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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
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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...
....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
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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...
....Read more...
Type: Permanent Location: Ventura, US-CA
Salary / Rate: Not Specified
Posted: 2024-04-12 08:05:03
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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...
....Read more...
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...
....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...
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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...
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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.
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-04-11 08:13:26
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We are seeking a Member Relationship Specialist for the Park Ten Financial Health Center.
This level of work uses good, individual judgment, analysis, and decision-making in assessing & overcoming obstacles to produce outputs.
Accumulating data from which to draw conclusions, listening to evaluate and determine needs.
It involves dealing one-by-one with concrete situations as they arise and diagnosing a problem from a multi-factor model.
Offering an optimal solution taking into consideration multiple variables to enable additional opportunities to be realized while also considering immediate cause and effect impacts and associated impacts of up to 6 to 9 months in length.
Manage meaningful member relationships and continually improve the efficiency and effectiveness of the interaction, experience, and execution of transactions.
Making situational response decisions to schedule and prioritize actions.
Foreseeing developing issues based upon observations and taking action to eliminate or reduce their negative impact or maximize their positive impact.
The objectives include effective coordination, collective improvement, and efficiency to improve current processes.
The theme of the work is service.
If you have exceptional listening, verbal communication, good written communication, and problem-solving skills, you should apply right away!
Highlights:
* Embody sincere empathy for our members and display a deep passion for helping our members achieve financial health
* Develop and propose multiple decision alternatives to address and/or improve members' current financial situation, remedy past missteps, and develop an action plan to help members attain short-range financial goals (up to one year)
* Thoughtfully and thoroughly plan and prepare for upcoming meetings with members to ensure high-quality, high-value, high-yield interactions
* Actively leverage multiple established community partner relationships by supporting the partner's values and mission through service, volunteer, or engagement opportunities
* Participate in cross-functional project team environments
* Work effectively and cooperatively with full commitment to tasks assigned by their manager
Experience:
Required
* 3 years of face-to-face interaction experience
Education:
Required
* High School Diploma or Equivalent
Preferred
* Baccalaureate degree desired
Skills & Knowledge:
Required
* Exceptional listening skills
* Exceptional verbal communication skills
* Good written communication skills
* Good problem solving skills
Schedule: Monday - Friday, 8:30 am-5:30 pm
Level of Work: 2B
Credit Human provides employees with many benefits from insurance coverage to college tuition reimbursement.
To get to know Credit Human and learn more about our benefits, visit our careers page at www.credithuman.com/careers.
Credit Human conducts employment background checks that may be use...
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Type: Permanent Location: San Antonio, US-TX
Salary / Rate: Not Specified
Posted: 2024-04-11 08:12:59
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Company
Federal Reserve Bank of Atlanta
As an employee of the Atlanta Fed, you will help support our mission of promoting the stability and efficiency of the U.S.
economy and financial system.
Your work will affect the economy of the Southeast, the United States, and the world.
The work we do here is important, and how we do it is just as important as what we do.
We live our values of integrity, excellence, and respect every day.
We do the right thing, we do things right, and we treat people right.
A career at the Federal Reserve Bank of Atlanta gives you the chance to do work that touches lives and helps communities prosper.
We are a dynamic hybrid workplace environment that requires at least 2 days a week in the office.
Job Description:
Independently consults with business lines on complex issues to strengthen workforce capabilities for a high performing organization, with guidance only in the most complex situations. Collaborates with other HR areas and business lines to execute on strategies related to talent management and succession/workforce planning, onboarding and assimilation, engagement and culture as well as leadership and staff development. Identifies and directs solutions and interventions in support of the organization's goals and objectives.
Leads projects/project steps and has accountability for HR activities/objectives.
Acts as a resource for colleagues with less experience
Key Responsibilities:
Engagement and Culture:
* Consult key stakeholders to execute the people and culture elements of the organization's mission and strategy.
Coordinate identification, timeline, and resource requirements for enterprise-wide and department-specific projects and initiatives to ensure alignment with organizational goals and objectives.
* Design, develop and facilitate sessions/workshops and recommend and implement changes and improvements as needed.
Create success measures, monitors progress and provides follow-up to ensure development solutions effectively address business and individual needs.
* Facilitate design, implementation, and administration of Bank-wide engagement survey. Serve as liaison with survey vendor to ensure timely and accurate administration of survey.
* Consult with business lines in the design, development, and facilitation of solutions and interventions that address engagement survey results.
Onboarding & Assimilation:
* Develop, enhance, deliver and monitor programs to help new employees and leaders become effectively enculturated to their new role within the Federal Reserve Bank of Atlanta (i.e., learn about the Bank, our culture, values, mission, strategy as well as policies, procedures, benefits, systems, key contacts and other resources).
* In partnership with Talent Acquisition, consult Business Lines/Departments on their onboarding and assimilation process for new or promoted employees and leaders.
* Partner with the team to monitor the assessment of new empl...
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2024-04-10 08:43:51
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Company
Federal Reserve Bank of Chicago
The DevOps Engineer is a technical professional who leverages their expertise in design, development, testing, implementation, and support of the Cloud platform ecosystem, to streamline development and deployment of applications using modern DevOps practices.
The level of work required is considered intermediate and staff must be able to work under general supervision.
This job does not have direct reports.
* Support the design, development, and management of Cloud platform ecosystems and infrastructure
* Works closely with software development teams and other functional groups to assist in the development of a robust, flexible, and scalable platform
* Assists in the design and development of automated deployment tooling and infrastructure, code management, orchestration deployment, testing, and monitoring
* Participate in the development of common components and templates for resources deployed in Cloud environments using Infrastructure as Code
* Integrate on premise solutions with Cloud resources
* Build out solutions based on security, monitoring, logging, and alerting requirements
* Coordinate technical and end-user resources to execute moderately complex tests and analyze testing results.
* Provides assistance and technical support regarding architectural and procedural best practices both across departments and applications including rotational on call support
* Maintains technical documentation for designs and operational procedures
* Identifies opportunities for automation of operational tasks to increase efficiency and lower the human intervention of repetitive activities.
* Contributes to a culture of continuous improvement and proactively searches for ways to apply DevOps tooling and practices to increase productivity of engineering and operations teams
Your Background
* Bachelor's degree in Computer Science, Information Systems, or equivalent background or experience
* 2-3 years of experience working with cloud based platforms in an enterprise environment
* 2-3 years software engineering experience in a team based environment
* Experience with programming tools, computer interfaces, and application architectures
* Experience deploying, managing, operating and monitoring of applications in scalable, highly available and fault tolerant data centers (both on-premise and hosted), AWS
* Experience learning, sharing, and implementing best practices with the ability to define operational processes, implement DevOps, deployment checklists
* Experience with Python or Node.js
* Experience with source code management tools; Git
* Experience developing solutions in an iterative (Agile) approach
* Experience with Continuous Integration Continuous Delivery tools and technologies; GitLab, CloudFormation, Terraform
* Basic knowledge and experience of scripting languages
* Knowledge of basi...
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Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:43:47
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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: Williston, US-VT
Salary / Rate: Not Specified
Posted: 2024-04-10 08:27:40
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Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
About the Role
In support of continuous improvement in Mining and Alcoa’s environmental performance, we have a unique opportunity for a suitably qualified Environmental Research Scientist to join the team that are driving improvements in rehabilitation processes and practices.
Reporting to the Environmental Research Superintendent, you will be working with a close-knit team of scientists based at Alcoa’s Huntly Central location and contributing to improving plant and soil aspects of rehabilitation performance.
The key aspects of the role will include:
* Designing, implementing, monitoring, analysing and writing up field trials to improve plant recruitment and survival in rehabilitation, e.g.
fencing, irrigation, ripping, and topsoil management.
* Investigating plant health to understand and overcome limitations to plant survival.
* Undertaking soil testing and analysis.
* Communicating results to internal and external stakeholders.
* Liaising with external research scientists to facilitate site access and field trials.
* Supervising higher degree by research students.
What’s on offer
* Career development opportunities to pursue your passion
* Performance related bonus (variable)
* Enjoy additional time off with a monthly Leisure Day
* 16 weeks paid primary parental leave scheme
* Paid annual volunteering hours
* Social and diversity focused engagement opportunities
What you can bring to the role
* PhD in restoration ecology, land rehabilitation, soil science or ecohydrology.
* Research experience post-PhD studies with exposure to soil testing.
* Capable in installing and monitoring large-scale field trials with minimum supervision.
* An analytical mind that can solve complex datasets using appropriate statistical methods.
* Skilled in publishing papers in peer reviewed journals.
* Previous experience in mining rehabilitation, knowledge of the WA flora and GIS will be considered desirable.
Application Closing Date
Sunday, 5 May 2024
Additional information
* Interviews may progress prior to the closing date, although all applications will be considered.
* You will only be contacted if you are shortlisted for an interview, this process can take up to four weeks from the closing date.
#LI-JR1
About the Location
As an Alcoan you are part of a global team committed to advancing sustainability and delivering excellence and innovation.
Join in and become an essential part of our purpose: to turn raw potential into real progress.
The power is in your hands to shape the things that matter to us all.
We are values led, vision driven and united by our purpose of transforming raw potential into real progress. Our commitments to Inc...
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Type: Permanent Location: PINJARRA, AU-WA
Salary / Rate: Not Specified
Posted: 2024-04-10 08:23:07
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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.
As a member of the MSAT (Manufacturing Science & Technology) Team Ibex Visp responsible for the successful transfer, scale up, supervision and optimization of biopharma processes.
As a very experienced professional, you are regarded as an expert in process science and manufacturing aspects.
In this role, you significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.
Key Responsibilities
* Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals
* Act as the interface between the process donor (external customer, process development) and operations.
Responsible to ensure process scalability and manufacturability
* Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control
* Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements.
This includes on call duty
* Responsible for execution of GMP risk analysis for the manufacturing processes
* Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance
Key Requirements
* PhD (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related disciplines
* Working experience in biopharma manufacturing and / or process development preferable in of Mammalian Manufacturing
* Deep understanding of GMP and bioprocess technology
* Very good communication skills and interaction with all kinds of interfaces within customers and the project organization
* Fluency 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...
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Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:18:55
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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.
For Drug Product Services (DPS), our successful DP focused branch located in Basel, Switzerland and Stein, Switzerland, we have exciting opportunities.
Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for Principal Scientist/Group leader Formulation Development.
Key responsibilities:
* Lead formulation development activities related to liquid and lyophilized parenteral drug products of large molecule biologics(e.g.
monoclonal antibodies, novel formats, ADCs, peptides), vaccines and small molecules.
* Design, plan, execute and deliver formulation studies as well as characterization studies based on contracted terms and scientific inputs relevant to product
* Supervises the analyses of formulations in context of the product development using analytical and pharmaceutical test methods
* Author technical documents and support preparation of regulatory documentation
* Manage group of technicians, engineers and/or scientists and collaborate across departments
* Ensure safety and health protection following lab and safety instructions as well as basic GMP qualification
* Contribute to improvements, explore new technologies and lead integration of activities
* Enable innovation and technical strategy projects, generate IP and evaluate and implement new methods and technologies
Key requirements:
* Ph.D.
in pharmaceutical sciences, chemistry, biochemistry, or related fields
* Significant work experience in biotech / pharma industry
* Experience with technical issues and requirements for development of drug product formulation and/or processes of biologics.
* Knowledge of lyophilization, primary packaging, aseptic product manufacture (protein or vaccine drug products and/or protein analytics is desirable)
* Excellent communication skills, excellent command of English both written and oral
* Excellent leadership and interpersonal as well as planning skills
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, ...
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Type: Permanent Location: Basel, CH-BS
Salary / Rate: Not Specified
Posted: 2024-04-10 08:18:38
-
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.
As a member of the MSAT (Manufacturing Science & Technology) Team Ibex Visp responsible for the successful transfer, scale up, supervision and optimization of biopharma processes.
As a very experienced professional, you are regarded as an expert in process science and manufacturing aspects.
In this role, you significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.
Key Responsibilities
* Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals
* Act as the interface between the process donor (external customer, process development) and operations.
Responsible to ensure process scalability and manufacturability
* Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control
* Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements.
This includes on call duty
* Responsible for execution of GMP risk analysis for the manufacturing processes
* Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance
Key Requirements
* PhD (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related disciplines
* Working experience in biopharma manufacturing and / or process development preferable in of Mammalian Manufacturing
* Deep understanding of GMP and bioprocess technology
* Very good communication skills and interaction with all kinds of interfaces within customers and the project organization
* Fluency in English; German nice to have
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 proble...
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Type: Permanent Location: Visp, CH-BL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:16:03
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SUMMARY:
The person in this role will oversee all Safety Activities and be responsible for the field training and mentoring of Engineering Services employees as it relates to MOW technical procedures, specifications, safety guidelines as required by FRA, OSHA, MSHA and company policies regarding machinery and hand tools to ensure safe and efficient operating procedures, usage, and maintenance.
RESPONSIBILITIES:
* Be familiar with all state, federal, and local safety regulations governing all aspects of the rail industry.
* Establish a safety culture foundation based on compliance with GWI safety rules, regulations and environmental responsibilities
* Supervise and set the example for all safety training and work with the Corporate Safety Team.
* Create a professional and safe environment that is conducive to the development of all employees
* Respond to reported incidents to evaluate current best practices and recommend changes where necessary.
* Ensure the safety of the workplace by coordinating, administering and implementing comprehensive training programs in occupational, industrial and environmental safety.
Support the design, delivery and continuous improvement of equipment training programs as well as ongoing learning opportunities across the organization, in support of the organization’s needs
* Assist in the administration of the company's On-The-Job Injury Policy and return to work issues.
* Implement regional and corporate safety initiatives and policies.
Conduct audit assessments and provide feedback to regional leadership.
* Participate in corporate and regional safety calls with the ability to intercede in any operational activity that may be deemed an improper/unsafe job procedure.
* Conduct safety audits and inspections to ensure compliance with occupational and environmental health and safety requirements.
* Evaluate employees to measure their progress in achieving proficiency in specific tasks.
Ensure accurate record keeping of training conducted
* Deliver training via oral and hands on demonstration in a field and classroom environment
* Conduct initial and follow up training sessions with employees and provide feedback on developmental needs
* Other projects and duties as assigned.
REQUIRED SKILLS AND/OR EXPERIENCE:
* Demonstrate an ability to lead and direct, plan work schedules, assign or delegate work on a daily basis, develop and mentor employees and take corrective actions when necessary.Creates and maintains a positive and professional learning environment.
* Ability to identify problem safety areas and set up a solution to resolve.
* Good oral and written communication skills.
Excellent communication, team building, and leadership skills.High level of interpersonal skills to work effectively with others, motivate employees and elicit work output.
* Must have a good understanding of rail industry and its goals and object...
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: Not Specified
Posted: 2024-04-10 08:11:41
