat fü...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-06-02 07:51:46
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DESCRIPTION
Michael Baker International is currently seeking a Project Accountant to provide full life-cycle project support to our Project Managers.
This position is Remote but should be based in the Eastern or Central Time-Zone.
Other major responsibility includes gaining an understanding of and providing project analysis as well as assisting with requests for information as needed.
RESPONSIBILITIES
* Perform data analytics at a project level to monitor project performance and provide high level comments regarding the financial status of projects.
Utilizing these analytics, identify potential project performance issues and notify Regional Project Accounting Manager.
* Coordinate completion of project setups with the Project Manager to ensure that the project is in accordance with the terms of the contract and MBI Approval Authority Policy.
Responsible for reviewing the contract and understanding the contract terms regarding project type, scope of work and invoicing terms.
* Responsible for monitoring and addressing project maintenance within Oracle and budget/funding updates as needed.
* Responsible for monthly reporting to the Regional Project Accounting Manager including detailed comments on project status that meet exception reporting and projects marked as significant for unbilled and unearned revenue.
* Actively participate in project performance reviews and provide financial commentary on projects where applicable.
* Provide support and assist with requests from the Project Managers and/or Department Managers.
These requests may include financial information for proposals, price estimates throughout the life cycle of the project, annual budget process support, audit requests (external and/or client) or special projects as requested by the Business Management Team.
* Monitoring outstanding receivables and supporting project managers with collections.
* Coordinate with the Project Manager to identify any invoicing issues and assist the Project Manager with developing a corrective action plan to rectify any conditions which are hindering timely payment.
* Work with the Project Managers to ensure project revenue is recognized in accordance with company policies.
PROFESSIONAL REQUIREMENTS
* Bachelor’s degree preferred in Accounting or Finance.
* 0-3 years of experience within accounting, finance, or similar role.
* Must have effective oral and written communication skills including strong interpersonal skills to effectively work with Project Managers and Department Managers.
* Required intermediate knowledge of Microsoft Excel.
* Preferred experience with Oracle Project Accounting Modules-Beginner Level (or equivalent ERP system).
* To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
COMPENSATI...
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Type: Permanent Location: Pittsburgh, US-PA
Salary / Rate: Not Specified
Posted: 2026-06-02 07:48:21
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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
Unser Team
Unser Team ist ein integraler Teil der globalen Sites Networks von Roche und betreut die großen Produktionsstandorte Mannheim und Penzberg (München).
Wir gestalten die strategische Ausrichtung und organisatorische Entwicklung dieser Standorte.
Mit einer umfangreichen strategischen Agenda treiben wir zahlreiche Initiativen und Projekte im Site Management voran, immer mit dem Ziel, messbaren Fortschritt und Verbesserung zu erreichen.
In unserem aufgeschlossenen und ambitionierten Team wirst du in Zusammenarbeit mit lokalen, globalen und Konzernfunktionen standortübergreifend innovative Ideen und Lösungen entwickeln sowie umsetzen.
Deine Rolle
In dieser Schlüsselfunktion bringst du deine eigenen Ideen direkt ein.
Durch die enge 1:1 Zusammenarbeit mit dem/der Chief of Staff nimmst du eine aktive Sparringspartner-Rolle ein, um zentrale Managementthemen des Sites Networks erfolgreich mitzugestalten.
Als Teil des Stabs der Geschäftsführung unterstützen wir zudem bei allen relevanten Gremien (u.a.
Betriebsrat, Wirtschaftsausschuss) und Terminen von Roche Diagnostics.
Deine Aufgaben in unserem Team setzen sich wie folgt zusammen:
* Konzeption und Umsetzung eines Dashboards von Business-relevanten KPIs zur Performancesteuerung im Site Management.
Dabei gehört die kontinuierliche Reflektion von Optimierungspotenzialen zu deinen Aufgaben
* Durchführung von verschiedenen Analysen und Auswertungen laufender Initiativen im Site Management, wie beispielsweise Marktanalysen und Stakeholderanalysen
* Analyse der Voraussetzungen und Ausarbeitung eines ganzheitlichen und zielgerichteten Ansatzes für ein unternehmerisches Ökosystem in der Pharmabranche in Deutschland.
Hierbei arbeitest du eng mit den Fachbereichen zusammen
* Eigenständige, konzeptionelle Vor- und Nachbereitung von Workshops, Meetings, Reportings und Entscheidungsvorlagen für das Management und Gremiensitzungen
* Mitwirkung bei der Koordination, Konzeption und Umsetzung von strategischen Projekten in direkter Abstimmung mit dem/der Chief of Staff
* Aktive Unterstützung des Managements bei der Weiterentwicklung von Business, Strategie und Innovation
Dein Profil
* Ein Master-Studium der Betriebswirtschaftslehre, Wirtschaftswissenschaften oder einem vergleichbaren Studiengang
* Relevante praktische Erfahrung durch mindestens zwei Praktika in der Unternehmensberatung, in strategischen Konzernrollen, einem Start-up oder ähnlichen Bereichen, in denen analytis...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-06-02 07:47:46
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ERM is hiring a Lead Biological Environmental Inspector to oversee environmental compliance during the construction phase of our client’s transmission and distribution project in northern Nevada and southern Idaho.
This is a full-time (60-72 hours per week) limited-term role for a duration of 18 months, with the possibility of extension.
RESPONSIBILITIES:
* Preparing and conducting environmental training for construction personnel.
* Conducting field inspections, conducting environmental inspection of construction activities, and field survey work as directed.
* verifying that the limits of authorized construction work areas and locations of access roads are properly marked before clearing;
* Interacting with and serving as a point of contact with agency officials, regulatory agency staff, landowners, contractors, clients and other project members and conducting required agency notifications.
* Reviewing and implementing project documents and providing direction, support and critical judgment on environmental compliance issues.
* Providing technical leadership, support and direction to field staff. This includes the coordination of daily Environmental Inspector and Resource Monitor schedules and conducting morning construction meetings.
* Critically assessing environmental conditions in the field to evaluate potential environmental impacts from construction.
* Evaluating potential issues and concerns ahead of construction activities.
* Overseeing the proper implementation of mitigation measures.
* Conducting environmental sampling (hydrostatic test water, soil, etc.).
* Overseeing and verifying flagging and signage of waterbody and wetland boundaries, cultural and biological resources exclusion zones, refueling zones, or areas with special requirements within the construction work area.
* Inspecting and documenting compliance with a project's environmental requirements by preparing daily written inspection reports that provide up-to-date and consistent written and photo documentation of activities observed in the field.
* identifying, documenting, and overseeing corrective actions as needed to bring an activity back into compliance.
* identifying erosion/sediment control and soil stabilization needs.
* Participating in various construction meetings.
* Preparing documentation to support requests for variances from environmental permits.
* Evaluating restoration activities and conducting compaction testing as required.
* Compliance with ERM’s rigorous safety program.
* Performing additional tasks as assigned or required.
REQUIREMENTS:
The role of a Lead Biological Environmental Inspector requires meticulous oversight by highly skilled individuals stationed in the field throughout construction to ensure compliance with federal, state and local environmental regulations.
Qualifications of individuals to be considered will include:
*...
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Type: Permanent Location: Elko, US-NV
Salary / Rate: Not Specified
Posted: 2026-06-02 07:35:23
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ERM is hiring a motivated hands-on Senior Environmental, Health and Safety (EHS) Consultant to join our growing Performance & Assurance technical team in Sunnyvale, California. This position is expected to involve working a minimum of 3 days on-site. This is a fixed-term, full-time role (40 hours a week) for a duration of 4 months, renewable.
The ideal candidate will have experience developing and supporting implementation of Cal/OSHA requirements, Standard Operating Procedures, Job Hazard Analysis/ Risk Assessments, Emergency Response Plans, Behavioral Safety Programs and Contractor Safety Management. Candidates should also have familiarity with research laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* Oversee and direct team members to effectively manage tasks for on-time delivery and quality of their deliverables.
* Perform compliance audits to assess client compliance with applicable health and safety or environmental regulatory requirements, client standards, or management systems.
* Support our clients’ desire to improve safety performance by providing training, field coaching, and targeted EHS assessments.
* Identify follow-up corrective actions to close audit findings.
* Provide technical assistance on EHS compliance and EHS management system projects on a range of areas such as R&D laboratory safety, chemical safety, machine guarding, laser safety, robotics safety, hazardous materials use/storage/waste, EHS auditing.
* Develop and implement EHS compliance procedures, plans, permits, and reports.
* Manage tasks within assigned scope/budget/schedule and ensure quality standards on project deliverables.
* Build client relationships and nurture repeat business by continuously striving to exceed their expectations.
* Support ERM Partners and Project Managers to effectively manage and deliver projects.
* Build strong collaborative relationships with other ERM employees.
REQUIREMENTS:
* BS in engineering, environmental science, occupational health and safety, or related discipline preferred.
* A minimum of 7 years of applicable experience providing EHS support with an emphasis on health and safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to succeed in a fast-paced consulting environment, handling multiple assignments, meeting strict deadlines, and being able to re-prioritize tasks as-needed.
* Valid driver’s license and good driving record.
Pay Transparency:
For the Environmental, Health and Safety (EHS) Consultant position, we anticipate the annual base pay of $76,000– $97,400, $36.54/hr - $46.82/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on ...
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Type: Permanent Location: Sacramento, US-CA
Salary / Rate: Not Specified
Posted: 2026-06-02 07:34:55
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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!
Your role:
This role supports the needs of the Global Procurement Analytics team with a focus on analyzing complex data sets, generating actionable insights, and implementing strategies to help drive informed Category Strategy decisions.
You will work closely with stakeholders across various departments in Procurement Analytics to understand their data needs, develop analytics solutions, and present findings clearly and concisely.
Your Responsibilities:
* Analyze large and complex data sets using BI tools and methodologies to identify trends, patterns, and correlations.
* Build and manage end-to-end ETL workflows and data models using Power Query, Alteryx, or similar platforms to enable efficient and scalable analytics.
* Support data and system integration initiatives across enterprise platforms such as SAP, GCP, and other cloud-based applications, leveraging APIs, connectors, and direct data connections.
* Design and develop high-quality data models that align with business logic, governance standards, and reporting requirements to drive meaningful business insights.
* Partner cross-functionally with Finance, Procurement, and IT teams to understand business challenges, define technical requirements, and deliver effective data transformation and reporting workflows.
* Continuously monitor, troubleshoot, improve, and enhance existing workflows and data solutions to meet changing business priorities and ensure long-term sustainability.
* Interpret data to provide actionable insights that support strategic and operational decision-making
* Design and implement user-friendly interfaces to facilitate data-driven decision-making across Strategic Sourcing Team
* Establish and maintain data governance standards to ensure data accuracy, consistency, and security.
* Implement measures for data quality assurance and compliance with Category Strategies
* Work closely with the Data Analytics Leader to understand and maintain focus on the Procurement data need, including identifying critical metrics and KPIs, integrating Mkt Intelligence data and deliver actionable i...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2026-06-01 07:59:12
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Lead the future of cultural resource management and shape meaningful outcomes across complex, high-impact projects.
ERM is seeking a Managing Consultant, Archaeologist (Colorado-based or Remote – United States) to join our Cultural Resources Services team.
This role sits at the intersection of technical expertise, regulatory strategy, and client partnership—offering the opportunity to lead archaeological projects that directly influence responsible development and environmental stewardship.
As a management-level professional, you will play a key role in guiding project delivery, mentoring teams, and contributing to the growth of ERM’s cultural heritage practice across the U.S.
Why This Role Matters
Cultural resources are essential to understanding and preserving our shared history.
In this role, you will help ensure that infrastructure, energy, and development projects move forward responsibly—balancing progress with preservation.
Your expertise will help clients navigate complex regulatory landscapes while protecting culturally significant sites and resources.
This is an opportunity to lead, influence, and make a lasting impact on both communities and the environment.
What Your Impact Is:
* Serve as a trusted technical expert in archaeology and cultural resources for diverse projects across the United States
* Lead and deliver archaeological studies that meet federal, state, and local regulatory requirements
* Strengthen ERM’s client relationships by providing thoughtful, strategic guidance on permitting and compliance
* Mentor and guide junior staff, fostering a collaborative and high-performing team environment
* Contribute to business growth through proposal development and expanding client partnerships
* Support cross-functional collaboration across ERM’s national practice areas
What You'll Bring:
Required
* Graduate degree in Anthropology, Archaeology, or closely related field of study or 6 to 8 years of related paid experience
* Colorado archaeological experience as a field director
* Demonstrated experience completing inventory, survey, testing, and/or data recovery
* Experience as primary author on agency-reviewed technical reports
* Demonstrated business development abilities
* Experience interacting with regulatory agency personnel
* Strong attention to detail in documentation of work
* Excellent communication and computer skills
* Ability to work within a team as well as independently
* Strong proficiency in Microsoft Office Suite
* Must be locally available for projects
* Ability and willingness to frequently travel to field sites located in and out of state
* Ability to walk long distances (up to ten miles per day) in varying terrain under adverse conditions, including inclement weather and wildlife encounters; ability to lift and carry up to 50 lbs.; ability to excavate shovel tests
* Driver's License Required: T...
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Type: Permanent Location: Denver, US-CO
Salary / Rate: Not Specified
Posted: 2026-06-01 07:18:52
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Own the impact of cultural resource stewardship—lead complex archaeological projects that shape sustainable development across the U.S.
This is an opportunity to step into a leadership role where your expertise not only shapes projects—but helps preserve cultural history while enabling future development.
Why This Role Matters
As a Managing Consultant, Archaeologist at ERM, you will play a critical leadership role in advancing responsible development while protecting cultural heritage.
Your expertise will guide clients through complex regulatory environments, ensuring archaeological compliance while delivering high-quality, defensible results.
This role directly influences project success, environmental stewardship, and ERM’s continued growth in cultural resources consulting.
What Your Impact Is:
* Lead and deliver archaeological investigations that meet federal, state, and local regulatory requirements (including NHPA Section 106 and NEPA).
* Serve as a trusted advisor to clients, providing strategic guidance on permitting, compliance, and cultural resource management.
* Drive project execution from research and fieldwork through technical reporting and client delivery.
* Strengthen ERM’s cultural resources practice by contributing to business development and cross-functional collaboration.
* Mentor and lead team members, fostering a high-performing and safety-focused field and office environment.
What You'll Bring:
Required
* Graduate degree in Anthropology, Archaeology, or closely related field of study plus 6 to 8 years of related paid experience.
* Demonstrated experience completing inventory, survey, testing, and/or data recovery.
* Experience as primary author on agency-reviewed technical reports.
* Must have strong attention to detail in documentation of work.
* Experience interacting with regulatory agency personnel.
* Excellent communication and computer skills.
* Demonstrated business development abilities.
* Ability to work within a team as well as independently.
* Strong proficiency in Microsoft Office Suite.
* Must be locally available for projects.
* Ability and willingness to frequently travel to field sites that will be located in and out of state.
* Must be able to walk long distances (up to ten miles per day) in varying terrain under adverse conditions, including inclement weather, wildlife encounters, and able to lift and carry up to 50 lbs., and able to excavate shovel tests.
* 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
* Registered Professional Archaeologist (RPA).
* Ability to be listed on BLM cultural resources use permits.
* ...
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Type: Permanent Location: Albuquerque, US-NM
Salary / Rate: Not Specified
Posted: 2026-06-01 07:18:50
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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: 2026-05-31 08:14:20
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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: 2026-05-31 07:52:49
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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:
Being the customer service company in the world.
OUR PURPOSE:
Creating packaging solutions for life’s essentials.
Job Requisition #:
034382 Apprentice Quality Engineer (18+) (Evergreen) (Open)
Job Description:
Location: Greif, Ellesmere Port
Apprenticeship Duration: 2 Years
Career Progression: Quality Engineer
Do you have an interest in quality, engineering, and manufacturing? Do you enjoy problem-solving? Do you like understanding how things work and how to make them better?
We are recruiting an Apprentice Quality Engineer to join our Quality team at Ellesmere Port.
This is an excellent opportunity to develop a long-term career in Quality Engineering within a high-volume manufacturing environment.
Our Apprentice Quality Engineer role gives you the chance to learn on the job, gain a nationally recognised qualification, and progress into a professional Quality Engineer role in a manufacturing environment.
This is a hands-on, paid apprenticeship with real responsibility, mentoring, and clear career progression.
What You’ll Learn - Over 2 years, you’ll gain experience in:
✅ Quality inspections and testing
✅ Manufacturing processes (steel drums & IBCs)
✅ Problem-solving and root cause analysis
✅ UN packaging regulations
✅ Quality systems (ISO 9001 & ISO 17025)
✅ Continuous improvement projects
You’ll be supported every step of the way by experienced Quality Engineers.
What We’re Looking For - You don’t need experience — just the right attitude.
✅ Interest in engineering, quality, or manufacturing
✅ Good attention to detail
✅ Willingness to learn and develop
✅ Enjoys working as part of a team
✅ GCSEs (or equivalent) in Maths & English
What We Offer
· Fully supported apprenticeship programme
· On-the-job training in a real manufacturing environment
· Mentoring from experienced Quality Engineers
· Clear progression to Quality Engineer on successful completion
Interested applicants should email their CV and covering letter to lois.griffiths@greif.com Closing dates for applications 2nd June 2026
Please note we will be advertising internally and externally to recruit for the above role, and all applications will be considered equally.
At Greif, we believe that our colleagues are the center of our success.
Our Total Rewards have a compreh...
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Type: Permanent Location: Ellesmere Port, GB-CHE
Salary / Rate: Not Specified
Posted: 2026-05-30 09:00:00
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
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!
Le site d’Elanco à Huningue (68) recherche ses nouveaux Préleveur-Contrôleur de l’équipe Contrôle Qualité Matières Premières et Articles de conditionnement.
Poste en CDI et en 2x8, du lundi au vendredi.
Vous serez un acteur primordial du flux de matières premières en réalisant leur prélèvement dès leur réception au magasin.
Vos Responsabilités :
* Effectuer, dans le respect du planning, les prélèvements des matières premières suivant le plan d’échantillonnage
* Effectuer les premières manipulations d’identification IR de matières premières et articles de conditionnement.
* Effectuer le contrôle des articles de conditionnement
* Assurer l’archivage des prélèvements dans l’échantillothèque
* Gérer le stock des éléments nécessaires aux prélèvements
* Préparer les documents nécessaires aux opérations et à la traçabilité
* Respecter strictement les Bonnes Pratiques de Fabrication (BPF) et les consignes de sécurité (HSE) lors de toutes les manipulations.
* Participer aux démarches d'amélioration continue intra et interservices avec la supply chain et la logistique
* Maintenir les différents éléments du poste de travail en bon état de fonctionnement et de propreté
Ce dont vous avez besoin pour réussir (qualifications minimales) :
* Niveau Bac Pro ou Baccalauréat
* Expérience requise d’un an minimum en prélèvement de matière
* Rigueur documentaire et de travail, autonomie et sens de l'organisation
* Aptitude à la conduite de transpalette électrique (la formation CACES 2 sera délivrée si nécessaire)
Ce qui est un plus :
* Expérience préalable en industrie, idéalement dans un environnement pharmaceutique ou réglementé
* Connaissance des techniques d'échantillonnage
* Capacité à lire et comprendre des documents techniques en anglais
* Maîtrise du Pack Office et connaissance SAP
Les avantages du poste
* 26 jours de congés payés + 15 RTT/an
* Part variable sur tous les postes
* Intéressement & Participation
* Épargne salariale ...
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Type: Permanent Location: Huningue Cedex, FR-68
Salary / Rate: 34000
Posted: 2026-05-30 08:51:16
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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!
Your Role: R&D Quality Assurance Auditor
This role provides quality oversight and consultative support for Elanco’s R&D Clinical Development organization, serving as the GLP Test Facility Quality Assurance Unit to ensure regulatory compliance for non-clinical safety studies.
Based at the Fort Dodge site, the position oversees regulated activities including VICH GL9 standards to support global product approvals for veterinary medicines.
By partnering closely with R&D stakeholders, the role proactively drives compliance through the implementation of Elanco Quality Standards, specialized training, and strategic quality input.
Your Responsibilities:
* Regulatory Execution & Leadership: Execute the site Quality Assurance program in strict compliance with FDA GLP (21 CFR Part 58) and vGCP (VICH GL9) standards, while serving as the ERDQA representative to the R&D Site Lead Team.
* Comprehensive Auditing: Plan and conduct end-to-end internal and third-party audits—including protocol, in-life, data, and final report reviews—to ensure total adherence to regulatory requirements and Elanco Quality Systems.
* Sponsor & System Oversight: Provide critical Sponsor oversight for non-clinical safety and clinical studies conducted at third parties, while maintaining quality standards for R&D GXP equipment, systems, and site procedures.
* Quality Management & CAPA: Manage the Quality Management System (QMS) by authoring site Quality procedures, leading investigations into deviations, and overseeing the implementation and suitability of Corrective and Preventive Actions (CAPA).
* Stakeholder Engagement & Training: Act as a primary liaison for regulatory authority inspections and external stakeholders, while developing and delivering compliance training to R&D and ERDQA teams to foster a culture of quality.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor's of Science Degree in biology, animal science, pharmacy, or a related field.
* Experience: At least 10 years of experience in a quality oversight or monitoring role for veterinary clinical and safety studi...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 155000
Posted: 2026-05-30 08:51:04
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Senior Legal Counsel, Malaysia & Singapore (12 months contract)
Job Description
Join the team behind iconic brands like Huggies®, Kotex®, Poise® and Depend®.
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
You perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring. You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.
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.
This is a single contributor role and will have end-to-end responsibility for all legal matters in Malaysia and Singapore.
He/she will provide legal strategy to accomplish the objectives of the business units while ensuring compliance with all applicable laws and regulations.
The successful candidate will be the legal business partner to the Managing Director of Malaysia & Singapore, and be the representation of legal leadership and capability within the Malaysia & Singapore Leadership Team.
This role will also support the APAC Global Business Services team based in Malaysia.
Key Responsibilities
* Prepared to travel within Malaysia (including to Kluang where the plant is located), Singapore and regionally / globally as needed.
* Legal business partner to the Malaysia and Singapore leadership team.
Identify legal risks, propose changes required and where relevant lead the implementation of the changes.
* Contracts: Review and participate in the negotiation, review and approval of material contracts.
* Marketing and digital / social commerce: Provide guidance, advice on product developments and approval of marketing claims and commercial initiatives (including digital and social commerce initiatives)
* Employment: Provide legal advice on employment-related issues, work closely with HR to ensure country practices, polices and work rules comply with relevant labour regulations and to maintain harmonious relationship with Union, advise on employment disputes.
* Disputes / Litigation: Lead and manage legal disputes including marketing claim challenges and regulatory inquiries and investigations.
* Regulatory: Legal guidance to manufacturing / plant team on dealings with regulatory agencies during inspections, inquiries, or investigations.
Advise on legal risks regarding accid...
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Type: Permanent Location: Petaling Jaya, MY-10
Salary / Rate: Not Specified
Posted: 2026-05-30 08:11:44
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PRINCIPLE ACCOUNTABILITIES
* Work alongside the Safety Manager to develop, coordinate and support the safety program and activities through safety contacts, observations, inspections, and accident/incident investigations.
* Assist with creating safety training materials including, policies and procedures, monthly safety training presentations, etc.
* Leads safety orientations for new or existing employees.
* Tracks and maintains safety program, policies and procedures.
* Conduct work area safety audits.
* Assist with onsite injury management and case management.
* Trains personnel on assigned safety subjects such as personal protective equipment, fall protection, etc.
* Engage in communication with department personnel, both management and hourly workers, to address safety concerns promptly.
This includes investigating accidents and incidents and preparing detailed reports with corrective actions and recommendations.
* Conduct or assist with major incident analysis.
* Contribute to achieving facility compliance with OSHA and other relevant regulations by applying federal, state, and local safety standards.
* Inspects equipment and work areas for proper operation and safety requirements.
Converses with operating and maintenance crews to check for unsafe conditions and notifies proper personnel when deficiencies are found or reported by other personnel.
* Coordinates emergency response drills and/or emergency evacuation plans.
Conducts follow-up evaluation and critique of the response with involved employees.
* Conducts the gathering and preparation of information for safety meetings and ensures adherence to monthly topics for reporting.
Assists in the preparation and production of various safety videos used in safety training.
* Audits facility chemicals, reviews SDS documents to ensure all new products are documented & employee acknowledgment and training is completed.
* Collaborate with engineering and operations teams to design and implement engineering controls for hazard mitigation.
* Stay informed about emerging safety technologies and industry best practices, and recommend their adoption where appropriate.
* Perform other duties as assigned.
JOB KNOWLEDGE/SKILLS AND EXPERIENCE
* Bachelor’s degree in occupational safety or related field preferred.
A minimum of 2-3 years of experience in a manufacturing environment.
* Communicates details of safety procedures clearly to employees.
* Demonstrates strong leadership, problem-solving and analytical skills and attention to detail, proficiency in computer skills to include, MS Office and database management.
* Exhibits ability to think practically and creatively to implement the best safety practices.
* Responds quickly and efficiently to emergency situations.
* Exercises caution and alertness at all times.
* Knowledge of OSHA standards as well as local and state requirement...
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Type: Permanent Location: Keokuk, US-IA
Salary / Rate: Not Specified
Posted: 2026-05-30 07:57:52
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Job Description
The Musculoskeletal Control and Dynamics Lab at Stevens Institute of Technology is conducting research to evaluate the feasibility of using music-based biofeedback to assist persons with Parkinson's disease in their gait training.
We welcome applications for a postdoctoral fellow to take a lead role in this newly funded NIH research project (Grant # 1R34AT013265-01A1).
Qualifications
* PhD, MD, or equivalent doctoral degree in Neuroscience, Biomedical Engineering, Biomechanics, or a related field
* Candidates in ABD (“all but dissertation”) status will also be considered
* Required Knowledge, Skills, and Abilities
+ Excellent written, verbal and computer skills
+ Excellent communication and interpersonal skills
+ Strong ability to work independently and collaboratively
+ Excellent critical thinking and problem-solving skills
+ Demonstrated ability to organize and execute human subjects research experiments
+ Experience working in a fast-paced environment
* Preferred Qualifications:
+ Prior clinical or research experience with persons with Parkinson’s disease
Responsibilities
* Under the direction of the Principal Investigator, the Postdoctoral Fellow will be responsible for the planning, analysis, interpretation, and presentation of experiments regarding the NIH-funded study of the use of musical biofeedback to train postural control in persons with Parkinson’s disease.
The Postdoctoral Fellow will also be responsible to contribute to the study design and execution of related projects in the lab.
* The Postdoctoral Fellow will collect, document, organize, analyze, and present data and results from human subject experimentation.
* In addition, the Postdoctoral Fellow will provide research guidance to junior trainees, including graduate students and student research assistants in the laboratory.
* The Postdoctoral Fellow is responsible for the scientific operations of the laboratory regarding the new NIH study.
* The Postdoctoral Fellow will lead manuscript preparation for peer-reviewed journals and presents findings at conferences.
* The Postdoctoral Fellow will contribute to submitting fellowship and grant applications to obtain further funding for the lab as well as leading submissions to secure independent research funding.
* This position requires a fully on-site work arrangement.
Department
Biomedical Engineering
Compensation Range
In compliance with the New Jersey Wage Transparency Act, the annual base range for this position is $63,000 - $67,000.
This range represents the University’s good faith estimate of possible compensation at the time of posting.
Stevens Institute of Technology determines compensation based on factors including the position’s scope and responsibilities, the candidate’s experience, education, skills, internal equity, market data, and organizational ...
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2026-05-30 07:54:56
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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 dipendenti.
Siamo alla ricerca di un/una Quality Control Analyst che si unisca al nostro QC Team di Pessano con Bornago.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Quality Control Analyst svolge le attività analitiche e affini all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP e dalle Procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, ed altri regolamenti interni, riportando direttamente al/alla Quality Control Laboratory Supervisor.
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.
* Tiene in ordine ed aggiornati i propri quaderni di laboratorio e i propri documenti analitici.
* Esegue operazioni di base di laboratorio, quali: preparazione di reattivi e soluzioni, campionamenti di materie prime, prodotti semilavorati e prodotti finiti, ecc.
* Segue scrupolosamente le disposizioni impartite dai superiori.
* Esegue analisi con tecniche analitiche semplici e complesse, seguendo metodi definiti, in autonomia operativa.
* Valuta criticamente i dati ottenuti nello svolgimento del lavoro a lui/lei assegnato.
* Stila ove richiesto rapporti sul lavoro svolto.
* Sovrintende, ove preposto/a, alle operazioni analitiche di tecnici meno esperti.
* Esegue calibrazioni strumentali e analisi di standard secondari.
* Si occupa della stesura, revisione, archiviazione e gestione della documentazione tecnica.
* Ove preposto/a, adempie alle funzioni di Standar...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2026-05-30 07:44:04
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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
* Premio di partecipazione
Siamo alla ricerca di un un/una Quality Control Compliance Junior Specialist (tempo determinato 12 mesi) che si unisca al nostro Quality Control Compliance Team di San Giuliano Milanese.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE:
Il/la Quality Control Compliance Junior Specialist risponde alla responsabile del Quality Control Compliance Team e si occupa di assicurare la corretta applicazione delle GMP e l’aderenza alla compliance nel laboratorio Controllo Qualità, supportando il responsabile di reparto nelle attività principali.
COMPITI E RESPONSABILITA’:
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati:
* Organizzazione e gestione dei training del personale del Controllo Qualità, svolgendo, quando necessario, la funzione di docente.
* Redazione, revisione, archiviazione e gestione della documentazione del Controllo Qualità.
* Stesura, revisione, archiviazione e gestione della documentazione tecnica quale: procedure Operative Standard, Procedure Analitiche Standard, metodi di analisi, specifiche, rapporti di validazione, ABR, protocolli e report tecnici.
* Revisione dei dossier nella parte che compete le attività analitiche e del Controllo Qualità.
* Aggiornamento dei documenti analitici in conformità alle principali farmacopee ed ai dossier di riferimento
* Monitoraggio e gestione delle CAPA, dei Change e delle indagini all’interno del laboratorio QC
* Supporta il corretto svolgimento delle investigazioni di laboratorio e della gestione delle deviazioni in conformità alle procedure aziendali e ai requisiti GMP.
Individua-zione delle CAPA e stesura dei report delle investigazioni di laboratorio.
Valutazione dei trend degli eventi, individuazione di eventuali ricorrenze e valutazione delle azioni correttive dedicate.
* Agisc...
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Type: Contract Location: San Giuliano Milanese, IT-25
Salary / Rate: Not Specified
Posted: 2026-05-30 07:44:02
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Shape the Future of Decarbonization and Air Quality Strategy for Global Industry
At ERM, we’re looking for a Consulting Associate, Climate Change (Mid-Atlantic, U.S.) who is ready to step into a dynamic, high-impact role supporting complex environmental challenges.
In this position, you’ll partner with leading organizations across the energy, oil and gas (O&G), power, chemical, and technology sectors—helping them navigate evolving regulations, advance decarbonization strategies, and deliver measurable sustainability outcomes.
This is more than a technical role—it’s an opportunity to contribute to meaningful, large-scale change while learning from some of the top experts in the field across ERM’s global network.
Why This Role Matters?
Organizations today are under increasing pressure to meet climate commitments while maintaining operational performance.
This role sits at the intersection of environmental compliance, climate strategy, and technical execution—helping clients move from ambition to action.
Your work will directly support regulatory compliance, emissions reductions, and long-term sustainability strategy.
What Your Impact Is:
* Support clients in developing and implementing climate and air quality strategies that drive real, measurable outcomes
* Contribute to greenhouse gas inventory development, emissions reduction initiatives, and regulatory compliance programs
* Help organizations navigate complex permitting processes and environmental regulations
* Deliver high-quality technical insights that inform critical business and environmental decisions
What You'll Bring:
Required:
* Bachelor’s of Science in chemical, environmental, or mechanical engineering and related engineering degree; or equivalent experience
* Recent graduate to 3 years of direct consulting or industry experience involving greenhouse gas or emission inventory support, product carbon foot printing, life cycle analysis, and/or Clean Air Act permitting and compliance
* Strong hands-on spreadsheet and database comprehension
* Excellent written and verbal communication skills
* Ability to succeed in a fast-paced consulting environment, handling multiple project assignments, meeting strict deadlines, and traveling to client facilities, as needed
* Enthusiasm, initiative, flexibility, and a desire to work in a growing team
* Strong problem-solving skills with a high desire to learn and apply new concepts
Preferred:
* MS and/or EIT
* 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
* Local or regional candidates preferred
* Advanced Excel such as: Queries, Pivot Tables, Macros
* This position is not eligible for immigration sponsorship.
Key Responsibilities:
* W...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2026-05-30 07:37:19
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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
Eine gesündere Zukunft.
Das ist es, was uns bewegt, innovativ zu sein.
Wir bringen die Wissenschaft ständig voran und sorgen dafür, dass alle Menschen heute und in Zukunft Zugang zur Gesundheitsversorgung haben, die sie brauchen.
Eine Welt zu schaffen, in der wir alle mehr Zeit mit den Menschen haben, die wir lieben.
Das ist es, was uns zu Roche macht.
In der R&D-Abteilung Process Technologies and Material Science (Teil von Roche Diagnostics Solutions) entwickeln wir chemische Einsatzstoffe für das gesamte diagnostische Produktportfolio.
Das Team Bioorganic Development & Transfer besteht aus 8 Mitarbeitenden mit wissenschaftlichem und technischem Hintergrund.
Wir arbeiten an organisch-chemischen Synthesen und Up-scale Projekten und gehen dabei flexibel und zielorientiert vor, um maßgeschneiderte Moleküle für unsere Projektpartner zu entwickeln.
Dabei legen wir Wert auf eine hohe Qualität und den Spaß an der gemeinsamen Arbeit.
Deine zentralen Aufgaben
In dieser Rolle bringst Du Deine fundierte Labor-Expertise direkt in die Entwicklung innovativer Diagnostika ein:
* Synthese & Herstellung: Du planst und führst eigenständig organisch-präparative Synthesen im Bereich niedermolekularer Verbindungen und deren funktionellen Bausteinen durch
* Up-Scale Arbeiten: Darüber hinaus bist Du für die Maßstabsvergrößerung chemischer Reaktionen vom Milligramm- bis in den Multigramm-Bereich verantwortlich
* Chromatographie & Downstream Prozesse: Du bringst Deine Expertise in die Aufreinigung komplexer Reaktionsmischungen ein (z.
B.
Flash-Chromatographie, HPLC) und optimierst Downstream-Prozesse
* Charakterisierung: Du isolierst die Zielverbindungen und nutzt moderne analytische Methoden (z.
B.
NMR, MS, HPLC/UV) zur Strukturaufklärung und In-Prozess-Kontrolle
* Prozessoptimierung & Transfer: Du optimierst etablierte Syntheseprozesse, um einen reibungslosen Transfer in die Produktion vorzubereiten und erstellst die entsprechenden Verfahrensanweisungen
* Dokumentation & Innovation: Du dokumentierst Deine Ergebnisse präzise, präsentierst diese im Team und setzt Dein Spezialwissen ein, um Projekte innerhalb von Roche Diagnostics voranzutreiben
Dein Profil
* Du hast ein erfolgreich abgeschlossenes Hochschulstudium in Chemie (Bachelor) mit Schwerpunkt Organische Chemie oder eine Ausbildung zum Chemielaborant mit Weiterbildung zum Techniker oder eine vergleichbare Qualifikation
* Darüber hinaus bringst Du tiefgreifende Kenntnisse und ...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2026-05-30 07:34:02
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Strategic Healthcare Programs (SHP) is a leader in analytics and performance management solutions serving the post-acute market. We are an industry leader in helping Home Health, Hospice, and Skilled Nursing providers improve their financial and quality performance while complying with many regulatory requirements Additionally, we connect the post-acute world to the broader provider markets to allow for optimal management across the continuum of care.
The Survey Processor plays an integral role in the timely and accurate processing of survey data.
Duties and Responsibilities:
* Receive and log inbound mail deliveries in a timely and organized manner.
* Sort, open, and process incoming mail according to established procedures.
* Prepare and organize daily mail carts to support workflow efficiency.
* Coordinate shredding preparation by relocating shred bins to designated areas in advance of scheduled pickups.
* Stage empty trays and carts outside of the office for vendor collection and reuse.
* Accurately handle mail by opening, extracting, and categorizing contents in accordance with processing guidelines.
* Scan survey documents and supporting materials, ensuring image quality and proper file indexing.
* Operate computer systems and scanning equipment for data entry, verification, and quality control.
* Maintain and organize archive rooms, including the daily filing of completed survey trays.
* Prepare materials and workspace for the following day’s processing volume to ensure operational continuity.
* Perform end-of-day cleanup procedures, including securing all bins, equipment, and restricted office areas.
* Available to work weekends.
Knowledge, Skills and Abilities
* Able to follow specific instructions and procedures without deviation
* Excellent attention to detail
* Excellent communication is a must
* Proficient in core computer skills (Excel, Word, Outlook, Microsoft Teams, etc.)
* Able to lift up to 30 lbs.
* Able to push and pull 65-gallon shred containers on wheels, weighing up to 300 lbs.
* Able to push and pull mail carts on wheels, weighing up to 400 lbs.
* Deliver work that meets defined quality, accuracy, and performance standards.
Schedule: June 15th - July 8th, and July 20th - August 12th
Pay: $19.00 per hour.
Benefits: We value work/life balance.
Temporary part-time employees are not eligible for health benefits, but are eligible for paid vacation, sick time, and holidays.
This position is not eligible for immigration sponsorship.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
Administration
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Type: Permanent Location: Goleta, US-CA
Salary / Rate: Not Specified
Posted: 2026-05-29 08:30:18
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Advanced Utility Systems, a division of Harris; is seeking a VP of Sales & Marketing to lead a focused, high-performing team of four sales professionals and two marketing specialists.
This is a senior leadership role reporting directly to the Executive Vice President of Advanced. The VP sits on the executive leadership team and operates as a peer to leaders across Customer Support, Research & Development and Professional Services.
This leader will have regular engagement with Harris leadership for strategic and business operations engagements.
The VP of Sales & Marketing is expected to lead, coach, enable, and develop the team to deliver results - not compete with their own sales people for deals.
However, the VP is expected to be actively engaged in key closing activities to ensure the team delivers against its commitments.
This remote role welcomes candidates anywhere in Canada and the US.
Travel is required as needed, approximately 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.
Preference will be given to candidates who can work in EST or CST timezone.
Salary:
125K
OTE:
240K - 250K incl base
What your impact will be:
Sales Leadership & Performance
* Own and deliver the annual sales bookings target of $12M, currently comprising approximately 2/3 install base expansion and upgrades and 1/3 new customer acquisition, and prepare Advanced's growth engine for renewed emphasis on new customer acquisition
* Drive consistent pipeline development, opportunity management, and forecast accuracy across the sales team
* Lead weekly forecast reviews and maintain rigorous Salesforce CRM hygiene and reporting discipline
* Develop and execute territory and account strategies that balance installed base health with new logo growth
* Support the sales team in key closing activities, executive relationships, and deal strategy - without displacing the salesperson's ownership of the opportunity
Coaching, Development & Retention
* Recruit, hire, onboard, coach, and retain top-performing enterprise software sales professionals
* Build and sustain a high-performance sales culture rooted in accountability, continuous improvement, and winning behaviors
* Actively coach the team on the MEDDICC sales framework, ensuring consistent and disciplined application across all active opportunities
* Identify performance gaps early and respond with structured coaching plans, training, and resources
Marketing Leadership
* Oversee the two-person marketing team to develop and execute targeted marketing campaigns, a robust event and tradeshow schedule, sales collateral, and guerrilla marketing programs appropriate to the municipal utility vertical
* Align marketing activity closely to pipeline and revenue goal...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2026-05-29 08:28:43
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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!
Your Role: Affiliate Health, Safety, and Environment Advisor
As the Affiliate Health, Safety, and Environment Advisor, you will be a key guide in our Global Health, Safety, and Environmental (HSE) team, instrumental in shaping the future of safety across our global and US/Canada commercial operations.
You will take ownership of transforming our affiliate safety program, refreshing it from its foundations to a best-in-class model that truly fits Elanco's mission and maturing culture.
Partnering with affiliate and commercial leadership, you will act as a trusted advisor and coach, providing critical expertise on a wide range of HSE topics, while playing a leading role in hazardous waste management for our US warehouses.
This is a high-impact role where your strategic vision and ability to translate data into actionable insights will directly protect our people and enhance our operational excellence worldwide.
Your Responsibilities:
* Provide strategic direction and direct oversight for HSE programs across US and Canadian affiliates, acting as the primary expert for all regional HSE issues, including the comprehensive management of hazardous waste for US commercial warehouses.
* Drive, own and uphold the global transformation of the Affiliate HSE program, designing and implementing a fit-for-purpose framework that aligns with Elanco’s strategic objectives, leverages existing and new digital technologies and fosters a maturing safety culture.
* Establish and manage a robust system for tracking HSE performance; analyze key performance indicators (KPIs) to identify trends and deliver reliable, data-driven reports to senior leadership to inform strategic decisions.
* Drive the continuous improvement of the safety culture by training, coaching, and influencing affiliate management and HSE representatives on best practices and line ownership of safety.
* Collaborate with regional fleet managers to integrate critical HSE elements into the fleet program, ensuring driver safety and regulatory compliance.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor's degree ...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-05-29 08:23:53
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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!
Your Role: Vice President, Research & Breakthrough Innovation
As Vice President, Research & Breakthrough Innovation, you will be part of the global R&D leadership team to deliver Elanco’s long-term scientific vision.
In this role, you’ll be responsible for leading the discovery organization, managing breakthrough innovation portfolios, and translating complex scientific concepts into sustainable commercial value for the enterprise.
Your Responsibilities:
* Lead the identification and validation of novel scientific platforms and therapeutic modalities to fuel Elanco’s long-term research pipeline.
* Oversee the management of global research portfolios, making high-impact decisions on resource allocation and financial oversight for innovation budgets.
* Drive breakthrough innovation initiatives by identifying and evaluating unique scientific challenges and providing guidance to teams to develop pioneering solutions.
* Build and extend strategic relationships with global external innovation ecosystems, regulators, and partners to enhance Elanco’s competitive edge in research.
* Direct the translation of early-stage research into commercially viable assets, ensuring a robust bridge between scientific discovery and market readiness.
What You Need to Succeed (minimum qualifications):
* Education: Advanced degree (PhD, DVM, or equivalent) in a relevant scientific field.
* Experience: A minimum of 12 years of experience in research leadership and breakthrough innovation management within the animal health or pharmaceutical industry.
* Expertise in managing large-scale research portfolios and visionary leadership in discovery operations.
What will give you a competitive edge (preferred qualifications):
* Experience with both large and small molecules and/or monoclonal antibodies.
* Proven track record of successful external innovation partnership development and global regulatory navigation.
* Demonstrated ability to influence at the executive level and drive cross-functional alignment across a global organization.
* Significant experience in financ...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 344000
Posted: 2026-05-29 08:23:49
