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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: Head of Small Molecule Discovery
As Head of Small Molecule Discovery, you will lead our efforts in identifying and developing novel small molecule therapeutics for animal health.
The successful candidate will be a visionary leader, responsible for driving strategic direction, scientific excellence, and operational execution of our small molecule discovery programs from target validation through to candidate selection.
This role requires a deep understanding of diverse discovery technologies, a proven track record in drug discovery, and the ability to inspire and mentor a high-performing team.
Your Responsibilities:
* Provide strategic leadership and scientific oversight for all small molecule drug discovery programs, ensuring alignment with Elanco's R&D pipeline goals.
* Lead, manage, and develop a team of talented medicinal chemists and discovery scientists, fostering a culture of innovation, collaboration, and scientific rigor.
* Drive the implementation and application of cutting-edge discovery technologies, including DNA-Encoded Libraries (DEL), Artificial Intelligence/Machine Learning (AI/ML) approaches, and advanced medicinal chemistry techniques.
* Oversee the design, synthesis, and optimization of novel small molecules, guiding hit identification, lead generation, and lead optimization strategies.
* Collaborate cross-functionally with biology, pharmacology, ADME, toxicology, and research / development teams to ensure seamless progression of discovery candidates.
* Identify and evaluate new technologies, and external collaboration opportunities to enhance our small molecule discovery capabilities and pipeline.
* Ensure robust data analysis, interpretation, and decision-making throughout the discovery process.
* Represent Elanco's small molecule discovery efforts internally and externally, including presentations at scientific conferences and interactions with key opinion leaders.
* Contribute to the overall discovery strategy and portfolio management, providing expert insights into small molecule opportunities and challenges.
What You Need to Su...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-12-17 07:29:24
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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: Scientist, In vitro Assay and Method Development
As the In vitro Assay Development Scientist, you will be responsible for method transfer and the training of junior scientists in the design, development, optimization, and execution of cell-based and biochemical assays.
You will work in a collaborative, cross-functional environment focusing on the characterization of small molecule compounds and the elucidation of their mechanism of action.
This role offers an exciting opportunity to provide critical data to guide medicinal chemistry efforts and contribute directly to the advancement of our innovation pipeline.
Your Responsibilities
* Lead method transfer and training of junior scientists in cell-based and biochemical assay development and optimization
* Collaborate cross-functionally in the build-out of new Discovery Bioassay capabilities at our new Indianapolis HQ
* Design, develop, and validate novel and robust cell-based and enzymatic assays suitable for high-throughput screening (HTS).
* Characterize protein inhibitors by determining IC50 values, potency (Ki), and their mechanism of inhibition (e.g., competitive, non-competitive, reversible, irreversible).
* Implement and execute screening funnels to evaluate compound libraries, generating high-quality, reproducible data to drive structure-activity relationship (SAR) analysis.
* Collaborate internally and externally with protein production to ensure the availability of high-quality, active protein preparations for use in assays.
* Proactively research and implement new assay technologies, detection methods (e.g., absorbance, fluorescence, luminescence), and instrumentation to increase assay quality and efficiency.
* Analyze, interpret, and present complex experimental data to colleagues within project teams.
* Troubleshoot assays to ensure high-quality, reproducible results.
* Stay current with scientific literature and proactively evaluate new technologies, instrumentation, and methodologies to improve assay performance and throughput.
* Maintain records of experimental designs, prot...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-12-17 07:29:23
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Nous sommes à la recherche d'une personne qui désire relever de nouveaux défis, qui est organisée et dynamique.
Notre clientèle regroupe les villes, les municipalités, ainsi que des entreprises diverses principalement situées au Québec, mais aussi en Ontario, dans les Maritimes et en Colombie-Britannique.
Ainsi, tu devras accompagner nos clients dans l’apprentissage de nos différents logiciels de gestion des loisirs, et ce, en étant un joueur clé dans l’atteinte de leurs objectifs d’apprentissage.
Voici l'occasion de faire partie d'une équipe passionnée et polyvalente !
Description du poste :
Dans un environnement de travail stimulant axé sur la collaboration et le travail d’équipe, tu auras la possibilité de réaliser tes objectifs professionnels.
Sous la supervision du gestionnaire de projet, tu travailleras sur plusieurs dossiers stimulants et enrichissants.
Tes principales tâches seront :
* Conseiller et former nos clients sur l’utilisation de nos différents logiciels ;
* Assurer l’atteinte des objectifs d’apprentissage ;
* Élaborer des plans de cours ;
* Planifier la matière à voir lors des séances ;
* Participer à l’élaboration de webinaires ;
* Réaliser des capsules de formation;
* Être en mesure de te déplacer en clientèle (à l’occasion et sur demande seulement) ;
* Amener tes idées pour améliorer le processus d’apprentissage ;
* Offrir un soutien et une aide au service à la clientèle.
Ce que nous offrons comme avantages :
* 3 semaines de vacances dès la 1ère année, 4 semaines après 3 ans et 5 semaines après 7 années de service dans l’entreprise ;
* 5 jours de congés personnels et 1 journée de bénévolat payés par année ;
* Des assurances collectives payées à 100 % par l’employeur dès le premier jour ;
* Un programme de REER collectif avec cotisation de l’employeur ;
* Environnement de travail 100 % en télétravail avec possibilité d’horaires flexibles lorsque tu n’es pas en rendez-vous client
* Un programme de vie active (prime annuelle) ;
* Un programme d’aide aux employés avec Inkblot ainsi qu’un accès à la télé médecine avec Maple ;
* Un cadeau te sera envoyé à ton anniversaire ;
* Remplacement d’ordinateur aux 4 ans que tu pourras conserver pour usage personnel ;
* Programme de prêt pour l’achat d’un ordinateur personnel neuf ;
* Programme d’encouragement à l’achat d’action de la compagnie.
Aptitudes professionnelles :
Si tu possèdes un diplôme collégial/baccalauréat pour toute discipline jugée pertinente ou une expérience équivalente comme formateur ainsi que les aptitudes suivantes :
* Démontrer de bonnes capacités pédagogiques ;
* Détenir de bonnes capacités à coordo...
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Type: Permanent Location: Quebec City, CA-QC
Salary / Rate: Not Specified
Posted: 2025-12-17 07:29:17
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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: Senior / Principal Scientist, Downstream Process Development
The Biopharma Technical Development team located in Indianapolis, IN is seeking a Senior / Principal Research Scientist to provide scientific and technical expertise for the development and launch of new biological drug substances in an innovative and fast-paced organization.
This role is focused on downstream process development with an emphasis on monoclonal antibodies, therapeutic proteins, and other biological modalities.
You will be responsible for leading downstream process development activities at bench and pilot scales, supporting scale-up, technical transfers, process implementation, and clinical material production at both internal and external manufacturing sites.
In addition to technical excellence, this position requires strong organizational management, communication skills, and cross-functional collaboration across departments and geographies.
As a subject matter expert in downstream process development, you will have the potential to lead both projects and people.
Your Responsibilities:
* Provide scientific expertise in downstream process development for early- and late-stage biologic programs (mAbs, therapeutic proteins, and other modalities) using phase-appropriate development strategies.
* Apply Quality by Design (QbD) principles to process development and process characterization.
* Lead and contribute to risk assessments supporting product development stage-gate reviews and robust manufacturing control strategies.
* Develop representative scale-down models from commercial-scale operations and apply prior knowledge to guide development studies.
* Author and review source documents for regulatory submissions; respond to CMC questions from regulatory agencies.
* Partner with R&D, Technical Services/Manufacturing Sciences (TS/MS), supply chain, Quality, Manufacturing, Launch Leaders, external CDMOs, and other stakeholders to ensure successful tech transfers and commercialization.
* Serve as a technical resource to Biopharma Technical Development, TS/MS, CMOs, and manufacturing operati...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: 171000
Posted: 2025-12-17 07:28:54
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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!
Position Description:
The role of Biostatistician is to support the biostatistics and statistical analysis in terms of analysis dataset creation, statistical analysis and creation of statistical analysis tables and summaries in collaboration with statistical and programming colleagues, physicians, veterinarians, and/or medical colleagues.
Functions, Duties, Tasks:
* Prepare statistical analysis plans, including table under the supervision of senior statistical staff.
* Use SAS or other software to develop custom programming code to generate tables, data listings, graphs and derived datasets as specified in the protocol/statistical analysis plan.
* Generate randomization schedules from provided specifications under guidance from senior statistical staff.
* With mentoring, provide sample size calculations and review protocols for completeness and appropriateness of statistical sections.
* Ensure that outputs meet quality standards and project requirements.
* Perform validation programming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
* Keep project team members informed of programming progress and issues requiring their attention.
* Follow applicable SOPs and relevant regulatory guidelines.
* Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload.
* Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others.
* Display willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
* Negotiate and establish accurate time estimates for completion of study activities with internal team members and statistical management, and complete project activities within timeframe allotted.
* Assist in drafting regulatory submissions.
* Effectively utilize current technologies and available tools for conducting the analyses.
* Keeping...
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Type: Permanent Location: Bengaluru, IN-KA
Salary / Rate: Not Specified
Posted: 2025-12-17 07:28:52
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Your Job
The Product Development Strategist is responsible for developing and executing product design strategies, pipelines, and roadmaps for assigned brand.
This role serves as the primary point of contact in product development for their brand, ensuring alignment with business goals and market needs, and driving market share growth through deep consumer and competitive insights.
What You Will Do
* Serve as the primary point of contact for assigned branded products, including in-market support.
* Develop and communicate product strategies, pipelines, and roadmaps.
* Lead and coordinate technical project teams for product initiatives.
* Oversee consumer connection model development/updates, intellectual property strategy, project opportunity initiation, competitive intelligence point of view, and specification approval processes.
* Apply deep consumer knowledge and competitive market insights into product development.
* Collaborate with manufacturing and brand vision teams to achieve financial and strategic goals.
* Influence decisions through strategic and economic thinking.
* Develop and communicate points of view for product direction.
* Foster category influence and ensure a range of alternatives are explored for product solutions.
* Drive household or market share growth and/or loss avoidance for assigned brands.
Key Performance Indicators (KPIs)
* Market share gain or loss avoidance for assigned brands.
* Effectiveness of product strategies and roadmaps.
* Depth and impact of consumer and competitive insights applied.
* Successful execution of project technical lead responsibilities.
Who You Are (Basic Qualifications)
* Deep technical and organizational knowledge applied to solve consumer needs.
* Strategic and economic thinking with strong influencing skills.
* Ability to develop and communicate clear POVs.
* Consumer empathy and category influence.
* Strong collaboration and communication skills.
What Does Success Look Like?
* Market share gains and strong category influence for assigned brands.
* Strategic thinking and deep technical knowledge applied to deliver consumer solutions better than competitors.
* A robust pipeline of product alternatives and innovations.
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Milit...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-12-17 07:27:29
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Quality Manager - Warren, OH
Job Description
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.
The Plant Quality Manager is a key leadership position within a manufacturing facility with accountability to establish and maintain a robust Quality Management System (QMS) complaint with FDA Class 1 Medical Device and Consumer Product requirements and consistently capable of shipping product conforming to the Finished Product Specification (FPS) and other regulatory and customer requirements.
This role is key in building talent and quality system capabilities throughout the manufacturing facility aligned with K-C core values of putting quality into everything we do.
The plant quality manager drives the culture of quality across the entire site in alignment with the strategic quality plan and supporting the business objectives.
The incumbent should have a strong background in managing Medical Device Quality Management Systems, leadership skills in building quality talent throughout a manufacturing facility and have a strong track record of meeting business objectives as a key business partner.
This position reports to the Senior Quality Manager (staff) with a dotted line to the Warren Plant Manager. This position will manage a total staff of approximately 2-4 salary and 8-12 hourly employees.
In this role, you will:
* Develop and deploy the facility quality plan ensuring alignment with the K-C North America Quality Objectives and Supply Chain Strategic Business Plan.
* Ensure adequate resources are available and trained to implement the facility quality plan and required day-to-day activities.
* Engage with and influence the facility management team and other stakeholders such as product development, logistics and suppliers to maintain a focused quality culture within the facility.
* Provide mentorship and direction for quality professionals plant-wide. This includes, but is not limited to, providing strategic guidance and coaching to the system skill roles responsible for supporting plant quality systems and standards.
* Manage yourself, your team and your interactions with others in accordance with the principles and tenets of the plant’s High Performance Work System and expected K-C Values: We Care, We Own, We Act and Ways of Working: Focus on Consumers, Play to Win, Move Fast and Grow our People
* Establish and maintain the facility QMS, ensuring it is capable of consistently meeting FDA Medical Device requirements for Class 1 products and other customer requirements.
* Serves a...
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Type: Permanent Location: WARREN, US-OH
Salary / Rate: Not Specified
Posted: 2025-12-17 07:25:02
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Especialista de EHS Pleno
Job Description
Nosso objetivo é oferecer um Melhor Cuidado para um Mundo Melhor e isso requer pessoas e equipes que se preocupam em fazer a diferença todos os dias.
Aqui, você irá contribuir com a sua experiência profissional, talento e motivação para continuar a levar nossas marcas cônicas e inovadoras para a vida de milhões de pessoas.
Nessa função, você vai nos ajudar a impactar a vida de milhões de pessoas ao redor do mundo.
Tudo isso começa com VOCÊ!
Nesse papel de Especialista de Sistema de Gestão Integrada você irá garantir a eficácia e conformidade dos sistemas de gestão de segurança do trabalho, promovendo um ambiente seguro e saudável para todos os colaboradores, alinhado às normas legais e aos padrões internacionais.
Principais Responsabilidades:
* Dissemina as diretrizes corporativas programas, padrões, políticas globais da empresa;
* Gerenciar e prestar suporte no atendimento dos requisitos legais através do sistema SOGI.
* Implantar, manter e aprimorar o Sistema de Gestão de Segurança do Trabalho (SGST) de acordo com a ISSO 45001.
* Monitorar indicadores de desempenho de segurança e propor ações corretivas e preventivas.
* Desenvolver e revisar procedimentos, instruções de trabalho e políticas de segurança.
* Coordenar treinamentos e campanhas de conscientização sobre segurança.
* Investigar incidentes e acidentes, propondo medidas de mitigação.
Sobre nós
Você já conhece nossas marcas Huggies®.
Intimus®.
Poise®.
Plenitud®.
e os produtos da Kimberly Clark não existiriam sem profissionais talentosos como você.
Aqui, você fará parte de uma equipe comprometida em impulsionar a inovação, o crescimento e o impacto de nossas atividades.
Temos mais de 150 anos de liderança de mercado e estamos sempre em busca de novas e melhores formas de desempenho – portanto, esse é o seu momento de aproveitar nossas oportunidades em aberto.
Esperamos por você na Kimberly Clark.
Somos inspirados por um propósito e guiados pelo desempenho.
Somos uma empresa comprometida com a inclusão, a equidade e a diversidade, para impulsionar nossos resultados de negócio e impactar positivamente a vida de pessoas colaboradoras, consumidoras, fornecedoras e comunidades.
Trabalhamos todas as nossas vagas visando promover uma cultura inclusiva, ou seja, respeitamos e abraçamos a diversidade de gênero, raça, orientação sexual, religião, nacionalidade, idade e deficiência.
Acreditamos no talento e no potencial das pessoas e para nós, é importante termos equipes diversas, que nos permitam atingir nossas ambições de crescimento e contribuir ativamente na representatividade de diferentes perspectivas, opiniões e histórias, para que aconteça a transformação que tanto queremos.
Sobre você
Você atua no mais alto nível possível e aprecia uma cultura de desempenho alimentada por um cuidado autêntico com as pessoas ao seu redor,...
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Type: Permanent Location: Camacari, BR-BA
Salary / Rate: Not Specified
Posted: 2025-12-17 07:24:58
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Hybrid
Employee Value Proposition:
At Taiho Oncology, we are leaders in cutting-edge science and technology, from chemistry to pharmacokinetics.
This expertise and our unique vision allow us to consistently pursue and develop life-changing innovations.
As Senior Director of Scientific & Medical Communications, you’ll play a pivotal role in shaping how our therapies are understood across the globe.
This is your opportunity to lead a team, connect disciplines, and elevate the clarity and impact of our science at every stage of the product lifecycle.
Position Summary:
The Sr.
Director, Scientific & Medical Communications (SDSMC) leads the strategic development, implementation, and global dissemination of scientific communication platforms across all therapeutic assets and disease areas.
This role ensures alignment with broader therapeutic area strategies and drives impactful scientific engagement through robust communication planning.
This role fosters strong internal and external partnerships with medical experts and stakeholders to enhance scientific dialogue and engagement.
The individual ensures compliance with regulatory policies, oversees vendor and budget management, and leads strategic pilots to measure and optimize the impact of scientific communication efforts across the scientific community.
The successful individual will have a strong commitment to achieving corporate objectives while maintaining the highest ethical, regulatory, and scientific standards.
Performance Objectives:
* Lead the development of omnichannel communication strategies that embody Taiho’s scientific integrity and long-term vision.
* Direct publication planning and execution, including abstracts, posters, manuscripts, and congress presentations, ensuring scientific rigor and alignment with strategic goals.
* Cultivate cross-functional collaboration among Clinical, Medical Affairs, HEOR, Commercial, and Communications teams to driv...
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Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2025-12-17 07:19:23
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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
Unsere Pharma-Vision
Medikamente schnell zu den Patienten zu bringen und das beste Ergebnis für unsere Kunden zu schaffen.
Das ist es, was uns in Sterile Drug Product Manufacturing (SDPM) in Mannheim antreibt.
So tragen wir auch dazu bei, bis 2029 unser Ziel zu erreichen: 20 bahnbrechende Medikamente zur Behandlung der Krankheiten mit der größten gesellschaftlichen Belastung bereitzustellen. Unsere Arbeit, unser täglicher Einsatz und unser Engagement bedeuten für sehr viele große Hoffnung und Zuversicht und deswegen müssen wir anders denken und arbeiten.
Mit dem Patient im Fokus setzen wir auf eine neue Organisation und zwar #WIRGEMEINSAM in SDPM!
Verantwortlichkeiten | Das erwartet Dich
Als Head of Biotesting (m/w/d) bist Du für die disziplinarische Führung der Organisationseinheit (ca.
45 Mitarbeitende in 3 Laborgruppen) unter Beachtung der geltenden Arbeitssicherheitsvorschriften verantwortlich.
Du übernimmst die Verantwortung für die Einhaltung aller rechtlichen und behördlichen Anforderungen für die Themengebiete Bioassay und Mikrobiologie.
Ziele für Biotesting und QC, die als Beitrag zur Erreichung der Standort-Ziele dienen, werden von Dir etabliert, visualisiert und nachgehalten.
Budget-, Kennzahlen- und Qualitätsziele werden kontinuierlich von Dir überwacht sowie steuernde Maßnahmen geplant, die in der Organisation abgestimmt und ausgeführt werden.
Zudem vertrittst Du die Abteilung bzw.
den Standort in lokalen und globalen Gremien sowie Projektgruppen.
Du agierst als Coach und Mentor und förderst demnach die stetige Entwicklung deiner Mitarbeiter (individuelle Zielvereinbarungen, Leistungsbeurteilung, Job Responsibilities, Job Exchanges).
Darüber hinaus übernimmst Du folgende spannende Aufgaben:
* Du trägst die Verantwortung für die Einhaltung aller rechtlichen und behördlichen Anforderungen gemäß AMG, AMWHV, Arbeitssicherheit, IFSG § 44 ff, GenTG und weitere bei Bedarf
* GMP konforme und termingerechte Planung und Durchführung aller relevanten Tätigkeiten (u.a.
Release/Stabilty Testing, EMT, IPC) des Bereiches und Sicherstellung der Compliance
* Verantwortlichkeit für Behördenanfragen unter anderem bei Inspektionen, CLO für interne und externe Kunden
* Auswahl, Beauftragung und Überwachung von Auftragslaboratorien sowie Verantwortung von Prüfergebnissen
* Sicherstellung der crossfunktionalen Zusammenarbeit (inkl.
Peer-Coaching) innerhalb der Einheit als auch mit den externen Partnern...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-12-17 07:13:09
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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
Die Qualitätskontrolle (QC) Direct Materials ist ein zentraler Bereich innerhalb unserer globalen Herstellungsprozesse.
Unser Team ist verantwortlich für die zeitgerechte und GMP-konforme Freigabe aller direkten Materialien, die für die Herstellung unserer pharmazeutischen Produkte benötigt werden.
Werden Sie Teil eines dynamischen Teams, in dem Präzision, Zuverlässigkeit und die Einhaltung höchster Qualitätsstandards im Fokus stehen.
Als Laborant (m/w/d) in der QC Direct Materials übernehmen Sie folgende spannende Aufgaben:
* Sie führen selbstständig die physikalisch-chemischen Eingangskontrollen (Identitäts-, Reinheits- und Gehaltsprüfungen) für unsere Direktmaterialien (Hilfstoffe, Verpackungsmaterialien) gemäß GMP-Richtlinien und gültigen SOPs durch.
* Sie wenden verschiedene analytische Techniken an, wie z.B.
Titration, UV/Vis-Spektroskopie, IR- und RAMAN-Spektroskopie.
* Sie dokumentieren alle Ergebnisse lückenlos, präzise und nachvollziehbar im LIMS (Labor-Informations- und Managementsystem) und/oder in papiergebundenen Prüfprotokollen.
* Sie sind für die Wartung, Kalibrierung und das qualifizierte Arbeiten an den zugeordneten Analysegeräten zuständig.
* Bei Abweichungen, OOS- oder OOT-Ergebnissen führen Sie entsprechende Erstuntersuchungen und Recherchen durch und leiten notwendige Maßnahmen in Abstimmung mit dem Vorgesetzten ein.
* Sie unterstützen aktiv bei der Überarbeitung und Erstellung von Prüfanweisungen und SOPs im Rahmen des kontinuierlichen Verbesserungsprozesses.
Ihr Profil
* Eine erfolgreich abgeschlossene Ausbildung als Chemielaborant (m/w/d), Pharmazeutisch-technischer Assistent (PTA) oder eine vergleichbare naturwissenschaftliche Ausbildung.
* Idealerweise mindestens 2 bis 3 Jahre Berufserfahrung in der Qualitätskontrolle oder einem vergleichbaren analytischen Laborumfeld, vorzugsweise in einem GMP-regulierten Umfeld.
* Fundierte Kenntnisse und praktische Erfahrung mit gängigen nasschemischen und instrumentellen Analysenmethoden.
* Sehr gute Kenntnisse der Good Manufacturing Practice (GMP) und Good Laboratory Practice (GLP).
* Sicherer Umgang mit MS Office; Erfahrung mit LIMS oder SAP ist von Vorteil.
* Sie arbeiten äußerst präzise, zuverlässig und selbstständig.
Sie sind teamfähig, flexibel und verfügen über ein hohes Maß an Verantwortungsbewusstsein.
* Gute Englischkenntnisse (in Wort und Schrift) sind für die Dokumentation erforderlich.
Abte...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2025-12-17 07:10:16
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ERM is hiring a motivated, hands-on Environmental, Health and Safety (EHS) Consultant to support a key client in Milpitas, California. This is a part-time (36 hours a week), limited-term role with a duration of 2 months, extendable.
The ideal candidate will have experience developing and supporting the 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 laboratory safety requirements, waste management (hazardous, non-hazardous, universal/ electronic), environmental reporting (HMBPs), and chemical safety requirements.
RESPONSIBILITIES:
* 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 3 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 EHS Consultant position, we anticipate the annual base pay of $88,236 – $132,849, $42.42/hr.
– $63,86/hr. USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may...
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Type: Contract Location: Walnut Creek, US-CA
Salary / Rate: Not Specified
Posted: 2025-12-17 07:09:22
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ERM is hiring an Environmental Compliance Specialist in New Orleans, Louisiana to assist an essential ERM Client.
This Environmental Compliance Coordinator ensures and maintains business unit or department environmental and regulatory compliance with Federal, State and Local regulations.
This is a full-time (40+ hours a week) limited-term role, with a duration of 6 months and the possibility of extension.
RESPONSIBILITIES:
* Ensure the assigned department’s compliance with environmental permits, as well as other regulatory permits and requirements.
* Confirms required monitoring is conducted and data acquisition occurs, verifies recordkeeping systems are implemented and records are maintained in order to meet both site standards and agency requirements.
* Track and monitor waste management activities within the assigned area, to include the manifesting of generated waste, proactively schedule transportation and disposal of industrial solid waste.
Work with site waste specialist / environmental engineer to sample, obtain lab analysis, generate waste profile, manifest, and schedule transportation and disposal of Hazardous Waste.
* Interacts with site personnel, including but not limited to operations management and supervision, engineering, maintenance, operators, and contractors to discuss, resolve, and provide direction on environmental compliance issues.
* Attend and participate in assigned department’s meetings, as a representative of the HSSE Department, specifically to address any environmental concerns and related customer needs.
* Prepares environmental and regulatory reporting for submittal to federal, state, and local agencies.
* Completes monthly monitoring of key metrics related to environmental performance.
* Reviews and ensures the departmental operating procedures include required environmental compliance aspects.
* Conducts incident investigations, participates in Root Cause Analysis, and drives action items to closure.
* Performs housekeeping, compliance audits, and gap analysis within the assigned department at recurring frequency, as well as participates in site-wide compliance audits.
Develops action plans in coordination with central environmental staff to drive HSSE performance to a world-class level.
* Participates in the site EOC duty rotation for emergencies as the site environmental contact and environmental liaison to government agencies.
REQUIREMENTS:
* A BS Degree and 3 years of experience in a chemical manufacturing, refinery, or other related industrial environment are preferred.
* Knowledge of EPA and LDEQ air, water, and waste regulations, as well as industrial compliance experience.
* Proficiency in Microsoft Office products, including but not limited to Word and Excel.
* Experience as an environmental engineer, environmental coordinator, or environmental specialist assigned to a petrochemical process unit is highly desired.
...
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Type: Permanent Location: Metairie, US-LA
Salary / Rate: Not Specified
Posted: 2025-12-17 07:09:21
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Your Job
Georgia-Pacific is seeking a curious, hands-on Material Testing Engineer to join our cutting-edge team at the GP Innovation Institute® in Norcross, GA.
In this role, you'll help shape the future of sustainable packaging and materials performance for one of the world's leading manufacturers.
As a Material Testing Engineer, you'll play a key role in testing and analyzing containerboard, corrugated boxes, and recyclable mailers.
You'll support customer projects, lead quality investigations, and provide technical insights that influence product design and performance.
This is a great opportunity for an engineer who enjoys hands-on lab work, data-driven analysis, and turning test results into real-world improvements.
Our Team
At the Innovation Institute®, we push boundaries to make packaging stronger, smarter, and more sustainable.
Our engineers collaborate with customers and cross-functional teams to uncover creative ways to reduce supply chain costs, improve shelf performance, and drive measurable sustainability gains - using a proven 5-step process built around innovation and value creation.
What You Will Do
* Collaborate with project teams to define testing plans and objectives
* Perform hands-on material and packaging tests using established methods and lab equipment
* Record, analyze, and interpret data to uncover trends and insights
* Identify and troubleshoot anomalies in test results
* Communicate findings and recommendations clearly through reports and presentations
* Maintain lab equipment, uphold safety standards, and support process improvements
* Manage time effectively and contribute to a high-performing, collaborative team
Who You Are (Basic Qualifications)
* Bachelor's Degree in a Science or Engineering discipline; OR an Associate Degree in a Science or Engineering discipline with 2 or more years of experience in laboratory physical property testing and analysis
* Experience analyzing data sets and drawing conclusions
* Experience with Microsoft Excel, Word, Power Point, and Outlook
* Ability to multi-task, prioritize workload, and utilize excellent time management skills to meet deadlines
* Experience working in a lab and following standard operating procedures for testing and housekeeping
* Experience with experimental design, laboratory procedures, and writing technical reports
What Will Put You Ahead
* Bachelor's Degree in Packaging Science, Materials Science, or Mechanical Engineering
* Two or more years of laboratory testing experience
* Experience communicating test plans, test results, and recommendations across all levels of the organization
* Knowledge of statistics including using software packages such as JMP, Minitab, or Power BI
* Experience developing new test methods
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for ou...
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Type: Permanent Location: Norcross, US-GA
Salary / Rate: Not Specified
Posted: 2025-12-17 07:08:57
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General Summary
Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken.
Benefits and Culture
We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future.
Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees.
Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options.
We strive to be your Employer of Choice.
As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career.
Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits
Principal Duties and Responsibilities
• Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken
• May assist with pre-operational inspection of production plant and equipment and completion or related documentation
• Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan.
• Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan.
• Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions.
• Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products.
• Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products.
• Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned
• Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned
• As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s).
Job Specifications
• Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience.
• Basic knowledge of GMP's, Food Safety, and Safety requirements
• Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc.
is required.
• Basic computer ...
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Type: Permanent Location: Topeka, US-KS
Salary / Rate: Not Specified
Posted: 2025-12-16 08:51:58
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Company
Federal Reserve Bank of Dallas
We are dedicated to serving the public by promoting a strong financial system and a healthy economy for all.
These efforts take a team of dedicated individuals doing many different jobs.
Together we’re creating a workplace where talented people can thrive, and we welcome your unique background and perspective to help present the best possible solutions for our partners.
Location: #LI-Onsite.
If you need assistance or a reasonable accommodation, please notify your Talent Acquisition Consultant.
Hold
ABOUT THE DALLAS FED:
At the Dallas Fed we serve the public by partnering with communities and businesses, promoting jobs and stable prices, and keeping your money safe and available.
We welcome different perspectives, ideas, and experiences.
As part of the nation’s central bank, we are committed to improving the economy and our communities.
Are you ready to make a difference?
Learn more about the Dallas Fed: www.dallasfed.org/fed
ABOUT THE INTERNSHIP PROGRAM:
We offer paid, full-time summer internships for many majors, with fulfilling work and opportunities to grow.
To help launch your career, we provide dedicated staff mentors.
You’ll also learn from senior leaders and industry experts.
As part of the Federal Reserve System, you’ll be connected to a professional network that spans the nation.
You will begin in early June 2026 and will be based in the [Insert location] office.
Learn more about our internship program: www.dallasfed.org/internships
ABOUT YOUR TEAM:
This individual will support our outreach in Ausin and our Government Relations function. There are 3 people involved in Austin-area outreach and 3-4 people on our Government Relations team. They will report to the Bank’s Regional Executive in Austin.
WHAT YOU’LL DO:
* Develop and maintain a database of key Austin-area contacts and stakeholders, including for firms in the technology and financial technology sectors
* Support the Austin Regional Executive’s engagement with these stakeholders, including in organizing both virtual and in-person roundtables
* Devise metrics to track the volume and effectiveness of our outreach to stakeholders, and suggest new approaches to improve our effectiveness
* Assist in the production of reports related to legislative developments, to keep internal stakeholders apprised of important developments
WHAT YOU BRING:
* Experience with MS Office Suite (Word, Excel, PowerPoint, Outlook); familiarity with Stata and R a plus
* Strong data management and analytical skills
* Basic research skills for stakeholder mapping and audience identification
* Excellent verbal and written communication skills
* Strong interpersonal abilities and professional demeanor for engaging with business and community leaders
* Self-motivated with ability to work independently and as part of a team
* Willingness to travel within the 11th District...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-12-16 08:48:13
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
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!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
Your Role: Senior Specialist - Upstream Operations Technician
The Upstream OpTech is technical process leader on the Upstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of cellular expansion from benchtop through production bioreactor processes.
Your Responsibilities:
* Executes the operation with team serving as process lead, coach, trainer, and responsible party.
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Serve as the operations representative and subject matter expert for cross-functional process support team.
* Real-time problem solving, process intervention, and technical experiment delivery, and continuous improvement.
* Ensure process documentation is prepared and completed with accuracy and concurrence.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: minimum of 3 years experience with cellular growth/expansion processes.
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Fermentation
* Proficiency with SAP
* GMP manufacturing
* Aseptic experience
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
* Shift: 12 hour Day shift 5a-5:15p 2 week rotation (M,T,F,Sa,Su,W,R)
+ This role currently operates on an 8-hour shift schedule.
Starting in July 2025, the position will transition to the 12-hour shift schedule stated above.
+ Please note that weekend work will have a 4% premium and work outside of your shift hours will have 10% premium.
* Qualified candidates must be legally authorized to be employed in the United States.
Elanco does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Don’t meet every s...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 30
Posted: 2025-12-16 08:31:07
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper & world-shaper.
As a Research Technologist at Alcoa Technical Center (ATC) located in New Kensington, PA, you will be an integral member of the production team responsible with leading projects from design through implementation by organizing, delegating, coordinating, and directing activities within the scope of functional specialization.
This role will be part of a pilot-scale production team focusing on manufacturing and testing advanced proprietary materials for the development of innovative technology.
About the Role:
* Maximize production capacity through process improvements by minimizing ergonomic issues, while meeting customer demand and deliver on-time performance.
* Provide technical direction to technicians and support personnel in ceramic processing, including powder mixing, milling, spray drying, pressing, machining, firing and quality control.
* Track current production performance and improvement to determine effectiveness.
* Responsible for the quality of work performed by others.
Assignments involve initiating, designing, developing, testing, and installing equipment for projects or programs.
* Provide operational troubleshooting and problem solving.
* Manage equipment design and product line design.
* Coordinate and take part in manufacturing audits.
* Provide technical direction to support products and processes.
* Coordinate daily tasks to achieve operational goals.
* Coordinate and execute production planning maintenance tasks.
* Provide CAD/CAM programming when needed.
* Produce reports and presentations.
What you can bring to this role:
* Associate of Science with 5 years of work experience in ceramics, chemical or material processing
* In lieu of a degree, 5-10 years of experience in a manufacturing/process environment
* Effective written and verbal communication skills and the ability to interact with individuals at all levels of the organization.
* Experienced in ceramic operations.
* Independently conducts and directs processes.
* Demonstrated ability to physically perform work in laboratory and industrial environments.
* Strong interpersonal and communication skills required.
* Ability to work with resources within and outside the program team to accomplish the work required.
* Strong organization and analytical skills for data management, and analysis.
Preferred Qualifications:
* Computer and design skills as well as experience with Allen Bradley PLC/HMI Software (RS Logics, etc.) as well as CAD/CAM software (SolidWorks or AutoCAD).
* Experience in managing projects (equipment installation, upgrades, etc.).
* Six Sigma or Lean Manufacturing certification.
What we offer:
* 401(k), employer matc...
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Type: Permanent Location: Alcoa Center, US-PA
Salary / Rate: Not Specified
Posted: 2025-12-16 08:29:21
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Position Title: Multi-Watershed Monitoring Crew Member- Americorps
Conservation Legacy Program: Southwest Conservation Corps
Site Location: Four Corners Office- Durango, Colorado
Terms of Service:
* Start Date: May 25, 2026
* End Date: November 13, 2026
* AmeriCorps Slot Classification: 900
Purpose:
The Southwest Conservation Corps (SCC) is an AmeriCorps Program of the non-profit service organization, Conservation Legacy.
It is built on the legacy of the Civilian Conservation Corps (CCC) that operated from 1933 – 1942. SCC provides youth and young adults opportunities to complete conservation projects on public lands.
While serving with SCC, members receive training of job skills, conflict resolution, leadership, teamwork, and environmental stewardship.
Programs are developed using a step ladder approach to provide a progression of skill development based on a member’s needs.
Members receive a weekly living allowance, training, and an AmeriCorps Education Award.
SCC’s Watershed Program engages motivated young adults, ages 18 - 30, to complete challenging and impactful vegetation monitoring and restoration projects on multiple watersheds in the Four Corners region.
SCC’s Watershed Program is based in the Four Corners office in Durango, CO.
SCC’s Multi-Watershed Monitoring Crew will work with watershed groups across the Southwest to perform vegetation surveying along streamside habitat in 3 watersheds in Colorado, Utah, and Arizona.
Watershed groups include the Dolores River Restoration Partnership, Escalante River Watershed Partnership and Friends of the Verde River.
Vegetation monitoring is crucial to informing river restoration efforts across these watersheds that have been severely impacted by invasive species and other stressors. The crew will also engage in riparian restoration work in the Summer or Fall.
Description of Duties:
This is an AmeriCorps position. The crew member will participate on a 2-person crew (1 leader, 1 member).
While working (i.e. on-hitch), the crew will camp together, prepare all meals together, and work together as a team to complete all projects and chores.
Hitch schedules will vary between 4 days on, 3 days off or 8 days on, 6 days off depending on the watershed the crew is working in. SCC does not provide off-hitch accommodation and crew members will be responsible for their own accommodation during that time.
The primary responsibility of this crew is to collect vegetation monitoring and species inventory data according to each watershed’s rapid monitoring protocol. This crew will tie in and work closely with field staff from each watershed group in order to collect data. This crew is designed to be flexible to meet the evolving needs of each partnership.
Flexibility, adaptability, and the ability to work in remote areas are essential for this crew member position.
Qualificat...
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Type: Contract Location: Durango, US-CO
Salary / Rate: Not Specified
Posted: 2025-12-16 08:23:59
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Title: Watershed Strike Team Crew Leader (Formally known as the DRRP Strike Team)
Conservation Legacy Program: Southwest Conservation Corps Four Corners
Reports to: Watershed Programs Coordinator
Location: Based out of Durango, CO.
Dates of Employment: April 6, 2026- November 13, 2026
Status: Seasonal, Full-time, Camping Program
Wages: $1025-$1125/week, depending on prior experience and certifications
Benefits: Health Benefit Eligible
5 paid days off structured in August between seasons
3 additional days of PTO
Food provided while in the field
Uniforms and protective equipment
Access to Mental Health Consultant and Employee Assistance Program
Training: U.S.
Forest Service recognized Chainsaw training (Certificate awarded upon completion of program)
Colorado pesticide applicator examination and licensure
Leadership skills trainings
Housing: SCC will provide camping location for leaders and CLDP’s during the spring season.
Off-hitch accommodation will not be provided during the regular season.
Host-housing and a partnership with a local hostel may be available during the off-hitch.
More information will be provided during the interview process.
Deadline: Application closes December 31, 2025
Program Summary:
The Southwest Conservation Corps (SCC) is a program of the non-profit service organization, Conservation Legacy, that is built on the legacy of the Civilian Conservation Corps (CCC) that operated from 1933 – 1942.
SCC provides youth and young adults opportunities to complete conservation projects on public lands.
While serving with SCC, members receive training in job skills, conflict resolution, leadership, teamwork, and environmental stewardship.
Programs are developed using a step ladder approach to provide a progression of skill development based on a member’s needs.
Members receive a weekly living allowance, training, and an AmeriCorps Education Award (for qualifying individuals).
Position Summary:
The Watershed Strike Team Crew Leader position is an opportunity to make a difference in young peoples’ lives while completing conservation projects on public and private lands.
Leaders will be mentors, educators, and facilitators for young adults, working to promote the health and resiliency of our land, air, and water.
Standard schedule generally consists of 4 days on-hitch (out in the field as a crew unit) and 3 days off with some exceptions.
Crew Leaders may also be required to come in for an additional day each hitch cycle to complete administrative duties and check-ins with program staff.
On-hitch, crews camp together, prepare all meals together, and work together as a group to complete all projects and chores.
The Watershed Strike Team Crew Leader position requires patience, a consistently positive mental attitude, mentorship, technical aptitude, focus on efficiency, and a high level of competence in the outdoors.
It also involves an administration r...
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Type: Permanent Location: Durango, US-CO
Salary / Rate: Not Specified
Posted: 2025-12-16 08:23:56
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Westminster Suncoast, a beautiful active living retirement community located in St.
Petersburg is currently seeking an On-Call Occupational Therapist.
Provide patient/resident assessment, care planning, direct treatment and consultation to a general rehab caseload.
Participate in the interdisciplinary team process.
Provide teaching and training to care giving staff.
Involvement
with the clinical program development.
Supervise other therapists, assistants, technicians, aides and students as
required.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
1.
Evaluate, identify and treat physical and cognitive deficits that interfere with the resident’s ability to perform daily life activities.
Follow recommendations on MD’s orders.
2.
Design restorative programs and train residents in the use of adaptive equipment.
3.
Develop and enter Care Plans in the system for each of the resident’s needs.
Maintain timely and accurate documentation.
4.
Perform Resident Home Assessments as part of the discharge process.
5.
Perform Resident’s screening during the admission process and quarterly & annual screening to determine the need for therapy.
This job description is not to be construed as a complete listing of the assignments and responsibilities assigned to
any employee; nor are such assignments restricted to those precisely listed in the description.
This job description may change from time to time as the needs of the organization change.
To learn more about our culture and what it is like to work at Westminster Communities of Florida, follow us on our social channels (Facebook and Instagram) at @WestminsterCareers.
EOE, DFWP – “We honor those who have served.”
Experience
Preferred
* 2 year(s): Two years clinical experience preferred
Education
Preferred
* Masters or better in Occupational Therapy or related field
* Bachelor's Degree or better in Occupational Therapy or related field
Licenses & Certifications
Required
* Occupational Therapist
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
See job description
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Type: Permanent Location: St. Petersburg, US-FL
Salary / Rate: Not Specified
Posted: 2025-12-16 08:21:08
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Voyant 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, and 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
Ensures accuracy and reliability in laboratory testing and analysis.
The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards.
What you will do
* Conduct quantitative and qualitative analysis of raw materials and products.
* Collaborate with production teams to troubleshoot production issues.
* Ensure compliance with industry standards and regulations.
* Prepare technical documents and reports.
* Develop and validate analytical methods.
* Calibrate and maintain analytical instrumentation.
* Manage standard chemical inventory and safety protocols.
* Some duties may vary slightly by location.
Education Qualifications
* Bachelor's Degree in Chemistry or related scientific discipline (Preferred)
Experience Qualifications
* 1-3 years Analytical chemistry in a manufacturing environment (Preferred)
* 1-3 years Method development and validation (Preferred)
Skills and Abilities
* Analytical Chemistry (High proficiency)
* Quality Control (Medium proficiency)
* Laboratory Safety (Medium proficiency)
* Technical Documentation (Medium proficiency)
* Regulatory Compliance (Medium proficiency)
* Data Analysis (Low proficiency)
* Instrumentation Calibration (Low proficiency)
* Method Validation (Low proficiency)
* Chemical Handling (Low proficiency)
* Collaboration (Low proficiency)
To Staffing and Recruiting Agencies:Our company does not accept unsolicited curriculum vitae’s or applications from agencies.
We are not responsible for any fees related to unsolicited curriculum v...
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Type: Permanent Location: Countryside, US-IL
Salary / Rate: 70628.5
Posted: 2025-12-16 08:21:06
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Intertek (BML) is a commercial laboratory which specializes in recovery of base and precious metals from raw mineralization.
We are looking for dedicated technicians to join our team.
General Responsibilities
To ensure that all required tasks are performed safely, accurately and on schedule.
Specific Responsibilities:
* Carry out method statements for all required assays and equipment
maintenance/operation in an efficient manner, including proper documentation.
* Analyze and report data in a safe and timely manner.
* Uphold quality control standards to ensure accuracy of analyses.
* Perform fire assaying duties as required.
+ These include fluxing, fusing, deslagging, cupelling, digesting and reading
samples.
* Troubleshooting instruments/equipment as needed.
* Other duties as assigned.
Skill Experience Requirements
* Bachelor of Science, BCIT Assayers Certification or equivalent.
* 1 year lab experience.
* Ability to work independently or as a team.
* Working knowledge of Excel and Word.
* Good communication and interpersonal skills.
Salary & Benefits Information
The base wage or salary range for this position is $22.00 to $28.00 per hour.
Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.
In addition to competitive compensation packages, Intertek (BML) employees are eligible for a variety of benefits including vacation, paid sick days, medical benefits and more.
Intertek’s Commitment
Intertek (BML) is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts.
With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth.
Our Culture of Total Quality Assurance
Intertek (BML) promotes a culture where motivated, customer-oriented employees can flourish, experience professional fulfillment, and reach their highest potential.
At Intertek (BML) we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.
A career with Intertek (BML) offers rewarding opportunities to help companies around the world develop products that are used safely by millions of people every day.
Intertek (BML) is the trusted advisor to many of the world’s leading brands, companies, and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence.
Working at Intertek (BML) means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustai...
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Type: Permanent Location: Kamloops, CA-BC
Salary / Rate: Not Specified
Posted: 2025-12-16 08:18:43
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ERM is hiring an experienced Startup and Validation EHS Team Lead for onsite support of our client’s new greenfield pharmaceutical manufacturing facility in Lebanon, IN.
The ideal candidate will bring strong leadership, technical EHS expertise, and a proven ability to manage health, safety, and environmental programs through system startup and validation activities.
In this role, you will lead the EHS Startup and Validation Team, ensuring consistent practices across all manufacturing areas, alignment with client standards, and readiness for operational handover.
This is a full-time (40 hours per week) limited-term role, with a duration of 36 months.
Responsibilities
* Serve as the on-site lead for EHS during system startup and equipment validation activities.
* Develop and implement consistent safety strategies and procedures across all manufacturing areas.
* Oversee Lockout/Tagout (LOTO) strategies, training, and audits for startup operations.
* Lead and mentor area-based EHS Managers and Specialists supporting startup and validation phases.
* Review and approve EHS-related documentation, including JHAs/JSAs, PSERs, PFTSRs, and PSSRs.
* Conduct audits and inspections to ensure compliance with client and regulatory standards.
* Track and report EHS performance metrics, including incident trends and corrective actions.
* Lead incident investigations and develop root-cause analysis and preventive recommendations.
* Coordinate environmental permit preparation and reporting in collaboration with the site’s environmental team.
* Interface regularly with project management, engineering, and contractor teams to maintain safe startup execution.
Requirements
* Bachelor’s degree in Safety, Occupational Health, Environmental Engineering, or related field.
* Minimum 7 years of EHS experience in pharmaceutical or related manufacturing startup and commissioning projects.
* OSHA 30-hour Construction or General Industry certification required; CSP, CIH, or equivalent preferred.
* First Aid/CPR/AED certification preferred.
* Strong understanding of process safety management (PSM), startup readiness, and validation safety requirements.
* Demonstrated ability to lead multi-disciplinary EHS teams and standardize practices across complex operations.
* Excellent written and verbal communication skills with the ability to engage all levels of stakeholders.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us...
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Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2025-12-16 08:05:42
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ERM is hiring a Protected Species Specialist to support our client in New Haven, Connecticut.
In this critical role, you will be responsible for observing, recording, and reporting wildlife during construction.
This is a full-time (40+ hours/week), limited-term role for a duration of 1 year, extendable.
RESPONSIBILITIES:
* Conduct initial project sweeps, including inspection of isolation barriers, proximate species habitat boundaries, and record the status of species of concern.
* Provide daily sweeps, oversight, and consulting services related to protected species within the area, including adhering to the Project Species Protection Plan and completing daily monitoring and observation reports
* Document protected species interactions and assist with data collection.
* Ensure that all staff are adhering to safe practices.
REQUIREMENTS:
* Bachelor of Science in a related field preferred.
* A minimum of 2 years of experience as a herpetologist, biologist, or wildlife specialist.
* Has or will obtain a Connecticut Scientific Collectors Permit to work with State-listed species.
* Strong knowledge of Endangered Species Act (ESA).
* Good observational skills and attention to detail.
* Strong communication and reporting skills.
* Basic computer proficiency for data entry and report generation.
* Must work safely and follow instructions as per Client and ERM policies.
* Ability to regularly lift 25 lbs.
and occasionally lift 50 lbs.
* Valid driver’s license.
Pay Transparency:
For the Protected Species Specialist position, we anticipate the annual base pay of $ 74,000– $96,901, $/35.57hr – $46.58/hr USD, limited-term, non-exempt. An employee’s pay position within this range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, and business or organizational needs. We also may have instances where employee’s fall outside of the range based on the factors noted above. This job may be eligible for bonus pay (casual and fixed term/Flexforce employees are NOT bonus eligible).
We offer a comprehensive package of benefits including paid time off, medical, dental, vision, 401(k), life & disability insurance to benefits eligible
* employees.
*Benefits Eligibility is limited to Regular employees regularly scheduled to work 20 or more hours per week. Fixed-Term employees (including Flexforce) who are regularly scheduled to work 20 hours a week or more are eligible for a limited benefits package. Casual employees are NOT benefits eligible.
See your recruiter for more details.
You can apply for this role through https://www.erm.com/careers/apply/ or through the internal careers portal if you are a current employee.
Note: No amount of pay is considered to be wages or...
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Type: Permanent Location: Hartford, US-CT
Salary / Rate: Not Specified
Posted: 2025-12-16 07:57:48
