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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 Austin, 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.
* Relevant consulting experience with multimedia environmental compliance and management systems.
* 4+ years (7 years preferred) of experience.
* Experience in managing projects, including scope, schedule and budgets, communications, and interactions with clients.
5 years minim...
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Type: Permanent Location: Austin, 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/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:
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:
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,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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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
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PURPOSE AND SCOPE:
The Field Service Technician performs client-site installation, service and maintenance on company manufactured and/or distributed equipment within the assigned regional area(s). The incumbent provides technical support in the diagnosis of operational and/or technical issues of applicable equipment. The Field Service Technician performs all responsibilities in compliance with company policies and procedures intended to meet health and safety, compliance and regulatory guidelines.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Performs all assigned equipment installation, service and/or maintenance in compliance with company policies and procedures.
* Provides high level technical in-service support for cross-divisional teams and/or customers as requested.
* Handles various confidential patient and/or health information in compliance with company policies and procedures, HIPAA, and other regulatory requirements.
* Ensures data accuracy and integrity within applicable systems throughout the documentation process of all completed services performed.
* Processes applicable documentation and corresponding parts in compliance with company policies and procedures on a routine basis.
* Maintains field service inventory in compliance with management recommendations; ensuring accountability for the usage and/or dispersal of assigned inventory.
* Maintains assigned company vehicle, credit card(s) and other business accounts in compliance with company policies and procedures.
* Contributes to the improvement of ongoing operations within the assigned function(s) to maximize efficacy and efficiency in alignment with company goals and objectives.
* May be required to provide cross-coverage of additional regional area(s) to meet business needs.
* Assists with various projects as assigned by direct supervisor.
* Other duties as assigned.
Additional responsibilities may include focus on one or more departments or locations. See applicable addendum for department or location specific functions.
PHYSICAL DEMANDS AND WORKING CONDITIONS:
* The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
+ Participation in the District On Call Technician (DOCT) and National After Hours On Call Technician (NACT) call rotations required.
+ Must be available for inclusion in a rotating 24-hour call coverage schedule.
+ Must be available to work overtime as required.
+ Exposure to blood borne pathogens and/or hazardous materials possible.
+ Routinely lift and/or move up to 70 pounds.
* Extensive travel may be required.
EDUCATION:
High School Diploma required; Associate’s Degree desirable; and Bachelor’s ...
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Type: Permanent Location: St Louis, US-MO
Salary / Rate: Not Specified
Posted: 2025-04-16 08:22:19
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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:
Supply Chain Manufacturing
Job Sub Function:
Multi-Family Supply Chain Manufacturing
Job Category:
People Leader
All Job Posting Locations:
Leiden, Netherlands, Ringaskiddy, Cork, Ireland
Job Description:
Janssen Supply Chain is recruiting for a Global Lead, Site Engineering Biotherapeutics to be located in Leiden, Netherlands, Zug or Schaffhausen, Switzerland or Cork, Ireland.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Switzerland - Requisition Number: R-001569
Netherlands, Ireland -R-009372
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
#Li-Hybrid
At Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress.
That’s why for more than 130 years, we have sought to keep people well at every age and every stage of life.
Today, as the world’s largest and most broadly- based healthcare company, we are committed to using our reach and size for good.
We strive to improve access and affordability, build healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.
Every day, our more than 130,000 employees across the world are blending heart, science and resourcefulness to profoundly change the trajectory of health for humanity.
Position Summary:
The Global Lead, Site Engineering Biotherapeutics will be a key member of the Global Engineering Leadership Team, responsible for supporting and executing the engineering strategy across all Biotherapeutics manufacturing sites.
This role will be pivotal in enhancing operational excellence, asset reliability, and technical standardization while ensuring alignment with network strategy and global engineering priorities.
The role will support global engineering initiatives, ensuring alignment with evolving business needs and technological advancements.
It will require strong stakeholder management and influencing leadership skills to collaborate across Manufacturing, Quality, MSAT, Facilities, EHS and the broader global engineering function.
#Li-Hybrid
Key Responsibilities:
* Global Engineering...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:57
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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:
Quality
Job Sub Function:
Quality Control
Job Category:
Business Enablement/Support
All Job Posting Locations:
Santa Rosa, California, United States of America
Job Description:
Job Description
About MedTech
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
An internal pre-identified candidate for consideration has been identified.
However, all applications will be considered.
We are searching for the best talent for QA Technician III to be in Santa Rosa, CA.
The Quality Technician III is responsible for assuring that company products have been manufactured, inspected, and tested using company approved procedures.
Work with manufacturing and QA to implement solutions to quality related problems.
Description of Work
Perform a wide variety of audits, inspections, checks, tests, and sampling procedures to ensure quality of manufactured goods and adherence to quality procedures.
Maintain “qualified” status on all quality audits, inspections, testing, and equipment procedures.
Coordinate training/cross-training of new and/or existing employees.
With direction from supervisor, coordinate quality activities (i.e., inspections, testing, audits) based on manufacturing and/or Research & Development activities.
Alert supervisor and/or department engineer of any situation that prevents the Quality Technicians from achieving optimum efficiency.
Work with department engineers on development/modification of test methods for new and/or existing products.
Write and update inspection procedures and checklists as required.
Propose document changes, as necessary, to supervisor or engineers to ensure GMP compliance.
Check lot history records for completeness, accuracy, and conformance to SOP.
Monitor calibration and maintenance of all test equipment and fixtures and operation of equipment.
In partnership with manufacturing, implement visual standards and limit samples related to WIP and final inspection of product.
Maintain thorough knowledge of all testing related to set-up, in-process, final inspection, and lot release testing.
Support implementation of corrective actions related to internal/external audits.
Required Skills & Experience
* High school diploma
* 5+ yea...
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Type: Permanent Location: Santa Rosa, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:55
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America, US059 DC Washington - 1350 I St NW
Job Description:
Johnson & Johnson is hiring for a Field Clinical Specialist for Shockwave Medical Inc.
located in Washington.
DC.
This position is fully remote and you must be located n the DC area.
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 Field Clinical Specialist is a visible position that will provide case support to physicians within certain territories. Case support will be done on peripheral and coronary interventional procedures in the pre-market and post-market phases of product development with the Shockwave Medical Intravascular Lithotripsy (IVL) ® technology.
The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection for clinical programs. Case support may be required to support other territories at certain times.
Essential Job Functions
* Physician and hospital staff training, and procedural case coverage to ensure the safe and effective use of medical devices.
* Effectively meet the needs of internal and external customers with a sense of urgency and dr...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:51
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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:
MedTech Sales
Job Sub Function:
Clinical Sales – Hospital/Hospital Systems (Commission)
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
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
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
This position is fully remote and you must live in the West Virginia area
Purpose:
Established and productive individual contributor, who works under moderate supervision.
Helps implement projects, programs, and processes in support of the organization's overall Clinical Sales - Hospital/Hospital Systems strategy.
Applies practical knowledge of the Clinical Sales - Hospital/Hospital Systems field to administer best in class policies, procedures, and plans for the area.
Territory Managers are responsible for cold calling, prospecting, and building relationships that will increase account revenue growth and customer satisfaction within specified product lines and geography.
Focus areas will include driving new business with responsibility for achieving sales expectations in an assigned territory while providing exceptional service and support to physicians to meet their patient’s needs.
The Territory Manager is responsible for case coverage in catheter labs while w...
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Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-16 08:09:47
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ERM is seeking a motivated Consultant, Environmental Scientist to join our global consulting firm in our Cincinnati, OH office.
As a consultant at ERM, you will gain a wealth of experience across different sectors, clients, geographies and services, all of which will help shape your future career path at ERM. In this role, you will work closely with Project Managers on a variety of projects in the energy industry including renewable energy and electric transmission. ERM's collaborative culture provides knowledge sharing of best practices and ongoing learning opportunities for our consultants, allowing you to build your own individualized career path.
RESPONSIBILITIES:
* Provide technical assistance on environmental impact assessments and sustainability-related projects.
* Prepare plans, permits, and reports for wetlands, storm water, NPDES, and wastewater programs.
* Perform environmental compliance assessments and implement follow-up corrective actions to ensure compliance with federal, state, and local regulations.
* Conduct field work, including ecological field studies.
* Provide general environmental compliance support to clients, including on-site assistance, as needed.
* Compile and evaluate data and assist in report preparation.
* Perform project tasks within scope/budget/schedule expectations and ensure quality standards on project deliverables.
* Support ERM Partners-in-Charge and Project Managers to deliver exceptional client value on projects.
REQUIREMENTS:
* BS in biology, environmental studies, or related science degree.
* 2+ years of relevant environmental experience.
* Strong commitment to safety.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Strong hands-on spreadsheet and database comprehension.
* Detail-oriented with mechanical aptitude and hands-on troubleshooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
* 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.
* Ability to lift up to 30 pounds.
* Local candidates preferred.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
At ERM we know that creating a diverse, equitable and inclusive work environment is an essential part of making our company a great place to build a career.
We also see our diversity as a strength that helps us create better solu...
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Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-16 08:08:14
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Primary Function
At Ardurra, the Senior Recruiter is a blend of a strategic and detailed hands-on role responsible for applying and participating in enhancing talent resources solutions that align with our growing organization’s goals and supporting our culture and a great employee work environment.
Our company’s organic growth and acquisitive growth strategies require a successful Senior Recruiter to have a deep understanding of both technical and business aspects to identify and address hidden issues that may impede the company’s talent acquisition success.
Strong collaboration and communication skills are essential to effectively interact with hiring managers and candidates at all levels and to positively influence organizational and/or regional outcomes.
The Sr.
Recruiter works in a collaborative culture, identifying and delivering high performing candidates within the Architectural, Engineering, and Construction (AEC) industry.
Serving as a trusted advisor to internal business teams, guiding the hiring process in a highly competitive industry.
This includes offer negotiation, understanding the psychology of selling and hiring, navigating non-compete agreements, and managing external recruiting agencies.
The ideal candidate will have experience in a professional services or engineering, architectural and construction organization.
The right candidate will be energized by the talented individuals who make up our entrepreneurial workforce.
Primary Duties
* Manage full life-cycle recruitment including creating search strategies, actively sourcing candidates, pre-screening, interviewing and presenting qualified candidates to hiring managers, negotiating offers and facilitating the hiring processes
* Involvement on all aspects of the hiring process, including hiring strategies, recruitment cycle timing and guidance on best practices and sourcing trends
* Build relationships and communicate consistently and proactively throughout the recruitment process to ensure all participants in the hiring process are updated and well informed
* Create a positive candidate experience throughout the entire recruiting process
* Creation of offer letters and keeping candidate files updated
* Update and maintain administrative responsibilities such as applicant tracking system data entry and Excel report
* Follows compliance standards throughout process
Education and Experience Requirements
* Bachelor’s Degree plus 7 plus years of related recruiting experience or equivalent
* Solid experience recruiting for positions in Engineering required (Transportation, Water/Wastewater, Environmental, Structural or Civil)
* Architectural, Engineering, and Construction (AEC) industry experience (required)
* Experience with LinkedIn Recruiter and working within an ATS (required)
* Must have successful track record in sourcing passive candidates
* Creative sourcing techniques and cold c...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2025-04-16 08:07:38
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About Us
Founded in 1908, Merz is a successful, family-owned specialty healthcare company with a rich history.
As a leading global aesthetics business, our award-winning portfolio of injectables, devices, and skincare products empowers healthcare professionals to enhance confidence through aesthetic medicine.
Our purpose is to fuel confidence by helping people look better, feel better, and live better.
We believe you do not have to choose between living life and making a living.
Live your best life with Merz Aesthetics.
A Brief Overview
Serves as a key role within the Merz Aesthetics Clinical Research and Development team, the Clinical Scientist is responsible for contributing scientific and strategic expertise to our global clinical programs.
Liaising with cross-functional study teams, this position requires a highly motivated, scientifically driven leader to contribute to the development of clinical strategy including study design and execution, and data analysis and interpretation, delivering clear, consistent, and comprehensive results toward the registration of new aesthetic products and/or novel aesthetic indications.
What you will do:
* Accountable for contributing scientific expertise to the trial design phase of clinical projects under development:
+ Provide scientific and strategic input across various stages of clinical development to achieve market approval for new products and/or novel indications.
o a.
Duties performed as a member of a cross-functional team of internal and external experts and in support of the medical director.
o b.
Projects are focused on devices, drugs, biologics, and/or other products for human use.
o c.
Projects may span from in-development to post-marketing studies and products.
+ Coordinate and integrate data and information from a variety of sources (e.g., internal and external studies, research documentation, and published literature) to support various clinical development initiatives.
+ Consolidate input from internal and external contributors to develop appropriate key messaging.
+ Provide scientific guidance and technical expertise within teams, across departments, and across functions by providing strategic, actionable direction, creating a strong sense of team unity and identity, and providing positive, constructive feedback.
+ Proactively identify and troubleshoot study-specific issues, competing priorities, and clinical or scientific challenges; propose and enact solutions, developing contingency plans as needed.
+ Ensure effective, accurate, and timely communication of key issues and progress to the team and senior management.
+ Support planning and preparation for internal and external stakeholder meetings (e.g., workshops/summits, investigator meetings, scientific advisory boards, and regulatory meetings).
* Accountable for authorship of various clinical documents, i...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-15 08:29:25
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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
Your Department and Team:
The Analytical Development and Quality Control (ADQC) unit is located in the Gene Therapy Development Center (GTDC) in Penzberg, Germany.
The ADQC department consists of 40 - 50 persons working to develop and implement novel analytical technologies for pre-clinical studies until market authorization and launch of gene therapeutic modalities.
The sub-team focusing on analytical ultracentrifugation (AUC) technologies consists of one subject matter expert (SME) and one part-time analyst.
We are looking for a highly motivated scientist (m/f/d) with a specific focus on/ or interest in analytical ultracentrifugation technologies for the testing and characterization of gene therapy vectors.
Key Responsibilities:
* Scouting, evaluation, development and implementation of innovative, cutting edge analytical ultracentrifugation technologies and workflows for the analysis and characterization of viral vectors (predominantly rAAV) for gene therapeutic applications
* Driving and advancing the science to characterize and quantify viral vectors with a highly enthusiastic and agile, interdisciplinary team
* Independent, self-organized hands-on execution of experiments: method development, equipment qualification and assay validation under GMP requirements as well as testing
* Contribution to the development and definition of control and testing strategies for gene therapy vectors (e.g.
rAAV payload, full/ empty ratio, process related impurities)
* Independent interpretation, evaluation, and documentation of data and the generation of analytical reports in accordance with current regulations
Who you are:
* You have a track record and knowledge (theoretical as well as hands-on) in analytical ultracentrifugation technologies such as e.g.
MWL-AUC method, operating Optima-AUC, UltraScan, Sedfit software solutions, as well as developing and applying respective IT and data management tools
* You have knowledge in the area of gene therapeutic modalities (AAV, Lentiviruses, etc.).
* You have knowledge and experience with principles of GMP (e.g.
data integrity, equipment qualification, assay validation)
* You have a high degree of self-motivation, responsibility, result-orientation and you are an excellent team player
* You are fluent in English and German language skills (written and spoken)
Advantages:
* Flexible time management
* 2092 Euro salary per month for a full-time internship > 3 months
* Reduce...
....Read more...
Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-15 08:07:23
