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Position Title: Postdoctoral Fellow
Required Skills & Qualifications:
· Ph.D.
in Biology or a related field within the life sciences.
· Demonstrated history of high-quality peer-reviewed publications in relevant areas.
· Experience in laboratory mouse handling and work with human pluripotent stem cells.
· Exceptional writing proficiency.
* Capable of rapid learning and independent operation with minimal supervision; highly self-motivated.
Postdoctoral researchers will work on projects related to the above, using stem cells, cultured cells, genetically modified model mice, etc., in collaboration with their supervisors and co-researchers.
They will also aim to provide guidance to undergraduate students at UCLA within the laboratory, participate in academic conferences, and publish research papers.
We are seeking individuals with a collaborative spirit.
Description of Duties:
Multiple postdoctoral researcher positions are available at the Yoshihara Laboratory within the Lundquist Institute at Harbor-UCLA Medical Center.
Our research is focused on understanding the molecular genetics of pancreatic islets, the underpinnings of metabolic diseases, inflammation (including autoimmune diseases and diabetes), and leveraging this knowledge to develop regenerative medicine and small-molecule therapies.
We are actively seeking a highly motivated postdoctoral fellow with an interest in the molecular mechanisms of developmental biology and physiology, aiming to innovate therapeutic approaches for type 1/type 2 diabetes and related disorders, such as neurodegenerative diseases and cancer.
The Yoshihara Laboratory utilizes multi-omics analyses (genomics, metabolomics, proteomics), animal models, and stem cells as powerful tools to investigate diabetes, metabolism, and to pinpoint therapeutic targets for metabolic diseases.
While experience with next-generation sequencing, mouse models, and stem cells is preferred, it is not a mandatory requirement.
Ideal candidates will be in the final stages of obtaining or have already obtained a doctoral degree (Ph.D., M.D./Ph.D., or M.D.), have a proven track record of productivity evidenced by peer-reviewed publications, and possess excellent communication skills.
Interested applicants are encouraged to submit a cover letter, CV, and contact information for three references to janet.perez@lundquist.org.
Reference
https://eijiyoshiharalab.com/publications
Salary Range: $66,560-$75,000
*MON
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Type: Permanent Location: Torrance, US-CA
Salary / Rate: Not Specified
Posted: 2024-03-27 07:11:06
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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.
As QA Operations Manager for Drug Product Services (DPS) in Visp, you will represent Quality Assurance in cross-functional teams, including but not limited to Manufacturing, MSAT, QC, Engineering, Supply, Qualification/Validation and others to effectively execute tasks related to Drug Product processes.
Key responsibilities:
* Act as point of contact for Drug Product QA related questions and issues related to the manufacturing operations
* Ensure shop floor QA oversight (regular presence in the cleanroom)
* Assess, review and approve GMP documents and quality records e.g.
SOPs, risk assessments, deviations, investigation, CAPAs, change controls, complaints, APR/PQRs, protocols, executed MBRs
* Act as QA representative during the conduction of internal / customer / regulatory inspections and audits
* Provide GMP-related trainings to Operations personnel
* Support continuous improvement programs to establish an effective Quality Management System for DPS Visp
Key requirements:
* Master of Science in biotechnology or a related field
* Significant work experience in the GMP regulated environment, in relation with aseptic manufacturing activities and preferably within a Quality Unit
* Experience working with stakeholders from different departments and management levels
* Fluent in English (written and spoken), German language is an advantage
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
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Type: Permanent Location: Visp, CH-VS
Salary / Rate: Not Specified
Posted: 2024-03-27 07:10:10
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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
Deine Abteilung
Wir sind ein Team, bestehend aus Laboranten, Laborassistenten und Gruppenleiter.
Wir freuen uns auf ein hilfsbereites und flexibles, neues Teammitglied, das Spaß an der täglichen Arbeit hat und eine positive Arbeitsatmosphäre unterstützt.
Wir möchten Dir als Praktikant (m/w/d) einen Einblick in das „Daily business“ eines Mitarbeitenden im Qualitätskontrollumfeld geben.
Außerdem wirst Du die Möglichkeit haben Dich selbstständig mit Compliance-Themen zu beschäftigen und bei der Bearbeitung von SOPs und Testvorschriften mitzuwirken.
Deine Aufgaben
* Chemische bzw.
mikrobiologische Analytik von Einsatzstoffen im diagnostischen Umfeld
* Mitwirkung bei der Überarbeitung von SOPs und Testvorschriften
* Selbständige Durchführung von kleineren Projekten im Umfeld der Qualitätskontrolle
Dein Profil
* Du bist aktuell in einem naturwissenschaftlichen Studium (z.B.
B.Sc.
/ M.Sc.
Chemie oder Biochemie) immatrikuliert oder Du befindest Dich in Deinem Gap-Year
* Kenntnisse in der physiko-chemischen Analytik sind von Vorteil
* Du bist motiviert, neugierig und möchtest Dich in der Qualitätskontrolle einbringen
* Solide Deutsch-Kenntnisse sind erforderlich
Deine Vorteile
* Flexible Zeiteinteilung
* 2025 € Vergütung im Monat für ein Vollzeitpraktikum > 3 Monate
* Vergünstigte Essenspreise (-50 %) in unserer Mitarbeiterkantine
* Fitnesszentrum auf dem Roche-Campus
* Vernetzung mit anderen Studierenden (online/offline)
* Weiterbildungsmöglichkeiten und spannende Gastvorträge
* Möglichkeit der Unterbringung im Roche Boardinghaus
* Gut organisierte Verkehrsanbindung nach München mit unserem Roche-Shuttle
Deine Bewerbung
Bitte lade nur Deinen Lebenslauf online hoch.
Denke daran, dass sich dieses Praktikum an Studierende (m/w/d) bei laufender Immatrikulation richtet oder alternativ an Personen im Gap-Year.
Zeitraum: ab sofort oder nach Vereinbarung für die Dauer von 6 Monaten
Wir freuen uns auf Deine Bewerbung!
Your contact to us! With people.
For people.
Do you need more support?
Our Talent Acquisition Team welcomes your questions.
Please send an email to
germany.talent_acquisition@roche.com
Who we are
At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare.
Working together, we’ve become one of the world’s leading research-focused healthcare groups.
Our success is built on innovation, curiosity and diversity.
Roche at Penzberg, near Munich, employs more than 7,000 people.
Th...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-03-27 07:08:08
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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 Contract Development and Manufacturing Organization (CDMO) 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 the position as QA Expert Equipment Qualification and Validation, CSV and DI 80-100% (m/f/d) being responsible to implement and maintain the commissioning, process validation, qualification of equipment and computerized systems (CQV) in the manufacturing site of Lonza DPS Stein.
Key responsibilities:
* Design an E2E DI/CSV Roadmap for the IT infrastructure and pertaining systems for the Growth Facility, ensure proper Quality Systems Design as well as Quality Oversight
* Act as Single Point of Contact providing Quality Oversight for all DI/CQV (Life Cycle Management) Projects executed for the Growth Project
* Ensure implementation and Quality oversight for the Risk Management Process and periodical reviews pertaining to the DI / CQV Strategy in Line with LEAN Design Principles
* Continuously improves the DI Maturity Level of the Dolphin Facility towards Excellence
* Review, Assess and Approve all Documents pertaining to CQV Projects and DI
* Establish a robust review mechanism to ensure maintaining the validated status of DI / CSV over given review cycles
* Providing guidance, expertise and coaching, assisting sites and their teams for policies, procedures and specifications.
* Serve as a Coach / Mentor for Network Key Talents in order to ensure talents development
Key requirements:
* Academical degree (Bachelor or higher) in a Life Sciences, Engineering; IT Systems, Industrial Engineering or related science discipline
* Strong experience in CSV and Data Integrity within a GMP regulated environment
* Significant working experience in a QA role within the pharma industry
* Aseptic production experience
* Fluency in English, German would be an asset
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 a...
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Type: Permanent Location: Stein, CH-VS
Salary / Rate: Not Specified
Posted: 2024-03-27 07:08:01
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ISP Freetown Fine Chemicals Inc
Benefits & Perks:
* Team recognition rewards, sponsored lunches and monetary incentives based on performance
* Comprehensive Benefit package, Medical, Dental and Vision
* 401(k) plan with company match
* Rotating shift – 14 days off/month
The responsibilities of the position include, but are not limited to, the following:
* Performs a variety of routine tests or experiments within parameters defined by supervisors. Observes and adjusts variables as necessary.
* Operates a wide range of analytical equipment including GC’s, HPLC’s, FTIR, UV/Vis spectrometer, auto-titrators, particle size analyzers, viscometers, pH meters, Nitrogen Analyzers etc.
* Provides analytical support to production operations and becomes familiar with basic process chemistries to put analytical testing into the proper context.
* May perform tests and experiments of a non-routine nature in response to various production situations or in accordance with supervisors’ instructions.
* Demonstrates basic competence in experimental techniques.
* Conducts all observations and adjusts variables as instructed making a variety of specified measurements and manipulations as necessary.
* Recognizes irregularities in equipment, tests, and experiments, bringing them to the attention of the supervisor.
* May perform minor adjustments and repairs of instruments, mostly under the guidance of the supervisor.
* Summarizes results using appropriate mathematical techniques, maintaining data in appropriate form for interpretation by supervisors.
* Maintains complete record of work.
* Provides data for formal reports composed by supervisors.
* Performs other related duties as required.
In order to be qualified for this role, you must possess the following:
* Bachelor's Degree in Chemistry or related field with 0-2 yrs.
experience; or Associate's degree in related field with 1-4 yrs.
experience; or technical certification/military training in science field with 3 – 5 yrs.
experience.
* Ability to follow written and verbal instructions, detail oriented.
* Ability to analyze problems.
* Ability to recognize the cause of inconsistent or unexpected analytical results.
* Ability to learn or a basic knowledge of LIMS, various analytical instrument software and other databases.
* Proficient with MS Word and Excel.
* Excellent oral and written communication skills.
* Must work a rotating shift schedule.
The following skill sets are preferred by the business unit:
* Experience with Laboratory Instrument Management
In more than 100 countries, the people of Ashland LLC.
(NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow.
Our chemistry is at work every day in a wide variety of markets and applications, inc...
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Type: Permanent Location: ASSONET, US-MA
Salary / Rate: Not Specified
Posted: 2024-03-26 07:36:19
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Summary:
The COI team is seeking a paid summer intern who is prepared to assist with multiple quality engineering projects.
The TekniPlex City of Industry plant specializes in plastic medical tubing manufacturing.
The intern will assist with identifying processes within the manufacturing process, provide summaries and make corrections to current manufacturing instructions.
Responsibilities and Learning Opportunities:
* Assessment of the manufacturing and quality process and provide a SWOT analysis.
* Assist with quality department documentation with task such as filing, follow-up and reporting
* Work on multiple quality department projects: reviewing processes, streamlining processes.
* Work closely with operations department to assess and gather data; includes walking the production floor and gathering data from operators.
* Create presentations for management and supervisor teams summarizing strategic and corrective action opportunities
Minimum Skills, Knowledge and Ability Requirements:
* Current pursuit of a full-time undergraduate degree in Manufacturing Engineering, Medical Devices Engineering, Material Sciences, Quality Engineering, or similar.
* Demonstrated initiative, uncompromised integrity, and a results-oriented mindset
* Excellent written and verbal communication skills
* Acute attention to detail with strong quantitative and analytical skills
* Working knowledge of Microsoft Excel, PowerPoint, and Word
* Strong motivation and work ethic and the ability to work independently, ability to balance multiple projects and competing deadlines
* Third year students or above with prior internship experience preferred
PHYSICAL DEMANDS:
While performing the duties of this job, the employee is regularly required to see, sit, stand, walk, talk, and hear.
The employee must be able to frequently lift and/or move up to 10 pounds and infrequently lift up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, and the ability to adjust focus.
WORK ENVIRONMENT:
Duties will be primarily based in a production environment. Most of the job will be performed in a manufacturing environment.
A frequent amount of time may be required on the production floor interfacing with key stakeholders to identify/resolve issues and/or develop solutions. Travel may include tours, observations and/or troubleshooting in the company’s and/or customer’s production environments.
The job duties, physical demands and work environment characteristics described are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Where possible, reasonable accommodation may be made to enable individuals with disabilities to perform the essential job functions where it does not cause undue hardship or safety risks to the company and/or the employee.
TekniPlex is committed to a d...
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Type: Permanent Location: City Industry, US-CA
Salary / Rate: Not Specified
Posted: 2024-03-26 07:35:44
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Company
Federal Reserve Bank of Chicago
The Federal Reserve Bank of Chicago is recognized as one of the most influential, trusted and prestigious financial institutions in the world.
We serve the Seventh District encompassing Iowa and most of Illinois, Indiana, Michigan, and Wisconsin, and is one of the 12 regional Reserve Banks in the United States.
Together with the Board of Governors in Washington, D.C., the 12 Banks constitute the nation’s central bank.
Who we are:
One of the most influential, trusted and prestigious financial institutions in the world.
The Federal Reserve Bank of Chicago, serving five states, is one of the 12 regional reserve banks in the United States.
The twelve banks, along with the Board of Governors in Washington, D.C., make up the nation’s central bank.
What makes us unique? We are a regulatory bank.
This internship gives you the opportunity to intern for a bank that supervises other banks.
Job Description
The economic research internship program offers a number of summer research opportunities across each of our departmental teams, inclusive of – but not limited to:
* Macroeconomics
* Microeconomics
* Finance & Insurance
* Community Development & Public Policy
* Regional Analysis
This program provides students with the opportunity to gain valuable research experience, network with peers in the field, and to work side-by-side with our economists and research assistants to support research and policy work.
The program is designed to help students develop quantitative analysis, critical thinking, and writing skills throughout the summer experience.
Summer projects typically ask interns to:
* Support economists in their basic and applied research – inclusive of collecting data, conducting moderately complex statistical analysis, writing code for model estimations and organizing the presentation of results
* Assist economists with their research and analysis of public policy issues and events
* Prepare a variety of charts, tables, and descriptive text for staff economists and department management.
Internship Program Details:
The Federal Reserve Bank of Chicago Summer Intern Program is a paid internship that is open to undergraduate, graduate and PHD students. It begins in June and continues for 12 consecutive weeks.
Interns work 40 hours per week and are assigned to one department.
These internships are ideal for students looking to build their research portfolios, who have a potential interest in graduate school, or who are considering applying for the Chicago Fed’s Research Assistant program after graduation.
Economic Research Interns are given priority consideration for 2024 RA openings providing positive recommendations regarding performance throughout their internship experience.
Job Requirements:
* Currently pursuing at least a Bachelor’s degree, graduating Fall 2024 or later, in economics, finance, or related field (e.g.
statistics, com...
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Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2024-03-26 07:34:20
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SmartWorks is seeking a talented and motivated Technical Consultant who can balance their business knowledge, technical skills and strong interpersonal skills.
The Technical Consultant will interact with our customers, development teams and third-party software vendors to gather and document requirements, deploy applications and provide implementation support and training.
As a Technical Consultant, you will be required to travel throughout North America approximately 30% of the time when safe and appropriate.
While you're not traveling throughout Canada and the US, you will be able to work remotely from home or out of any of the Harris offices.
This role is available remotely within Canada and the US.
This role requires travel up to 30% in North America.
A valid passport is required.
What your new role will be:
* Design and implement SmartWorks solutions to meet customer requirements
* Integrate SmartWork’s application suite with 3rd party software interfaces
* Develop and maintain project documentation, standard operating procedures, and other documentation as required
* Lead or assist in training sessions with SmartWork’s customers and provide implementation support
* Act as a liaison between SmartWorks, customers, 3rd party vendors and industry consultants
* Provide consulting services based on knowledge of Smart Metering infrastructure and best practices on analysis of corresponding data
* Provide the Project Manager with regular updates on progress, issues and ideas for resolution, and successes
What we are looking for:
* Experience in the technical field (for example, Electric or Computer engineering, Computer Science) or a degree/diploma in the related field
* Strong grasp of SQL and one or more Enterprise Database Software such as SQL Server, Oracle etc
* Comfortable working in Linux and Windows
* Ability to travel in North America up to 30% of the time
* 5+ years of relevant work experience in software implementation
* Strong working knowledge of object-oriented design (C/C++ or Java)
* Previous experience in the Utilities industry
What will make you stand out:
* Possess strong analytical skills to understand requirements
* Demonstrate excellent verbal and written communication skills in English
* Can work independently, but most importantly, as a team player
* Demonstrate positive attitude and determination
* Previous experience in training customers and writing technical documents
What we can offer:
* 3 weeks' vacation and 5 personal days
* Comprehensive Medical, Dental, and Vision benefits starting from your first day of employment
* Employee stock ownership and RRSP/401k matching programs
* Lifestyle rewards
* Remote work and more!
About us:
SmartWorks empowers utilities to navigate change and unleash the potential of the smart infrastructure.
At SmartWorks we are committed to delighting our cust...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: Not Specified
Posted: 2024-03-26 07:34:10
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world.
And that’s the kind of work we want to be part of.
Lonza Walkersville is hiring a Manufacturing Associate I who will be responsible for participating in upstream and/or downstream aseptic manufacturing of Endotoxin Testing products in a ISO 5 environment according to company and departmental SOPs.
Successful candidate will also perform set-up and operate production equipment in the Filling and Finishing areas.
Performs product inspections and final kit packaging of finished goods.
The work schedule for this 3rd shift position is Sunday 11:30 PM - Friday 8:00 AM at our Walkersville, MD site.
Eligible for 15% 3rd shift differential and an additional 10% once gown and APS qualified
Key responsibilities:
* Understand basic level of Endotoxin Operations process flow
* Completion of Endotoxin Operation Cleanroom General Training
* Aseptic processing/gowning
* Cleanroom Equipment Set-Up and Usage
* Environmental Monitoring
* Completion of Endotoxin Operation Finishing General Training
* GMP Documentation practices
* Inspection Proficiency Testing
* Perform job functions with minimal operator related deviations
* Maintain training compliance to meet yearly target
* Must be able to demonstrate GMP documentation practices (minimal
* document errors)
* Comply with all safety policies and general regulations
* Perform other duties as assigned
Key requirements:
* High School Diploma / GED or equivalent required.
Associate degree in Science or similar, preferred
* Experience working in a GMP (Good Manufacturing Practices) environment, a strong plus
* Solid Communication skills
* Effective problem solving skills
* Results driven
* Self-motivated, requiring minimal Supervision
* Knowledge/understanding of Inventory management, desired
* Familiarity with Environmental & Personnel Monitoring, desired
* Knowledgeable of Microsoft Applications (Word, Excel, Teams, Outlook)
* Must have the ability to work in a fast paced, high workload environment, and be able to manage multiple projects and objectives for on-time event closure
* Must work well on a team, and be able to trouble shoot and problem solve in across-functional team setting
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 suc...
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Type: Permanent Location: Walkersville, US-MD
Salary / Rate: Not Specified
Posted: 2024-03-26 07:26:14
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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.
This position is responsible for creation and maintenance of MES authoring principles and practices across the Lonza site in Portsmouth, NH.
This position is responsible for ensuring that all projects and processes use consistent and innovative design and implementation of MES solutions.
Position is expected to operate with a high degree of autonomy.
Key responsibilities:
Safety
* Performs all work safely and meets the requisite training requirements
Manufacturing Support
* Act as MES engineering lead for tech transfer of new processes into the facility
* Develop technical knowledge on manufacturing equipment and process automation systems
* Responsible for resolution of all equipment breakdowns and quality issues in the suites
* Provide SME support to Manufacturing and other departments for the design and operation of process automation equipment
* Conduct troubleshooting and technical analyses on manufacturing equipment and process automation systems including PI data analyses, CIP/SIP circuit development and review, flow path analyses, code review/troubleshooting, etc.
* Complete change request lot assessments to support lot release
* Participates in IPT/JPT meetings and customer ad hoc meetings as MES/Engineering SME
* Represents group at Engineering DMS meetings
* Participates in audits and inspections as MES SME
Projects
* Planning and execution of plant projects involving complex automation changes and significant process improvements including lump sum and CAR capital projects
* Execute test scripts (design , execution, simulation, wet testing)
* Own change requests and complete change request tasks to support project completion
* Perform change request assessments
Deviations / RCAs
* Assist the Quality department with deviation investigations
* Performs MES review/approval of deviations
* Participate in RCAs as MES representative
* Owns and executes completion of CAPA actions
* Approver of action plans for non-regulatory CAPA
* Participates/Leads quality risk assessments
Documentation
* Review/revise MES and Manufacturing related SOP’s, Functional Specifications, and work instructions as a result of CAPA, equipment/process changes, error prevention activities, etc.
* Complete MES review/approval of batch records, deviations, commissioning protocols, and validation protocols
Perform other duties as assigned.
* Assists in department recruiting efforts as an interviewer
* Mentors le...
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Type: Permanent Location: Portsmouth, US-NH
Salary / Rate: Not Specified
Posted: 2024-03-26 07:25:08
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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.
Our Senior Process Engineer’s primary responsibility is to support ongoing operations at Porriño site (Biologics BU), through technical assistance as it relates to manufacturing, utilities and process systems.
The focus of the role is on ensuring manufacturing equipment and facilities are operating as intended to meet the requirements for biopharmaceutical manufacturing.
Responsibilities of the Senior Process Engineering function include both tactical support of ongoing plant operations and strategic implementation of engineering projects to meet the changing needs of the business.
Key responsibilities:
* Develop technical knowledge on manufacturing equipment and processes.
Identification and/or evaluation of new technology and/or equipment that improves manufacturing processes from a cost, time, or yield perspective
* Execute and / or oversee the design, implementation and commissioning of the different projects that are executed in the site to improve safety, quality, cost and capacity.
* Responsible to assure adherence to cGMP and safety requirements throughout all phases of Capital Project execution.
* Execute and / or oversee of the installation qualification (IQ).
* Actively collaborate with other areas and departments of Porriño (Production, MSAT, Quality, Program Management, etc ...), to resolve quality and production issues.
* Provide SME support to other areas / departments for the design and operation of process equipment, deviations investigations and for audits and inspections.
* Assist with tech transfer of new processes into the facility.
* Deliver 24x7x365 support rotating on-call schedule (as required) to manufacturing operations by troubleshooting equipment, systems, and processes to resolve issues that may arise during manufacturing campaigns.
* Perform other duties as assigned.
Key requirements:
* Degree / MSc Chemical Engineering
* + 5 Years of experience of Process Engineer in the Biotech Sector
* Spanish and English Business Fluent
* Broad knowledge -SME level- of typical mammalian unit operations (CIP/SIP, Chromatography, UFDF, Bioreactors, Centrifugation, HVAC, Utilities, etc…)
* Broad experience in the design and operation of Biopharmaceutical facilities, both manufacturing and support systems.
* Experience in Project Management and coordination associated with the execution of projects in an industrial environment required.
* Experience with fluid processing (pumps, valves, piping systems, tanks an...
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Type: Permanent Location: Porriño, ES-GA
Salary / Rate: Not Specified
Posted: 2024-03-26 07:20:08
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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 Process Engineer gesucht.
Diese Stelle unterstützt den Support mit verschiedenen Arbeiten beim PRAUF und Monatsabschluss.
Ihre Aufgaben
* Koordination von allen PRAUF-Abschlüssen im PCP
* Führt alle Daten für eine PRAUF-Analyse zusammen
* Enge Zusammenarbeit mit Supply Chain und Betriebslogistik bei der Materialabbuchung
* Zuständig für die zeitnahe Materialabbuchung
* Verbucht Anlage- und Personalkosten
* Hilft bei Monats- und Jahresabschlüssen mit und erstellt mit Hilfe vom Controlling eine Prognose der PRAUF-Abweichungen während dem Jahr
Ihr Anforderungsprofil:
* Sie verfügen über eine abgeschlossene Ausbildung
* Mehrjährige Berufserfahrung in der Chemie und Pharmaindustrie
* Hohes persönliches Engagement sowie selbstständige und pflichtbewusste Arbeitsweise
* Einwandfreie Deutschkenntnisse in Wort und Schrift, (Englischkenntnisse von Vorteil)
* Gute Office-Kenntnisse runden Ihr Profil ab
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: 2024-03-26 07:19:00
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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
Wer wir sind:
Roche in Mannheim ist mit rund 8.000 Mitarbeitenden drittgrößter Standort des Roche Konzerns.
Mannheim ist Sitz des Geschäftsbereiches Diabetes Care, Drehscheibe des weltweiten Diagnostika-Geschäftes sowie Sitz des Vertriebes für Diagnostika-Produkte.
Vom ersten Tag an werden Sie bei Roche von einem kollegialen Team aufgenommen und unterstützt.
Neben zahlreichen Entwicklungsmöglichkeiten, flexiblen Arbeitszeitmodellen und einer attraktiven Vergütung erwarten Sie Angebote zum Thema Familie & Beruf.
Roche ist ein Arbeitgeber, der die Chancengleichheit fördert.
Die Position Das Team des Strategic Planning Analytics Management Team verantwortet die Gestaltung, Betreuung und Weiterentwicklung der strategischen Aktivitäten in Global Operations.
Hierzu zählen u.a.
die Standorte Mannheim und Penzberg.
Gemeinsam mit unseren Partnern in den operativen Betrieben arbeiten wir als Team kontinuierlich daran, besser zu werden.
Unsere Ziele erreichen wir als Team durch die Anwendung von agilen Methoden und kreativen out of the box Ideen.
Mögliche Aufgaben sind:
● Du unterstützt das Digital Core Team bei der Erstellung von adressatengerechter Kommunikation und der Messung des Erfolgs dieser Kommunikation
● Du stimmst dich dabei eng mit dem Kommunikationsteam für Global Operations ab
● Du arbeitest aktiv an der Implementierung von Initiativen und Projekten mit
● Du hast die Möglichkeit, eigene Projekte zu planen und umzusetzen
● Du gestaltest deine Themen und treibst diese voran
● Deine Energie bringst Du dort ein wo Du mit deinen Talenten den größten Impact generieren kannst
Wer Du bist:
Du möchtest Effizienz in der Produktion aktiv mitgestalten.
Das sind deine Stärken:
● Du hast Spaß daran auf Menschen zuzugehen und gemeinsam mit einem Team Konzepte zu erarbeiten
● Deine Kombinationsgabe ermöglicht es dir verschiedene Ziele und Wünsche zu vereinen und geeignete Lösungen zu finden
● Du kannst komplexe Sachverhalte in einfache Inhalte und spannende Formate übersetzen
● Du bist ein digital affin und bezeichnest dich selbst als Digital Native
● Du bist fit im Google Workspace (Gmail, Google Docs/Slides...)
● Du bist kreativ und setzt deine Ideen gerne in die Tat um
● Du kannst dich eigenständig organisieren und dir deinen Arbeitsalltag strukturieren
● Du hast Interesse daran in einem operativen Umfeld zu arbeiten und dich in interdisziplinäre Inhalte einzuarbeiten
● Du hast bereits einige Erfahrungen in der Umsetzung von Projekten erworben
● Du bist immatrikulierter Student (m/w...
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Type: Permanent Location: Mannheim, DE-BW
Salary / Rate: Not Specified
Posted: 2024-03-26 07:16:11
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At American Career College, we share a passion for students and transforming healthcare education! As an associate for a certified Great Place to Work, you will join a collaborative, student-centric culture valuing academic integrity, mutual respect, student learning, service, responsiveness, innovation, diversity, and stewardship. As a part of this team, you will guide students to do more than change their own lives – you will help change the lives of every patient they care for throughout their career.
At American Career College, you will have the opportunity to share your expertise and passion with the next generation of nurses.
You will make an impact by:
* Provide each nursing program(s) with the necessary Assessment Technologies Institute (ATI) management and oversight to help each cohort achieve or exceed ACC's outcomes.
Benchmarking 90% of each graduating cohort to achieve the green light and the program.
* should achieve each quarter a 90% or better first-time pass rate on the NCLEX.
* Collaborate with the Director of Nursing (DON), overseeing a comprehensive success plan that evaluates the effectiveness of ATI initiatives, creates new methods to improve specific ATI student/graduate and faculty performance,
* Developing/implementing administrative systems and procedures to monitor and improve ATI effectiveness and provides analysis and remediation strategies to help ensure students/graduates are actively engaged in their ATI program and that graduates pass NCLEX with a satisfactory level of performance on their first attempt.
* Serves as the campus ATI champion to support both existing students and graduates until NCLEX is passed.
Your Experience Includes:
* A minimum of at least one (1) year previous experience with program management.
* Knowledge in technological support and delivery of educational programs and services.
* Knowledge and evidence of strong management skills, and administrative systems management as applicable to specialized program area.
* Knowledge of state, federal and local laws/regulations relating to programs, governmental compliance, and other regulatory standards such as ABHES, BVNPT, BRN, and other accreditation standards.
* Experience: ATI product experience.
* A minimum of one to two years of professional testing and/or statistical data experience involving database management.
* Experience working with nursing programs.
* Experience with Blackboard Learning Management System.
* Experience with Campus Vue.
Education:
* Bachelor's degree from an accredited college or university that includes course work in education or business administration OR equivalent experience required.
* Master's degree in nursing preferred.
LICENSES/CERTIFICATIONS:
* Registered nurse licensed required.
Must meet faculty requirements.
Compensation:
$85,402.45-$123,807.03
#LI-MJ1
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Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: 10460474
Posted: 2024-03-25 06:55:56
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At Harris' SmartWorks, we are committed to delighting our customer base, and we do that by ensuring our customers receive maximum enduring value from their investment in our solutions.
A big part of ensuring they receive value is the satisfaction and resolution they receive from our support services throughout the use of our SmartWorks Product Suite.
While our customers evolve their value, our Support Services team ensures they have a stable environment to meet their day-to-day operations, their planning, and the success of the utility.
We are looking for a Team Lead Software Support Analyst to join our dynamic team of smart, positive, and passionate people who are appreciated for their unique talents and empowered to do their jobs well.
We are looking for individuals with proven experience in client service, troubleshooting, and analytics to help us support our Utility Customers on the SmartWorks product they own.
As part of the team, you will be troubleshooting and designing new solutions for customers while continuously increasing customer satisfaction.
We highly value team members who communicate clearly and concisely and who work to build a positive and enjoyable workplace.
As a Team Lead Software Support Analyst, your role will encompass a wide range of responsibilities to ensure the efficient resolution of customer issues and the seamless coordination between internal departments.
Our head office is located in Ottawa, ON, however a significant percentage of our management and staff work remotely from their homes.
This position is open to qualified individuals living anywhere in the US or Canada and willing to work remotely from home.
Availability outside regular business hours (Mon-Fri, 8am-8pm EST) may be required occasionally for emergency situations, project-related tasks, or resolving service-impacting incidents.
Travel is required for departmental events approximately 2 times per year.
What your impact will be:
Support
* Monitor the support ticket queue and take ownership and/or re-assign new tickets
* Promptly address customer issues and consistently provide updates to ensure customers are informed of the progress in resolving their issues
* Provide timely and thorough resolution to customer issues within customer Service Level Agreement requirements
* Help develop, implement and review operational policies and procedures to improve efficiency wherever possible
* Help develop and implement support initiatives, including knowledge bases, technical and operational techniques, and documentation
* Document and share knowledge through Knowledge Base, Internal Articles, and Knowledge Exchange Training sessions
* Build alliances and partnerships and interact with a range of internal and external departments (i.e.
Infrastructure, Development, Professional Services, Sales, and other Harris Business Units and Vendors.) for ticket escalation and resolution
* Provide technical advice, ass...
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Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 82000
Posted: 2024-03-24 07:15:03
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Our Professional Services team has an exciting opportunity for a driven individual, and we're looking for a Project Manager that is passionate about providing IT transformation and implementation services for our clients.
It is mission-critical for the Project Manager to be a leader and a champion that will act as a conduit between the senior management team, key clients, and third-party vendors.
The Project Manager role is project-driven and will support clients by acting as the first point of contact to ensure that their organizational goals are met.
In addition, the Project Manager will be dedicated to monitoring and controlling the scope of work, engagement team priorities and project finances.
Finally, our Project Managers will have the opportunity to travel globally or regionally, based on client locations.
This remote role welcomes candidates from anywhere in Canada or the US.
This role requires travel up to 50% within Canada and the US; a valid passport or visa is required.
What your impact will be:
Project Planning, Scope Management, & PMO Improvements
* Demonstrate outstanding project control, ensuring that project plans/schedules, project budgets, and scope control all exceed expectations.
* Effective project management provided through, impact analysis, leading project scope negotiations, managing expectations of evolving project requirements
* Identify, analyze and assess business opportunities, processes, and workflows for PMO process improvements
Project Delivery & Critical Issue Resolution
* Adhere to the schedule of work for all phases (& refine as a project journey progresses) of the project including start-up and post-implementation follow-up.
* Be knowledgeable on project deliverables and contractual documentation to ensure obligations and expectations are met.
* Prioritize project needs based on tasks outstanding, obstacles or barriers, budgets, resources and deadlines.
* Coordinate resolution of project issues and/or delays to reduce the impact on the project and ensure timely implementation.
* Additional learning opportunities as the project evolves.
Client Management & Leadership
* Responsible for all aspects of the project delivery, including managing the scope of the project and changes to the project deliverables, while ensuring client satisfaction and organizational profitability.
* Regular communication of project updates, critical issues, implications, and progress to our clients and our leadership team.
What we are looking for:
* Ability to manage multiple projects concurrently.
* Strong communication skills.
* Ability to develop strong working relationships with internal and external stakeholders.
* Ability to firmly manage scope, schedule and budget.
What would make you stand out:
* Experience managing CIS implementation projects.
* Experience working in the Utility sector.
* CIS solutions knowledge & experience.
...
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Type: Permanent Location: Edmonton, CA-AB
Salary / Rate: 95000
Posted: 2024-03-24 07:14:55
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About the Company:
Merz is a family-owned medical device and pharmaceutical company headquartered in Germany.
Our Global Technical Operations based in WI manufactures, packages and ships several innovative products so that people all over the world can live better, feel better, and look better.
The Global Quality Systems Manager support the development, execution and delivery of global quality systems strategies for Merz Aesthetics.
They partner with Quality Site Heads, Global Quality Functions, R&D, Supply Chain, Operations & Marketing to assure Global Objectives are identified and fulfilled.
They drive continuous improvement in the overall quality systems infrastructure for Merz Aesthetics sites.
They provide support to other departmental activities as directed. They provide Subject Matter Expertise in evaluation and implementation of domestic and international regulatory GMP requirements.
Key Responsibilities:
Quality System Infrastructure
* Collaborate to ensure eQMS Software System(s) and their design, installation, qualification and deployment to Merz Aesthetics Global Manufacturing Sites and Affiliates fulfills global requirements and user needs.
* Support the development and execution of company-wide Quality Systems roadmap and define priorities in line with global stakeholder needs and requirements.
* Support creation of Quality Master Data Strategy and Execution into applicable systems (SAP, MES, eQMS, etc.)
Evaluate and implement new technology
* Evaluate and implement new technologies per Quality System Standards, Quality System Regulations, and other company procedures around which the Quality System is developed.
* Identifies new quality improvement initiatives / projects in accordance with cGMP expectations to improve compliance, quality levels (reducing defects), and improve operational efficiencies.
* Drive global data digitalization projects
Global alignment and Strategy
* Drive the implementation of company-wide eQMS tools and technologies in alignment with global strategy
* Collaborate to define global processes & support the site Quality teams to ensure execution on site level, supporting the site leaders as needed
* Facilitate the harmonization of quality system tools and ensure they are aligned across functions
* Collaborate with Global Site Quality Leaders to implement digital strategies for Global Quality and Compliance Data
Knowledge and Skills:
* Familiarity with of ISO13485 ISO14971, 21CFR 210,211, 820, European MDR and MDSAP.
Required
* Experience in use and configuration of electronic Quality System Software.
Required
* Solid experience in problem solving and statistics.
Required
* Demonstrated strong organizational skills including ability to prioritize tasks and adhere to agreed timelines.
Preferred
* Fluent in English; Additional Language proficiencies are an asset.
Required
* Ability to...
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Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2024-03-23 07:27:23
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ERM is hiring a Construction Safety Specialist for a key technology client in the San Diego, CA metropolitan area (Rancho Bernardo).
In this critical role, you will be responsible for establishing, implementing, managing, and continuously improving the safety programs for several ongoing construction projects.
The Construction Safety Specialist will have broad knowledge of Safety compliance programs and, where required, Safety specialty areas.
This is a tactical role for site-wide Safety systems, Safety regulations, and best practices.
This is a part-time (16-24 hours/week), fixed-term position for a duration of one year, renewable.
RESPONBILITIES:
* Champion a strong safety culture across the site and maximize personnel involvement in Safety related activities.
* Act as Owner’s representative while interacting with contractors.
* Provide daily observations of on-site safety practices.
* Provide timely, high quality Safety technical support.
* Carry out regular workplace inspections to monitor compliance with site rules, procedures, etc.
* Coordinate the completion of job safety analyses, risk assessments and pre-task plans.
* Prepare and submit local, State, and internal reports as needed.
* Review and track investigations of injuries, illnesses, environmental releases, non-injury accidents and near-misses to ensure that they are effective, and that they identify and resolve root causes.
Lead investigations into serious adverse events.
Monitor and analyze Safety performance and initiate action to support or correct trends.
REQUIREMENTS:
* Bachelor’s degree in safety, occupational health, engineering, or related degree is preferred.
* Minimum 5 years’ experience with H&S in the construction industry, preferably with commercial/office building construction or large projects.
CHST certification a plus.
* Bilingual Spanish a plus.
* Proficient with the management of high-risk activities including electrical safety, excavation, confined spaces, fall protection, material handling, rigging and crane operations.
* Experienced in communicating and problem solving as a team with sub-contractors is required.
* Experience with demolition preferred.
* Understanding of the complexities of multi-employer worksites.
* Experienced trainer on construction safety topics and comfortable working with a wide variety of trades.
* Demonstrated experience conducting construction site safety audits and inspections.
* Experience conducting incident investigations and can follow reporting processes.
* Excellent written and verbal communicator who understands the importance of timely communications and reporting.
Who We Are:
As the largest global pure play sustainability consultancy, we partner with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today wh...
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Type: Contract Location: Irvine, US-CA
Salary / Rate: Not Specified
Posted: 2024-03-23 07:26:56
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Qualified Mental Health Specialist (QMHS)
Are you looking for an organization where you can grow while making a positive impact on people's lives? At Signature Health, our purpose is to provide integrated healthcare for our community specializing in patients with mental illness and/or addiction because we want people to realize their highest potential.
Our core values are the foundation of who we are:
* People First mindset where we honor our colleagues and patients
* Striving for Excellence in our work each day
* Can Do approach where we roll up our sleeves in response to opportunities and challenges
In addition to a rewarding career, as a full-time employee, you will have access to the following employer/employee paid benefits:
Full Time:
* Medical, Dental, Vision
* Robust earned paid time off program (PTO)
* 401k match
* Various Life Insurance Options
* Short- and Long-Term Disability (Not applicable for school-based employees)
* Federal Loan Forgiveness Program (available on eligible on roles)
* HealthJoy - no cost medical and mental health online resources available Day 1 (coverage extends to family members living in the same household)
* Tuition & Professional Development Assistance
If you value the people around you, strive to be the best version of yourself and have a can do mindset, then Signature Health could be the best place for your next career.
Read below on how you can make a difference in our community and apply today!
SCOPE OF ROLE
Reporting to the Supervisor and Manager, Behavioral Health Services, the Qualified Mental Health Specialist (QMHS) will be key in the development and execution of patient treatment plans.
You will provide patients and their families with ongoing community support resources including transportation for access to identified resources.
The QMHS acts as an outstanding subject matter expert related to patient needs and will foster positive relationships to all patients, their families, and Signature Health team members.
HOW YOU’LL SUCCEED:
* Diligently develop, prepare and present treatment program work material to patients.
* Plan, coordinate, and provide reliable transportation to patients to access identified resources as part of their treatment plans.
* Maintains clear communication and professional boundaries with all patients.
* Act as a subject matter expert and provide support in accessing and developing a sober support network.
* Collaborates effectively with a patient's treatment team.
* Create an outstanding experience for both adult and child patients (SMD/SED, CD/Dual DX) by identifying support needed in the following areas: educational, medical, vocational, housing, and daily living skills resulting in patients becoming successful in their communities.
* Encourage, monitor, and follow-up on client engagement and participation in all treatment plan activities.
* Serve as a liaiso...
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Type: Permanent Location: Lakewood, US-OH
Salary / Rate: Not Specified
Posted: 2024-03-23 07:25:40
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Company
Federal Reserve Bank of Chicago
The Federal Reserve Bank of Chicago's Financial Markets Group is focused on advancing financial policy and robust market practices to promote the stability of the U.S.
financial system.
We analyze and advise on issues that affect the entire life cycle of activity in exchange-traded derivatives such as interest rate products, equities, commodities, and emerging asset classes like digital assets.
We are part of the Research, Policy, and Public Engagement function.
As part of a multidisciplinary and collaborative team of professionals, you will develop data-focused analysis and work alongside policy advisors to conduct applied research on policy issues affecting financial markets, with a focus on trading, clearing, and settlement of derivatives.
This is an outstanding opportunity for an experienced professional from industry, academia or a regulatory environment to produce high quality, impactful work directly connected to the responsibilities of the Federal Reserve.
#LI-Hybrid
Your Responsibilities
* Directly contribute to research and communicate findings to the public through published reports and presentations.
* Support development of internal policy analysis to support Bank objectives related to monetary policy and financial stability.
* Develop and maintain overview materials to educate internal stakeholders on key issues affecting financial markets.
* Support team deliverables to advise Reserve Bank President, other senior Bank leaders, and other policymakers on matters related to your area of expertise through written analysis and presentations.
* Develop and maintain strong relationships with financial industry leaders, focused on market makers, exchanges, and clearinghouses.
* Develop and maintain strong relationships with key internal and external stakeholders to advance Bank-level objectives.
* Oversee the data-driven analytical tools developed by the team’s analysts.
* Contribute to a highly collegial and collaborative work environment.
Your background
* Advanced degree in finance, economics, business, or public policy, or equivalent experience
* 5+ years of experience as an industry participant, regulator, or academic scholar
* Commitment to public service.
* Demonstrated ability to produce high-quality research or policy analysis.
* Experience working with and analyzing complex data sets using R, Python, and Tableau.
* Public speaking skills a plus.
Our benefits
* Comprehensive benefits package include medical, dental, vision, prescription drug coverage, 401k savings plan, retirement plan, paid time off, transit benefit, onsite gym and subsidized cafeteria
Requirements
* Travel approximately up to 10%
* This is a hybrid work model role in Chicago.
* This position requires access to confidential supervisory information and/or FOMC information, which is limited to "Protected Individuals" as defin...
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Type: Permanent Location: Chicago, US-IL
Salary / Rate: Not Specified
Posted: 2024-03-23 07:23:13
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Working on Denials with correct resolutions.
Finding ways to reduce denials.
Denial Analysis.
Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: 15000
Posted: 2024-03-23 07:21:08
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Working on Denials with correct resolutions.
Finding ways to reduce denials.
Denial Analysis.
Type: Permanent Location: Mumbai, IN-MH
Salary / Rate: 15000
Posted: 2024-03-23 07:21:07
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PRIMORIS POWER DELIVERY IS ON POINT IN 2024
With over 70 years of operating experience, Primoris Power Delivery services include engineering and design, installation and maintenance, material and equipment procurement, repair of electrical transmission, distribution, substation, wireless communication, and storm restoration.
Our experience ranges from small engineering and consulting projects to multi-million dollar turn-key distribution, substation, and transmission line programs.
The Total Rewards Proposition:
* Competitive compensation paid weekly.
* Best-in-class; Medical, Dental, Vision, and LTD/STD.
* 401(k) with company match, vested day-one.
* Employee Stock Purchase Plan [ESPP].
* Tuition Reimbursement.
* Paid Time Off, Holiday Pay, and Community Service Paid Time Off.
* Pet Coverage "For our Furry Friends"
* Legal Assistance Coverage
* Award winning safety programs.
* Overtime opportunities.
* Growth Opportunities.
* And more.
The Position Proposition:
Primoris Power Delivery is seeking a High-Voltage Estimator. This position is responsible for assisting in providing estimating services to deliver cost-effective and detailed estimates of Substation, Distribution, or Transmission construction projects dependent upon area of expertise.
This position is responsible for the successful estimating of projects accomplished through managing all aspects of estimate development including scope, schedule, cost, safety, and quality.
Summary
This role can be remote.
However, it will require travel once to twice a month.
Ideal candidate would be experienced in substation and transmission for EPC and experienced in this field.
Bid Win (B2W) software experience is a plus.
Key Responsibilities:
* Estimate projects in accordance with Primoris policies and procedures with oversight while learning estimating practices and processes.
* Responsible for assisting in and developing possible opportunities and marketing efforts to foster growth within the division.
* Prepare work to be estimated by gathering proposals, drawings, speci...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2024-03-23 07:15:31
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Looking for a chance to make a real difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.
Our “People first” approach means we also value our employees, who work relentlessly to help us execute our mission.
Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.
By following these guiding principles, we earn and maintain the confidence of our patients, our partners, and each other.
Together, we’re working to discover and develop innovative cancer treatments that address unmet patient needs and apply the science behind them in novel ways.
As the field of cancer treatment evolves, we evolve with it.
Advanced technology, dedicated investigators, and incomparable facilities: these vast resources empower us to redefine the way the world treats cancer.
It’s our work, our passion, and our legacy.
If the prospect of being part of this sounds exciting, we invite you to join us.
Territory Coverage: South Central - TX, AR, LA, and OK
Position Summary:
The Medical Science Liaison (MSL) is a field-facing representative of the Medical Affairs Department with a primary responsibility to engage in the exchange of scientific data, education of health care practitioners on Taiho products and relevant disease states, and facilitation of clinical research.
The MSL integrates clinical/scientific expertise and knowledge to ensure successful implementation of the medical affairs strategic plan within an assigned geographic region.
The MSL brings relevant insights from the field on research developments, treatment landscape and new concepts in medical treatment.
The role of the MSL is non-promotional in nature.
Responsibilities and Duties:
* Product/Therapeutic Area Support to External Stakeholders:
* Act as the primary clinical/scientific resource to HCPs in a specified geography for information pertaining to disease state and Taiho's product(s) and compounds to ensure awareness and understanding.
* Provides high quality scientific information to healthcare professionals (HCPs)
* Serve as a conduit for accurate and updated clinical, scientific and medical information between Key Opinion Leaders (KOLs)/investigators and the company's Medical Affairs and development groups.
* Establish, foster, cultivate and maintain peer relationships with KOLs and HCPs in the therapeutic areas in which Taiho has current and future interests.
* Share knowledge and participate in scientific exchanges and interactions with identified KOLs
* Present clinical and scientific data on Taiho’s products and relevant therapeutic areas as requested.
* Identify and report key scientific, clinical and research insights from KOLs and HCPs to Medical Affairs.
* Respond to unsolicited medical information requests in the field.
* Fulfill Pharmacovigilance responsibilities as define...
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Type: Permanent Location: Dallas, US-TX
Salary / Rate: Not Specified
Posted: 2024-03-23 07:13:21
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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.
Role Purpose:
This role is for a Principal Scientist position in the Bioprocess Analytics and Automation group within the R&D Protein and Process Analytics department.
It requires proficiencies in designing, planning and executing analytical studies and identifying, developing and establishing automated methods to replace manual processes in the lab.
Minimum requirements include hands-on experience with different automation equipment and/or liquid handling systems.
The position require the ability to analyze and interpret data, and outstanding team working skills.
Key responsibilities include to design and lead experimental work programs, and contribute to the development and implementation of new processes and procedures at a department level.
Key Accountabilities and Duties:
Drives innovation in emerging area of expertise, with use and knowledge of automation equipment and/or robotics
* Demonstrates scientific and technical leadership at a project level
* Is a “go to” person for less experienced scientists and actively provides support and development
* Reviews reports to ensure they address the right questions, are based on good science and present a high quality image of Lonza
* Collaborates with scientists in other Lonza business units, academia, and industrial partners to further the knowledge capital of Lonza
* Serve as a subject matter expert (SME) in automation• Working with the High Throughput Automation Team and other relevant stakeholders beyond the Protein and Process Analytics Team
* Experience of any of the following, Tecan, Hamilton, Biotek, Agilent, Thermo.
Qualifications:
Degree (required) Degree in Life Science or equivalent Field of Study Biology/Biomanufacturing or any related discipline.
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people and our environment.
Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences.
In return, we offer the satisfaction that comes with improving lives all around the world.
The satisfaction that comes with making a meaningful difference.
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Type: Permanent Location: Slough, GB-SLG
Salary / Rate: Not Specified
Posted: 2024-03-23 07:12:21
