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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.
Ihre Aufgaben:
* Instandhaltung und Störungsbehebung an technisch hochwertigen Anlagen
* Prüfen von Qualitäts- und Sicherheitseinrichtungen in bestehenden Anlagen
* Konfigurieren und Kalibrieren von EMR Geräten
* Inbetriebnahme von neuen Anlagen oder Anlageteilen
* Leisten von Pikettdienst
Ihr Anforderungsprofil:
* Eine abgeschlossene Ausbildung als Elektroinstallateur EFZ, Automatiker EFZ oder Automatikfachmann
* Grundkenntnisse in der Mess- und Regeltechnik sind von Vorteil
* Weiterbildung im EMR Bereich zu absolvieren sind für Sie ein Ansporn
* Sehr gute Deutschkenntnisse sind zwingend
* Selbständige und genaue Arbeitsweise
* Sie arbeiten kundenorientiert und sind offen für Neues
* Kommunikationsfähigkeit, Initiative und Belastbarkeit runden Ihr Profil ab
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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-13 08:03:52
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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.
Für unsere Konstruktionstechnik-Werkstatt in Visp suchen wir nach einem/r Anlage- und Apparatebauer/in.
Als Konstruktionstechniker gehört das Ändern, Reparieren und Herstellen von Chemieapparaten und Anlageteilen sowie Montage- und Demontage an den Geräten.
Suchen Sie eine spannende und abwechslungsreiche Aufgabe und bringen die benötige Flexibilität mit? Dann freuen wir uns auf Ihre Bewerbung.
Ihre Aufgaben:
* Fachgerechtes und wirtschaftliches Ändern, Reparieren, Herstellen und Montieren von anspruchsvollen und komplexen Werkstücken nach Skizzen oder Zeichnungen
* Mithilfe beim Umstellen von Anlagen
* Einfache Schweissarbeiten
* Kennt die SOP PED Richtlinie und Herstellung nach derselben
* Druckproben durchführen
* Anwendung von SAP/ Windows Office
* Bereitschaft zur Mitarbeit und Unterstützung aller Werkstätten der Lonza
* Pikettdienst / Winterdienst, Schneeräumung
Ihr Anforderungsprofil:
* Sie haben eine abgeschlossene Lehre als Anlage- und Apparatebauer Fachrichtung Konstruktionstechnik
* Mehrjährige Erfahrung ist von Vorteil
* Die Flexibilität, auch in anderen Abteilungen einsetzbar zu sein, bringen Sie mit
* Initiativ, Selbständigkeit und Belastbarkeit sowie Sicherheits- und Qualitätsbewusstsein zeichnen Sie aus
* Sie sind ein(e)Teamplayer(in), haben ein vernetztes Denkvermögen und haben ein wirtschaftliches und unternehmerisches Handeln.
Hohe Kommunikationsfähigkeit
* Sie beherrschen die Deutsche Sprache in Wort und Schrift
* Umgang mit SAP/ Windows Office
* Weiterbildung in spezifischen Fachgebiet
* Bedienung von Grossmaschinen
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, der das Leben vieler Menschen auf der ganzen Welt verbessern kann.
Dies bietet i...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-13 08:03:51
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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 Elektroinstallateur / Automatiker (m/w/d) gesucht.
Ihre Aufgaben:
* Instandhaltung und Störungsbehebung an technisch hochwertigen Anlagen
* Prüfen von Qualitäts- und Sicherheitseinrichtungen in bestehenden Anlagen
* Konfigurieren und Kalibrieren von EMR Geräten
* Inbetriebnahme von neuen Anlagen oder Anlageteilen
* Leisten von Pikettdienst
Ihr Anforderungsprofil:
* Eine abgeschlossene Ausbildung als Elektroinstallateur EFZ, Automatiker EFZ oder Automatikfachmann
* Grundkenntnisse in der Mess- und Regeltechnik sind von Vorteil
* Weiterbildung im EMR Bereich zu absolvieren sind für Sie ein Ansporn
* Sehr gute Deutschkenntnisse sind zwingend
* Selbständige und genaue Arbeitsweise
* Sie arbeiten kundenorientiert und sind offen für Neues
* Kommunikationsfähigkeit, Initiative und Belastbarkeit runden Ihr Profil ab
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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-13 08:03:50
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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.
Sind Sie bereit für eine neue berufliche Herausforderung im Fachbereich
EMR (Elektro-, Mess- und Regeltechnik) Suchen Sie eine spannende und abwechslungs-
reiche Aufgabe und bringen die benötige Flexibilität mit? Dann freuen wir uns
auf Ihre Bewerbung.
Ihre Aufgaben:
Zu Ihren Hauptaufgaben gehören Arbeiten im Bereich der Reinraumtechnik.
* Sie testen und nehmen Anlagen im Bereich Reinraumtechnik in Betrieb
* Selbstständig beheben Sie Störungen an Chemie-, Pharma- und Bio- Anlagen
* Sie führen Reinraummessungen durch
* Sie kalibrieren diverse elektrische Messmittel
* Sie führen vorbeugende Instandhaltungsarbeiten durch
Was wir von Ihnen erwarten:
* Sie verfügen über eine Grundausbildung im technischen Bereich mit EFZ
* Die Bereitschaft für dauernde Weiterbildung im Bereich Reinraummessungen / Messtechnik bringen Sie mit
* Die deutsche Sprache beherrschen Sie fliessend in Wort und Schrift
* Englischkenntnisse erwünscht
* Sie haben Freude an der interdisziplinären Arbeit und sind es als Teamplayer gewohnt, selbstständig und flexibel zu arbeiten
* Wichtig sind uns zudem Ihre Zuverlässigkeit, Initiative und Belastbarkeit
* Bei der Erledigung ihrer Arbeiten handeln Sie unternehmerisch und kommunizieren offen und direkt
* Sie sind belastbar und initiativ
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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-13 08:03:49
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Specialist, Disease Intervention
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 Director, Infectious Disease Services, the Specialist, Disease Intervention will work in collaboration with service providers to effectively coordinate medical, prevention and other support services for patients recently diagnosed or at a risk of contracting HCV and/or other infectious diseases while assuring access to and retention in care.
The Specialist, Disease Intervention will identify individuals who use drugs and are exposed to STI’s through high-risk behaviors.
The Specialist, Disease Intervention will provide education, and other risk reduction information about HCV prevention and care as well as care prevention for other Infectious Diseases and assure they are treated appropriately and follow ups completed.
HOW YOU’LL SUCCEED:
* Conducts time -limited linkage to care interventions to coordinate medical, prevention, and other support services for patients recently diagnosed or at a risk of contracting HCV and/or other infectious diseases while assuring access to and retention in care.
Provides education, and other risk reduction information about HCV prevention and care as well as care prevention for other Infectious Diseases and assure they are treated appropriately and follow ups completed.
* Develops and extracts reports from databases for delivery to internal and external candidates.
Enters infectious case information into the Ohio Disease Reporting System (ODRS...
....Read more...
Type: Permanent Location: Mentor, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-12 08:35:00
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Qualified Mental Health Specialist (QMHS)
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 and Manager, Behavioral Health Services, the Qualified Mental Health Specialist (QMHS) will be key in the development and execution of patient treatment plans.
You will provide patients and their families with ongoing community support resources including transportation for access to identified resources.
The QMHS acts as an outstanding subject matter expert related to patient needs and will foster positive relationships to all patients, their families, and Signature Health team members.
HOW YOU’LL SUCCEED:
* Diligently develop, prepare and present treatment program work material to patients.
* Plan, coordinate, and provide reliable transportation to patients to access identified resources as part of their treatment plans.
* Maintains clear communication and professional boundaries with all patients.
* Act as a subject matter expert and provide support in accessing and developing a sober support network.
* Collaborates effectively with a patient's treatment team.
* Create an outstanding experience for both adult and child patients (SMD/SED, CD/Dual DX) by identifying support needed in the following areas: educational, medical, vocational, housing, and daily living skills resulting in patients becoming successful in their communities.
* Encourage, monitor, and follow-up on client engagement and participation in all treatment plan activities.
* Serve as a liaiso...
....Read more...
Type: Permanent Location: Ashtabula, US-OH
Salary / Rate: Not Specified
Posted: 2024-04-12 08:34:57
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The Account Executive role is phone-based and focused on net revenue growth, retention, and relationship development within a defined portfolio of accounts.
Account Executives are responsible for renewing contracts, protecting against termination or loss of revenue, and growing their portfolio through upselling and cross selling.
This role requires superior communication skills, completing individual goals while working in a team environment, and the ability to multi-task while managing priorities.
The role is part client advocate, part sales professional, part support, and part product expert, leading our clients on their records and information management journey from initial transaction through expansion and renewal.
AEâs must demonstrate a capacity to make connections with all types of people and build rapport easily over the phone.
AEâs should have a strong desire to be trained and mentored, excited about building a team, have a track record of success, and motivated to build their careers from the ground up.
Primary Functions:
⢠Create valued business partnerships with clients within assigned account portfolio and convey a firm understanding of customersâ business
⢠Articulate compelling value propositions around Access services and solutions
⢠Deliver information on programs, promotions and products via phone, email, Teams, etc.
to pipeline of potential sales opportunities within assigned accounts
⢠Create account plans for action to support relationships, retention and revenue goals for assigned accounts
⢠Develop and maintain a sales pipeline to meet and exceed annual revenue quotas
⢠Follow Accessâ sales methodology to maximize revenue and profitability
⢠Utilize consultative selling techniques, ensuring customers recognize and agree our solutions meet their needs
⢠Use Salesforce automation tools to manage client interactions, pipeline, and forecast to ensure accurate reporting and dashboards for tracking and management visibility
⢠Prepare and distribute client communications & engagement including price increase notifications, issue resolution and follow-up
⢠Negotiate positive contract renewals, including at risk customer defense and client save efforts
⢠Host scheduled business reviews with assigned clients and proactively engage with client organizations
⢠Coordinate with Client Care team for service level requests and follow-up to ensure completion
Education and Years of Experience:
⢠2-4 years of relevant work experience in customer success, client experience or sales development
⢠1 year of Experience using Sales Automation tools such as Salesforce.com
⢠Bachelorâs degree in marketing, business, technology, or relevant field of study or equivalent experience
Knowledge, Skills and Abilities:
⢠Excellent organizational, time management, and follow-up skills
⢠Strong problem-solving skills with solution-oriented focus
⢠Exceptional phone/verbal and written communication skills
â...
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Type: Permanent Location: Salt Lake City, US-UT
Salary / Rate: Not Specified
Posted: 2024-04-12 08:32:03
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At Equity Residential, we're dedicated to creating thriving communities, and we invite you to be part of our team.
Embracing values like Diversity, Sustainability, and Total Wellbeing, we foster a workplace culture of authenticity and collaboration.
How We Deliver A Winning Performance:
* Question Authority
* Walk the Talk
* Share Knowledge
* Listen, Not Just Hear
* See the Glass Half Full
* Take Educated Risks
* Enjoy the Ride
* Share the Spotlight
* Do the Right Thing
* Test Your Limits
We Care About Your Total Wellbeing:
* Physical Wellbeing: Medical, dental, and vision care
* Social Wellbeing: 9 paid holidays, annual vacation time, paid sick leave, new parent benefits
* Financial Wellbeing: 401(k) Retirement Savings Plan, Rent Discounts, Competitive Compensation
* Community Wellbeing: Paid Community Service Hours
* Career Wellbeing: Leadership Development
* Learn more about our Total Wellbeing program here.
What You’ll Be Doing:
As a Maintenance Technician, your day-to-day will involve addressing resident service requests, performing diverse hands-on maintenance tasks, and ensuring market-ready apartments.
Additionally, you will perform preventative maintenance and maintain the grounds and common areas, reporting any concerns.
* Promptly addressing resident service requests
* Performing hands-on maintenance tasks, including plumbing, electrical work, and more
* Preparing market-ready apartments and maintaining community grounds
* Conducting regular community inspections to identify necessary repairs or replacements
What You’ll Need To Thrive:
* Hands-on maintenance experience in areas including, but not limited to plumbing, electrical, appliance, and HVAC is necessary.
* High School diploma or equivalent
* Valid driver’s license and good driving record along with auto insurance will be required when working between multiple sites that require driving throughout the day.
If you do not possess a valid driver’s license, you will be required to sign an addendum agreeing not to drive any form of registered motorized vehicle while at work/on the clock.
* Computer literacy, and must be able to effectively communicate both orally and in writing in English for all work-related purposes
* Knowledge of federal and state apartment housing laws
* Availability to work a flexible schedule, including weekends
* Must be able to respond to emergencies after normal business hours and on weekends when assigned on-call responsibilities; a telephone number where you can be reached after-hours must be provided to your manager
* Service team employees, with limited exceptions, are required to use their own smartphone to perform certain aspects of their job
Bonus Qualifications:
* Trade school certification/diploma
* EPA Section 608 Type I, Type II or Universal certification
* Resi...
....Read more...
Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2024-04-12 08:15:19
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As part of the quality team, help drive a positive plant Quality culture change by leading with a positive attitude and innovative thinking.
Actively coach plant personnel to continuously raise the standard of plant quality performance. Help in the execution of education and development programs for all employees including GMPs and food safety policies.
Support production when issues arise.
Responsible for overall Redzone quality checks to ensure first pass quality and consistent documentation completion.
Perform assigned Redzone quality inspection checks to ensure products meet the requirements of the Redzone/Master Manufacturing Records (MMR); Confirm product adheres to visual standards.
Responsible for Customer sample collection and inspection.
Quality lead for managing changeover process in the filler room.
Perform visual inspections, ATP swabs, and allergen swabs to minimize cross-contamination and cross-contact risk.
Verify proper line clearance.
Notify QA Supervisor/Production Supervisor and others as appropriate when ingredients or products do not meet specifications or there are food safety or quality concerns.
Responsible for controlling hold forms and system holds when a non-conformance occurs and assisting in rework on-line.
Responsible for reviewing batch record and rework packets prior to production.
Provide QA Label and Component Document Coordinator with non-conformance report on components used on packaging lines to ensure timely Supplier NCRs.
Follow plant GMP’s and safety guidelines to maintain a clean and safe work area at all times.
Responsible for training Line Technicians on quality functions.
Read and properly interpret documents such as swab results, GMP Manuals, HACCP programs and procedure manuals.
Complete all required documents in a timely manner.
Advise manufacturing personnel on compliance of GMP’s.
Assist with plant audits as needed.
OPEN
....Read more...
Type: Permanent Location: Wautoma, US-WI
Salary / Rate: Not Specified
Posted: 2024-04-12 08:11:18
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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 sind Sie als Anlage-Ingenieur (m/w/d) bei der Infrastruktur (Energie- und Entsorgungsbetriebe) zuständig für das Betriebsengineering der zugeteilten Anlagen.
Unter anderem betreiben wir Dampferzeugungs-, Wasseraufbereitungs-, Lösungsmittelrecycling-, Abwasserreinigungs- sowie Rückstands- & Abgasverbrennungsanlagen und deren Netz-Infrastrukturen.
Ihre Aufgaben:
* Gewährleistung, Vorbereitung und Koordination einer fachgerechten und wirtschaftlichen Durchführung der Instandhaltung unter Einbezug von internen und externen Dienstleistern / Partnern.
* Auftragserteilung, Kapazitätsplanung, Pflege Meldewesen in SAP.
Sicherstellung der Anlagenverfügbarkeit.
Zusammenarbeit im Fachübergreifenden Engineering Team, Unterstützung der Betriebsleitung.
* Hochhalten und Einhaltung von Sicherheit, Qualität, Hygiene, Umwelt in Bezug auf technische Einrichtungen und Infrastruktur.
* Kontinuierliche Optimierung der Anlagen, Instandhaltungsprozessen / Abläufen.
Mitarbeit an Risikoanalysen und Umsetzungen des Änderungswesen.
* Technische Projektleitung und/oder Mitarbeit in Kleinprojekten und Investitionsvorhaben.
Sicherstellung und Pflege der Anlagendokumentation / Spezifikation mithilfe der Systeme wie SAP / COMOS (Plant Engineering Software) sowie Fließbildpflege.
* Mitarbeit bei der Überwachung und Einhaltung des zur Verfügung stehenden Budgets (Unterhalt, Projekte und Investitionen)
Ihr Anforderungsprofil:
* Technikerschule (HF) oder Bachelor (FH) im Bereich Maschinenbau, Verfahrenstechnik, o.ä.
Ausbildungen in technischen Berufsfeldern
* Kenntnisse / Erfahrung der Instandhaltung in der Industrie von Vorteil
* Kenntnisse in SAP / COMOS von Vorteil, gute Kenntnisse Windows Office
* Fliessend Deutsch und Englisch von Vorteil
* Selbständiges und flexibles Arbeiten, ausgeprägte Teamfähigkeit, strukturiertes, fokussiertes und sehr gut organisiertes Arbeitsverhalten
* Zuverlässig und belastbar, lösungsorientiert, offen für neue Ideen, neue Tätigkeitsfelder, initiativ und hoch motiviert
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 ...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:10:12
-
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 sind Sie als Elektro, Mess- und Regeltechnik-Ingenieur (m/w/d) bei der Infrastruktur (Energie- und Entsorgungsbetriebe) zuständig für das Betriebsengineering der zugeteilten Anlagen.
Unter anderem betreiben wir Dampferzeugungs-, Wasseraufbereitungs-, Lösungsmittelrecycling-, Abwasserreinigungs- sowie Rückstands- & Abgasverbrennungsanlagen und deren Netz-Infrastrukturen.
Ihre Aufgaben:
* Gewährleistung, Vorbereitung und Koordination einer fachgerechten und wirtschaftlichen Durchführung der EMR Instandhaltung unter Einbezug von internen und externen Dienstleistern / Partnern.
* Auftragserteilung, Kapazitätsplanung, Pflege Meldewesen in SAP.
Sicherstellung der Anlagenverfügbarkeit.
Zusammenarbeit im Fachübergreifenden Engineering Team, Unterstützung der Betriebsleitung.
* Hochhalten und Einhaltung von Sicherheit, Qualität, Hygiene, Umwelt in Bezug auf technische Einrichtungen und Infrastruktur.
* Im Bereich EMR kontinuierliche Optimierung der Anlagen, Instandhaltungsprozessen / Abläufen.
Mitarbeit an Risikoanalysen und Umsetzungen des Änderungswesen.
* Technische Projektleitung und/oder Mitarbeit in Kleinprojekten und Investitionsvorhaben.
* Sicherstellung und Pflege der Anlagendokumentation / Spezifikation mithilfe der Systeme wie SAP / COMOS (Plant Engineering Software) sowie Fließbildpflege.
* Mitarbeit bei der Überwachung und Einhaltung des zur Verfügung stehenden Budgets (Unterhalt, Projekte und Investitionen)
Ihr Anforderungsprofil:
* Technikerschule (HF) oder Bachelor (FH) im Bereich Elektro-, Automations- oder Systemtechnik o.ä.
Ausbildungen
* Kenntnisse / Erfahrung der EMR Instandhaltung in der Industrie von Vorteil
* Kenntnisse in SAP / COMOS / DeltaV (Prozess Control System) von Vorteil, gute Kenntnisse Windows Office
* Fliessend Deutsch und Englisch von Vorteil
* Selbständiges und flexibles Arbeiten, ausgeprägte Teamfähigkeit, strukturiertes, fokussiertes und sehr gut organisiertes Arbeitsverhalten
* Zuverlässig und belastbar, lösungsorientiert, offen für neue Ideen, neue Tätigkeitsfelder, initiativ und hoch motiviert
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 errei...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:10:02
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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.
An unserem Standort in Visp, Switzerland suchen wir einen Senior Chemielaborant (m/w/d) QC ChemPharma.
Als Mitglied unseres Analytik Teams der QC FCC sind Sie unter Einhaltung der GMP- und Sicherheitsrichtlinien verantwortlich für die analytische Betreuung von Produktionskampagnen und arbeiten in Projektteams.
Aufgaben:
* Durchführung analytischer Methoden (HPLC, GC, Titrationen, IR) im GMP-Umfeld, sowie Transfer und Validierung neuer Methoden.
* Kontrolle und Freigabe von Resultaten
* Betreuung und Qualifizierung von Laborequipment
* Untersuchen von Abweichungen und unerwarteten Resultaten, Troubleshooting
* Verfassen und Bearbeiten von qualitätsrelevanten Dokumenten (Protokolle, Berichte, etc.)
* Evaluation und Implementierung neuer Techniken im Labor, Optimierungsprojekte
* Schulung der QC FCC Schicht
Anforderungsprofil:
* Abgeschlossene Ausbildung als Laborant, CTA (m/w/d) Fachrichtung Chemie und / oder BSc in Chemie
* Praktische Erfahrung mit HPLC und / oder GC ist ein Muss
* Kenntnisse im Bereich GMP ist von Vorteil
* Handlungs- und zielorientierte, motivierte Arbeitsweise
* Gute Deutsch- und Englischkenntnisse
* Erfahrung mit CDS Empower, LIMS, TIAMO und Dokumentum sind 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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:09:20
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Senior Validation Specialist, Physical-Chemical Quality Control
Full-time, temporary fixed-term contract position (12 months)
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 is looking for a Senior Validation Scientist Physical-Chemical Quality Control (m/f/d) for our site in Basel-Stücki for a 12-month fixed-term contract.
Key responsibilities:
* Provide support in the area of cGMP analytical method validation, verification and transfer activities within DPS QC Phys-Chem Analytics:
* Evaluate and implement analytical methods (e.g.
HPLC and CE-SDS purity methods, identity methods, content determination, compendial methods provided by a customer)
* Independently execute pre-validation, validation or transfer under cGMP (protocol writing, experiment execution or reviewing, and report writing)
* Oversee assigned tasks, including monitoring timelines, proper execution and reporting
* Ensure lab clean/maintenance and training status to cGMP standards
* Support Drug Product analytical infrastructure as assigned
Key requirements:
* Completed apprenticeship (CTA, BTA or equivalent) or academic degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related subject
* Advanced scientific knowledge of phys-chem analytical techniques
* Strong working knowledge in relevant analytical techniques in the lab
* At least 2-3 years experiences in GMP environment
* Experienced in large molecule analytics (advantageous)
* Very good planning, reporting, interpretation and documentation skills
* Good knowledge of written and spoken English
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: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:09:02
-
Senior Validation Specialist, Physical-Chemical Quality Control (m/f/d)
Full-time, permanent position.
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 is looking for a Senior Validation Scientist Physical-Chemical Quality Control (m/f/d) for our site in Basel-Stücki.
Key responsibilities:
* Provide support in the area of cGMP analytical method validation, verification and transfer activities within DPS QC Phys-Chem Analytics:
* Evaluate and implement analytical methods (e.g.
HPLC and CE-SDS purity methods, identity methods, content determination, compendial methods provided by a customer)
* Independently execute pre-validation, validation or transfer under cGMP (protocol writing, experiment execution or reviewing, and report writing)
* Oversee assigned tasks, including monitoring timelines, proper execution and reporting
* Ensure lab clean/maintenance and training status to cGMP standards
* Support Drug Product analytical infrastructure as assigned
Key requirements:
* Completed apprenticeship (CTA, BTA or equivalent) or academic degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related subject
* Advanced scientific knowledge of phys-chem analytical techniques
* Strong working knowledge in relevant analytical techniques in the lab
* At least 2-3 years experiences in GMP environment
* Experienced in large molecule analytics (advantageous)
* Very good planning, reporting, interpretation and documentation skills
* Good knowledge of written and spoken English
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: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:09:01
-
Classification:
Non-Exempt
We are Alsco Uniforms.
We’ve been working hard for our customers since 1889 when we invented the uniform and linen rental industry.
Alsco Uniforms has grown into a worldwide leader serving over 350,000 customers in 13 countries.
It’s our job every day to make every aspect of the customer experience better.
Whatever our customers need, Alsco Uniforms finds the answers that work for them.
Our employees are the heart and soul of Alsco Uniforms.
As a result, we have a long history of strong financial performance, continuous improvement, and customer service.
We’re seeking driven professionals with ambition to grow within our company.
We’d love to talk to you about how you can fit into our team of diverse individuals and how your hard work will be rewarded with competitive pay and benefits and ongoing career development.
Join our team and build your career with Alsco Uniforms!
Job Summary:
The Route Relief/Utility RSR supports the Service Department in its objectives to meet our customers needs through up-selling/cross-selling and providing superior customer service.
Main duties are to cover routes and perform service related tasks as required.
Reports to the District Manager.
Our full-time employees enjoy:
401K Plan with Company Match
Medical, Dental, Vision, FSA/HSA
Life Insurance, Disability Insurance
Vacation, Sick Time, Holidays
Choice of Global Cash Card or Direct Deposit
Career Advancement
Learning & Development Opportunities
Inclusive and Diverse Team Environment
Essential Functions:
- Perform all responsibilities of a Route Sales Representative and related tasks.
- Learn and support all routes.
Run routes as needed for holidays, vacations or other vacancies.
- When not on a route, assist in rush deliveries, renewals, audits, training and any other tasks assigned by supervision.
- Solicit new customers, up-sell/cross-sell/sample all lines of service or product and ensure a profitable product mix.
- Actively participate in promotions and contests, training and audits.
- Follow company policies/procedures regarding new customers, managing customer needs and all aspects of service.
- Ensure customer loyalty and outstanding customer service.
Build relationships, communicate openly, educate customers and proactively resolve concerns in cooperation with supervision.
- Safely operate a delivery vehicle on each trip, following all applicable laws and company policy.
Maintain vehicle cleanliness and perform regular vehicle inspections.
- Handle and process customer payments.
Keep route paperwork current.
- Ensure timely and correct deliveries of complete textile loads, pick up soiled textiles and maintain proper inventories in accounts.
Service items such as facility maintenance products.
- Monitor and report competitive activity.
Keep service agreements current and renewed.
- Return from route and off load soiled textiles in the receivi...
....Read more...
Type: Permanent Location: Ventura, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-12 08:05:03
-
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 Cleaning Validation Expert will own cleaning validation activities for the assigned biological assets at the Visp site.
The role includes preparation of validation documents and support of execution, presentation of cleaning validation topics in audits and inspections, tight collaboration with operations and quality to ensure successful and on time validation activities.
Key Responsibilities:
* Develop and prepare equipment cleaning validation documents
* Lead execution of equipment cleaning validations
* Support equipment cleaning harmonization and continuously develop the cleaning validation process (procedures, templates, R&R) in collaboration with site and global functions
* Keep up to speed with regulations and their implementation on site if applicable, development of risk based approaches to cleaning validation
* Work closely with Operations and Quality to ensure smooth delivery of work packages
Key Requirements:
* Master's degree preferred, or Bachelor's Degree plus relevant industry experience.
Area of study in Biotechnology or similar science related field.
* Intermediate previous experience working in the biotech industry
* Intermediate GMP experience
* Very good planning and organizing skills, including risk management skills
* Fluent in English
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: 2024-04-11 08:23:37
-
Manager, Maintenance Services
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 a Manager, Maintenance Services to lead at their Bend, OR location.
Key Responsibilities:
* Lead team of engineers and technicians in the planning, scheduling, and improvement of maintenance activities and equipment
* Direct and coordinate planning/scheduling of maintenance activities, reliability based maintenance improvements, engineering improvement projects, and assessment of spare parts requirements
* Coach and mentor team to build a methodology of maintenance improvement, troubleshooting, and problem solving
* Make recommendations to management to resolve maintenance issues, perform operational troubleshooting and identify opportunities for continuous improvement
* Develop maintenance plans and workflows, i.e.
work requests, work execution process, determining priority based on asset criticality and other criteria, developing corrective maintenance job plans, job kitting (Spare Parts, Permits, Tools, JHA, Production Availability, etc.)
* Use CMMS system (Blue Mountain RAM) for maintenance planning/scheduling. Develop metrics and reporting process utilizing data acquisition programs (Crystal Reports, Tableau, etc.)
* Perform evaluations for proper maintenance strategies for systems including predictive inspections, condition monitoring, and failure replacement
* Work with project teams for sourcing of appropriate process and utility equipment
* Constructively, courteously and professionally interact with peers and clients in manufacturing, maintenance, utility plants, analytical labs and contracted services
* Function effectively with peers and demonstrate a high degree of teamwork
* Perform other duties as assigned
Key Requirements:
* Bachelor’s degree in any Engineering discipline (e.g.
chemical, electrical, mechanical) preferred
* 5+ years experience in biotech/pharmaceutical engineering or combination of relevant education and experience, including management roles
* 3+ years of experience in reliability and maintenance
* Demonstrated ability to perform hands-on, detailed work, in a fast-paced manufacturing environment.
* Knowledge of computerized maintenance management systems, Microsoft Project, AutoCAD and Building Automation Systems preferred.
* Strong leadership, writing, and communication/presentation skills are required
* Must be independent, self-motivated, organized, able to multi-task in project environments, and s...
....Read more...
Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-11 08:23:26
-
Staff Position Description
Position Title: Business Applications Analyst 3 Position Code: AnalystBA3-8135
Department: Information Systems Safety Sensitive: Yes
Reports to: Business Informatics/Applications Manager Exempt Status: Yes
Position Purpose:
All KHI employees are expected to perform their respective tasks and duties in such a way that supports KHI’s vision of providing the region’s best clinical care and patient service through an environment that fosters respect for others and pride in performance.
The Business Applications Analyst 3 supports the core functions of the enterprise business systems to enable cost-effective, high quality and safe patient care.
The candidate assists customers with design, implementation, work-flow optimization, and issue resolution of supported applications.
Provides standardization direction for products aligning the application version and workflow with current standards.
The Business Application Analyst 3 will be responsible for providing support, and problem resolution within the Business Applications portfolio.
This position will help lead system implementations, perform project management, systems development\upgrades, and staff training.
May assist in budgetary and strategic planning, and will be a Financial\Business\Technical liaison.
Must be able to write detailed technical and non-technical documentation.
Must have excellent customer service skills, and the ability to effectively provide support remotely.
This position shares in the Business Applications on call rotation.
Key Responsibilities [List of material responsibilities and essentials duties which must be completed in achieving the objectives of the position]
This is a customer facing position responsible for providing support for his/her area of responsibility.
The Business Applications Analyst 3 will round with business department designees as assigned in support of high levels of customer service, systems administration, and development.
In support of upgrades and implementations, this person may help lead projects, assist in configuration, and the deployment of software and hardware.
This position is responsible for training technical and non-technical staff, as well as write detailed documentation and training materials.
This position is responsible for developing, creating, and modifying Business applications software or specialized utility programs.
· Obtains requirements through discovery, document analysis, business process descriptions and use cases, research scenarios, tasks and workflow.
· Pushes creative thinking beyond the boundaries of existing industry practices and client mindsets by asking thought provoking and clarifying questions.
· Evaluates and reconciles information gathered from multiple sources; distinguishes user requests from underlying needs, creates quality requirements documentation.
· Understands the necessity of project standards and apply them consistently; promote best practic...
....Read more...
Type: Permanent Location: Kingman, US-AZ
Salary / Rate: Not Specified
Posted: 2024-04-11 08:23:00
-
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 Cleaning Validation Expert will own cleaning validation activities for the assigned biological assets at the Visp site.
The role includes preparation of validation documents and support of execution, presentation of cleaning validation topics in audits and inspections, tight collaboration with operations and quality to ensure successful and on time validation activities.
Key Responsibilities:
* Develop and prepare equipment cleaning validation documents
* Lead execution of equipment cleaning validations
* Support equipment cleaning harmonization and continuously develop the cleaning validation process (procedures, templates, R&R) in collaboration with site and global functions
* Keep up to speed with regulations and their implementation on site if applicable, development of risk based approaches to cleaning validation
* Work closely with Operations and Quality to ensure smooth delivery of work packages
Key Requirements:
* Master's degree preferred, or Bachelor's Degree plus relevant industry experience.
Area of study in Biotechnology or similar science related field.
* Intermediate previous experience in cleaning validation
* Intermediate GMP experience
* Very good planning and organizing skills, including risk management skills
* Fluent in English
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: 2024-04-11 08:21:01
-
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 site in Visp, Switzerland is growing and for our Biologics organization, we are currently looking for a MSAT BioConjugates Process Expert.
Lonza has a strong track record in the manufacturing of BioConjugates from early clinical to large scale commercial supplies.
Our dedicated Protein Conjugation Plant facility (PCP) is recognized as a center of excellence for Antibody Drug Conjugates (ADC) as well as other classes of BioConjugates.
We are experiencing an increased demand in this area and as part of Lonza’s Ibex® Dedicate model, new BioConjugation suites were built out within a pre-existing shell.
In the position of MSAT Bioconjugates process expert, you will make a difference by being responsible for the successful supervision, support and life cycle management of BioConjugates processes running in Lonza’s facilities in Visp.
You will play a crucial role in the network between the different departments as manufacturing, development, quality assurance and control.
Become part of this exciting opportunity and apply now!
Key Responsibilities:
* Support of the commercial and clinical re-supply BioConjugates GMP campaigns in our Ibex® and Protein Conjugation Plant (small scale and large scale PCP) facilities
* Plan and supervise MSAT activities on project level to ensure that the processes deliver the required products with the required quality in a safely, timely and in a cost effective manner.
* eading process troubleshooting on the manufacturing floor as needed
* Change control management
* Supporting process validation activities
* Annual product review (APQR)
* Representing the facility during process specific inspections and audits as SME for area of responsibility
* The preparation of GMP clinical re-supply and commercial campaigns as part of a project team (tech transfer, scale up, GMP documentation, equipment)
Key Requirements:
* Master or PhD (preferred) in Bioconjugation, Biotechnology, chemical engineering, organic chemistry or related disciplines
* Significant experience in Bioconjugation, biopharma manufacturing and / or process development, preferably in the area of BioConjugates or DSP (Mammalian or Microbial)
* cGMP experience and deep understanding of Bioprocess technology
* Excellent communication skills for interaction with customers and within the project organization
* Fluent in English required, German fluency is desired
* Creative, agile, open-minded
Every day, Lonza’s products and services have a positive i...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-11 08:19:56
-
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 Kingston is hiring a Product Development Engineer or Mechanical Engineer for our Kingston, ON location where we have cutting edge technology such as the Cocoon® Platform.
The Cocoon® Platform is an automated, scalable, and functionally closed-process cell therapy manufacturing platform.
The Cocoon® is used to manufacture multiple types of cell therapy with applications in oncology (i.e., CAR-T), regenerative medicine (i.e., HSCs, MSCs) and tissue engineering (i.e., orthopedics).
The Product Development Engineer or Mechanical Engineer will be responsible for driving continuous improvements in the Cocoon® product line.
The Product Development Engineer or Mechanical Engineer also ensures the mechanical design for the Cocoon® Platform can be sustained for manufacture and distribution within regulated markets, and that field defects are investigated and addressed at the design-level.
Learn more at: https://pharma.lonza.com/technologies-products/cocoon-platform
Key responsibilities:
* Improves product quality and reliability, manufacturing efficiency and production yields through product design modification
* Investigates product complaints and non-conformances, performs root cause analysis of failures, and proposes corrective actions in a timely fashion
* Reviews existing product designs, identifies weaknesses, proposes and implements improvements
* Leads collaborative and complex design updates and implementations of corrective actions and backlog features related to product design within a cross-functional team
* Creates strategy for the verification of corrective designs, and participates in verification activities
* Generates and reviews technical documentation including investigative pursuits, conceptual design, mechanical drawings, and technical reports, all within a ISO 13485 Quality Management System
* Applies a risk-based approach to product design activities using xFMEA methodology
Key requirements:
* Bachelor’s degree in an Engineering discipline such as Systems, Mechanical, Biomedical or similar path of study; Master’s degree, preferred.
* Minimum of 7 years of experience with leading product design in a regulated industry; medical device or product design/manufacture field required.
* Must have an in-depth knowledge of manufacturing processes: machining, injection molding, 3D printing.
* Extensive understanding of CAD systems required – preferably SolidWorks.
* Design experience with a focus on Design for Manufacturing and ...
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Type: Permanent Location: Kingston, CA-ON
Salary / Rate: Not Specified
Posted: 2024-04-11 08:19:53
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Salary Range: $25.53 - $34.47
Anticipated Hiring Range: $25.53 - $30.05
Short Job Description:
The City of Greeley is seeking a Planning Technician to join the Development Review Division of the Community Development Department.
This position is a full-time, term-limited position funded for 2024.
The position is anticipated to continue in 2025 with the possibility of becoming permanent subject to future appropriations.
This position is benefit eligible.
Job Summary:
The City of Greeley is seeking a Planning Technician to join the Development Review Division of the Community Development Department. The Planning Technician will report to the Chief Planner – Development Review and is responsible for a variety of essential planning functions to assist the Department’s professional planners.
The technician is the point person for all new project intakes, checking development review submittals for completeness, and is the Department’s primary Planner On-Call.
Other duties include reviewing minor cases such as adjacent agency referrals and minor subdivisions; performing reviews of building and sign permits; responding to citizen and applicant inquiries; and providing information via walk-in, telephone, and email.
The ideal candidate understands that latitude is considered the most appropriate procedure or precedent to follow.
Standard operating procedures provide guidance for daily work; however, each project, permit, and question include unique aspects to take into consideration.
Experience, Knowledge, Skills:
* Detailed knowledge in a specialized field such as planning, environmental science, economics, etc.
* The ability to selectively extract, verify and compile data and/or operate specialized equipment to produce results.
Entry level for more specialized fields.
* Extensive knowledge of land use planning principles and zoning regulations to accurately convey requirements to external customers or demonstrated experience communicating highly technical information to non-technical customers.
* The ability to interpret data and the city development code, as well as an understanding of general planning principles.
* The ability to complete all activities associated with a site visit.
* Knowledge of the business and organizational structure of Colorado municipalities.
* Collaboration skills, including the ability to work with others from different areas and backgrounds to reach a common goal.
* Computer skills, including the ability to utilize Microsoft Office programs (i.e.
Word, Excel, PowerPoint, Outlook, etc.) and learn and experiment with new software and systems.
* Interpersonal skills, including the ability to facilitate interaction, communication, and teamwork between others.
* Oral, written, and listening communication skills, including the ability to accurately interpret what others are saying and convey messages, informa...
....Read more...
Type: Contract Location: Greeley, US-CO
Salary / Rate: 30
Posted: 2024-04-11 08:19:31
-
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.
Key accountabilities and duties
* Responsible for the generating, managing and reviewing documentation for Drug Product manufacturing campaigns in compliance to cGMPs, SOPs and applicable guidelines.
Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
* Generating, managing and reviewing the logbooks for Drug Product Operations in compliance to cGMPs, SOPs and applicable guidelines.
* Provides front line technical and procedural support, working with the manufacturing teams (operators), plant engineers and QA operations.
* Lead process related investigations and critical deviations and assists in decision making on production issues
* Lead process changes, CAPAs, and CAPA effectiveness checks related to manufacturing documentation within required timelines and through GMP systems (e.g.
Trackwise, MES, training, etc.)
* Supports the execution of process validations, liaising with all the relevant parties at shopfloor to ensure accurate execution
* Use scientific, process and statistical knowledge to analyze data to provide process understanding, and to identify root causes of product and process failures
* Provide training for assigned areas of responsibility, including documentation use and review.
* Acts as Subject Matter Expert during customer audits and visits, maintain their processes at inspection readiness level and to provide the necessary support
* Executes innovation and improvement projects comprising general manufacturing aspects for the production plant.
Qualifications and skills required
* Bachelor / Master Degree
* Preferred area of study: Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree
* 5-10 years of experience in Sterile Manufacturing on the shopfloor and/or QC/QA preferred
* Fluent in both German and English
* Familiarity with GMP requirements, quality procedures and SOP execution
* Good communication skills and interaction with a variety of interfaces within the organization and on the shopfloor
* Structured, focused and well-organized working attitude; open-minded for new ideas and suggestions
* High motivation and dynamic drive; solution-oriented
* Proven IT knowledge, knowledge in ERFP (SAP) or MES (Syncade) is an asset
* Prepared to work flexible working hours
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Type: Permanent Location: Visp, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-11 08:16:18
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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 site in Visp is growing and for Ibex™ Solutions, our recently launched unique biological manufacturing and development concept in Visp, Switzerland, we are currently looking for a Head of Downstream Processing (DSP) (m/f/d) for our Mammalian Operations in Visp.
In this role, you will manage a team of bioprocess engineers, automation engineers and shift team leaders for our Mammalian 1k2k single-use facility with full responsibility for all aspects of human resource management such as qualification, development, coaching, hiring, pay decisions and discipline issues.
You will manage/support the operational activities of a manufacturing DSP unit and be accountable for the execution of all production campaigns in the DSP manufacturing unit with regard to safety, quality and on-time-in full delivery.
Key responsibilities:
* Handling daily DS delivery with your teams, aligned with production planning and KPIs.
* Driver of solving production issues in the DSP manufacturing unit according to the common escalation guidelines; promote a great collaboration with the support functions MSAT, Production Support, QA and the USP production teams with expertise in solution finding and trouble shooting
* Representing the operational area in customer meetings, audits and regulatory inspections.
* Deputies the Head of Mammalian 1k2k Operations if needed
* As a member of the 1k2k Operations Leadership Team responsible for all aspect of general production management such as housekeeping, staff behavior and control of general processes and installations
* Execute innovation and improvement projects comprising general manufacturing aspects for the production plant.
* Empower people and make them grow.
Identified and coach talents.
* Promote lean management and lean initiatives
Key requirements:
* Master or Bachelor degree in Biotechnology, Bio-chemical engineering, Bioengineering or related disciplines (with equivalent experience)
* Significant experience in a leading position in Biopharma manufacturing
* Strong leadership skills and ability to communicate internally and externally at higher levels
* Very good understanding of business and financial processes
* Strong background in mammalian cell culture using single use systems
* Detail oriented with exceptional organizational skills and a structured and proactive working attitude
* Open-minded for new ideas with a highly collaborative and strong team oriented attitude
* Fluent in English, Germa...
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-11 08:13:27
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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.
Bewerben Sie sich als QC Laborant für das Team Stabilität 80-100% (m/w/d) an unserem Standort in Visp, Switzerland.
Sie sind Teil des Teams „QC - Stabilität“, welches sich mit der Untersuchung der Stabilität von biologisch, biotechnologisch und chemisch unter GMP hergestellten Produkten beschäftigt.
Zu diesem Zweck wird das Produkt unter verschiedenen klimatischen Bedingungen gelagert und in regelmässigen Abständen analytisch untersucht und ausgewertet.
Mit diesen Informationen werden die Stabilität und das Haltbarkeitsdatum des Produktes bestimmt.
Es erwartet Sie ein spannendes und hoch dynamisches Geschäftsfeld, an dessen weiterer Entwicklung Sie aktiv teilhaben können.
Aufgaben:
* Organisation von Stabilitätsproben (Start von neuen Studien und Probenverwaltung)
* Dokumentationen der Durchführung von Stabilitätsstudien unter GMP
* Verwalten der Stabilitätsstudien in entsprechender Software
* Verpacken von Stabilitätsproben
* Verantwortung von Geräten (z.B.
Kühlschränke, Waagen)
Anforderungsprofil:
* Sie verfügen über eine Laborantenausbildung im Bereich Chemie, Biologie oder vergleichbarer Fachrichtung
* Sie haben ein präzises und strukturiertes Arbeiten
* Sie haben Spass mit Computerarbeit (ca.
50% Arbeitsanteil)
* Erfahrung im GMP-Umfeld ist von Vorteil
* Gute Deutsch- und Englischkenntnisse
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, 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.
....Read more...
Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-11 08:13:26
