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Applications due by May 17, 2024
Position Description
Pay: $17.00 per hour
This position is eligible for Daily Pay! Work today, get paid today! We’ve partnered with DailyPay, a voluntary benefit to offer employees access to their pay on their own schedule.
Work Schedule: Monday - Friday 8am to 4:30pm or 9am to 5:30pm
This Full-Time job is eligible for Medical, Dental, Vision, Retirement, Long Term Disability, Short Term Disability, Life and Accidental Death and Dismemberment, Flexible Spending Accounts, and several voluntary supplemental benefit offerings. In addition, this position is eligible for paid time off in the form of vacation, sick, holiday, floating holiday, jury duty and bereavement leave.
OBJECTIVE:
The Programs Case Manager II assists in the design and delivery of program activities for person with mental, physical, and/or intellectual/developmental disabilities. This position will be responsible for continuous support to the Employment and Community based programs. This role serves as a champion and model of Goodwill’s values.
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION AND EXPERIENCE:
Applicable field or equivalent combination of training and experience in a social service, counseling or rehabilitation setting, providing direct services to persons with physical, emotional and/or developmental disabilities will also be considered. A valid Colorado driver’s license, vehicle insurance, and willingness to use personal vehicle for community work is required.
OTHER REQUIREMENTS/PREFERENCES:
It is preferred that the incumbent have excellent written and verbal communication skills and demonstrate the ability to interact with various types of internal and external customers.
It is also preferred that the incumbent have the ability to relate effectively to people with disabilities, their parents, host home providers and guardians and be empathetic toward their needs.
The incumbent must have the ability to work independently, cooperatively and to exercise effective planning. The Case Manager II, Programs must demonstrate flexibility within the framework and pressure of established deadlines. The incumbent must be able to write clear, concise and accurate reports and plans, submit them in a timely fashion and possess excellent time management skills. The incumbent must have a working knowledge of community resources, have the ability to program, train and be creative in motivating Participants toward individual success.
The incumbent must also conduct self in a professional manner and maintain a professional appearance that enhances the firm’s reputation.
Overtime may be required as w...
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Type: Permanent Location: Colorado Springs, US-CO
Salary / Rate: 17
Posted: 2024-05-03 08:44:28
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Today Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Ibex® Solutions (www.ibex.lonza.com) is a modular build complex to develop and manufacture biological products.
It enables companies to get access to a complete solution, gaining speed and achieving a simplified value chain.
The Ibex® Complex is our contribution to the medicine of tomorrow and possibly the next step in your career? Start your career with Lonza today.
Key responsibilities:
* Review of the executed Batch Records (e.g.
cleaning logs, production documentation review, temperature reports, test procedures (HEPT, FIT), Autoclave and Washing machine protocols, used material, calibration records, sample results recorded in LIMS, logbooks, etc.)
* Support preparation of documentation package to enable fast release by QA
* Review comments added to the executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
* Initiate and support accomplishment of Deviations and investigations for Batch Record review related observations
* Support the initiation of CRs and TCRs
Key requirements:
* Previous experience in GDP and GMP regulated pharmaceutical / API industry is an advantage
* Ability to identify non-compliance and gaps from quality standards
* Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation
* Structured, focused and well-organized working attitude
* Open-minded for new ideas and suggestions; solution-oriented
* Agile, highly motivated and dynamic drive
* Ability to produce reliable results under stress
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: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-03 08:43:42
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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.
Ibex® Solutions (www.ibex.lonza.com) is a modular build complex to develop and manufacture biological products.
It enables companies to get access to a complete solution, gaining speed and achieving a simplified value chain.
The Ibex® Complex is our contribution to the medicine of tomorrow and possibly the next step in your career? Start your career with Lonza today.
Key responsibilities:
* Review of the executed Batch Records (e.g.
cleaning logs, production documentation review, temperature reports, test procedures (HEPT, FIT), Autoclave and Washing machine protocols, used material, calibration records, sample results recorded in LIMS, logbooks, etc.)
* Support preparation of documentation package to enable fast release by QA
* Review comments added to the executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
* Initiate and support accomplishment of Deviations and investigations for Batch Record review related observations
* Support the initiation of CRs and TCRs
Key requirements:
* Previous experience in GDP and GMP regulated pharmaceutical / API industry is an advantage
* Ability to identify non-compliance and gaps from quality standards
* Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation
* Structured, focused and well-organized working attitude
* Open-minded for new ideas and suggestions; solution-oriented
* Agile, highly motivated and dynamic drive
* Ability to produce reliable results under stress
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: 2024-05-03 08:43:41
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Georgia Pacific is seeking a Sr.
R&D Engineer/Scientist at our building products laboratory in Decatur, GA.
The role creates value by identifying, developing, and commercializing market-focused innovative solutions for GP Building Products.
We use creative and inventive skills to conceptualize and engage the scientific method to profitably translate existing and new technologies into our marketspace.
The ideal candidate will have experience or a scientific background in a field that relates to building products.
This role is based out of our Decatur Technical Center (just outside Atlanta, GA).
The Decatur center primarily focuses on Georgia-Pacific building products R&D efforts and includes a state-of-the-art analytical lab with extensive application testing capabilities.
As a market leader, Georgia-Pacific has the analytical, statistical and process tools, assets, and commitment for you to be a successful contributor and create value.
At Georgia-Pacific, you will play a key role in the product development cycle from idea generation through new product commercialization.
If you aspire to use your critical thinking skills and creativity to drive innovation, we are interested in learning more about you!
*
*
*This role is not eligible for visa sponsorship
*
*
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What You Will Do
* Demonstrate the virtues consistent with Georgia-Pacific's Principle Based Management (PBM®)
* Ensure laboratory safety is our number one priority
* Participate in voice of customer initiatives to identify valuable problems worth solving
* Lead technology scouting initiatives and brainstorming of innovative solutions
* Lead experimental design/statistical data analysis to prototype/test brainstormed solutions, with the goal of discovering those that are economically viable and technically feasible
* Work with and mentor technicians/associates to conduct well designed experiments at both the laboratory scale and pilot scale
* Participate in scaling-up and launching developed solutions
* Lead intellectual property strategy
* Communicate project results with key stakeholders of various levels across multiple capabilities within GP Building Products, including senior leadership
Who You Are (Basic Qualifications)
* PhD with 3+ years of research and development experience
-OR-
Master's degree with 3+ years of research and development experience
-OR-
Bachelor's degree with 5+ years of research and development experience
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Bachelor's Degree or higher in Materials Science, Chemistry, Chemical Engineering, or Building Science
* Research and development experience in material science related disciplines (e.g., polymers/chemistry, composites, ceramics)
* Experience communicating technical information to non-technical audiences
* Experience advancing projects through the stage gate process (ideation, research, development, and commercialization)
* Experience with design of experiments (DOE) and statistic...
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Type: Permanent Location: Decatur, US-GA
Salary / Rate: Not Specified
Posted: 2024-05-03 08:34:51
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Your Job
Georgia-Pacific is recruiting for a Research Chemist at our Neenah Technical Center (NTC).
This individual will become a recognized internal expert in tissue making chemistry, take on challenging problems and develop solutions to fill the technology pipeline, and advance our company's executional excellence.
NTC, located in Neenah, WI, is the central site for research, development, and lab services for Georgia-Pacific's North American Consumer Products business.
Our consumer brands are household names throughout North America - Quilted Northern® and Angel Soft® bath tissue, Brawny® paper towels, Dixie® plates and bowls, and many others.
We also produce products such as enMotion® towels and dispensers, as well as SmartStock® cutlery dispensers for commercial markets.
Many of the store-brands at your favorite retailers are our products too!
Flexible work options for this position are offered depending on business need, such as occasional work from home.
Travel will also be a part of this role for up to 25% of the time.
Relocation assistance is offered for candidates that need to relocate.
What You Will Do
Innovation: Bring your creativity to solve challenging problems and develop chemistry solutions.
From concept to commercialization, you will shape the future of our operations and products.
Technical Support: Provide technical recommendations for wet end chemistry and assist with skill-building and teaching within the organization.
Collaboration: Work with product development, operations, sourcing, and product stewardship to uncover new opportunities and deliver unique solutions.
Partner with external vendors to develop and commercialize new technologies.
Entrepreneurship: Take ownership of your projects and work within a supportive team environment to bring your new ideas to life.
Experiment at the lab-scale and pilot-scale then translate those learnings as you provide hands-on operational support.
Career Development: Leverage the internal network within GP and Koch Industries to share your technical expertise and learn from a diverse group of scientists within the organization.
We'll help match your individual strengths and passion areas to high value projects.
Who You Are (Basic Qualifications)
* Bachelor's or advanced degree in Paper Science, Chemistry, or Engineering and two (2) or more years of work experience in a papermaking or chemical R&D environment.
* Experience working in a Research & Development environment with demonstrated results independently leading research.
* Able to travel 25% of the time.
* Ability to lift and carry samples routinely weighing up to 50 lbs.
What Will Put You Ahead
* Experience and knowledge of the tissue making process.
* Experience and knowledge of process and functional papermaking chemicals.
* Experience in project management and team leadership.
About the Neenah, WI Area
Our facility is the Georgia-Pacific Innovation Institute® in Neenah, ...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-05-03 08:34:41
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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 Stability Manager will supervise the daily activities of the QC Stability team with responsibility for implementing and maintaining cGMP Stability for all phases of development, clinical, and commercial drug products.
Primary responsibility will include managing stability studies for client projects and stability data analysis. May oversee additional areas of responsibility within the Quality Control Lab such as Lab Support, Data Review, Raw Materials, or Product Analysis, as required.
Key responsibilities:
* Manage and coordinate Lonza Tampa stability study program on development, clinical, and commercial drug products, summarize stability results to ensure scientific and technical execution.
* Manage stability database, and perform data trending, forecasting, and reporting of metrics.
* Creation, revision, and approval of SOPs, stability protocols, and reports in accordance with current GMP, FDA, EU, Global, and ICH guidelines and regulations.
* Facilitates and executes stability study protocols strategy and design including calculation and execution of stability study set downs and pulls independently and through direct collaboration with cross-functional teams and clients.
* Ensure Quality Control test methods, lab equipment maintenance/repair, calibrations, and record keeping are done in accordance with established procedures.
* Record test results, disposition of raw materials, intermediate and finished goods.
* Support validation of new/revised test methods and/or equipment, investigation of nonconformances, and new product launch activities.
* Support the development of data for Quality Control specifications for new products, optimizing existing specifications and test methods.
* Manages QMS records for QC Stability which includes deviations, change controls, CAPA, and other applicable stability-related investigations and events.
* Ensure that the GMP stability program continuously aligns with FDA, ICH, and other international agencies.
* Provide support, leadership, and training for members of the QC Chemistry department when necessary.
* Managing laboratory projects as required.
* Actively participates in customer and regulatory audits.
* Provide strong teamwork in establishing a quality culture and shared accountability.
* Perform other responsibilities to support the business as requested.
* Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustai...
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Type: Permanent Location: Tampa, US-FL
Salary / Rate: Not Specified
Posted: 2024-05-03 08:25:48
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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.
Das QC 24/7 Analytical Services Team ist der erste Kontaktpunkt für alle analytischen Proben aus der Biologics-Produktion am Standort Visp.
Das Team erhält rund um die Uhr Proben, aliquotiert sie gemäß den Vorschriften für die weitere Verarbeitung und führt vor allem zeitkritische Analysen für alle Technologien durch (Chromatographie, Biochemie, Mikrobiologie und Physikalische Chemie).
Als Analyst in unserem Quality Control (QC) 24/7 Analytical Services Team haben Sie die Möglichkeit, sich auf eine der verschiedenen Technologien zu spezialisieren oder ein breites Wissen über unser umfangreiches Portfolio an analytischen Tests zu erlangen (Bioburden, Endotoxine, SEC, HPLC, ELISA, TOC, UV, pH usw.).
Aufgaben:
* Arbeit im Qualitätskontrolle Labor
* Aliquotieren von Proben unter aseptischen Bedingungen
* Durchführung und Dokumentation von zeitkritischen IPC-Analysen (Bioburden, Endotoxine, HPLC, TOC, UV, pH, usw.)
* Alle Tätigkeiten werden unter Einhaltung der GMP Richtlinien ausgeführt
* Arbeiten mit hochaktiven Wirkstoffen (AHSK 4/5)
Anforderungsprofil:
* Abgeschlossene Berufsausbildung (Naturwissenschaftlich-technisches Fachgebiet wie pharmazeutische Technologie, Biotechnologie, Chemie, Verfahrenstechnik bevorzugt), zB Lehre, CTA/BTA oder BSc
* Hohe Lern– und Einsatzbereitschaft sowie Flexibilität
* Sicherheits- detail- und pflichtbewusstes Arbeiten
* GMP Kenntnisse sind ein Plus
* Sehr gutes Verständnis von technischen Zusammenhängen
* Verhandlungssichere Deutschkenntnisse, Englischkenntnisse sind ein Plus
* Bereitschaft zur Schichtarbeit (4-Schicht-Betrieb)
Das können Sie von uns erwarten:
* Während des Trainings und der Einarbeitungszeit stehen Ihnen erfahrene Mitarbeiter zur Seite, zum schnellen Erwerb aller evtl.
fehlenden Kenntnisse oder Erfahrungen
* Weiterbildungs- und Aufstiegsmöglichkeiten je nach individuellem Schwerpunkt Ihrer Fähigkeiten (e.g.
Ausbildung zum Trainer einer Technologie)
* Leere Skihänge oder Wanderwege wenn Sie unter der Woche frei haben dank des 4-Schicht-Betriebs 😊
Wenn Sie eine neue spannende Herausforderung suchen und bereit sind, Teil eines dynamischen Teams zu werden, bewerben Sie si...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-03 08:24:46
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist.
Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen.
Unsere wichtigste wissenschaftliche Lösung sind talentierte Mitarbeitende, die zusammenarbeiten und Ideen entwickeln, die anderen Unternehmen helfen, Menschen zu helfen.
Im Gegenzug steuern unsere Mitarbeitenden ihre Karriere selbstständig.
Denn ihre Ideen, ob gross und klein, verbessern die Welt.
Und das ist die Art von Arbeit, an der wir Teil haben möchten.
Am Standort Visp wird ein Chemiker (m/w/d) für den Bereich Launch Plant gesucht.
Ihre Aufgaben:
* Funktionale Leitung multidisziplinärer Projektteams inkl. aller Herstellungsaspekte der zugewiesenen Produkte.
* Vorbereitung und Durchführung der Risikoanalyse für die zugewiesenen Produkte und die Umsetzung und Kontrolle der definierten Massnahmen.
* Dokumentation der Prozesse und des Prozess-Know-hows mit den entsprechenden Berichten gemäss den anlage- oder produktspezifischen Anforderungen.
* Verantwortlich für die Kostenkalkulation zur Planung der Produktion und die Kostenübersicht während der Produktion.
* Schulung der Operatoren für die Herstellung der zugeordneten Produkte.
* Unterstützung des Produktionsleiters, der Anlageteamleiter und des Leiters des Produktionspersonals bei Schulungs- und Planungsaufgaben.
* Unterstützung und Durchführung von Innovations- und Verbesserungsprojekten, welche die allgemeinen Herstellungsaspekte für die Produktionsanlagen umfassen.
Ihr Anforderungsprofil:
* Bachelor- / Master-Abschluss, vorzugsweise in Chemie, Chemieingenieurwesen, Biotechnologie oder verwandten Disziplinen.
* Sehr gute Kommunikationsfähigkeiten und Interaktion mit allen Arten von Schnittstellen innerhalb der Organisation (Teamplayer).
* Sehr gute Deutsch- und Englischkenntnisse.
* Erfahrung in der chemischen oder biotechnischen Herstellung (z.
B.
als Produktionschemiker / Biologe, MSAT-Experte, Ingenieur) und GMP-Kenntnisse von Vorteil.
Lonzas Produkte und Services wirken sich täglich positiv auf Millionen von Menschen aus.
Für uns stellt dies nicht nur eine grosse Ehre, sondern auch eine grosse Verantwortung, dar.
Wie wir unsere Geschäftsergebnisse erreichen ist für uns genauso wichtig wie unsere Erfolge selbst.
Bei Lonza wird Respekt grossgeschrieben und wir schützen sowohl unsere Mitarbeiter als auch unsere Umwelt.
Erfolg für uns bedeutet moralisch vertretbarer Fortschritt.
Zu Lonza kommen Menschen, die Herausforderungen annehmen und mit ihrer Kreativität im Bereich Life Science neue Ideen für komplexe Problemstellungen entwickeln.
Zusammen leisten wir einen Beitrag, der das Leben vieler Menschen auf der ganzen Welt verbessern k...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-03 08:24:40
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Are you looking for a new scientific challenge?
We advance science so that we can spend more time with the people we love.
In pharma Research and Early Development (pRED) of Roche, we are united by the vision to advance and realize protein-based therapies, translating scientific progress into life-changing experiences for patients.
The core business of the Bioprocess Research department, located in the Large Molecule Research area, is to develop innovative purification processes for complex, mostly antibody-based protein therapeutics for groundbreaking therapies.
In addition, we support the development of new modalities such as gene therapeutics and antibody conjugates.
In this environment, we are looking for you to strengthen our motivated and dynamic team, which operates in a flexible matrix organization.
The position
As a Principal Associate in laboratory automation for the purification of therapeutic proteins (m/f/d), you will work in an expert team in the field of bioprocess development for protein-based therapies.
The main goal of your work is the development, establishment, and execution of automated screens and workflows to make bioprocess development faster and better.
Your impact
* You independently adapt, develop, and establish existing or new workflows for automated screens for protein purification (Downstream Processing (DSP) robotics)
* You take responsibility for the planning, execution, and evaluation of DSP robotics experiments (TECAN robotics)
* You program TECAN robots and support IT experts in establishing data workflows
* You work in a cross-functional team to support the development of bioprocesses that enable new drugs to quickly reach the clinic.
These processes should also be feasible in a production environment later on.
Your profile
* Most importantly - you have at least five years of practical experience in laboratory automation, ideally in laboratory automation for bioprocess development.
In addition, you ideally bring knowledge about proteins and protein purification.
* You have experience in programming laboratory robots (ideally TECAN robots).
Moreover, you are excited about new technologies.
* Independent data evaluation and discussion of data with other experts is also not new to you
* The scientific basis for your activity is a master's degree in biology, biotechnology, biochemistry, mechatronics, or a similar field.
We ask students with PhD to refrain from applying.
With a doctorate, you are above the educational profile required here.
* Fluent English skills in...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-05-03 08:23:22
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Roche fosters diversity, equity and inclusion, representing the communities we serve.
When dealing with healthcare on a global scale, diversity is an essential ingredient to success.
We believe that inclusion is key to understanding people’s varied healthcare needs.
Together, we embrace individuality and share a passion for exceptional care.
Join Roche, where every voice matters.
The Position
Was wird Sie erwarten?
Verstärken Sie unser Entwicklungsteam Zellkultur als Prozessassistent / Senior Associate Scientist (m/w/d) in dem Bereich Pharma Technical Development, welcher das Bindeglied zwischen der Pharma Forschung und Produktion darstellt.
Zu Ihrem Verantwortungsgebiet zählen die Entwicklung, Optimierung und Validierung von Zellkulturprozessen zur Herstellung therapeutischer Antikörper und anderer biologischer Modalitäten.
Sie tragen maßgeblich dazu bei, neue innovative Therapeutika zur Zulassung zu bringen und damit dringend benötigte Arzneimittel für die Patienten verfügbar zu machen.
Dabei berichten Sie an den Gruppenleiter Prozessentwicklung Zellkultur bzw.
einen Projektleiter im Rahmen einer Matrix-Organisation.
Was beinhaltet Ihre neue Stelle?
* Sie entwickeln, optimieren und validieren robuste industrielle Zellkulturprozesse zur Herstellung von therapeutischen Antikörpern durch Planung und Auswertung von Experimenten vom Labor- bis zum Pilotmaßstab.
* Sie planen Experimente mit komplexen Designs (unter Verwendung von „design of experiment“-Strategien), koordinieren die Durchführung und werten die Experimente unter Verwendung fortschrittlicher Datenanalysemethoden (statistische Datenanalyse, Datenvisualisierung) aus.
* Die Mitarbeit bei der Übergabe /Transfer der Fermentationsverfahren an den jeweiligen GMP Betrieb zählt ebenfalls zu Ihren Aufgaben.
* Die Erstellung der erforderlichen Projekt-, Entwicklungs- und Zulassungsdokumentation rundet Ihr Aufgabengebiet ab.
* Sie arbeiten an abteilungsübergreifenden und globalen Themen und unterstützen mit ihrer Fachexpertise die kontinuierliche Einführung von Innovationen.
* Sie arbeiten in lokalen und globalen Teams und präsentieren in diesen Teams die von Ihnen erarbeiteten Resultate.
* Sie entwickeln neue und optimieren bestehende Technologien für den Einsatz in Fermentations- und Ernteprozessen und implementieren diese.
Sie können sich mit den folgenden Aussagen identifizieren?
* Abgeschlossenes Masterstudium der Fachrichtung Biotechnologie, Biologie, Biochemie, oder einer vergleichbaren Fachrichtung.
Alternativ haben Sie ein Bachelorstudium oder eine berufliche Ausbildung mit mindestens 3-jähriger Berufserfahrung idealerweise im industriellen Umfeld.
* Für die Durchführung der genannten Arbeiten sind umfassende Kenntnisse im Umgang mit tierischen Zellkulturen , der Verfahrensentwicklung und Fermentation erforderlich.
Außerdem sind ein sicherer Umgang mit der EDV (u.a.
MS Office, Tibco Spotfire, SAS JMP) u...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-05-03 08:22:06
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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.
Head QC Microbiology in Visp, Switzerland.
Key responsibilities:
* Assume overall responsibility for departmental budget
* Provide leadership to a multilayer organization of leaders, technical supervisors and lab technician to ensure organizational readiness to absorb current and future growth business specifically
* Ensuring workforce planning, and ensuring organizational readiness to absorb the growth curve inline with forecast
* Developing an effective and cohesive teamwork, fostering close collaboration with internal and external customers and stakeholders
* Supporting and maintaining robust and reliable product supply to our customers
* Ensuring an inspection readiness state for the site to meet expectations from customers and regulators
* Developing and maintaining a robust communication and escalation process to internal and external stakeholders and customers
* Driving a lean mindset and establishing mechanisms to continuous improvement initiatives to be executed in line with plan
* Ensure main laboratory management systems are in place and developed to the next level
* Develop strategy and plan to ensure Laboraory Capacity and Assets are fit for purpose (short-, mid-, and longterm)
* Main and develop the Laboratory IT Infrastructure inline with global standards
* Orchestrate main Quality Systems and ensure adherence to main regulations (ICH, PIC/S, HMG, CFR, GMP Regulations)
* Establish a continuous improvement mindset
* Oversee and manage departmental performance and quality metrics
* Assume a “Customer First Mindset” and ensure technical and compliance positioning is accurate
Key requirements:
* University Bachelor’s degree in Science with a major in Microbiology and/or Virology with at least 10 years of experience in GxP positions with progressive experience in Biologics/Biopharmaceutical/Pharmaceutical industry or MSc/Ph.D degree with at least 8 years in GxP positions
* Strong pharmaceutical microbiology experience, specifically in dealing with Biologics
* Demonstrated, well developed analytical and problem-solving skills
* Comprehensive knowledge of global GMP regulatory requirements for microbial contamination controls, quality control laboratory operations, environmental and critical utility monitoring and data integrity
* In depth knowledge of requirements of GxP Regulations and guidance of Health Canada, US-FDA, EU in particular data integrity and various compendia (USP,...
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-05-03 08:19:57
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ERM is seeking a Managing Consultant, Corporate Sustainability & Climate Change to join our growing corporate sustainability and climate change advisory services practice in across North America.
In this role, you will be a key contributor to a team developing and growing ERM’s corporate sustainability and climate change business.
ERM delivers a wide range of climate change services including decarbonization strategy development, creation of Scope 1, 2, and 3 carbon inventories, Task Force on Climate-related Financial Disclosure (TCFD) analysis and reporting, strategy development, policy and regulatory analysis, target setting, and benchmarking.
We help clients, including global companies, electric and natural gas utilities, and financial institutions, develop and implement climate change programs across a broad range of industry sectors and contribute to climate, clean energy, and clean transportation policy development.
This is an excellent opportunity for an experienced professional looking to play a key role working with an expert consulting team on leading-edge climate advisory projects for Fortune 500 and privately held clients.
RESPONSIBILITIES:
Managing Clients and Projects
* Demonstrates expertise in the evaluation of oil and gas, chemical, and/or manufacturing processes to evaluate GHG emissions.
* Advises and manages climate-related projects including the design and development of GHG inventories (Scopes 1, 2 and 3) analysis of emission reduction levers (e.g.
energy efficiency measures, renewable energy, decarbonized fuels), and strategic policy assessment and design.
* Supports development of climate change strategy, action planning, and/or modeling with regards to mandatory or voluntary drivers.
* Builds strong and trusted relationships with clients and/or business partners
* Thinks strategically in order to influence decision-makers and outcomes.
* Distills complexity from detail to effectively coach colleagues to deliver high-quality outputs.
* Demonstrates strong project management skills and oversight through the project lifecycle, including scoping, budget and delivery.
* Demonstrates strong analytical skills, excellent writing and presentation skills, and a mastery of impactful client communication.
Teamwork and Organization
* Demonstrates strong people management skills; particularly the ability to support, coach and celebrate others to advance employee engagement and achieve results.
* Mentors junior staff in the proper planning and execution of projects, and in directing or conducting independent technical reviews of deliverable work products.
* Manages a team of two to five junior consultants.
* Identifies, evaluates, cultivates and manages partnerships and relationships with senior clients, external stakeholders and key opinion leaders.
* Effectively collaborates internally to bring our services to existing clients.
* Enhances ERM’s capabil...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2024-05-02 08:39:08
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RESPONSIBILITIES:
* Ensure consistent adherence to, and execution of, Company safety and environmental standards.
* Provide technical support in management of EHS related topics including: Lockout, Confined Space, Emergency Response, Hazard Communication, Overhead Cranes, Mobile Equipment, Cardinal Safety Rules, Waste Management, Spill Response, Storm Water etc.
* Perform onsite safety audits of employees, processes, contractors, vendors, etc.
* Recognize process safety conditions and coach operations staff accordingly.
* Manage HSE incident investigations and reporting, including root cause analysis, development of corrective action strategies, maintaining statistical information, recommending program revisions as appropriate and issue required reports to Management.
* Provide technical support and problem solving in troubleshooting safety and environmental issues
* Coordinate and instruct safety-related training classes, and act as subject matter expert for Safety meetings.
* Vendor interface for company policy communications & expectations
* Know and follow all Health, Safety and Environmental (HSE) policies always.
* Always know and use appropriate Personal Protective Equipment (PPE).
* Exercise stop work authority in the event of unsafe conditions or situations.
* Assist in writing technical and management systems reports and documents
* Establish and maintain EHS controls and documentation procedures
* Assist with internal compliance audits and program evaluations
* Oversee department sub-contractor support as needed
* Support the EHS department as a valuable and knowledgeable resource
* May conduct other tasks as required
EXPERIENCE, SKILLS, AND KNOWLEDGE:
* HSE regulatory knowledge
* Environmental regulatory knowledge
* Outstanding communication skills
* Highly organized and able to successfully manage multiple projects
* Capable of working independently in a self-directed environment
EDUCATION, TRAINING, AND CERTIFICATIONS:
* Associate of Science degree in Safety or any HSE-related discipline
* First responder/CPR trained (desired)
* Experience with OHSAS 18001, ISO 14001, Integrated Management Systems, and associated documentation and audits (desired)
* Minimum of 2 years’ experience in safety experience preferred
* Experience working within manufacturing industry preferred
* Bilingual (English and Spanish) preferred
Other
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Type: Permanent Location: Houston, US-TX
Salary / Rate: Not Specified
Posted: 2024-05-02 08:33:16
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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: Destin, US-FL
Salary / Rate: Not Specified
Posted: 2024-05-02 08:26:57
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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!
The Technical Services & Manufacturing Science (TSMS) Scientist is responsible for providing technical support for commercial operations at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. The position is a subject matter expert with respect to mAb products and processes and is engaged in tech transfer, scale-up, process optimization, validation, monitoring, troubleshooting and continuous improvement activities. The TSMS scientist plays a key role in day-to-day operations and delivery of technical projects.
Functions, Duties, Tasks:
Technical Ownership of Product and Process
* Provide technical and on-floor support for the commercialization, manufacture, and life-cycle management of monoclonal antibody products.
* Work with R&D, Manufacturing, and Quality teams in execution of technical / development studies, validation activities and technical transfer programs.
* Provide on-floor support to the Manufacturing teams regarding product and process troubleshooting. Participate in product and process related technical investigations and root-cause analyses of process deviations, complaints, and OOS/OOE events. Ensure issues are identified and captured in the relevant quality management system and that proper root cause analysis is performed with appropriate corrective and preventative actions assigned.
* Act as product and process subject matter expert in Process Teams, project teams and committees.
* Use scientific and statistical analysis tools to improve process understanding, ensure manufacturing processes are capable and operating in a state of control, and identify opportunities for process improvements.
* Develop / execute projects to address process performance issues and deliver on improvement opportunities.
* Provide support in resolution of technical and compliance issues. Prepare technical assessments and responses for site quality, internal inspection bodies, and relevant Health Authorities.
* Author and provide critical review of technical documents including, but n...
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Type: Permanent Location: Elwood, US-KS
Salary / Rate: 94000
Posted: 2024-05-02 08:23:26
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EHS Mill Manager מנהל/ת בטיחות
Job Description
כמנהל/ת בטיחות באתר עפולה תוביל/י שיפור במעורבות והתערבות פרואקטיבית של מנהלים ועובדים ליצירת תרבות פרואקטיבית עם עמידה ביעדי ה- EHS.
בנייה ושיפור מתמיד של תשתית מקצועית רגולטיבית ופרואקטיבית ליצירת סביבת עבודה בטוחה ללא פציעות.
עלינו
האגיס®.
קלינקס®.
קוטקס®.
דיפנד®.
קימברלי-קלארק פרופשנל® המותגים האייקונים שלנו בטוח כבר מוכרים לך - וכך גם לשאר העולם.
למעשה, מיליוני א.נשים בעולם משתמשים במוצרי קימברלי-קלארק מדי יום.
אנו יודעים שהמוצרים האלה של קימברלי-קלארק לא היו קיימים ללא א.נשים מוכשרים, כמוך.
בקימברלי-קלארק תוכלי.י לעבוד עם הצוותים הטובים ביותר שמחויביים לחדשנות, צמיחה והשפעה.
יותר מ-150 שנה כחברה מובילה ועדיין - ואנחנו תמיד מחפשים דרכים טובות יותר להמשיך ולצמוח – אז יש כאן דלת פתוחה להזדמנות, הכל כאן עבורך.
הכל מתחיל בך
תחומי אחריות עיקריים (Principal Accountabilities)
1.
ניהול ותפעול מערך EHS מפעלי לעמידה מלאה בכל דרישות החוק ודרישות KC .
2.
הכשרה, אימון והדרכה- בניית יכולות מקצועיות בבטיחות לעובדים ומנהלים.
3.
בניית תכניות עבודה ומעקב אחר ביצוען.
4.
הטמעת גישות חדשות ופרויקטים בEHS
5.
בניית שגרות לווידוא עבודה בהתאם להנחיות נהלים וחוקים.
6.
חניכה אישית ובניית יכולות למנהלים ועובדים.
דרישות התפקיד (Position Requirements)
השכלה :
אקדמאי, רצוי מהנדס / הנדסאי תעו"נ \מכונות.
ממונה בטיחות מדופלם עם כשירות בתוקף.
הסמכות מקצועיות -מדריך עבודה בגובה, מכין תוכנית בטיחות וכו..
יתרון.
ניסיון מקצועי :
ניסיון מעשי בניהול EHS בתעשייה בחברה גלובאלית (יתרון )
שליטה טובה מאוד באנגלית ( קריאה, כתיבה, יכולת שיחה מקצועית )
שליטה מלאה ב Office
יחסי גומלין עם תפקידים אחרים (Working Relationships)
ממשקי עבודה מול כלל המחלקות יצור, לוגיסטיקה, איכות, אחזקה, מטה.
ממשקי עבודה רציפים מול מנהלים עמיתים בהנהלת המפעל.
מחוץ לארגון (בארץ ובחו"ל): עבודה שוטפת מול ג...
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Type: Permanent Location: Afula Elit, IL-Z
Salary / Rate: Not Specified
Posted: 2024-05-02 08:21:28
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Executive Assistant- Adult & Feminine Care- Remote
Job Description
You’re not the person who will settle for just any role.
Neither are we.
Because we’re out to create Better Care for a Better World, and that takes a certain kind of person and teams who care about making a difference.
Here, you’ll bring your professional expertise, talent, and drive to building and managing our portfolio of iconic, ground-breaking brands.
In this role, you’ll help us deliver better care for billions of people around the world.
It starts with YOU.
Looking for a self-directed, team oriented, innovative, hardworking individual to provide a full range of administrative support to the Kimberly-Clark North America Adult Care team in Chicago, IL.
This includes the Adult Care Vice President/General Manager, the Adult & Feminine Care Regional Sector Lead, their team leaders, and team members. This role requires the ability to act independently, organize workload, set priorities, work well under deadline pressures, adapt to change, and handle confidential material. In addition, the incumbent must have the ability to exercise independent problem solving and decision making with a high degree of initiative and self- coordination.
Executive Assistants at Kimberly-Clark manage access to the director, maintain and modify the director’s schedule, and ensures the director is made aware of issues that need immediate attention.
They provide a broad range of highly skilled and highly confidential administrative support to the director, additional team members, and others as needed.
The incumbent must be highly organized, maintain strong interpersonal relationships at all levels of the organization, be highly detail oriented with excellent communication skills, and work independently to efficiently resolve issues.
Influence: This role will regularly interact with executives and senior leaders on behalf of the Vice President/General Manager and Regional Sector Lead
Responsibilities:
Project & Task Management:
* Provides a high level of administrative skills, normally acquired through an accredited college and/or prior work experience.
* Handles confidential business matters, works independently on special assignments, and maintains smooth operation of the office responsibilities of the department.
* Operates independently in absence of the director, calling on staff and works collaboratively with other administrative assistants when required.
* Assists and advises the director of any problems arising during absence.
* Sets priorities independently and maintains a comprehensive understanding of department policies, procedures and department members’ methods of operation to effectively and efficiently conduct duties and responsibilities.
Schedule Management:
* Manages senior leader calendars, responding to requests for time and rescheduling when necessary.
* Managing team leader calendar/scheduling requests, as needed.
...
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Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2024-05-02 08:21:27
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Seeking Compassionate Per Diem Therapists for The Mobile Crisis Team
About Us:
Liberty Resources is a dynamic and growing human services agency that is a great place to work! Working for Liberty Resources means you’ll have access to great career opportunities, benefits and a fun atmosphere.
Our employees have passion around our values of excellence, integrity, diversity, self-determination, service, innovation and fiscal responsibility.
Our rapid growth is providing exciting opportunities in all areas of our organization.
Our employees have passion around the services they provide and our corporate values of excellence and staff support.
We pride ourselves on high quality, integrated, community-based services that meet the evolving needs of our communities.
We’re committed to building a diverse workforce that values contributions of all team members and work to recognize cultural beliefs, values, traditions, language preferences, and health practices of the communities that we serve and how they apply to provision of positive health outcomes.
About The Mobile Crisis Team:
Mobile Crisis is a trained response team that is available to deescalate crisis, divert unnecessary hospitalizations or arrests and link folks to needed services in the community.
Mobile Crisis is designed to provide a rapid crisis response, telephonically or in the community for adults and youth experiencing a behavioral health/substance use crisis.
As part of crisis stabilization, the team provides Telephonic and/or Mobile Crisis follow-up.
The Mobile Crisis team continues to build strong relationships and a successful reputation with providing efficient and quality crisis services within a five county region.
We serve Cayuga, Cortland, Madison, Onondaga, and Oswego counties.
Mobile Crisis Therapist Position Summary:
Under the direct supervision of the Program Supervisor and Program Director, the Mobile Crisis Therapist is primarily responsible for responding to mental health crisis either telephonically or in-person and providing clinical assessment and crisis intervention for individuals identified through Mobile Crisis Hotline.
Additional follow-up services may be provided depending of level of need.
Mobile Crisis Therapist Responsibilities:
* Provide telephonic or in-person crisis response to adults and youth
* Provide and perform clinical assessment and referrals to community based programs when necessary
* Utilize diagnostic and assessment information, crisis care plan in collaboration with the mobile crisis team.
* Effectively perform crisis intervention including de-escalation, crisis planning and implementation.
* Design appropriate referral recommendations using available community resources.
* Maintain effective professional relationships with other service providers and community organizations in the interest of clients’ and program goals.
* Make competent decisions about the need for an emergency petition ...
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Type: Permanent Location: Oneida, US-NY
Salary / Rate: Not Specified
Posted: 2024-05-02 08:21:10
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Your Job
We are currently recruiting for a Lab Technical Specialist for our Technical Center in Neenah, WI.
This person will be responsible for performing physical testing of products received from mills and consumers to ensure compliance and quality throughout the product lifecycle.
Our Team
Our Neenah Technical Center® is the central site for research, development, and lab services for Georgia-Pacific North American Consumer Products division.
The research and development areas include: Commercial and Retail towels, tissues, napkins and dispensers, Dixie® products and process development.
What You Will Do
* Physically testing products submitted by lab's clients
* Physically testing products from the paper machine and converting lines in the pilot plants
* Inputting test results, verifying data and reporting out results to clients
* Assuming Primary Person Responsible duties for several instruments in the lab to include maintenance, training and measurement control charting
* Supporting trial work at the mill locations when necessary
Who You Are (Basic Qualifications)
* Previous experience in a lab setting
* Able to travel up to 20% of the time
What Will Put You Ahead
* Associate Degree or higher in a physical science discipline
* 1+ years of lab experience
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
Learn more about our hiring philosophy here .
Who We Are
As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses.
Our more than 30,000 employees in over 150 locations are empowered to innovate every day - to make everyday products even better.
At Koch, employees are empowered to do what they do best to make life better.
Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Our Benefits
Our goal is for each employee, and their families, to live fulfilling and healthy lives.
We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing...
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Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2024-05-02 08:14:52
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Greif offers a great working environment and the opportunity to make an immediate impact at a company where your ideas are always welcome.
Job Requisition #:
027437 EHS Manager (Open)
Job Description:
Manages colleagues who perform Environmental Health & Safety work.
Typically supervises professional colleagues who exercise latitude and independence in assignments.
Key Responsibilities
* Manages the EH&S function and ensures the effective operations of the Environmental Health and Safety units.
* Oversees EH&S programs to ensure safe operating and working environments.
* Directs and reviews policies to ensure compliance with established standards.
* Direct supervision of professional staff including, recruitment, training, and performance reviews.
* Establishes and manages accident statistical basses for internal and external reporting.
* Prepares and presents a variety of reports, communications, and other documents.
* Develops and implements inspection policies and procedures, and a schedule of routine inspections.
* Develops health and safety procedures for necessary areas of the company.
* Performs other duties as assigned.
Education and Experience
* Typically possesses a Bachelor's degree (or equivalent) and 10 or more years of relevant experience.
Knowledge and Skills
* In-depth knowledge of relevant safety regulations.
* Demonstrated administration, planning and organization skills.
* Takes an analytical approach to complex issues and problem solving.
* Excels at training and coaching professional level colleagues.
* Exceptional interpersonal, communication and leadership skills.
* Demonstrated ability to analyze data pertaining to program functions and interpret other management information.
#LI-NG1
40
EEO Statement:
https://www.greif.com/wp-content/uploads/2023/04/HR-101-Equal-Employment-Opportunity-Policy-English.pdf
We offer a competitive salary, excellent benefits and opportunity for growth.
Greif, Inc.
is an equal opportunity employer.
We will not discriminate against any applicant or employee on the basis of sexual orientation, gender identity, race, gender, religion, age, national origin, color, disability, or veteran status.
EOE/Minority/Female/Disabled/Veteran.
For more information read Greif’s Equal Opportunity Policy.
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Type: Permanent Location: Delaware, US-OH
Salary / Rate: Not Specified
Posted: 2024-05-01 08:45:40
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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: Sr.
Analytical Scientist, API Characterization
As Sr.
Analytical Scientist, API Characterization, you will be a vital part of our global team, contributing to the advancement of new chemical entities to market through your expertise in analytical method development and validation.
Your Responsibilities:
* Lead technical efforts in small molecule API analytical development, enabling the design, development, and implementation of analytical methodologies for small molecule characterization and analysis, including peptides.
* Establish analytical control strategy and specifications for API that can be transferred into manufacturing and successfully registered globally, requiring cross functional collaboration with manufacturing, development, and regulatory affairs
* Oversee the development and validation of analytical methods in third-party organizations, ensuring adherence to quality standards.
* Design and implement VICH-compliant stability studies conducted by external partners.
* Author analytical submission documentation and coordinate the CMC sections of dossiers for worldwide registrations, including responding to technical questions from Health Authorities.
* Serve as the Analytical Subject Matter Expert for global project development teams.
* Ensure adoption of state-of-the-art technologies and QbD (Quality by Design) development concepts as well as adherence to quality standards
What You Need to Succeed (minimum qualifications):
* Education: PhD in a scientific discipline (e.g., Analytical Chemistry or equivalent)
* Required Experience: A minimum of 5+ years of related experience in industry
* Top 2 skills: Strong understanding of pharmaceutical analytical chemistry and analytical techniques, such as HPLC/UPLC, NMR, SSPC, GC, IR, UV.
Familiarity with ICH and/or VICH guidance and GMP regulations.
What will give you a competitive edge (preferred qualifications):
* Experience in planning, designing, and evaluating Health Authority registrat...
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Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:33
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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!
In this position, the incumbent will be trained in the set-up, operations, and troubleshooting of the equipment in the production areas. Additional duties will include documentation of work and specific computer functions.
Must integrate company initiatives such as LEAN into work practices.
Responsible for safely producing vaccines which meet all product specifications in accordance with current Good Manufacturing Practice standards.
NOTE: This position is offering a $2,500 Sign-On Bonus!
Basic Minimum Qualifications:
* High School Diploma/GED plus 4 years relevant experience
* Basic computer skills with Word, Excel and Electronic Management Systems
* Ability to read, interpret and conform to batch records, Quality and Safety requirements.
* Ability to operate applicable ERP system.
* Requires basic knowledge of manufacturing function, acquaintance with and general understanding of aspects of the production process and ability to apply this knowledge to situations ordinarily encountered.
* Ability to work Sunday - Thursday, 6pm-2:30am
Job Responsibilities:
* Perform duties associated with aseptic processes, weighing, measuring, counting, calculations, sampling, and verifications required for biological production processes in accordance with batch production records (BPR) and in compliance with current good manufacturing practice (cGMP) standards, all current safety standards and site procedures.
* Understands, performs and teaches others basic operation of production equipment and ensures all equipment, instruments and production materials are released and available for use.
Look up and perform transactions within the electronic inventory management system.
* To oversee production processes, cleaning, environmental monitoring and personnel and perform in-process batch quality checks per the written procedures.
Knows and follows safety rules, wears appropriate safety equipment and maintains proper safety practices at all times.
* Basic computer skills to create and update standard operating procedu...
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Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:31
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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!
Primary Function
* 了解并满足客户的需求，为客户提供有竞争力和有价值的服务
* 执行公司的业务发展战略，完成公司在当地的销售计划，实现公司的利益.
Primary Accountabilities/Responsibilities
* 执行公司业务发展战略，完成/超越销售指标
* 拜访养殖单位/客户，提供有价值的服务，体现公司的服务理念
* 建立并保持良好的分销渠道（经销商、兽药店）
* 组织技术研讨会，主讲小型的技术讲座
* 调查、反馈市场信息，与公司相关部门合作进行市场推广及市场分析
* 拓展公司在当地的业务，建立公司品牌和产品品牌
* 制定区域市场发展计划
* 管理当地销售团队和第三方销售员(TPS)，如有
Minimum Qualification:
* 动物科学、动物医学、动物营养及相关专业本科以上学历
* 3年以上农场或动保行业销售工作经验
* 熟悉猪饲料添加剂，功能性添加剂，饲料和动保市场
* 普通话流利，基本英语听、说、读、写能力
* 熟练操作电脑
* 居住在广西和湖南为尤佳
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
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Type: Permanent Location: Shanghai, CN-31
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:29
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Chemielaborant Analytische Entwicklung SMTD (Small Molecule Technical Development) (m/w/d)
Wir suchen zum nächstmöglichen Termin eine/n Chemielaborant/in/Chemotechniker/Bachelor in der Chemie in der analytischen Entwicklung SMTD (m/w/d) am Standort Monheim am Rhein, Deutschland.
Die Position:
Als Chemielaborant der analytischen Entwicklung von Small Molecules Technical Development ist man Teil eines funktionalen Teams und arbeitet eng mit angrenzenden Disziplinen zusammen (Formuliertechnologie, Verpackungstechnologie, Wirkstoffentwicklung).
Zentral ist hierfür das eigenständige Umsetzen von wissenschaftlichen Protokollen unter Anwendung verschiedener analytischer Techniken mit dem Schwerpunkt Chromatographie.
Zu den Kernaufgaben zählen die analytische Methodenentwicklung, Methodenvalidierung und -transfers, sowie die Durchführung von Entwicklungsstabilitätsstudien und registrierrelevanten Stabilitätsstudien unter GMP.
Ihre Aufgaben und Verantwortlichkeiten:
* Praktische Versuchsdurchführung zur Entwicklung/Validierung analytischer Prüfverfahren für die Qualitätskontrolle neuer Tierarzneimittel
* Analytische Begleitung der Formulierentwicklung
* Prüfung von Stabilitätsmustern unter Berücksichtigung der relevanten Richtlinien
* Eigenständige Planung, Organisation, Durchführung und Dokumentation von Versuchsreihen
* Datenanalyse zur weiteren Versuchsplanung sowie Unterstützung bei der Ergebnisinterpretation
* Unterstützung beim Erstellen von Berichten, Arbeits-, Prüf- und Verfahrensanweisungen
* Präsentation von Ergebnissen bei Team-, Projekt- oder Gruppenbesprechungen
* Intensive Zusammenarbeit mit Kollegen im F&E Umfeld zum Wissensaustausch
* Berücksichtigung externer und interner Richtlinien (z.B.
SOPs, GxP, HSE).
* Pflege der Laborinfrastruktur und der organisierten, sauberen und sicheren Arbeitsumgebung.
* Planung / Durchführung der Wartung von Instrumenten / Geräten sowie Evaluierung neuer Laborgeräte
* Arbeiten unter Verwendung der entsprechenden Sicherh...
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Type: Permanent Location: Monheim, DE-NW
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:29
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Global Clinical Development Scientist
Join our innovative team and take the lead in developing groundbreaking parasiticide products for pet health! As the Global Clinical Lead, you'll spearhead the planning, coordination, and implementation of top-tier clinical effectiveness and target animal safety programs.
Dive into exciting pilot and pivotal studies, ensuring compliance with global regulatory standards like GLP, vGCP, and VICH guidelines.
Play a pivotal role in driving the future of pet health innovation!
Your Responsibilities:
* Serve as Global Clinical Lead, representing Global Clinical Development on R&D Project Teams.
* Formulate comprehensive clinical development plans for new products, fostering cross-departmental relationships.
* Focus primarily on parasiticide product development, with potential involvement in therapeutics.
* Execute clinical programs, designing protocols for efficacy studies in collaboration with other teams.
* Coordinate study monitoring to ensure compliance with regulations and company policies.
* Analyze and interpret study results, collaborating with Regulatory Affairs for submission to regulatory agencies.
* Ensure quality assurance and regulatory compliance through administrative activities and process development.
What You Need to Succeed (minimum qualifications):
* Education: DVM or Ph.D.
in an animal health related field preferred, MS with experience considered.
* Required Experience: Three or more years of experience in product development within or closely associated with the pharmaceutical industry preferred.
* Top 2 skills: Proficient in strategic planning and forward-thinking, with a consistent focus on achieving desired outcomes.
Basic understanding of research and development processes.
What will give you a competitive edge (preferred qualifications):
* Keen interest in parasitology or significant practical experience in the discipline.
* Experience working with regulatory authorities.
* Knowledge of GCP/GLP/GMP and quality sta...
....Read more...
Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2024-05-01 08:20:28
