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As an In-Home Installation and Health Technician, you’ll be responsible for the delivery, installation, integration, and troubleshooting tech products such as home theater, computing, smart home, networking and health technology.
This role also requires technical expertise in health device installation and support including all appropriate HIPAA and health-related requirements Outside of delivery and installation, you’ll find the right solutions for customers’ lifestyles and technology needs based on your conversations.
You’ll partner with other Geek Squad Agents, service partners, retail employees and supply chain employees to drive performance to meet Best Buy’s strategy and yearly initiatives.
What you’ll do
* Provide a seamless customer experience by advising and fulfilling on lifestyle recommendations regarding products and services
* Maintain phone and in-person contact with customers to reveal diagnostic discoveries and make recommendations
* Provide feedback, coaching and training to Best Buy store teams
* Provide a variety of fulfillment duties including delivery, installation, integration, networking and troubleshooting consumer electronics devices
* Take the lead on two-person jobs and perform other work alone
* Manage inventory and vehicle maintenance, process paperwork and payment, provide feedback and training opportunities, and follow safety guidelines
Basic qualifications
* Must be at least 21 years old
* Current, valid driver’s license
* Have and maintain a driving record which meets Best Buy safety standards
* Ability to acquire and maintain any state or local licensing, as required to perform job effectively
* Ability to acquire any health-related certifications (e.g., HIPPA), as required to perform the job effectively within 90 days of hire
* Ability to lift weight up to 75 pounds with or without reasonable accommodation and up to 150 pounds as part of a team with or without reasonable accommodation
* Ability to lift weight up to 250 pounds as part of a team with the support tools such as harnesses or lifts
* 2 years of consumer electronics delivery, installation, integration and troubleshooting experience
* 1 year of customer service experience
Preferred qualifications
* 1 year of experience in installation, integration and troubleshooting of advanced or complex consumer electronics products
What’s in it for you
We’re committed to helping our people thrive at work and at home.
We offer generous benefits that address your total well-being and provide support as you need it, especially during key moments in your life.
Our benefits include:
* Competitive pay
* Generous employee discount
* Financial savings and retirement resources
* Support for your physical and mental well-being
About us
As part of the Best Buy team, you’ll help us fulfill our purpose to enrich lives through technology.
We bring...
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Type: Permanent Location: Lynchburg, US-VA
Salary / Rate: Not Specified
Posted: 2024-04-12 08:22:43
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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...
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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
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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 ...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:10:12
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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 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...
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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.
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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.
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-12 08:09:02
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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
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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...
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Type: Permanent Location: Ventura, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-12 08:05:03
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Line Cooks/Prep Cooks/Dishwashers Needed - Hiring Immediately!
Ted's Montana Grill isn't your ordinary restaurant, so we aren't looking for ordinary people.
While we’re Premium, Polished and Professional, we’re also Cool (known as 3 PC).
We live by “The Big Sky Spirit” which is our cultural compass and is evident in everything that we do.
Pay Rate Range: $15-$18/hr Based on Experience.
PREMIUM FOOD COOKED IN A SCRATCH KITCHEN
The little things are the big things in our kitchens.
Each of our menu items are made in small batches to ensure the premium freshness of our flavors.
Our on-premise butcher shop allows our team to hand carve and grind (daily) to ensure the peak freshness and premium flavor of our beef and bison.
At Ted’s Montana Grill, our Heart-of-House team members are highly valued members of our team.
A TMG Line Cook/Prep Cook not only prepares our made-from-scratch food but displays showmanship and interacts with our Guests in our display kitchens.
WHY WORK FOR TED'S?
· Competitive wages!
· Flexible schedules
· Medical benefits
· 401(k) plan with matching
· Scratch kitchen & no microwaves - be proud of where you work!
· Career advancement opportunities - half of our managers started as Team Members
To help promote family and quality of life for our teams, Ted's Montana Grill closes our restaurants on July 4th, Thanksgiving, Christmas Eve and Christmas Day.
REQUIREMENTS
· Full-service restaurant kitchen experience is desired.
· Great team player.
· Ability to multitask.
· Passionate about great food!
ESSENTIAL PHYSICAL REQUIREMENTS
Daily physical requirements and/or number of pounds that may need to be lifted on the job.
· Stands during entire shift.
· Frequent bending, stooping, reaching, pushing, and lifting.
· Lifts and carries tubs, trays, and cases weighing up to 100 lbs.
up to 20 times per shift.
· Frequent exposure to smoke, steam, high temperatures, humidity and extreme cold.
We invite you to become part of the team by applying today!
Ted’s Montana Grill is proud to be an Equal Opportunity and e-Verify employer.
HOSPITALITY
We take great pride in ensuring all guests receive a warm and memorable experience leaving them feeling better than when they came in.
From a bowl of half sours to our two-dollar bills, we empower each team member to deliver Big Sky Moments in ways that are natural and effortless to Ted’s and our guests.
THE EXPERIENCE
Our restaurants represent classic saloons of the 19th century where cattlemen and land barons found a little relaxation after a hard day’s work.
SUSTAINABILITY
We believe in leaving a better world for future generations.
You’ll see this in our commitment to local growers, the paper straws, the Boraxo soap in our restrooms and sustainable choices in our kitchen operations.
We are steadfast in our commitment to people, product and prosperity.
Ted’s Montana Grill develops and encourages people to become leaders and engage the hearts and minds of our teams.
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Type: Contract Location: Cumming, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-11 08:29:46
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: HSE Professional – Skyline Transition
As HSE Professional – Skyline Transition, you will be part of Greenfield HSE team.
In this role you’ll be responsible for advancing the transition to the new headquarters in Indianapolis from Greenfield IN.
This position is not permanent.
It is for a fixed duration of up to 18 months, with the potential to extend based on project needs.
Your Responsibilities:
* Draft new or revised HSE SOPs applicable to the new HQ.
* Generating LOTO ESI for operations.
* Facilitating R&D lab and office moves.
* Support HSE commissioning of new site, including life safety and emergency response.
* Support decommissioning of existing Greenfield site.
* Training and Safety Communications?
What You Need to Succeed (minimum qualifications):
* Education: Bachelor’s degree in occupational safety, environmental health or related science.
* Required Experience: A minimum of 5 years of experience in Environmental Health and Safety
* Excellent technical writing skills
* Excellent communication skills
* Experience with Microsoft office suite software.
What will give you a competitive edge (preferred qualifications):
* CSP
* Laboratory experience
* Broad Generalist HSE skills
* Regulatory experience
Additional Information:
* Location: Global Elanco Headquarters - Greenfield, IN - Hybrid Work Environment
* This position is not permanent.
It is for a fixed duration of up to 18 months, with the potential to extend based on project needs.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on fina...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 120000
Posted: 2024-04-11 08:25:01
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At Elanco (NYCE: 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!
IT Operations Analyst
Work Location: Position is in our corporate headquarters, which is currently in Greenfield, IN.
Elanco Animal Health will be moving to a new headquarters in downtown Indianapolis in 2025 (Q1 2025).
The Desktop Support Analyst will support local Information & AV Technology infrastructure and services including hardware, software, video conferencing, networking, printing as well as support internal stakeholders in our U.S.
and Canadian affiliates.
Responsibilities:
* Accountability for IT workplace and infrastructure operations (workplace technologies, conference rooms & AV technologies, user & executives support, assets, incidents, office apps and systems) in the USA and Canada.
* Provide standard and non-standard technical support to end-users in response to specific requests. Utilizes established operating procedures to review and resolve end-user technology issues; troubleshoots and resolves standard and non-standard hardware and software problems, as well as coordination of IT service providers when needed.
* Provide training on hardware and software for end-users; performs and supports testing and documentation activities. Documents operational problems; communicates with vendors, users, and other IT staff.
* Provide dedicated ("white glove") support for members of top management (executives) including in-the-office and outside-the-office board-, shareholders- and executive meetings.
* Ensure PRINT services in NA with contribution to the Global PRINT.
* Ensure MS Teams support model.
* Perform moves, adds and changes.
* Partner with site(s) & business stakeholders (especially Executives, Facility, Communications, IT)
* Own, manage and execute local IT infrastructure projects (including Workplace and AV domains within the “Skyline-New Head Quarters” /new office project).
* Advise and coordinate the work of a “last mile hands on support” representative in Canada.
* Manages and maintains local assets and configuration items in ServiceNow.
* Ensure local ...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 85000
Posted: 2024-04-11 08:24:48
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As a leading global animal health company, Elanco delivers innovative products and services to improve the health of pets and farm animals around the world because we believe making animals' lives better, makes life better.
Since 1954, we have provided solutions that support veterinarians, farmers and pet owners to advance our vision of Food and Companionship Enriching Life.
Elanco's promise to employees: Together, we foster an inclusive culture where everyone can make a difference, encouraging ownership, growth and well-being.
Position Description
Biopharma Technical Development has an exciting opportunity for an analytical scientist to join our product development organization in Greenfield, IN USA.
The scientist will drive development of chromatographic, electrophoretic and LC/MS analytical methods for a wide variety of biopharmaceutical product portfolios.
This position is laboratory-based and will require routine interaction with scientists across multiple discovery and core research laboratories at Elanco. The incumbent scientist will be expected to support multiple projects at any given time.
The scientist will independently plan, perform, interpret and report results of scientific experiments.
Responsible for leading validation, verification and method transfer strategies within Elanco and across the global sites as well as at CRO’s.
The scientist will also act as a mentor to other laboratory scientists by providing training and reviewing various methods and making recommended changes to scientific protocols and procedures.
This position will also be responsible for implementing R&D strategies to optimize analytical methods through principles of quality by design (QbD).
Functions, Duties, Tasks
* Perform assay development and optimization of chromatographic, electrophoretic methods for biopharmaceutical and therapeutic vaccine products and their characterization.
* Develop innovative and novel chromatographic solution to deliver analytics for wide variety of formulations for drug substances and drug products.
* Contribute to the development of analytical control strategy and setting specifications.
Must have ability to think critically, demonstrate curiosity, trouble shoot and solve complex problems.
* Provide rapid and timely analytical support for up- and down- stream bioprocesses along with formulation development activities.
* Develop method validation and verification strategies.
Provide guidance within Elanco global sites and work with CRO’s to achieve business objectives.
* Participates in technical teams by presenting results at team and business unit meetings.
* Author reports, prepare SOPs/working procedures.
Review technical documents including analytical test procedures, qualification protocols, development reports and stability protocols.
* Train and coach other associates and scientists globally to facilitate knowledge exchange to ensure consistent practices between sites...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: 153600
Posted: 2024-04-11 08:24:48
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As a leading global animal health company, Elanco delivers innovative products and services to improve the health of pets and farm animals around the world because we believe making animals' lives better, makes life better.
Since 1954, we have provided solutions that support veterinarians, farmers and pet owners to advance our vision of Food and Companionship Enriching Life.
Elanco's promise to employees: Together, we foster an inclusive culture where everyone can make a difference, encouraging ownership, growth and well-being.
The Dissolution Expert Analytical Development directly supports Elanco’s Technical Development (TD) organization and reports to the Head of Analytical Development SMTD.
This position is broadly responsible for analytical development activities of animal health products with a concentrated expertise in dissolution control strategy.
As part of technical development teams, the role is expected to support drug development with a diverse range of responsibilities.
These responsibilities include analytical development activities from the pipeline entry to regulatory approval: Quality by design development and optimization of analytical dissolutions methods as well as validation and release analytics in compliance with industrial (GxP) and regulatory requirements (VICH/ICH) are focus areas of this role.
In-depth scientific dissolution expertise and communication skills are expected for partnering with manufacturing and regulatory representatives to successfully drive drug product commercialization activities and technical submissions to global health authorities.
The Dissolution Expert will take on responsibility of problem solving for questions related to dissolution, cooperating within interdisciplinary and international teams and support ensuring launch readiness for analytical activities including transfer of methods to commercial organizations.
This role will also be responsible for driving evaluation and implementation of new technologies in the field of dissolution, applying the latest scientific thinking in dissolution testing to help bring new drug products to market.
Responsibility for dissolution strategy, identification of future capability needs, support of identification and selection of Contract Research/Development/Manufacturing Organizations (CRO/CDMO) and technical oversight of CRO/CDMO development work are also crucial part of the role.
The acceptable candidate should have relevant experience in authority interactions within technical sections of dossier submissions focusing on dissolution of orals solid dosage forms and other formulation types e.g.
suspensions.
Responsibilities will include but are not limited to:
* Develop and deliver relevant dissolution methods and specifications.
* Interpret results, evaluate data and draw relevant conclusions.
* Report and present scientific/technical results internally, may create external publications and patents and may present at scientific con...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2024-04-11 08:24:43
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At Elanco (NYCE: 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!
Functions, Duties, Tasks:
* Provide statistical input to the design, analysis, reporting and interpretation of clinical studies and contribution to publications.
* Use SAS or other software to develop custom programming code to generate tables, data listings, graphs and derived datasets as specified in the protocol/statistical analysis plan.
* Ensure that outputs meet quality standards and project requirements.
* Perform validation programming and work with other Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
* Keep project team members informed of programming progress and issues requiring their attention.
* Follow applicable SOPs and relevant regulatory guidelines.
* Manage scheduling and time constraints across multiple projects at a time, set goals based on priorities from management, and adapt to timeline or priority changes by reorganizing daily workload.
* Prepare in advance for internal meetings, contribute ideas, and demonstrate respect for opinions of others.
* Display willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
* Negotiate and establish accurate time estimates for completion of study activities with internal team members and statistical management, and complete project activities within timeframe allotted.
* Assist in drafting regulatory submissions.
* Effectively utilize current technologies and available tools for conducting the analyses.
* Keeping up-to-date with current literature and research new methodologies.
* Identifying, developing and implementing novel statistical methodologies in support of medicine development
* Ensure scientific integrity and animal welfare in all activities.
* Interact with global statisticians and implement recommendations locally.
* Create and maintain standard macros and applications to improve the efficiency of the department.
* Proactively participate in and/or lead process/quality impro...
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Type: Permanent Location: Bangalore, IN-KA
Salary / Rate: 580000
Posted: 2024-04-11 08:24:41
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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 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
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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...
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Type: Permanent Location: Bend, US-OR
Salary / Rate: Not Specified
Posted: 2024-04-11 08:23:26
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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...
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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
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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, 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...
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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...
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Type: Contract Location: Greeley, US-CO
Salary / Rate: 30
Posted: 2024-04-11 08:19:31
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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.
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
