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ERM is seeking a Managing Consultant, Environmental, Health, & Safety Management Systems and Compliance to join our Sustainable Operations technical team in Houston, Texas.
In this role, you will manage and contribute technically to challenging environmental compliance, management systems, auditing, and compliance assurance projects and programs for clients locally, nationally, and internationally.
The successful candidate will also network with ERM's national management systems and compliance technical teams to share consulting opportunities, business relationships, and the application of best practices to address client needs.
This is an excellent career opportunity for a mid-level professional looking to advance their career with a global environmental leader, and to make a significant impact in successfully implementing ERM's global strategy.
RESPONSIBILITIES:
* Provide leadership and strategic direction for expanding ERM's management systems and compliance service area and client base. Identify and develop new opportunities, prepare effective technical proposals, and take active leadership role in developing new business with new and existing clients. Develop and expand client relationships that generate repeat business.
* Direct strategic management systems and compliance assurance programs for a variety of clients with complex technical/regulatory issues. Work closely with clients and develop strong relationships to understand specific processes and develop compliance strategy to help clients maintain maximum operating flexibility.
Achieve client’s expectations for scope, budget, schedule, and quality.
* Serve as a senior technical resource on management systems, compliance, and/or auditing programs.
* Capitalize on existing client relationships to expand ERM’s profile and market share in the regional and global management systems and compliance markets (through a combination of excellence in technical delivery and business development).
* Mentor junior and mid-level staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Support the general growth and development of ERM’s global services. Collaborate with other ERM global practitioners to execute projects, including participating on teams comprised of management systems and compliance professionals from multiple offices around the global organization.
REQUIREMENTS:
* BS/MS in engineering (chemical, mechanical, environmental), environmental science, or related degree.
Or equivalent experience.
* Experience or interest in supervising direct reports.
* 4+ years (7 years preferred) of relevant consulting experience with multimedia environmental compliance and management systems.
* 4+ years (7 years preferred) of experience in managing projects, including scope, schedule and budgets, communications, and interactions with clients....
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-18 08:09:46
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Associate, Global Lab Informatics
The Global Lab Informatics Sr.
Associate is accountable for delivery and maintenance of Elanco global laboratory informatics systems, including selection, implementation, lifecycle management, and technical support.
This role is a key global point of contact for site QC labs, Global Quality, and Elanco MQ and IT leadership.
This role will provide business leadership and project management oversight for the Elanco laboratory informatics program.
Your Responsibilities:
* Strategic Deployment of Laboratory Informatics Solutions: provide program leadership and establish appropriate timelines, provide routine progress reports/metrics, and escalate issues as appropriate.
* Key contact for site leadership and staff to ensure successful deployment of systems, including negotiation of resources and elimination of barriers
* Define and implement support strategy for sustainable lifecycle management of lab IT solutions
* Collaborate with MQIT to define system requirements to ensure that they accurately reflect business needs; ensure business requirements are included in system development
* Collect key learning from deployment activities to incorporate improvements and best practices into downstream deployments
* Business Process Owner for designated global laboratory informatics solutions.
Ensure systems are in compliance with CSQ/CSV requirements.
* Define, develop, and implement business processes to help ensure most effective use of lab informatics solutions; Refine business requirements in collaboration with SMEs and stake holders as needed to gain maximum value from IT solutions.
* Represent business requirements in vendor discussions
* Comply with all company local and global policies including Quality frameworks, Code of Conduct, Corporate Citizenship, anti-discrimination, harassment, and health, safety and environment (HSE) policies.
What You Need to Succeed (minimum qualifications):
* Bachelors degree in Chemistry, Biology, Engineering, information t...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:41:17
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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.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Chemielaborant Analytische Entwicklung SMTD (Small Molecule Technical Development) (m/w/d)
Wir suchen zum nächstmöglichen Termin eine/n Chemielaborant/in/Chemotechniker in der analytischen Entwicklung SMTD (m/w/d) am Standort Monheim am Rhein, Deutschland.
Die Position:
Als Chemielaborant der analytischen Entwicklung von Small Molecules Technical Development ist man Teil eines funktionalen Teams und arbeitet eng mit angrenzenden Disziplinen zusammen (Formuliertechnologie, Verpackungstechnologie, Wirkstoffentwicklung).
Zentral ist hierfür das eigenständige Umsetzen von wissenschaftlichen Protokollen unter Anwendung verschiedener analytischer Techniken mit dem Schwerpunkt Chromatographie.
Zu den Kernaufgaben zählen die analytische Methodenentwicklung, Methodenvalidierung und -transfers, sowie die Durchführung von Entwicklungsstabilitätsstudien und registrierrelevanten Stabilitätsstudien unter GMP.
Ihre Aufgaben und Verantwortlichkeiten:
* Praktische Versuchsdurchführung zur Entwicklung/Validierung analytischer Prüfverfahren für die Qualitätskontrolle neuer Tierarzneimittel
* Analytische Begleitung der Formulierentwicklung
* Prüfung von Stabilitätsmustern unter Berücksichtigung der relevanten Richtlinien
* Eigenständige Planung, Organisation, Durchführung, Auswertung und Dokumentation von Versuchsreihen
* Datenanalyse zur weiteren Versuchsplanung sowie Unterstützung bei der Ergebnisinterpretation
* Unterstützung beim Erstellen von Berichten, Arbeits-, Prüf- und Verfahrensanweisungen
* Präsentation von Ergebnissen bei Team-, Projekt- oder Gruppenbesprechungen
* Intensive Zusammenarbeit mit Kollegen im F&E Umfeld zum Wissensaustausch
* Berücksichtigung externer und interner Richtlinien (z.B.
SOPs, GxP, HSE).
* Pflege der Laborinfrastruktur und der organisierten, sauberen und sicheren Arbeitsumgebung.
* Planung / Durchführung der Wartung von Instrumenten / Geräten sowie Evaluierung neuer Laborgeräte
* Arbeiten unter Verwendung der entsprechenden Sicherheitsausrüs...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: 5905
Posted: 2025-04-17 08:41:00
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Harris is seeking an experienced Product Manager to steer the development and success of our innovative software solutions within Caliber Public Safety.
The product manager role is vital in ensuring our products meet the evolving needs of law enforcement, fire, and emergency response agencies.
The ideal candidate will have a passion for public safety technology, effective leadership skills, and experience driving value-driven, customer-focused solutions.
If you are passionate about building technology that makes a difference in public safety, we want to hear from you!
What You’ll Do:
* Own and drive the product roadmap, ensuring alignment with customer needs, business goals, and market trends.
* Work with engineering, sales, and customer success teams to define and deliver innovative, high-impact solutions.
* Serve as the voice of the customer, gathering insights from end-users, industry trends, and key stakeholders.
* Develop and maintain product requirements, user stories, and acceptance criteria to guide development teams.
* Conduct market research to ensure our products remain leading in public safety technology.
* Partner with marketing and sales to develop go-to-market strategies, messaging, and training materials for product launches.
* Define and track key performance metrics to measure product success and adoption.
* Stay informed on public safety industry regulations, emerging technologies, and customer challenges to drive innovation.
What We’re Looking For:
* 5+ years of experience in Product Management, ideally within public safety, enterprise software, SaaS, or related industries.
* Knowledge of agile development methodologies and experience working with software development teams.
* Proven ability to translate customer challenges into clear, actionable product requirements.
* Excellent communication and stakeholder management skills.
* Data-driven mindset to product outcomes and prioritization.
* Familiarity with Computer-Aided Dispatch (CAD), Records Management Systems (RMS), Mobile solutions, or Offender Management software is a plus.
Why Join Caliber Public Safety:
* Impactful Work: Be part of a company dedicated to helping first responders and public safety agencies with mission-critical technology.
* Growth Opportunities: Join a team that values innovation, partnership, and professional development.
* Excellent Team Culture: Work alongside passionate, experienced professionals in a helpful and purpose-driven environment.
Who We Are:
At Caliber Public Safety, we are dedicated to delivering mission-critical software solutions that empower first responders and public safety agencies across North America and beyond.
Our suite of CAD, RMS, Mobile, and Offender Management solutions ensures that public safety professionals have the tools they need to respond faster, communicate efficiently, and protect communities.
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Type: Permanent Location: Austin, US-TX
Salary / Rate: 110000
Posted: 2025-04-17 08:40:13
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PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. For a defined Area, responsible for supervising the overall operation, condition, maintenance, and repair of all water treatment, physical plant, medical equipment, mechanical/electrical systems in the centralized program so as to ensure safety of the patients as well as the staff operating the equipment. Ensures all decisions, actions and activities of Technical Department Personnel are compliant with company standard operation procedures and with all pertinent local, state and federal regulatory requirements. Oversees OSHA and regulatory compliance related issues ensuring appropriate actions taken to ensure required resolution. Demonstrates pride in the quality of work, regulatory compliance, and the environmental cleanliness of the facilities in the Centralized Technical Program.
DUTIES / ACTIVITIES:
CUSTOMER SERVICE:
* Responsible for driving the FMS culture through values and customer service standards.
* Responsible for outstanding customer service to all external and internal customers.
* Develop and maintains relationships through effective and timely communication.
* Take initiative to respond to, resolve and follow up on customer issues in a timely manner.
* PRINCIPAL RESPONSIBILITIES AND DUTIES:
* Overall management of Technical Services for an area.
Area will typically consist of 10 to 25 clinics and 7 to 15 exempt and non-exempt employees.
* Works with Area Managers and/or Directors of Operations to ensure that operational, financial and regulatory requirements associated with Technical Service are met.
* Collaborates with area Quality and Education personnel on cross functional initiatives.
* Responsible for management and oversight of Area financial metrics i.e.
TAP, maintenance parts cost, travel and expenses.
* Responsible for data integrity for management systems at the Area level i.e.
PeopleSoft, Kronos, and Service Database.
* Responsible for piloting and implementation of new systems and processes as needed.
* Responsible for the following supervision and oversight activities for a defined Area:
* Repair and maintenance activities on water treatment equipment, dialysis equipment, ancillary equipment, test equipment, and the physical plant as recommended by the manufacturer and by procedures established by FMCNA Clinical/Technical services as documented in the FMCNA Policies and Procedures.
* Document all repair and maintenance activity per applicable policies and/or procedures.
* Purchase and maintain inventory of service parts.
* Ensure defective parts with associated RGA and warranty parts are returned in a timely manner.
* Actively support and participate in the Quality Assessment and Process Improvement (QAPI) proces...
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Type: Permanent Location: Aurora, US-CO
Salary / Rate: Not Specified
Posted: 2025-04-17 08:39:34
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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 Quality Control Packaging Supervisor 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 Packaging Supervisor coordina le attività analitiche e affini all’interno del reparto packaging del 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 Manager.
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 e assicura che il lavoro dei collaboratori a lui/lei affidati avvenga nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* È responsabile di garantire il corretto e tempestivo svolgimento delle attività di laboratorio demandate al proprio settore nel controllo qualità, coordinando il team, assegnando compiti e monitorando le performance.
* Supervisiona le attività di controllo qualità relative al packaging dei prodotti farmaceutici, garantendo la conformità agli standard GMP e alle normative FDA, EU-GMP e linee guida ICH.
* Assicura la corretta gestione dei campioni in ingresso in laboratorio provenienti dal reparto produttivo, magazzino e altri siti Adare ed effettua controlli in-process sul confezionamento primario e secondario.
* Forma e aggiorna il personale sulle procedure e sulle best practice di controllo qualità nel packaging.
* Verifica e approva la documentazione analitica inerente a batch...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:59
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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 Quality Control Packaging 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 Packaging Analyst svolge le attività analitiche e affini all’interno del reparto packaging del 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 Packaging 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
* Ha cura del proprio banco di lavoro, dei materiali e delle attrezzature affidatigli anche solo temporaneamente.
* Esegue in maniera corretta e tempestiva lo svolgimento delle attività di laboratorio packaging seguendo scrupolosamente le disposizioni impartite dai superiori.
* Tiene in ordine ed aggiornata la documentazione analitica.
* Esegue operazioni di base propedeutiche allo svolgimento delle attività all’interno del laboratorio packaging.
* Esegue controlli analitici sui materiali di confezionamento primario e secondario secondo le normative GMP.
* Effettua controlli in-process durante le fasi di packaging per verificare la conformità ai requisiti di qualità.
* Controlla etichette, foglietti illustrativi, astucci e materiali di imballaggio per garantire l’assenza di difetti e conformità agli standard aziendali.
* Segnala...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:58
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Sei pronto/a ad entrare a far parte di un’organizzazione in crescita, globale, specializzata nella produzione e sviluppo farmaceutico, che mette le persone al primo posto? Unisciti ad Adare! Noi lavoriamo a stretto contatto con i nostri partner nell’industria farmaceutica durante tutte le fasi di sviluppo e produzione dei farmaci destinati alla commercializzazione, con l‘intento di migliorare le vite dei/delle pazienti e dei farmaci essenziali per le persone di tutto il mondo.
Ogni ruolo all’interno di Adare ti offrirà un’esperienza unica e personalizzata nonché l’opportunità di avere un grande impatto, fondamentale per il successo della nostra azienda. Con l’aiuto di persone come te che si dedicano alla nostra missione, Adare migliora vite migliorando la somministrazione dei farmaci !
Unisciti alla nostra missione, unisciti ad Adare!
La nostra proposta:
* Assicurazione sanitaria
* Piano pensionistico
* Benefit previsti da accordo interno
* Crescita professionale e opportunità di avanzamento all’interno dell’azienda
* Premio di partecipazione
* Programma di riconoscimento dei/delle dipendenti
Siamo alla ricerca di un un/una Analytical Method Validation Analyst che si unisca al nostro Team di Quality Control Compliance.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE:
Il/la Analytical Method Validation Analyst svolge le attività di convalida di metodi analitici su API, intermedi e prodotti finiti all’interno del reparto di Controllo Qualità, in accordo con quanto previsto dalle GMP, dalle normative ICH e dalle Procedure Operative Standard, riportando direttamente al/alla Quality Control Compliance Lead.
COMPITI E RESPONSABILITA’:
Le attività e le responsabilità principali di questa posizione includono quanto segue.
Altri incarichi potranno comunque essere assegnati.
* Svolge il proprio lavoro nel rispetto delle procedure aziendali e delle disposizioni di legge in materia di sicurezza sul lavoro e delle Norme di Buona Fabbricazione.
* Partecipa e fornisce supporto, per quanto di competenza, al Transfer di nuovi Progetti, elaborando una valutazione di fattibilità e successivamente Protocolli e Report della convalida.
* Convalida metodi analitici per API, intermedi di produzione e prodotti finiti in bulk o in confezionamento di mercato.
* Consulta in autonomia linee guida, quali ICH, EurPh e documentazione inerente alla convalida di metodi analitici, ne assicura la corretta applicazione individuando eventuali disallineamenti tra i metodi esistenti e le richieste regolatorie o linee guida.
* Revisiona i dossier nella parte che compete le attività analitiche e del Controllo Qualità in collaborazione con il reparto Affari Regolatori.
* Aggiorna i documenti analitici in conformità alle principali farmacopee ed ai dossier di riferimento in caso di cambi.
* Monitora e redige peri...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:57
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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 Junior Analyst (tempo determinato 12 mesi) 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 Junior 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.
* Adempie alle funzioni per la corretta gestione dei reagenti in accordo alle specifiche procedure.
* Lavora in modo efficace nel rispetto delle scadenze.
* Agisce come rappresentante dell'azienda mostrando rispetto e come ambasciatore /ambasciatrice delle convinzioni e dei comportamenti aziendali.
* Rispetta le politiche, le procedure e le normative in vigore in azienda.
* Svolge ...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:45
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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 Senior Analytical Scientist che si unisca al nostro Team di Pharmaceutical Development.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Senior Analytical Scientist svolge le attività concernenti lo sviluppo, la convalida e l'applicazione di metodi analitici per materie prime, prodotti in corso di lavorazione e prodotti finiti, compresa la preparazione di documenti di sviluppo, convalida e caratterizzazione.
Gestisce i progetti in cui è coinvolto in autonomia.
Inoltre, fornisce formazione, affiancamento e tutoring a scienziati meno esperti.
La posizione riporta direttamente al Director I, Pharmaceutical Development.
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.
* Gestisce i progetti di ricerca a lui affidati
* Definisce la strategia degli studi analitici da attuare, in base delle sue conoscenze scientifiche
* Gestisce/effettua lo sviluppo e convalida di metodi analitici per prodotti farmaceutici
* Gestisce/fornisce supporto analitico per lo sviluppo di formulazioni e preparazione/rilascio lotti destinati a studi clinici.
* Effettua la stesura e la preparazione di metodi, procedure e documenti a supporto dei progetti e dei documenti normativi.
* Partecipa alle riunioni di progetto con i clienti o interne, fornendo input e dati appropriati per la parte di competenza.
* Assiste nelle funzioni quotidiane del laboratorio lavando la vetreria, preparando le soluzioni di labo...
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Type: Permanent Location: Pessano Con Bornago, IT-25
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:42
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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 Senior Formulation Scientist che si unisca al nostro Team di Pharmaceutical Development.
Se ti identifichi in questa descrizione, saremo davvero lieti di conoscerti!
DESCRIZIONE DELLA POSIZIONE
Il/la Senior Formulation Scientist svolge le attività concernenti lo sviluppo formulativo di prodotti solidi orali dalla scala pilota alla scala industriale, ivi inclusi lotti destinati a studi clinici.
Prepara la documentazione tecnica ed interagisce con i clienti.
Inoltre fornisce formazione, affiancamento e tutoring a scienziati meno esperti, oltre che interagire con i clienti in riunioni dedicate.
La posizione riporta direttamente al Director I, Pharmaceutical Development.
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.
* Elabora ed esegue studi di sviluppo formulativo mirati allo sviluppo di forme solidi orali definite dai clienti o dal Management
* Sviluppa nuovi prodotti impiegando le tecnologie nuove o disponibili dalla pre-formulazione alla produzione su scala industriale
* Esegue in autonomia o supervisiona la produzione di lotti destinati a studi clinici
* Esegue in autonomia attività di technology transfer
* Collabora con le funzioni di Project Management e Business Development nelle attività di progetto quali sviluppo formulativo o technology transfer
* Collabora con Operation, Quality e Regulatory nelle attività di scale up di prodotti dalla fase pilota alla fase industriale
* Esegue in autonomia la stesura di procedure...
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Type: Permanent Location: Pessano Con Bornago, IT-MI
Salary / Rate: Not Specified
Posted: 2025-04-17 08:26:38
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Trial Project Management
Job Category:
Professional
All Job Posting Locations:
New Brighton, Minnesota, United States of America, Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Sr.
Principal Clinical Research Associate - Shockwave Reducer (Remote) to join our team.
The position is FULLY REMOTE and can sit anywhere in the US.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
Position Overview
The Sr.
Principal Clinical Research Associate (Sr.
Principal CRA) is responsible for the day-to-day management of a global clinical study.
The Sr.
Principal CRA will be accountable for project management activities, oversight of multiple vendors and for conducting a global clinical study in compliance with applicable clinical and regulatory standards and in alignment with business needs.
The Sr.
Principal CRA is a subject matter expert in clinical research and this work is accomplished with minimal oversight, requires frequent contact with internal and external customers, and is critical to the success of the business.
Essential Job Functions
* Responsible for the day-to-day management of domestic and global clinical studies for pre- and post-market products. Responsible for organizing, communicating and evaluating team objectives for clinical studie...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:22:40
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Warsaw, Masovian, Poland
Job Description:
MEDICAL SCIENTIFIC LIAISON (oncology)
Location.: Poland
Full time job
To be a therapeutic area (TA) scientific expert, responsible for discussing our products, patients’ treatment trends and studies in TAs in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (LS) and to be considered a trusted scientific counterpart and partner and seen as scientific face of Janssen.
Through scientific interactions with LSs, champion medical value of our products fairly based on the risk- benefit profile of our drugs and contribute to foster innovative therapeutic approaches to benefit patients.
Through activities in line with the Medical Affairs Plan, the MSL is jointly responsible for the realization of short-term and long-term company goals.
Essential duties and responsibilities:
Medical and scientific knowledge development
* Continuously update their knowledge of products, patient’s treatment trends and clinical activities and studies within the TA and patient`s treatment trends in the region
* Identify evolving scientific concepts with future clinical implications.
Development and maintenance of a contact network with local Leading Specialists (LS)
* LS interactions during F2F meetings, congresses/scientific meetings and Medical Education events.
* Understand their needs, key value drivers, practical treatment patterns and scientific activities within the therapeutic area.
* Develop and execute an external stakeholder management plan in close collaboration and coordination with other functions including: MAF, HEMAR, Commercial
* Communicate the value of company products, contribute to e.g.
market access activities and formulary discussions.
* Through scientific interactions, champion the medical value of our products fairly based on the risk-benefit profile of our drugs and contribute to the fostering of innovative approaches.
* Collects medical insights including scientific & treatment trends and provides feedback as input for strategic TA & Medical teams.
* Recognize and nurture relationships with rising stars within the scientific community.
Proactive and reactive communication of medical scientific data to LSs
* Communicate directl...
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Type: Permanent Location: Warsaw, PL-MZ
Salary / Rate: Not Specified
Posted: 2025-04-17 08:22:37
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Legal & Compliance
Job Sub Function:
Health Care Compliance
Job Category:
People Leader
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson is currently recruiting for a Director, Health Care Compliance Officer for the Innovative Medicine business with responsibilities for areas within the Global Commercial Strategy Organization (GCSO) and Global Business Development.
This position is located in Raritan, NJ.
The Director, Health Care Compliance Officer will set strategic direction, provide oversight, lead compliance efforts, ensure an effective compliance and risk management program, and drive operational excellence across multiple therapeutic areas, brands and/or functions.
The Director will serve as an internal compliance expert to senior leaders and key stakeholders exercising judgment to mitigate business risk and manage the allocation of resources to support business initiatives and enterprise projects.
Responsibilities:
* Provide strategic guidance and compliance support for assigned areas; provide HCC oversight for business activities based on risk profiles; partner with colleagues to ensure compliance with HCC laws, regulations and industry standards related to the strategy and promotion of health care products and services, interactions with health care professionals (HCPs) and/or government officials (GOs) related to a number of areas including but not limited to:
+ Collaboration with business partners in the development and review of commercial and medical strategies, business plans, new business models, HCP/GO engagements, and company material to facilitate compliant growth.
+ Serving as a member or ad-hoc partner to business leadership team(s) to represent HCC and provide input during strategy discussions and business planning. Providing regular updates to business leadership and collaborating with stakeholders to effectively anticipate, prevent, detect issues and correct violations of laws, regulations, or company policies.
+ Performing risk assessment, root cause analysis, risk mitigation planning and execution, and regular risk reviews to ensure compliance program effectiveness.
+ Fostering a culture of accountability at all levels of the organization with a focus on credo-based decision making and operational excellence.
+ Partnering with business partners ...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-17 08:22:15
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Epidemiology
Job Category:
People Leader
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for the role of Associate Director, Oncology Epidemiology. We have a preference for this position to be located in either Raritan, NJ or Horsham, PA.
Remote work options in the US may be considered on a case-by-case basis and if approved by the Company.
The Associate Director, Oncology Epidemiology role is accountable for working independently, and in this role will also function under the supervision of more senior members of the department.
Primary responsibilities:
* Assist with identifying research study needs, drafting proposals and protocols, and contributing to epidemiology strategy and study conduct across the clinical development program.
* May conduct fit for purpose database and study feasibility assessments and execute analyses across the product cycle.
* Conduct literature reviews and synthesis; provide assistance to clinical teams with study design; and identify and evaluate data resources to meet therapeutic needs.
* Work closely with colleagues in the Observational Health Data Analytics group when defining research questions, developing epidemiological protocols, and implementing solutions.
* Provide epidemiological and/or statistical consulting, education and support to product teams, and disseminate technical information through technical reports, presentation, and publication in peer-reviewed literature, as agreed by the team.
* Research natural history of diseases, both within and outside of existing electronic databases, to understand the inherent risks associated with the indication; statistical risk assessment; using historical clinical trial data and other observational databases to develop an understanding of potential safety issues for new medications, ...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-17 08:21:58
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
Johnson & Johnson is currently seeking a Sourcing Process Intern to join our Global Procurement, Electronics Systems Group located in Danvers, MA.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
Requirements:
Improve your skills with J&J knowledge with one of the fastest growing business segments which supports critical products which save lives.
Organizations that embed strategic sourcing into their procurement processes put their teams in to competitive positions to decrease spending, increase operational efficiencies, and work with top-not suppliers.
Optimizing the entire supply chain- not just the purchasing element by evaluating suppliers, managing relationships, and considering long-term costs and risks, organizations can achieve greater value and efficiency in their sourcing activities.
* Provide analytical support during each of the procurement steps including, but not limited to
* Demand/consumption forecasting
* Supplier Capacity: Gap analysis and mitigation plan.
* Supplier market analysis.
* Supplier assessment.
* Comparative bid analysis: RFI, RFP.
* New Product Introduction, supplier vetting
Qualifications:
* Pursuing a degree in business, supply chain management, business administration, finance or a related field.
* Technical proficiency in major Microsoft products: outlook, excel, PowerPoint, etc.
* Strong communication and interpersonal skills, with the ability to work in a team environment
* Problem-solving mindset with a customer-first approach
* Basic knowledge of data analysis and metrics to evaluate market research
* Familiarity with supply chain management software or ERP systems is a plus.
Permanently authorized to work in the U.S., must not requir...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:21:53
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Market Access
Job Sub Function:
Health Economics Market Access
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Distinguished expert individual contributor and organizational thought leader.
Advises top leadership of ongoing execution of comprehensive market access strategies and performance against key department goals.
Contributes to the body of knowledge of the organization's best practices to develop and produce successful go-to-market health economics market access deliverables.
Identifies new methods of data-driven and researched insights to leaders and staff members on economic studies.
Leads the industry in the design and implementation of health research studies and evaluates value of products based on analysis and customer requirements.
This is a fully remote position.
The Director of Market Access & Reimbursement is responsible for directing and executing the overall US reimbursement strategy for Shockwave’s existing and future products.
The individual has in-depth expertise in developing and implementing strategic and tactical reimbursement/market access initiatives in the US.
A key focus of this position is pursuit of coding, coverage and payment for Shockwave’s novel intravascular lithotripsy (IVL) therapy.
Candidates should have a proven track record of success, including direct contributions in securing access for novel technologies, participation within the CMS rule making process, and a legacy of strategy development within the medical device market.
Experience with influencing private payor coverage
policies is required and, successful payor communication tools and messages is essential.
The role will also incorporate communication to, and with, third party payers, government entities and other market access partners and trade associations.
Strong capabilities in areas such as influence, communication, collaboration and partnership working are critical to this position.
The individual is highly skilled at developing relationships and experience working with KOLs, physician specialty societies, CMS and senior management.
Reporting directly to the Vice President of Market Access and Reimbursement, this person will be in a highly visible and critical role as we launch new products and applications for IVL in the United States.
Essential Job Functions
·Strategic Access & Reimbursement: Lead ...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:21:50
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At Johnson & Johnson,â¯we believe health is everything.
Our strength in healthcare innovation empowers us to build aâ¯world where complex diseases are prevented, treated, and cured,â¯where treatments are smarter and less invasive, andâ¯solutions are personal.â¯Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.â¯Learn more at https://www.jnj.com
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Zhengzhou, Henan, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
â¢Â      Actively identify, develop, and engage key KOLs at regional level.
â¢Â      Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
â¢Â      Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
â¢Â      Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
â¢Â      Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
â¢Â      To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
â¢Â      To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
â¢Â      To organize and moderate advisory boards in cooperation with TA groups.
â¢Â      To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
â¢Â      To collect insights from external customers and feedback timely to shape Brand/medical strategy    Â
Scientific Communication Effectiveness with external/internal customers
â¢Â      To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
â¢Â      To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
â¢Â      Support medical affairs program and activities at local and regional level.
â¢Â      Ensure program implementation 100% in compliance.     Â...
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Type: Permanent Location: Zhengzhou, CN-41
Salary / Rate: Not Specified
Posted: 2025-04-17 08:21:29
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At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Beerse, Antwerp, Belgium, Cambridge, Massachusetts, United States of America
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
Johnson & Johnson's Innovative Medicine - Research & Development (JRD) is seeking to recruit a Postdoctoral Scientist, for a fixed term of 2 years, specializing in Artificial Intelligence (AI) based solutions for Neuroimaging Data.
The most preferred location for this position is Cambridge, Massachusetts USA or Beerse, Belgium.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
The AI/Machine Learning and Digital Health team within Johnson & Johnson Innovative Medicine R&D designs cutting-edge insights and solutions employing various data sources across multiple disease areas.
We are in search of an exceptional postdoctoral scientist with key responsibilities:
* Design, develop, and implement cutting-edge AI and computer vision solutions to address high-priority scientific challenges in biomedical imaging.
Your work will directly contribute to advancements in drug discovery and healthcare.
* Develop and optimize state-of-the-art models to extract actionable insights from complex, unstructured biomedical image data.
* Contribute to the development of scalable core technologies that enable the deployment of advanced computer vision solutions across a variety of imaging modalities, including radiology, and brain imaging.
* Develop and deploy models using containerization technologies such as Docker and Kubernetes to ensure scalable and efficient deployment in production environments.
* Utilize high-performance computing resources and techniques to manage and process large-scale datasets and complex models efficiently.
* Clearly articulate complex technical methods and results to diverse audiences, including scientists, stakeholders, and decision-makers, to facilitate informed decision...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:21:18
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ERM is looking for a hands-on Consulting Associate, Environmental Engineering, Geology, or Science to join our growing team.
Working under the direction of project managers and partners, the successful candidate will work on a wide variety of site investigation, remediation, compliance, and hazardous waste management projects throughout office service area; however, opportunities for travel throughout the United States and globally may also occur.
This is a great opportunity to work with ERM's technical experts to implement the latest investigation and remediation technologies as well as more sustainable approaches, while building the required experience to obtain your professional registration.
RESPONSIBILITIES:
* Conduct field work, including soil, sediment, groundwater, surface water, soil vapor, and indoor air sampling, aquifer testing, drilling oversight and soil logging, soil boring and monitoring well installation, well development, purging and sampling, remedial and wastewater treatment pilot tests, and remedial system operation and maintenance.
* Assist in groundwater and wastewater system performance monitoring.
* Perform Phase I and II environmental assessments to support property transfer transactions.
* Compile and evaluate data and assist in report preparation.
* Prepare environmental compliance work plans, permits, and reports for air quality, hazardous waste, spill prevention, storm water, and wastewater.
* Assist in ensuring compliance with all federal, state and local regulations.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Bachelors in geology, hydrogeology, engineering, environmental science or related environmental discipline; Masters a plus.
Minimum 3.0 GPA.
Or equivalent experience.
* Recent graduate to 2 years of experience.
* Willingness/interest in field assignments; ability to perform field work standing or walking for full field days.
* Strong commitment to safety, including following established Health and Safety protocols.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to work independently and as part of a team.
* Detail-oriented with solutions and results-oriented aptitude and hands-on trouble-shooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
* Ability to lift at least 40 pounds
* 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.
* 40-hour OSHA HAZWOPER certification a ...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-04-17 08:20:42
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Associate, Immunochemistry
The Quality Assistant performs bio-analytical testing (primarily ELISA) on various sample types (raw materials, in-process, release, stability) following regulatory guidelines (9CFR, EU, VICH) and company SOPs.
This role involves initiating, executing, and completing assays while ensuring timely communication with supervisors regarding testing progress, compliance, or scheduling challenges.
Additionally, the Quality Assistant maintains a safe work environment and adheres to GMP documentation practices, with further duties assigned based on experience level.
Your Responsibilities:
* Performs ELISA and PCR testing on in-process, release, and stability samples.
* Prepares reagents and maintains calibrated equipment essential for testing.
* Analyzes test results and reports data using designated software systems.
* Manages inventory, orders necessary kits/supplies, and monitors critical reagent consumption.
* Reviews, updates standard methods, and collaborates with relevant personnel (QC Media Kitchen, Senior Scientists, Supervisors, Managers, Directors) for support and problem-solving.
What You Need to Succeed (minimum qualifications):
* Bachelor’s degree in scientific discipline (e.g., Biology, Biochemistry, Microbiology, etc.) (preferred), Associate degree with laboratory experience, or equivalent laboratory experience in lieu of degree
* Strong understanding of scientific principles, basic lab techniques and immunochemistry processes.
* Ability to performs and document work following established methods, SOP's, GLP/GCP and/or cGMP.
What Will Give You the Competitive Edge (preferred qualifications):
* Problem solving within the scope of responsibilities with some guidance from Supervisor.
* Strong ability to document lab results / data in a lab notebook following applicable regulations.
Additional Information:
* Laboratory work: 80% Lab work, Documentation 20%
* Location: Fort Dodge, Iowa
Don’t meet every single requirement? Studies ...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:25:18
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Director – Internal Manufacturing Procurement
As Global Director Internal Manufacturing Procurement, you will lead a team responsible for strategic sourcing and procurement activities across Elanco’s global manufacturing operations, focusing on Raw Materials, Packaging, and Consumables categories.
In this pivotal role, you’ll report to the Senior Director of Internal Manufacturing, Logistics, and R&D, collaborating closely with stakeholders to optimize costs, enhance quality, and manage supplier relationships effectively.
Your Responsibilities:
* Lead and manage a global team of 4-8 procurement professionals specializing in strategic sourcing for Raw Materials, Packaging, and Consumables categories, ensuring alignment with Elanco’s business objectives to reduce costs, improve quality, and manage procurement risks.
* Drive continuous improvement initiatives by actively seeking and implementing cost reduction and avoidance opportunities across procurement activities, leveraging market insights and strategic supplier partnerships.
* Develop and operationalize comprehensive sourcing strategies and options aimed at enhancing efficiency, mitigating risks, and achieving cost savings, collaborating closely with cross-functional teams to secure approval and execute plans effectively.
* Oversee team to ensure strong management of contractual agreements with key suppliers to ensure robust commercial relationships; map risks and opportunities while fostering strong partnerships with internal stakeholders, including strategy, engineering, and site teams, to drive innovation and operational excellence
* Oversee market analysis and maintain a strong understanding of the supply base to identify potential sourcing solutions, and oversee the preparation and execution of RFIs, RFPs, and tender projects, and prepare team members to lead complex negotiations for products and services to optimize value and terms.
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s degree in busines...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-04-16 08:25:17
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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.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Process Operator – Product Finishing
As a Process Operator for Product Finishing, you will play a key role in the granulating, blending, and bagging of animal health products.
In this role, you'll be responsible for meeting departmental goals, ensuring quality, quantity, and cost targets while maintaining safety, compliance, and industry standards.
This posting will offer a one-time sign on bonus of $2,500!
Your Responsibilities:
* Operate large-scale processing equipment and troubleshoot issues as they arise.
* Drive a fork truck and handle 60-pound bags as part of routine operations.
* Ensure all production operations align with cGMP and ISO 9000 standards.
* Follow proper documentation, verification guidelines, and safety procedures.
* Suggest and implement safety and process improvements to enhance efficiency.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma or equivalent.
* Required Experience: Experience operating industrial processing equipment and working in a manufacturing environment.
* Top 2 skills: Troubleshooting and problem-solving skills
What will give you a competitive edge (preferred qualifications):
* Familiarity with fork truck operation.
* Experience in the animal health or related industry.
* Previous experience with cGMP and ISO 9000 standards.
* Strong initiative and ability to work independently.
Additional Information:
* Location: Clinton, IN Manufacturing Site\
* 12-Hour Rotating Shift (Days/Nights)
This position is a fixed duration employee with a one-year contract, annually renewable for up to 4 years with a potential for a full-time position, based on individual performance and business needs.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily...
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Type: Permanent Location: Clinton, US-IN
Salary / Rate: 23
Posted: 2025-04-16 08:24:58
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At EVRAZ, our strength starts with our people! As a team we collaborate to solve problems, contribute ideas and challenge each other to ensure growth and ultimately success for the business and our employees.
Job Description and Responsibilities
We are currently seeking a Safety Supervisor to join our Pueblo, Colorado team. As a Safety Supervisor you will ensure employee safety, OSHA compliance and EVRAZ Pueblo Safety Program Compliance.
EVRAZ is committed to maintaining and promoting a safe, healthy and injury-free environment. It is required for all jobs.
* Employee engagement regarding safety programs, concerns, and compliance
* Audit and inspect various safety programs and processes including fire extinguishers, fall protection, eye wash stations, incident investigation, and safety permits
* Provide technical safety support to assigned mill and work in conjunction with entire safety department to ensure proper application of and compliance with regulatory, plant, and mill requirements
* Participate in the tracking and communication of mill safety statistics
* Conduct safety training
* Participate in the safety improvement and risk assessment processes related to the EVRAZ Business System continuous improvement program.
* Other duties as assigned
Requirements
* High school diploma or equivalent, 2- or 4-year college degree with an emphasis in occupational health and safety preferred
* Valid Driver’s License
* 2 years of occupational health and safety experience and training, with experience in a manufacturing facility preferred
* Safety program management experience and training, with experience in a manufacturing facility preferred
* Experience supervising in a union environment preferred
* Knowledgeable of OSHA regulations
* Must be available to be on call and assist personnel in times of emergency and business needs
* Ability to professionally communicate, in written and verbal forms, with all levels of our organization
* Strong leadership skills
* Functional knowledge in Microsoft Excel, Access, Word, PowerPoint
* Proven ability to professionally organize, engage, and motivate teams for safe, high-quality results and maximum productivity
* Ability to effectively manage change
COMPENSATION
* $75,000 – $80,000
Open & Closing Dates: 1/16/25 - 5/15/25
Our total compensation package includes amazing benefits!
* Competitive wages and bonus opportunities
* Family medical, dental, and prescription coverage at minimal employee cost
* Short and long term disability programs
* Competitive retirement plans
* Flexible Spending and Health Savings Accounts
* Employer-provided and Voluntary Life Insurance options
* Paid vacation and recognized statutory holidays
* Apprenticeship and career advancement within the company
* Tuition reimbursement
* Wellness program
All applicants must be elig...
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Type: Permanent Location: Pueblo, US-CO
Salary / Rate: Not Specified
Posted: 2025-04-16 08:24:56
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* Recent dialysis experience required
PURPOSE AND SCOPE:
Supports FMCNA’s mission, vision, core values and customer service philosophy.
Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements.
Ensure provision of quality patient care while maintaining cost-effective clinical operations in accordance with all legal, compliance, and regulatory requirements and programs.
Adheres to all requirements of the FMCNA Compliance Program, and FMS patient care and administrative policies as the clinical leader, has the authority to make daily decisions to ensure continuity of care and patient and staff safety
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Manages the tactical execution of short- and long-term objectives through the coordination of activities with a direct responsibility for results, including costs, methods, and staffing.
* Provides leadership, coaching and development plans for all direct reports to maintain an engaged and productive workforce; partnering with Human Resources on employee matters.
* Technically proficient in the specific department and knowledge of industry practice and business principles.
Works on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current business trends.
Has a larger range within the department.
* Responsible for supporting and driving FMS quality standards through meeting all ESRD regulatory requirements and the practice of Quality Assessment and Improvement (QAI), including use of FMS QAI tools.
* Responsible for addressing and acting on adverse events and action thresholds.
* Oversees facility’s Home Therapies Program if applicable.
* Accountable for compliance with all applicable federal, state and local laws and regulations.
* Ensures all FMS Clinical Quality policies and procedures are communicated to and implemented by the facility staff.
* Maintains integrity of medical records and other FMS administrative and operational records.
* Complies with all data collections and auditing activities.
* Maintains facility environmental integrity, including safety.
* Experienced leadership required for multi-faceted environment; role primarily focuses on tactical execution.
Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals.
* An individual contributor will have significant project/process responsibilities.
Program or project responsibility generally within the function.
* Follows processes and operational policies in selecting methods and techniques for obtaining solutions.
Interprets and recommends change to policies and establishes procedures that effect immediate organization(s).
* Decisions have an impact on work processes and outcomes.
Erroneous decisions or failure to achieve results will add costs and may impact the short-term...
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Type: Permanent Location: Linwood, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-16 08:22:55
