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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Am Standort Visp wird ein/e Deviation Manager gesucht.
In dieser Position werden Sie in einer Support Funktion GMP gerechte Dokumentation im Auftrag für die Clean-Utilities Logistik und Betriebshygieneteams sicherstellen.
Informationsbeschaffung und Interpretation sind zentral für diese Schnittstellenfunktion.
Ihre Aufgaben:
* Bearbeitung von Abweichungen aus den Bereichen der Reinstmedien, der Betriebshygiene inkl.
Lüftungsanlagen, Environmental Monitoring und Logistik
* Support aller anfallenden GMP Dokumentation (z.B.
CAPAs, CRs, SOPs, PQ Berichte ect.)
* Vorstellen der Dokumentation während Audits und Inspektionen.
* Unterstützung und Koordination von PQs
* Schnittstellenmanagement von Schnittstellen zwischen Clean-Utilities / Betriebshygiene zu QA, QC Monitoring und Produktion
* Verantwortlich für die Schulung und Unterstützung von Mitarbeitern der Utilities und Betriebshygieneteams.
* Unterstützung von Innovationsprojekten (Datenanalysen z.B.
mit R, Erstellung von Power BI Dashboards)
Ihr Anforderungsprofil:
* Master-Studiengang oder PhD in einer relevanten Fachrichtung (z.B.
Biologie/Bioinformatik)
* Sehr gute Deutsch und Englischkenntnisse
* Freude am Verfassen technisch anspruchsvoller Texte (auf Englisch und Deutsch)
* GMP Erfahrung bevorzugt
* Lösungsorientierte, strukturierte und selbstständige Arbeitsweise
* Präzise Arbeitsweise und Auge fürs Detail
* Durchsetzungsfähigkeit, Motivation und hohe Belastbarkeit
* Ausgeprägtes analytisches Denken und Problemlösefähigkeit
* IT Affinität (Data Science)
Lonza’s Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich Life Science neue Ideen für komplexe Problemstellungen entwickeln.
Zusammen leisten wir einen Beitrag, der das Leben vieler Menschen auf der ganzen Welt verbessern kann.
Dies bietet ihnen die Gewissheit und die ...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:48
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The Deviation management Team responsible for GMP documentation of Environmental monitoring (EM) and Clean Utilities Systems (CU).
As a data scientist you will support the team and facilitate the automation of routine reporting and documentation processes.
Key responsibilities:
* Actively develop an R markdown Pipeline for EM/CU Trend reports
* Coordinate the interface with IT regarding data management and integration
* Work on innovation and automation projects
* Lead data visualisation and statistical analyses of EM/CU data
* Support complex investigations with data analytics and summary statistics
* Development of Power BI dashboards
* Teaching the team to use the pipeline or develop GUI (e.g.
shiny app)
Key Qualifications:
* Master's degree or PhD in a relevant discipline
* Proficient in developing R scripts
* Experience with R markdown reports
* Basic knowledge of GMP
* Good understanding of microbiological data
* Strong analytical thinking and problem-solving skills
* Good communication skills in an interdisciplinary environment
* Good coding practice
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:41
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Am Standort Visp wird ein Operations Manager Manufacturing (m/w/d) gesucht.
In dieser Position bist Du für die Leitung von Produktionsanlagen und die Herstellung pharmazeutisch-chemischer Produkte verantwortlich.
Deine Hauptaufgabe liegt in der zeitgerechten und kosteneffizienten Produktion von chemischen Wirkstoffen (API), unter Einhaltung der gesetzlichen Vorschriften bezüglich Sicherheit, Qualität und Umwelt.
Dein Aufgabenbereich:
* Du bist verantwortlich für die termingerechte, qualitativ hochwertige und kosteneffiziente Herstellung Deiner Produkte.
Dabei hältst Du die geltenden Vorschriften und Richtlinien in Bezug auf Sicherheit, Qualität und Umwelt ein
* Du leitest die Erstellung von Risikoanalysen, um Qualität und Sicherheit während des Produktion zu gewährleisten
* Du identifizierst Möglichkeiten zur kontinuierlichen Verbesserung
* Du koordinierst und leitest funktionsübergreifende Teams, und stellst sicher , dass unsere Kunden kosteneffizient und pünktlich beliefert werden
* Durch effektive Kommunikation, Leistungsbereitschaft und Teamfähigkeit schaffst Du ein vertrauensvolles und erfolgreiches Arbeitsumfeld in dem wir und unsere Kunden ein gemeinsames Ziel verfolgen
* Du passt Dich flexibel an sich ändernde Prioritäten an und bist in der Lage gleichzeitige mehrerer Projekte zu unterstützen
Dein Anforderungsprofil:
* Abgeschlossenes Studium (PhD/Master), vorzugsweise in den Fachrichtungen Chemie, Chemieingenieurwesen, Verfahrenstechnik oder verwandten Disziplinen
* Berufserfahrung in der chemischen und/oder pharmazeutischen Produktion sind von Vorteil
* Kenntnisse im Bereich GMP sowie betriebswirtschaftliche Kompetenzen sind von Vorteil
* Fliessende Deutsch- und Englischkenntnisse in Wort und Schrift.
* Ausgeprägte Teamfähigkeit und Kommunikationsstärke.
* Ein hohes Mass an Lernbereitschaft und die Fähigkeit, sich rasch in neue Aufgaben einzuarbeiten
* Proaktive und flexible Arbeitsweise und die Fähigkeit, in einem komplexen Aufgabengebiet unter Zeitdruck hervorragende Ergebnisse zu liefern
* Bereitschaft, Verantwortung zu übernehmen und sich kontinuierlich weiterzuentwickeln
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:39
-
Lonza ist ein weltweit führendes Unternehmen im Bereich Life Sciences, das auf drei Kontinenten tätig ist.
Obwohl wir wissenschaftlich arbeiten, gibt es keine Zauberformel dafür, wie wir dies tun.
Unsere beste wissenschaftliche Lösung sind talentierte Menschen, die zusammenarbeiten und Ideen entwickeln, die Unternehmen helfen, Menschen zu helfen.
Im Gegenzug überlassen wir unseren Mitarbeitern ihre eigene Karriere.
Ihre Ideen, ob groß oder klein, verbessern wirklich die Welt.
Und das ist die Art von Arbeit, an der wir teilhaben wollen.
In dieser Position sind Sie für die Leitung von Produktionsanlagen für die Herstellung von pharmazeutischen Wirkstoffen und Zwischenprodukten auf chemischem Wege verantwortlich.
Ihre Hauptaufgabe ist die termingerechte und kosteneffiziente Produktion unter Einhaltung der gesetzlichen Vorschriften hinsichtlich Sicherheit, Qualität und Umwelt.
In der von uns zu besetzenden Position spielt der Operations Manager Manufacturing eine wichtige Rolle im Rahmen des Bereichsprogramms "Planning for Quality, Control and Reliability" zur effektiven Fehlerreduzierung, proaktiven Risikominderung sowie nachhaltigem Wissensmanagement und kontinuierlicher Verbesserung.
Hauptaufgaben:
* Sie sind verantwortlich für die fristgerechte, qualitativ hochwertige und kosteneffiziente Produktion der Ihnen zugewiesenen Produkte unter Einhaltung der geltenden Vorschriften und Richtlinien in Bezug auf Sicherheit, Qualität und Umwelt.
* Sie bereiten Risikoanalysen vor und führen ihr Team durch diese, um Qualität und Sicherheit während des Produktionsprozesses zu gewährleisten.
* Sie ermitteln und nutzen Möglichkeiten zur kontinuierlichen Verbesserung der Produktionsleistung in allen Bereichen eines großen Fertigungsbereichs unter Anwendung etablierter Operational Excellence Methoden.
* Sie koordinieren funktionsübergreifende Teams, um Unternehmensziele wie Rentabilität und Liefertreue zu erreichen.
* Sie fördern ein effizientes und erfolgreiches Arbeitsumfeld und kommunizieren effektiv mit Teammitgliedern aus verschiedenen Abteilungen und mit Kunden.
* Sie passen sich an wechselnde Prioritäten zwischen verschiedenen Projekten an.
Qualifikationen und Erfahrung:
* Abgeschlossenes Studium (Promotion, Master) auf dem Gebiet der Chemie oder der Verfahrenstechnik.
* Fließende Deutsch- und Englischkenntnisse in Wort und Schrift.
* Ausgeprägte Team- und Kommunikationsfähigkeiten.
* Proaktive und flexible Arbeitsweise mit der Fähigkeit, unter Druck zu arbeiten.
* Bereitschaft, Verantwortung zu übernehmen und sich ständig weiterzuentwickeln.
* Mehrjährige Berufserfahrung in der chemischen und/oder pharmazeutischen Produktion erwünscht / hilfreich.
* Kenntnisse in GMP und Betriebswirtschaft sind von Vorteil.
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auc...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:23
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Lonza ist ein weltweit führendes Unternehmen im Bereich Life Sciences, das auf drei Kontinenten tätig ist.
Obwohl wir wissenschaftlich arbeiten, gibt es keine Zauberformel dafür, wie wir dies tun.
Unsere beste wissenschaftliche Lösung sind talentierte Menschen, die zusammenarbeiten und Ideen entwickeln, die Unternehmen helfen, Menschen zu helfen.
Im Gegenzug überlassen wir unseren Mitarbeitern ihre eigene Karriere.
Ihre Ideen, ob groß oder klein, verbessern wirklich die Welt.
Und das ist die Art von Arbeit, an der wir teilhaben wollen.
Als Ingenieur für Prozessverbesserung sind Sie dafür verantwortlich, eine Kultur der kontinuierlichen Verbesserung innerhalb der Produktion zu entwickeln und voranzutreiben und dabei das Engagement und die Einbeziehung aller Abteilungen sicherzustellen.
Sie werden eine Schlüsselrolle im Programm "Planning for Quality, Control and Reliability" (Planung für Qualität, Kontrolle und Zuverlässigkeit) für eine effektive Fehlerreduzierung, proaktive Risikominderung, nachhaltiges Wissensmanagement und kontinuierliche Verbesserung übernehmen.
Hauptaufgaben:
* Sie führen Verbesserungen in allen Bereichen eines großen Fertigungsbereichs unter Verwendung etablierter Operational Excellence Methoden ein.
* Sie leiten und unterstützen Ursachenanalysen bei Problemen mit Anlagen und Ausrüstungen, schlagen von Korrektur- und Vorbeugungsmaßnahmen vor und stellen sicher, dass diese in Übereinstimmung mit den lokalen Verfahren angemessen dokumentiert und genehmigt werden.
* Sie unterstützen multidisziplinäre Teams in technischen Belangen wie Konstruktionsprüfungen, Inbetriebnahme und Validierung von Anlagen und Ausrüstungen.
* Sei helfen bei der Inbetriebnahme neuer Anlagen und Ausrüstungen durch Festlegung der Benutzeranforderungen bis hin zur Beteiligung an der Inbetriebnahme, Validierung und dem laufenden Betrieb und der Wartung.
* Sie entwickeln, pflegen und verbessern Anlagen, Ausrüstungen und Verfahren, sodass alle Aktivitäten sicher und vorschriftsmäßig ablaufen.
* Sie führen Optimierungsstudien und detaillierte technische Analysen von bestehenden Anlagen, Systemen und Prozessausrüstung durch.
* Sie unterstützen das Produktionsmanagement-Team dabei, dass die Anlagen, Einrichtungen und Prozessausrüstungen sicher sind und den gesetzlichen Vorschriften und Unternehmensverfahren entsprechen.
Qualifikationen und Erfahrung:
* Abgeschlossenes Studium in einer technischen Disziplin (Bachelor, Master)
* Nachgewiesene Erfolge in Projekten in einer ähnlichen Funktion.
* Erfahrung mit der Untersuchung und Dokumentation von Anlagen- oder Prozessfehlern und der Durchführung von Korrektur- und Vorbeugungsmaßnahmen
* Erfahrung mit GMP und Six Sigma / Business Improvement-Techniken.
* Nachgewiesene Fähigkeit, zwischen mehreren Aufgaben zu priorisieren und dabei ein hohes Maß an Genauigkeit aufrechtzuerhalten
* Nachgewiesene Fähigkeit,...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:22
-
Lonza ist ein weltweit führendes Unternehmen im Bereich Life Sciences, das auf drei Kontinenten tätig ist.
Obwohl wir wissenschaftlich arbeiten, gibt es keine Zauberformel dafür, wie wir dies tun.
Unsere beste wissenschaftliche Lösung sind talentierte Menschen, die zusammenarbeiten und Ideen entwickeln, die Unternehmen helfen, Menschen zu helfen.
Im Gegenzug überlassen wir unseren Mitarbeitern ihre eigene Karriere.
Ihre Ideen, ob groß oder klein, verbessern wirklich die Welt.
Und das ist die Art von Arbeit, an der wir teilhaben wollen.
In dieser Position sind Sie für die Vorbereitung und Durchführung von Terminkampagnen als PMO in einem Multiprojektumfeld verantwortlich.
In der von uns zu besetzenden Rolle spielt der Operations Planner Manufacturing eine wichtige Rolle bei Einführung und Ausbau des Critical Chain Project Managements.
Hauptaufgaben:
* Sie sind verantwortlich für die Planung von Projekten nach CCPM (Critical Chain Project Management) mit einer entsprechenden Software.
Bei den Projekten handelt es sich um Produktionskampagnen für pharmazeutische Wirkstoffe und Zwischenprodukte.
* Sie helfen bei der Koordinierung von Ressourcen, um Multitasking und Vorlaufzeiten in einer Multiprojektumgebung zu minimieren.
* Sie berichten über den Projektfortschritt im Vergleich zum Plan, überwachen die Projektdisziplin und helfen Teammitgliedern und -leitern bei der Prioritätensetzung.
* Sie sind maßgeblich an der Einführung und Pflege eines Systems beteiligt, das es ermöglicht, durch die oben beschriebenen Aktivitäten eine bessere Einhaltung des Zeitplans zu erreichen.
Qualifikationen und Erfahrungen:
* Abgeschlossenes Studium (PhD, Master) in den Bereichen Chemie, Verfahrenstechnik, Ingenieurwissenschaften oder Logistik.
* Fließende Deutsch- und Englischkenntnisse in Wort und Schrift.
* Ausgeprägte Team- und Kommunikationsfähigkeiten.
* Proaktive und flexible Arbeitsweise mit der Fähigkeit, unter Druck zu arbeiten.
* Bereitschaft, Verantwortung zu übernehmen und sich ständig weiterzuentwickeln.
* Projektmanagement-Erfahrung (PMO) erwünscht.
* Mehrere Jahre Berufserfahrung in der chemischen oder pharmazeutischen Produktion sind hilfreich.
* GMP-Kenntnisse und betriebswirtschaftliche Kenntnisse sind von Vorteil.
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich Life Science neue Ideen für komplexe Problemstellungen entwickeln.
Zusammen leisten wir einen Beitrag,...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-05 08:12:15
-
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
The IT Infrastructure Security Engineer executes the implementation of IT Security Controls , supports the implementation of appropriate measures in terms of processes and technology. The role works in close collaboration with IT Infrastructure colleagues and IT Security & Compliance.
Furthermore the role is directly involved in the implementation of the corporate-wide information security management program, pertaining to IT Infrastructure, in regards to secure design and implementation of systems to ensure that Infrastructure assets are adequately protected.
This position contributes to reporting on quantifiable security KPIs and drives vulnerability management pertaining to IT Infrastructure.
The position holder designs solutions to improve IT security within the IT Infrastructure environment in a sustainable fashion in accordance with life science regulatory practices, advises respective subject matter experts within Lonza and its’ outsourced services. The role is part of a team of infrastructure security subject matter experts and reports to Head of IT Infrastructure Security Engineering.
Additionally, this team will support, as required, the Security Operations Center team in case of potential IT security incidents.
The position holder will also pro-actively collaborate and communicate with all relevant stakeholders (e.g.
IT Security, system owners, etc.).
The ideal candidate is an experienced security architect with extensive hands-on experience in the relevant IT fields (e.g.
network, virtualization, AD, SQL, etc.), preferably supporting Operational Technology in the life science or manufacturing industry that is subject to regulatory compliance.
A strong solution oriented engineering mindset is expected.
Remote work anywhere in Spain / Italy.
Key responsibilities:
* Support infrastructure security relevant projects by ensuring implementation of required security controls from the design phase and throughout the lifecycle of the systems.
Enforce secure configuration of new and existing assets, design and implement mitigating controls as required
* Define and fully implement effective vulnerability remediation measures on both procedural and technology layer (e.g.
system hardening, patching, lifecycle management)
* Drive security culture within IT Infrastructure
* Support IT Security related Infrastructure services and identify potential improvements
* Co-ensure that regulatory security and data protection requirements are fulfilled on the infrastructure level, e.g.
GxP and GD...
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Type: Permanent Location: Porriño, ES-GA
Salary / Rate: Not Specified
Posted: 2024-04-05 08:10:19
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
027179 Safety Co-Op (Open)
Job Description:
Key Responsibilities
* Attends internship events and functions including but not limited to social networking events and roundtables.
* May presents to Executive Leadership Team at the end of the internship.
* Assists with assignments the team is currently working on.
* Familiarizes oneself with the functions of the department.
* Contributes valuable work through delivering against performance goals and assigned projects.
* Performs other duties as assigned.
Education and Experience
* Typically working towards a Bachelor's degree in related fields.
Knowledge and Skills
* Takes initiative and is intellectually curious.
* An effective communicator, both written and oral.
* Some knowledge of the function related to the position.
40
EEO Statement:
https://www.greif.com/wp-content/uploads/2023/04/HR-101-Equal-Employment-Opportunity-Policy-English.pdf
We offer a competitive salary, excellent benefits and opportunity for growth.
Greif, Inc.
is an equal opportunity employer.
We will not discriminate against any applicant or employee on the basis of sexual orientation, gender identity, race, gender, religion, age, national origin, color, disability, or veteran status.
EOE/Minority/Female/Disabled/Veteran.
For more information read Greif’s Equal Opportunity Policy.
....Read more...
Type: Permanent Location: Taylors, US-SC
Salary / Rate: Not Specified
Posted: 2024-04-04 08:54:40
-
Job Description
Plans and conducts assigned and/or original research projects autonomously while working collaboratively with faculty, staff, postdocs and students.
Education: PhD in related technical, scientific or engineering discipline.
Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies.
Department
Department of Physics
General Submission Guidelines:
Please submit an online application to be considered a candidate for any job at Stevens.
Please attach a cover letter and resume with each application.
Other requirements for consideration may depend on the job.
Still Have Questions?
If you have any questions regarding your application, please contact Jobs@Stevens.edu.
EEO Statement:
Stevens Institute of Technology is an Equal Opportunity Employer.
Accordingly, Stevens adheres to an employment policy that prohibits discriminatory practices or harassment against candidates or employees based on legally impermissible factor(s) including, but not necessarily limited to, race, color, religion, creed, sex, national origin, nationality, citizenship status, age, ancestry, marital or domestic partnership or civil union status, familial status, affectional or sexual orientation, gender identity or expression, atypical cellular or blood trait, genetic information, pregnancy or pregnancy-related medical conditions, disability, or any protected military or veteran status.
Stevens is building a diverse faculty, staff, and student body and strongly encourages applications from people of all backgrounds.
Stevens is a federal contractor under the Vietnam Era Veterans' Readjustment Assistance Act (VEVRAA) and the Rehabilitation Act of 1973, as well as other federal statutes.
NSF ADVANCE Institution Stevens values diversity and seeks candidates who will contribute to a welcoming and inclusive environment for students, faculty, and staff of all backgrounds.
We are an NSF ADVANCE institution committed to equitable practices and policies and strongly encourage applications from women, racial and ethnic minority candidates, veterans, and individuals with disabilities.
Jeanne Clery Disclosure:
In accordance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), the Department of Public Safety is required to publish an annual security report which includes statistics mandated by the Clery Act.
Click here for a copy of this report.
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Type: Permanent Location: Hoboken, US-NJ
Salary / Rate: Not Specified
Posted: 2024-04-04 08:47:32
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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!
Elanco is a Global Leader in pet and farm animal health products. With almost $5 Billion in revenue, our 9000 employees manufacture and market over 200 brands in 90 countries. The Elanco Fort Dodge site manufactures multi-species vaccines for the Global market which accept USDA registrations. We produce over 200 different references of inactivated and modified live vaccine products. Our processes include fermentation and cell-based production of viral and bacterial antigens, inactivation, downstream processing, formulation, liquid filling, and lyophilization of finished products. The site sits on ~335 acres and is the second largest site in all of Elanco.
Fort Dodge is the only Elanco Biotech site to have Manufacturing & Quality (M&Q), Research & Development (R&D), and Animal Care in one location.
About Fort Dodge:
We are a Biotech Manufacturing and Research & Development site with approximately 420 employees. Though the region may be considered rural by most standards, the town has one community college and a large university 1 hour from the plant (Ames, IA). Ames is a short drive to a major metropolitan area—30 minutes to Des Moines (state capital). For nature lovers, you can visit hundreds of thousands of acres of public lands for hiking, fishing, camping, hunting, four-wheeling.
Your Role: Director, Analytical Sciences and Technology
This role leads the Analytical Science and Technology Team in supporting the QC Department, fostering effective collaboration and communication within the team, department, and with internal cross-functional partners within M&Q and R&D.
It designs, conducts, and supervises laboratory experiments, including analytical method development, validation, transfer, remediation, and optimization using techniques like ELISA, western blotting, SDS-Page, CE, bioassays, viral titrations, serological assay, immunofluorescence, and proof of inactivation.
The role ensures the scientific robustness, accuracy, and compliance of all tests and procedures to corporate standards, 9CFR, OSHA, EPA, USDA, cGMPs, and custom...
....Read more...
Type: Contract Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2024-04-04 08:32:23
-
Are you looking to help transform a company and an industry? As a Stewart employee, you’ll be joining a company that is committed to helping you own, develop, and nurture your career while growing our company.
We invest in your career journey because we understand that as you grow so does our company.
You will be part of a diverse and equitable work environment that reflects the customers we serve.
You’ll be empowered to use your unique experiences, passion and skills to help our company constantly evolve and improve.
Together, we can achieve our vision of becoming the premier title services company.
More information can be found at https://www.stewart.com, subscribe to the Stewart blog at https://blog.stewart.com or follow Stewart on Twitter® @stewarttitleco.
Job Description
Job Summary
Directly engages in field operations outside of core Title Operations.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill, and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Job Responsibilities
* Responsible for the quality review of data stored in client files and/or company production systems, ensuring information captured is error-free and accurate
* Reviews quality reports to identify trends, issues and root causes and makes recommendations for change
* Responsible for maintaining title plant dates 5-7 days or less of corresponding county records.
* Responsible for accurately keying and verifying all incoming document files recorded daily.
* Proven ability to work within tight deadlines and manage multiple projects
* Participates in implementing quality processes to ensure operations are of the highest quality
* Follows standard procedures and guidelines
* Understands how assigned duties relate to others within the team and how the team integrates with related teams
* Impacts own team through the quality of the support provided
* Recognizes and solves typical problems; selects solutions from established options
* Communicates moderately complex information in routine situations, typically within own team
* Works under general supervision with limited ability to modify approach
* Individual contributor having no supervisory responsibilities; manages own workload
* Performs all other duties as assigned by management
Education
* High school diploma required; Bachelor’s preferred
Experience
* Typically requires 0-2 years of related work experience
* Ability to type 45-50 wpm
Equal Employment Opportunity Employer
Stewart is committed to ensuring that its online application process provides an equal employment opportunity to all job seekers, including individuals with disabilities.
If you have a disability and need assistance or an accommodatio...
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2024-04-04 08:29:14
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Der Standort Visp sucht eine/n Laborantin/Laboranten (all genders) für die analytische Untersuchung von Rohstoffen für das gesamte Lonza-Werk Visp.
Als Mitglied unseres Analytik Teams der QC FCC sind Sie unter Einhaltung der GMP- und Sicherheitsrichtlinien verantwortlich für die analytische Betreuung von Rohstoffen und Stabilitätsstudien.
Diese Stelle ist zur Verstärkung unseres Teams vorgesehen, das mit einer steigenden Anzahl von Proben konfrontiert ist.
Ihre Aufgaben:
* Untersuchung von Rohmaterialien mittels HPLC und GC und zu einem kleiner Teil auch mittels Titrationen
* Durchführung von Stabilitätsstudien nach GMP
* Analytische Methodenoptimierungen
* Arbeiten im Team
* Untersuchen von Abweichungen und unerwarteten Resultaten, Troubleshooting
Ihr Anforderungsprofil:
* Abgeschlossene Ausbildung als Laborant, Fachrichtung Chemie, CTA oder BSc in Chemie
* Berufserfahrung im Bereich der Qualitätskontrolle (insbesondere mittels HPLC oder GC) unter GMP ist von Vorteil
* Sie arbeiten gerne im Team und planen ihre Arbeit eigenständig
* Sichere Deutsch- und Englischkenntnisse
* Erfahrung mit CDS Empower, LIMS und Dokumentum von Vorteil
Lonza’s Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich
Life Science neue Ideen für komplexe Problemstellungen entwickeln.
Zusammen leisten wir einen Beitrag, der das Leben vieler Menschen auf der ganzen Welt verbessern kann.
Dies bietet ihnen die Gewissheit und die Zufriedenheit, mit der eigenen Arbeit wirklich einen Unterschied zu machen.
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-04 08:25:25
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
.
Lonza Pharma and Biotech has an opening for an experienced Inhalation Principal Investigator in their Bend, OR location.
The Inhalation Principal Investigator is accountable for the formulation and process design, development and manufacturing for the inhalation technology platform, including client programs focused on the inhalation or intranasal drug delivery route specifically around dry powder inhalers.
As the Inhalation Principal Investigator, you will apply your knowledge of chemistry, material science, and engineering to solve drug delivery, formulation, process, and manufacturing challenges to progress client programs focused on early, late stage clinical and commercial development.
Oversees multiple cross functional product development teams for specific client programs to execute work plans against specific hypothesis and problem statements.
Reviews, interprets, and reacts to data to make tactical and strategic decisions in order to maintain or change product development plans specific for the client portfolio.
Key responsibilities:
* Accountable for technical success of client programs by working with the client and the internal Subject Matter Experts (SMEs) to define the program problem statements and technical program strategy
* Work with client to define and maintain appropriate Target Product Profile (TPP) to guide technical development strategy
* Primary client technical counterpart related to formulation, process, and analytical methods
* Present technical results and recommendations to the client. Serve as the primary technical point of contact for the client programs (internally and externally).
* Define Intellectual Properties (IP) strategy for each program (by working with legal IP) that maximizes value for the client and Lonza by recognizing and pursuing new IP, utilizing existing IP, and / or establishing Freedom to Operate (FTO)
* Lead, motivate, and mentor multi-disciplinary project team of internal SMEs, scientists, and engineers to meet technical milestones on appropriate timelines and provide technical feedback and recommendations at the project level
* Collaborate effectively between different technical lines and support cross line collaboration
* Identify and propose new technical opportunities while working on client programs
Key requirements:
* Bachelor’s degree in chemistry, engineering, pharmaceutical sciences or a related field are required. Masters or PhD preferred.
* Advanced knowledge of common inhalation analyt...
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-04 08:24:46
-
Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Am Standort Visp wird ein Anlageteamleiter PCP (m/w/d) gesucht.
In dieser Funktion unterstützen Sie das Wachstum der Bioconjugate durch den Aufbau und die Leitung einer neuen Produktionslinie.
Sie tragen die Gesamtverantwortung für die Herstellungsergebnisse in Bezug auf Qualität, Menge, Sicherheit und sind Mitglied des PCP Manufacturing Leadership Teams.
Ihre Aufgaben:
* Aufbau und Führung eines Teams aus Bioprocess Engineers (Chemiker, Biologen), Teamleads Manufacturing und Manufacturing Specialists
* Verantwortung für Ausführung aller Produktionskampagnen seiner Linie entsprechend der Sicherheits-, Qualitäts- und Umweltschutzrichtlinien
* Verantwortung für alle Personalthemen wie Qualifizierung, Entwicklung, Coaching, Neueinstellungen, Gehalts- und Disziplinarthemen
* Mitglied im Manufacturing Leadership Team
* Fachexperte und Ansprechpartner für alle Fragen der Produktionsplanung (S&OP Process), technischen Evaluierungen und technical evaluations and Machbarkeitsstudien
* Sicherstellung und Weiterentwicklung der regelmäßigen Leistungs- und Ergebniskontrollen, wie Weekly Reports, Dashboard, Hoshin Board und weitere Reportings
* Projektleiter oder Mitglied in CAPEX Projekten
Ihr Anforderungsprofil:
* Bachelor oder Master in Chemie, Chemieingenieurwesen, Biotechnologie oder verwandten Studiengängen
* Mehrere Jahre Berufserfahrung in der chemischen oder biotechnologischen Produktion, vorzugsweise in Führungspositionen, MSAT, Engineering oder ähnlich
* Sehr gute Englisch und gute Deutschkenntnisse
* Umfassende GMP-Kenntnisse
* Klare und gewinnende Kommunikation mit Geschick der Interaktion mit allen verschiedenen Ansprechpartnern innerhalb der Organisation
* Gutes Verständnis von Finanz- und HR-Prozessen und -themen
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich
Life Science neue Ide...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-04 08:18:51
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IFG is seeking a Remote Systems Technician to join our Lumberton team.
This position is onsite at our Lumberton mill.
It involves the remote operation of radial cranes, grapples and overhead cranes.
REQUIRED ESSENTIAL SKILLS & ATTRIBUTES:
* Ability to operate joist stick controls for a remote crane operation using monitors
* Lightweight Maintenance duties and Mission Planning
* Demonstrate attention to detail
* Safety-oriented attitude
* Great at problem solving
* Strong communicator
* Team orientated
* Comfortable with Heights
* Continuous improvement mindset with a drive to improve the operation
EDUCATION & SKILLS REQUIREMENTS:
* Associates Degree in Instrumentation or Computer Science-preferred
* Experience with HMI Interface-preferred
* Mechanical & electrical experience-preferred
* Light weight Maintenance Skills
* Troubleshooting Skills
PHYSICAL REQUIREMENTS:
* Move safely, quickly, and perform duties with repetitious movement.
* Sit and/or stand for shift, reach with hands and arms, stoop, squat, twist, push and pull, maintain balance, bend at the waist, kneel, walk varying distances, and climb stairs.
* Must be able to tolerate all weather elements, loud conditions, vibrations, and airborne particles (sawdust).
PRE-EMPLOYMENT REQUIREMENTS:
As a condition of employment, Idaho Forest Group requires employees to complete a variety of pre-employment screening processes which may include, but are not limited to: criminal background check, drug and substance test, reference check, prior work verification, driving history (MVR), education verification, aptitude/skills testing, and credit checks.
The depth of screening will vary based on the position.
WHY JOIN IFG - IDAHO FOREST GROUP:
IFG employees are the engine that drives our company’s culture and success.
We value the diverse backgrounds, perspectives, and identities that team members bring to the job and recognize that it is often these experiences that fuel innovation.
We are committed to building a workplace where diversity of thought, life experience, and family history are welcomed.
We recognize and highly value America’s veterans and especially believe the talents and ingenuity acquired through military service can help our company grow and thrive.
If you are an individual with disability and need a reasonable accommodation in the application or hiring process, please contact Human Resources at 208-762-6630 and/or hr@ifg.com.
https://ifg.com/careers/
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job func...
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Type: Permanent Location: Lumberton, US-MS
Salary / Rate: Not Specified
Posted: 2024-04-03 10:26:36
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
As a leader within Alcoa, you can help fulfill our purpose and realize our vision to reinvent the aluminium industry.
Be part of the team that is helping shape a better workplace with a better work-life balance and the equal opportunities that help everyone thrive.
You have the power to shape things and individuals to make them better.
About the Role:
Are you ready to play a crucial role in securing Alcoa of Australia’s ongoing license to operate? Join our team and become a key influencer in shaping our risk management strategy.
As the Regional Risk Manager, you will lead the charge in creating and implementing a robust risk management framework tailored to the Australian region.
Your expertise will ensure compliance with legislation and other requirements while prioritizing and integrating risks across our operations.
By coaching fellow professionals and fostering a culture of risk awareness, you will drive Alcoa towards sustainable success.
Core activities include:
* Design and implement an overarching risk management framework and strategy for Alcoa of Australia.
* Lead complex risk assessments and workshops to identify and mitigate potential threats to our business.
* Tailor risk reporting for various stakeholders, from board members to department heads.
* Integrate risk management with our capital and long-term plans, ensuring alignment and efficient resource allocation.
* Establish business continuity plans to address key risks and maintain operational resilience.
* Recommend and implement measures to recognize and accommodate risks, including insurance strategies.
* Conduct policy and compliance audits, collaborating with internal and external auditors.
* Support procurement activities by reviewing contracts and proposals to minimize new risks.
This role is pivotal in safeguarding Alcoa of Australia's license to operate, requiring adept decision-making and collaboration across all levels of the organization.
Challenges include interrogating established policies, engaging in crucial discussions, and representing Alcoa in industry and government forums.
Join us in shaping the future of risk management at Alcoa! Ready to embark on this exciting journey? Apply now and be part of our dynamic team at Alcoa of Australia!
What’s on offer:
* Career development opportunities to pursue your passion
* Car allowance
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing s...
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Type: Permanent Location: BOORAGOON, AU-WA
Salary / Rate: Not Specified
Posted: 2024-04-03 09:07:28
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza Pharma & Biotech has an excellent opportunity for an experienced Limited Supervising Electrician at their Bend, Oregon location.
Key Responsibilities:
* Responsible for safety of all electrical installations and electrical equipment in all Lonza-Bend facilities
* Install, troubleshoot and repair all electrical systems under the direction of the Sr.
Manager, Maintenance and Sr.
Manager, Engineering.
* Work through Change Control process and documentation for all GMP changes.
* Assist with electrical code review of electrical designs, installations, and upgrades as needed
* Assist with installation, troubleshooting, and design of new installations in coordination with Automation and Electrical Engineers.
* Utilize safe working practices and safe work permits in all situations.
Examples include lockout tag out, proper PPE, ladder safety, lifting equipment, and use of man lifts.
* Assist with identifying and writing necessary energy control procedures.
* Provide project management of electrical contractors.
* Maintain proper electrical spare parts and work area.
* Utilize work order system to plan and document work.
* Maintain continuing education as required by the State of Oregon
* Assist with Arc Flash program requirements.
* Provide updates to electrical drawings
* Direct authority to halt any and all operations, which pose unsafe electrical or mechanical hazards
* Maintains site electrical permit with City and County.
* May have technical oversight of and training for Journeyman, Limited Maintenance and Apprentice Electricians.
* Some heavy lifting required
* Ability to identify hazards
* Dispose of electrical items under Federal and local codes
* Perform other duties as needed
Key Requirements:
* State of Oregon Limited Supervising Electrician license or higher is required.
* Experience working as a Limited Supervising Electrician in an industrial/manufacturing facility is required.
* Maintenance experience a plus.
* Experience with Hazardous Area classifications (NFPA 70 Article 500) is required.
* Familiarity with computerized maintenance management systems a plus.
* Low voltage and controls experience a plus.
* May be required to work evenings and/or weekends
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just...
....Read more...
Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-03 08:55:46
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Virtual Heroes/ARA is looking for an exceptionally skilled technical artist with a focus in Unreal Engine 5 development.
The ideal candidate has extensive experience with various art and design tools of the Unreal Editor.
This person has a solid grasp of the 3D art pipeline from ideation to finished application.
* What you’ll do as an Intermediate Unreal Technical Artist
+ Establish custom workflows and techniques for other artists to utilize when authoring assets.
+ Create assets for real-time applications, including virtual reality.
+ Troubleshoot and help solve challenges with technical solutions.
+ Support a wide variety of projects across many different industries.
* Intermediate Unreal Technical Artist Requirements
+ US Citizenship is required.
+ Candidates selected may be subject to a government security investigation and must meet eligibility requirements for access to classified information.
+ Bachelor’s degree in a related field with 5-7 years of relevant work experience or 11+ years relevant experience in lieu of degree.
+ Experience in real-time 3D game development using Unreal Engine.
+ Understanding of Unreal Engine, including Blueprints, and a passion to apply it to solving real-world training and simulation challenges.
+ Proven ability to estimate art requirements for potential projects.
* Intermediate Unreal Technical Artist Preferences
+ Experience in business development from a technical art perspective.
+ Experience authoring, editing, and animating MetaHumans.
+ Experience in secondary areas such as Niagara, Lumen, and Chaos Physics.
Salary Range: $88,200 - $147,000 dependent upon experience, education & skills as determined during the interview process.
Company Information:
At Virtual Heroes, we leverage simulation and digital-games-based paradigms to create applications that teach critical skills.
As a division of Applied Research Associates (ARA), we work with scientists and engineers of many disciplines and diverse backgrounds to enhance the creativity and innovation of the mission-critical solutions we provide to our customers.
ARA is an employee-owned international research and engineering company recognized for providing technically superior solutions to complex and challenging problems.
Founded in Albuquerque, NM in 1979, ARA currently employs over 2,122 professionals and is rapidly growing.
Our culture supports our exceptional staff of valued employees and encourages professional growth through continued higher education, participation and publication at technical conferences, and membership in professional organizations.
As an ARA employee you are encouraged to generate new ideas and bring those ideas to life.
ARA offers competitive salaries and outstanding benefits including stock ownership, medical and dental coverage, long-term disability insurance, life ins...
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Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2024-04-03 08:53:07
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ABOUT THE ROLE
Means TransForm Products is now the newest business unit of the Amsted Automotive Group, a premier technology organization specializing in complex metalworking and high tech machining equipment and processes.
Amsted Automotive is a growing company that embraces the employee experience through driving a positive culture, respecting and implementing your ideas and providing opportunities for career growth.
As an employee owned company, you will share in the overall financial success of the business.
If this is attractive to you, join our Shelby Twp, MI team today!
This job posting is for Afternoon Shift (3:00 PM-11:00 PM, 15% Shift Premium) and/or Midnight Shift (11:00 PM-7:00 AM, 15% Shift Premium)
WHAT YOU’LL DO
Primary Function Summary
* Adapt and promote Lean Manufacturing principals
* Active participant in the Elimination of Waste Team meetings
* Support the Company’s Goals and Objectives
* Perform receiving, in process and final audit inspection as directed
* Record attribute and variable data on in process inspection record according to parts-specific dynamic control plans
* Verify that procedures are being followed and inspections performed by operators
* Responsible for supporting the team efforts of set up and operation of stamping presses as related to inspection tools, etc.
* Perform final audit inspection which requires tagging parts and dunnage properly for storage in work in process areas or for shipment to the customer
* Responsible for notifying press and/or production if non-conforming material is detected, suspect material is to be identified and isolated.
Assist in identification of “Clean Point”.
* Communicate findings, regarding trends or nonconforming parts or processes to appropriate personnel and participate in corrective action process
* Perform First piece and in-process inspections and log in process inspection record, as applicable, including contamination testing, as applicable
* Perform Last Off inspections, including provide part data to assist in tooling repairs on last off report
* Generate reports of nonconforming material or product(s)
* Identify nonconforming material and quarantine
* Assist in root cause analysis and problem solving tasks as assigned
* Assist in Gage R&R’s and Part Capability Studies as assigned
* Identify trends using basic statistical process control techniques
* Other duties as assigned by Quality Management
* May receive direction from Quality Engineers
* Communicates to next shift personnel
WHAT YOU’LL NEED TO SUCCEED
* All inspection work requires proficient use of measuring equipment (scales, micrometers, calipers) and checking fixtures, and metrology tools (surface testers, CMM’s, )
* Must be computer literate and have working knowledge of other workplace machinery such as a SAP hand held scanners calculators and printers
* Mu...
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Type: Permanent Location: Shelby Township, US-MI
Salary / Rate: Not Specified
Posted: 2024-04-03 08:39:16
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* Monitor finished product and ingredient testing daily.
* Review inventory reports of finished products, raw materials, and components.
* Communicate with internal lab and 3^rd party laboratories for status updates and retests.
* Coordinate closely with Quality Manager on specifications, testing, deviations, OOS resolutions, etc., ensuring product compliance.
* Communicate with MSG suppliers professionally, as needed.
* Integrate with Sales Support for status updates to customers.
* Utilize System 21 and LIMS databases.
* Monitor and adjust the first available dates (FAD) for accuracy for finished products and ingredients.
* Coordinate supplier NCRs and corrective action follow up with supply chain.
* Review supplier documentation, compile 3^rd party reports, and review results against specifications.
* Login samples as needed.
* Assist with the release of ingredients and components for production.
* Customer Service
* Primary liaison with customers for consumer complaints
* Receive and log complaints into the complaint tracker
* Investigate and compile complaint reports in a timely manner
* Coordinate with department leaders to establish effective CAPAs
OPEN
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Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-03 08:37:37
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Global Key Account Manager
ESSENTIAL DUTIES and RESPONSIBITLIES:
* Serves as liaison between customer and Intertek global operations to ensure correct understanding and consistent execution of customer’s requirements according to specified processes and protocols.
* Manages multiple key global accounts, including managing activities of customer on-site staff (Account Coordinator) where applicable.
* Documents and communicates client requirements and work instructions to Intertek global network of labs and offices.
* Provides creative and innovative ATIC solutions to support client business strategies.
Works to develop a strategic partnership between self, Intertek, and customer.
* Drives and generates opportunities for revenue growth consistent with Intertek global key account initiatives and strategies.
* Performs random review of test reports to ensure consistency and accuracy which are reported to management and lab network.
* Proactively organizes and leads formal Quarterly Business Review (QBR) meetings with global key accounts.
* Keeps current on relevant product regulatory, safety, and quality performance requirements; communicates and consults with customer on relevant information; provides technical regulatory support; directly or facilitating through Intertek network of experts.
* Participates and consults with customer(s) in routine quality and safety meetings with QA engineers and other stakeholders.
* Expedite projects as needed to ensure turnaround times and performance metrics are met.
* Create and deliver client presentations for quarterly business review meetings.
* Prepares sales reports, forecasts, and provide regular account status updates through established CRM system, including the development of account-based strategies (Strategic Account Plan) in consultation with Director / Senior Director of Global Account Management and appropriate Global Business Line leaders.
* Organizes seminars or webinars to provide training to the customers and vendors on both process and technical related topics.
This may include periodic travel to overseas countries to meet with vendors or overseas customer sourcing offices.
Why work at Intertek?
Intertek is a world leader in the $250 billion Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts.
At Intertek, we exercise our spirit of innovation, the passion of our people and our unmatched customer commitment to realize our purpose of making the world an ever better, safer, and more sustainable place for all.
Learn more about Our History and What We Do.
What we have to offer:
We offer a salary and benefit package competitively placed within the local market, including medical, dental, vision, life, disability, RRSP with company match, tuition reimbursement and more.
Intertek believes that Our People are our str...
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Type: Permanent Location: Mississauga, CA-ON
Salary / Rate: Not Specified
Posted: 2024-04-03 08:35:47
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Operations Expert Support – Drug Product (m/f/d)
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that is the kind of work we want to be part of.
The site in Visp, Switzerland is growing and for our Biologics organization, we are currently looking for experienced Operations Expert Support in Ibex® Solutions, our recently launched unique biological manufacturing and development concept, to join our Drug Product team.
Visp, also known as the sun center of Switzerland, is located in the Swiss Alps close to Zermatt, Saas Fee, Verbier and Crans-Montana – a beautiful area to go skiing in the winter or enjoying great views during hiking and biking tours in the summer.
Become part of this exciting opportunity and apply now!
Key responsibilities:
* Participate in Capital investment projects for building and commissioning of new manufacturing equipment
* Coordination of cross-functional process improvement projects as part of a ramp-up of a commercial aseptic filling line
* Drive continuous process improvement of the manufacturing process to support commercial life-cycle
* Apply formal processes and tools to manage the transfer of information, process related risks and change control to securing success during daily operations
* Proactively anticipate, evaluate and resolve technical challenges within area of expertise and give scientific / technological guidance within the department
* Take care of implementing process monitoring and process control strategy as well as complex data analysis
* Contribute to the development and implementation of standardized MSAT procedures and processes
* Lead/participate in change controls, change evaluations and investigations
Key requirements:
* Bachelor or Master in Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering or other related life sciences
* Extensive experience in the area of sterile manufacturing on the shopfloor and/or MSAT, QA/QC with proven process understanding in aseptic manufacturing
* Strong communication skills and interaction with all kinds of interfaces within project organization and customer
* Very good orientation and collaboration across groups within a matrix organization
* Structured, solution-oriented and well-organized working attitude
* Fluency in English, German is advantageous
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and pro...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-03 08:32:09
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Laboratory Support Technician
Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Our busy laboratory is seeking an organised and proactive Laboratory Support to join the team.
You will work alongside the Scientists to provide vital support services to the department.
You will be responsible for ensuring maintenance and calibration of equipment, that consumables and buffers are always stocked, and generally ensuring the high standards of the laboratory are maintained at all times.
Key responsibilities:
* Completion of periodic activities within the laboratory to maintain equipment in good service condition
* Accountable for reagent and consumable stock management; eg: pH/Conductivity Probes, label ribbons, till receipts and inventory management.
* Ordering consumables from internal stores using the Warehouse Management System (WMS)
* Glassware and plastic ware cleaning, maintaining high levels of cleanliness and tidiness in the washroom environment
* Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind
* Liaison point between scientists, service providers and the Asset Maintenance department for breakdowns, preventative maintenance or calibration control activities.
* Generation of buffers and media for laboratory methods and processes
* Completing of periodic equipment cleaning such as Biological Safety Cabinets and water baths.
Key requirements:
* Self-starter with good organisational skills and a good eye for detail
* Prior exposure to a laboratory environment is preferred
* Minimum qualifications: A
*- C in GCSE Maths, English and Science (or equivalent)
* Ability to work at our Slough site 5 days per week.
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
#LI-IG1
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Type: Permanent Location: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-04-03 08:32:08
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The Outside Sales Representative prospects for, identifies and establishes relationships with new customers, develops proposals and closes sales for new and repeat business.
He or she also nurtures, maintains and expands relationships with and increases sales to existing customers within an assigned geographical territory in Southern East and West of Louisiana, specializing in the sugar industry.
Essential Job Functions and Responsibilities:
* Promote and market all of Bray product lines to all of the customers and prospective customers within the Outside Salesperson’s assigned territory
* Develop and maintain relationships with existing and prospective customers in the assigned territory
* Visit customers’ sites to gain an understanding of their processes and needs and make suggestions as to how Bray product lines can meet or exceed the reliability, efficiencies and value of competitors’ products to improve the customers’ processes and operations
* Manage territory and accounts in a manner that will enable the Outside Salesperson to meet or exceed sales goals
* Become technically proficient with all of Bray product lines.
* Target growth industry in the Sugar Industry for 13 mills in So.
LA.
Qualifications and Core Competencies (Knowledge, Skills & Abilities):
* Must have previous experience selling valves and controls
* Must have sales experience in the sugar mill industry
* Local travel including but not limited to Lafayette, Morgan City and Baton Rouge, Louisiana.
+ Outside industrial sales experience of industrial valves, actuators, controls, and instrumentation; experience calling on sugar refineries.
* Must have knowledge of the fluid handling equipment industry (e.g.
valves, controls, piping, etc.)
* BS College degree (in Engineering, Business or related major), or high school diploma plus relative experience
* Exceptional organizational and communication skills
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant.
However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
41 CFR 60-1.35(c)
Outside Sales
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Type: Permanent Location: Gonzales, US-LA
Salary / Rate: Not Specified
Posted: 2024-04-02 08:58:56
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Counselor, School Based
Are you looking for an organization where you can grow while making a positive impact on people's lives? At Signature Health, our purpose is to provide integrated healthcare for our community specializing in patients with mental illness and/or addiction because we want people to realize their highest potential.
Our core values are the foundation of who we are:
* People First mindset where we honor our colleagues and patients
* Striving for Excellence in our work each day
* Can Do approach where we roll up our sleeves in response to opportunities and challenges
In addition to a rewarding career, as a full-time employee, you will have access to the following employer/employee paid benefits:
Full Time:
* Medical, Dental, Vision
* Robust earned paid time off program (PTO)
* 401k match
* Various Life Insurance Options
* Short- and Long-Term Disability (Not applicable for school-based employees)
* Federal Loan Forgiveness Program (available on eligible on roles)
* HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
* Tuition & Professional Development Assistance
If you value the people around you, strive to be the best version of yourself and have a can do mindset, then Signature Health could be the best place for your next career.
Read below on how you can make a difference in our community and apply today!
SCOPE OF ROLE
Reporting to the Supervisor, BH Services the Counselor, School Based will provide an array of services to support school students and staff.
These services may include education, consultation/training, prevention, crisis intervention, and ongoing treatment.
Ongoing treatment services will be developed in response to a student's needs, including complete diagnostic assessment, case management, and individual, group, and family counseling. You will be relied on to provide excellent and complete diagnostic client assessment.
You will formulate treatment plans by providing community, home, and school based counseling services to children and their families.
HOW YOU’LL SUCCEED:
* Working primarily in the school environment, will demonstrate excellent outreach and engagement skills, forming positive relationships with school staff, students, and parents.
* Conduct comprehensive diagnostic assessments for referred students, incorporating input from students, parents and educational staff. These will be conducted at a location convenient for the family, including school, office or home.
* Develop treatment plans to meet assessed needs, including specific goals, objective and interventions.
* Facilitate referrals to other Signature Health services and community resources as needed.
* Work with school staff to plan and implement early intervention activities, including screenings, classroom presentations, and discussion/ st...
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Type: Permanent Location: Willoughby, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-02 08:55:43
