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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
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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 macht unseren Bereich aus:
Diagnostics Operations Penzberg ist als Teil der Diagnostics Global Operations der wichtigste Produzent von qualitativ hochwertigen Einsatzstoffen bis hin zu speziellen Kits für die Diagnostik-Division von Roche.
Es erwartet Sie eine vielseitige, interessante und verantwortungsvolle Aufgabe im Bereich Manufacturing.
Hier werden biochemische und chemische Reagenzien und Einsatzstoffe für alle Geschäftsbereiche und vor allem die In-vitro-Diagnostik mehrerer Roche Geschäftseinheiten hergestellt.
Das Team:
Wir sind das Team der organisch-chemischen Produktion und sind stolz darauf für nahezu alle Einheiten der Division Diagnostics wichtige Produkte liefern zu können.
Die technologische Bandbreite reicht von der klassischen organischen Synthese im Technikums- und Labormaßstab bis zur Festphasenchemie im Milligrammbereich.
Wir stellen hochwertige Peptide und Oligonucleotide in einem kleinen Scale unter GMP Bedingungen her.
Unser Antrieb gilt der Produktion dieser qualitativ hochwertigen Produkte, der Einführung neuer Produkte und der ständigen Verbesserung unserer Produktionsprozesse.
Gestalte unseren Bereich für die Zukunft mit und unterstütze uns mit deinem Know-how:
* Als Chemikant oder Chemielaborant in der Peptid- und Oligonucleotidproduktion stellst Du Peptide und Oligonucleotide in kleinem Scale her.
Die Tätigkeiten finden in einem GMP Bereich statt.
* Neben der Abarbeitung von Produktionsaufträgen unterstützest Du unsere Gruppe bei folgenden Themen:
+ Mitarbeit bei der Übernahme neuer Verfahren und Implementierung neuer Produkte
+ Mitarbeit bei Erstellung und Überarbeitung von Vorgabedokumenten
+ Mitarbeit bei Validierungen und Qualifizierungen
+ Mitarbeit bei Prozessoptimierungen, Scale-Up und Troubleshootings
+ Geräteverantwortlicher
Für diese verantwortungsvolle und spannende Position suchen wir genau DU:
* Du hast eine Ausbildung als Chemikant oder Chemielaborant erfolgreich abgeschlossen.
* Du verfügst über theoretische und praktische Erfahrung im Bereich der organischen Chemie und/oder der HPLC Chromatographie (analytisch sowie präparativ).
* Du verfügst über theoretische und praktische Erfahrung im hochregulierten Produktionsumfeld (QS/GMP).
* Auf deine guten Englisch- und sehr guten Deutschkenntnisse sowie guten Kenntnisse gängiger EDV-Anwendungen können wir uns jederzeit verlassen.
* Eine strukturierte, gewissenhafte und selbstständige Arbeitsweise zeichnen Du aus.
* Du arbeitest auch gern...
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Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2024-03-23 07:10:03
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Today, Lonza is a global leader in life sciences operating across three continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
In exchange, we let our people own their careers.
Their ideas, big and small, genuinely improve the world, and that’s the kind of work we want to be part of.
For mRNA Business unit, located in Geleen, Netherlands 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 a (Principal/Senior) Scientist LNP.
Key responsibilities:
* Leadership: provide strong scientific, technical and regulatory leadership and for individual scientists and lab technicians on complex projects
* Representation: act as a deputy of the team manager when needed
* Projects: lead multi-disciplinary matrix teams on complex projects in the area of scientific expertise.
Lead problem solving and lessons learned activities
* Scientific tasks: design advanced experimental plans, lead the execution, data evaluation, write and review high quality reports
* Interactions: Assess novel technologies together with external partners
* Provide solutions to identified risks, issues, problems.
Report issues in a timely fashion
* Facilitate improvements to departmental business processes and contribute to the implementation of innovative technologies
* Demonstrate flexibility to support other activities within the department
* Proactive approach to own continuous professional development
Key requirements:
* Degree in Chemistry, Biochemistry, Pharmaceutical Sciences related field (e.g bioengineering, chemical engineering)
* In-depth knowledge with liposome/lipid nanoparticle formulations process
* Experience and strong hands-on power in encapsulation development for biomolecules, with preference experience with mRNA formulation in lipid nanoparticles
* Expert-level experience & understanding of handling, purification and processing of biomolecules.
* Experience with analyzing data derived from high-throughput screening and/or analytical characterization techniques (UV-Vis, fluorescence, particle characterization, chromatography etc.)
* Demonstrated ability to efficiently work in a fast paced and fluid environment, changes in priority and timeline restrictions
* Design DoE studies & high-throughput screen for lipid formulations
* Desirable: Experience with cell-based assays
* Fluency in English
Every day, Lonza’s products and services have a positive impact on millions of people.
For us, this is not only a great privilege, but also a great responsibility.
How we achieve our business results is just as important as the achievements themselves.
At Lonza, we respect and protect our people ...
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Type: Permanent Location: Geleen, NL-LI
Salary / Rate: Not Specified
Posted: 2024-03-23 07:08:20
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PURPOSE AND SCOPE:
Promotes quality patient care, ongoing customer support and case management for Fresenius Kidney Care (FKC) renal patient population (internal and external) by providing guidance, support, care coordination, education and other case management functions as defined by the pertinent program.
Manages the implementation of the pertinent program as assigned while acting as the subject matter expert and resource for patients, dialysis staff, physicians and other healthcare professionals.
Services are generally provided telephonically but there may be programs where on-site visits to clinics, medical office, hospital or visits to patient homes are required.
Programs include but are not limited to the Patient Onboarding, Continuity of Care, Hepatitis C Nurse Advocates and Anemia Case Management programs.
Will support FMS’s mission, vision, core values and customer service philosophy.
Adheres to the FMS Compliance Program, including following all regulatory and FMS policy requirements.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
* Utilizes clinical judgment, independent analysis, critical thinking skills, time management skills and detailed knowledge of case management program.
* Adheres to company, department, program policies and clinical guidelines to identify, review, assess and allocate patients for program participation according to their identified needs.
* Collaborates with the clinical staff, physicians and other members of the patient’s healthcare team, to develop an individualized and comprehensive plan of care according to the applicable program specifications.
* Ensures the coordination and integration of services as planned in the pertinent program while revising the plan as needed to provide high quality continuity of services and cost-effective service delivery.
* Utilizing the telephone and other technical and electronic communication formats to remotely monitor the care of the patient according to the program requirements.
There may be situations within the pertinent programs which require the case manager to meet the patient, the patient’s family and/or the physician face to face in the home, clinic or medical office setting.
+ Proactively contacts the patient and/or clinic on a frequent basis as specified in the program details to assess their situation, provide assistance, and answer questions as necessary.
+ Revises and adjusts the patient care plan as needed to fit the needs of the patient.
Provides updates to clinical staff, physician and/or family members as detailed in the program documents.
+ Identifies patient and/or clinic staff knowledge and understanding deficits regarding their specific program and situation.
Provides the appropriate education, support and materials to facilitate informed decision making and understanding.
+ Provides a strong and effective reciprocal communication process with patients (in applicable programs), clinic ...
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Type: Permanent Location: Waltham, US-MA
Salary / Rate: Not Specified
Posted: 2024-03-23 07:07:03
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Company
Federal Reserve Bank of Minneapolis
The Minneapolis Federal Reserve Bank's Research Division is seeking Research Assistants to join our Economic Analysis group (EA).
The Economic Analysis group at the Federal Reserve Bank of Minneapolis conducts research and provides analytic support for the Bank President, Research Director, and other Senior Bank Management on a broad range of policy-related topics.
The Research Assistant position is responsible for supporting staff economists in fulfilling this mission.
This position is expected to start in the Summer, 2024.
Onsite work is an essential function of this position, and you are expected to be in the office 5 days per week for meetings and team collaboration, unless directed otherwise by your supervisor.
To be considered, your application must include (attach all documents in upload link):
* Cover letter explaining interest in the position and plans for graduate study afterwards.
* Resume/ CV
* Transcript(s)
* Letters of Recommendation: (optional at the time of application but required after initial interview)
Responsibilities:
* Work independently to assist economists in a timely manner with Institute projects.
* Download and assemble data sets.
* Create advanced charts, tables, and presentations in support of economists’ Institute projects.
* Prepare clear verbal and advanced written reports.
* Use applicable statistical, econometric, and other software packages at an advanced level to program, perform analyses, model estimations and simulations, and assist with the preparation of memos.
* Compile literature reviews and conduct archival research, handle and configure data, present and maintain data in an esthetically and user-friendly format.
* Co-author and proofread articles with the oversight of economists.
Qualifications
* Bachelor's degree with coursework in economics, mathematics, statistics, or database analysis.
Advanced coursework in statistics/econometrics preferred.
* Strong analytic and problem-solving skills; effective oral and written communication skills; proficiency in Microsoft Excel.
* Demonstrated ability to meet strict deadlines and work cooperatively within a team environment.
* Verifiable experience with data collection, management, and analysis by using large databases and statistical packages (e.g., Stata, Matlab, R, SAS, Gauss) or other related computer programming experience is preferred.
Additional Information:
Salary Range: $ $56,900 - $71,130- $85,400 Annually.
Salary offer will be based on qualifications/experience of the candidate, alignment with market data, the needs of the position, our total compensation package, and internal equity.
Our total rewards program offers benefits that are the best fit for you at every stage of your career:
* Comprehensive healthcare options (Medical, Dental, and Vision)
* 401(k) match, and a fully funded pension plan
...
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Type: Permanent Location: Minneapolis, US-MN
Salary / Rate: Not Specified
Posted: 2024-03-22 13:34:11
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Great People Making Lifesaving Products
We are currently seeking a Quality Specialist to join our highly skilled, dynamic team.
Nortech Systems is a global leader in digital connectivity and data management engineering and manufacturing for medical device, aerospace, defense and industrial markets.
We are a low-volume, high-mix global manufacturer with centers of excellence in United States, Mexico and China.
Our expertise is in complex cable, PCBA and integrated higher-level assemblies.
Nortech Systems is a global market leader in digital connectivity, data management, engineering and manufacturing.
Our team is focused on delivering lifesaving products from medical devices which detect and treat cancer to mission-critical components for the U.S.
military. Nortech’s customers include some of the biggest names in industry, medical devices and aerospace and defense.
We’re very proud of our team’s role in making products that make a difference.
Are you looking for a position that requires flexibility, and a multi-faceted approach to your responsibilities? Do you like troubleshooting to get to the root cause of an issue? Are you looking for a role that lets you work on the quality system and how we can improve how the quality team does its roles? Are you a Quality Tech looking for career advancement? If you answered yes to any of these, please consider our Quality Specialist role!
The Quality Specialist will plan and conduct activities concerned with the quality management system (QMS) and the quality assurance of processes, materials and products by performing the following duties:
Responsibilities:
* Continually assesses the impact of industry and business process changes to ensure continued regulatory compliance of the QMS.
* Maintains a working knowledge of applicable international and domestic government and industry quality assurance standards and guidelines, such as 21 CFR 820, and ISO 13485.
* Identifies quality problems and concerns, performs effective root cause analysis, develops and implements appropriate corrective or preventive remedial action.
* Plans, performs, and reports the findings of internal and supplier quality audits.
* Supports external quality audits from regulatory bodies and customers.
* Evaluates and approves suppliers and monitors supplier quality performance.
* Plans and conducts the analysis, inspection, test, and/or integration to assure the quality of products, materials, and components; recommends appropriate product and process performance targets.
* Performs quality reviews and approvals of design and manufacturing documentation for compliance with stated requirements, including company quality records.
* Monitors and measures material, product, and process performance against established performance targets; recommends appropriate actions.
* Applies statistical process control (SPC) methods for analyzing data to evaluate the current proces...
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Type: Permanent Location: Milaca, US-MN
Salary / Rate: Not Specified
Posted: 2024-03-22 11:43:18
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Position Summary: The individual will assist in all aspects during the development of immunoassays, up to and including performing product feasibility tasks and supporting the necessary tasks to complete a Design Control project.
Responsibilities will include designing, planning and executing experiments in a GMP/GLP environment, interpreting results and summarizing data into project reports.
Essential Job Functions:
* Performs a major role in the initiation of development projects with technical focus on leading proof of concept and feasibility studies.
* Performs a major role in the generation and transfer of project/product information for the initiation of Design Control projects.
* Establishes Manufacturing processes and Quality Control (QC) procedures for new products.
* Performs and/or supports the necessary Design Verification studies to support new product launches.
* Performs and/or supports Design Validation studies to support new product launches.
* Performs and/or supports the scale-up of new manufacturing processes as needed.
* Supports the transfer of new technologies, products and/or manufacturing processes into and out of the company.
* Trains analytical development scientists, clinical personnel, and quality control technicians in specific areas of expertise.
* Serves as the subject matter expert member on risk assessment, investigation, and audit support teams, as needed.
* Follows all company environmental, health and safety policies, procedures and guidelines, and conducts work in a safe manner.
* Performs other duties as assigned.
Job Specifications (skills, knowledge, special training, certification, license requirements):
* B.S.
or M.S.
in Science/Engineering
* Minimum of 5 years of laboratory experience in the diagnostic or pharmaceutical industries
* Strong immunoassay development and manufacturing experience
* Strong technical problem-solving skills and discipline
* Strong organizational and time management skills desirable
* Analytical and preparatory chromatography experience
* Experience with automated immunoassay analyzers
* Protein modification/chemistry knowledge desirable
* Quality control experience desirable
* Excellent verbal and written communication skills
* Must be detail-oriented and thorough
* Ability to lead technical project teams
* Ability to work with various software packages
* Ability to make presentations to various groups of individuals
* Ability to travel nationally and internationally
* Ability to work with potentially hazardous materials
* Manual dexterity and ability to do visual inspections
...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2024-03-22 07:32:38
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Join the SilverBlaze team and be part of an exciting rapidly growing, international software development organization specializing in Customer Web Portals for the Utilities industry.
Harris is currently searching for an enthusiastic, quick learner to work in the SilverBlaze organization to provide implementation expertise to new and existing customers using the SilverBlaze Smart Forms software platform.
This person will interface with our utility customers, Harris sister companies and our development team, to assist in installing and configuring our product suite and resolving technical issues.
As a member of our highly respected team, this person will have an active role in providing exceptional customer support that is helpful and timely.
The ideal candidate should be a team player with strong interpersonal skills.
Candidates need to be self-motivated, self-learning, and detail-oriented.
This remote role welcomes candidates anywhere in Canada and the US.
SilverBlaze head office is located in Richmond Hill, Ontario.
Remote work opportunities are available.
The successful candidate will be working in the EST timezone.
What your impact will be:
* Operate as front line and primary support liaison to our clients and effectively respond to inquiries of both a product and technical nature received by telephone or electronically submitted tickets
* Assess a variety of situations, reviewing software configuration, set-up and software code and identify the correct resolution or escalate according to departmental guidelines
* Report detailed information within the client tracking system and document processes, routines, and programs by following the defined guidelines and team goals & objectives
* Regularly review the database of submitted items and proactively follow up with clients to ensure that their inquiries and/or issues have been satisfactorily resolved
* Work closely with other team members as part of a cohesive group in exchanging knowledge through training sessions and peer to peer interaction
* Maximize and maintain current knowledge and awareness of applications and related technologies
* Sound understanding of API and web services technologies and functions
* Email technology troubleshooting
* Sound knowledge of engagement delivery and software troubleshooting techniques with a high focus on first call resolution
* Ability to interpret requirements, and recommend solutions that best address clients' needs
* Excellent analytical, research and problem solving skills with a strong ability to multi-task and prioritize work effectively
* Exceptional attention to detail and the ability to grasp concepts quickly
* Other duties as assigned by management
What we are looking for:
* HTML, CSS, JavaScript knowledge
* Understanding the key concepts of web development and deployment
* Working with VMs
* VPN connectivity
* BA/BSc, related College Technical d...
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Type: Permanent Location: Richmond Hill, CA-ON
Salary / Rate: 65000
Posted: 2024-03-21 07:12:30
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An exciting opportunity to join the risk management team leading the coverage for Equity Derivatives within Mizuho Americas – a fast growing business.
The individual will partner with the Front Office, Quants, IT and other control functions to enable growth within the Equity Derivatives product offering at Mizuho Americas.
The main existing product offering is Margin Loans, Call-Spread Overlay, Collars and Autocallables but the business seeking to expand into multiple new markets.
Key Responsibilities include:
* Becoming primary contact for the Derivatives trading desk.
* Understanding the direction and prioritization of the business for future growth.
* Understanding of the underlying models used within pricing.
* Work with Trading and Quants to ensure risk dynamics and risk representation of both new and existing structures are as expected.
E.g.
as the desk expands into VIX ensure the exposure can be viewed in both VIX and SPX terms.
* Ensure limit structure is robust to capture any new product, and getting agreement from management and the Front Office to enhance gaps.
* Ensure appropriate content within risk reports to display key risks to management.
Leverage the junior members of the team to bring to market.
* Develop a suite of pre-trade analytics to provide management with transaction oversight.
* Partner with Finance to ensure understanding of IPV, Back-testing, PnL explain.
* Work with Risk IT to ensure VaR model handling products correctly.
* Work with the junior members to design and build out additional reporting views – e.g.
barrier concentration, correlation risk etc.
* Work with the junior members to enhance quality of the reporting commentary to be targeted and precise.
* Attend and present the risk profile within regulatory meetings with the SEC.
* Perform targeted scenario analytics on the portfolio to uncover pockets of risk.
Key Requirements:
* Solid understanding of Derivative products – ideally Equity underlying.
* Confidence talking to trading and quants about the pricing models and risk dynamics, coupled with hedging strategies.
* An ability to simplify the technical and explain to management in layman terms.
* Comfortable handling data.
The expected base salary ranges from $144,000 - $235,000.
Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications and licenses obtained.
Market and organizational factors are also considered.
In addition to salary and a generous employee benefits package, successful candidates are eligible to receive a discretionary bonus.
#Hybrid
Other requirements
Mizuho has in place a hybrid working program, with varying opportunities for remote work depending on the nature of the role, needs of your department, as well as local laws and regulatory obligations.
Company Overview
Mizuho Financial Group, Inc.
is...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2024-03-21 07:04:43
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Riverside Presbyterian Apartments (RPA), a high rise senior living facility located in the beautiful Riverside area of Jacksonville, is seeking a full-time Certified Occupancy Specialist (COS).
The occupancy specialist performs leasing and occupancy duties that support and maintain maximum occupancy levels while maintaining positive interactions with applicants, residents, RPA staff and management.
This position requires in depth knowledge of the U.S.
Department of Housing and Urban Development (HUD) regulations thus, COS Certification is required within 6 months of hire.
Responsibilities include:
* Performs leasing and occupancy tasks.
* Certifies and recertifies applicants and tenants.
* Builds and maintains resident files and ensure they are in compliance with regulations.
* Uses customer service skills to take resident requests, address resident concerns, and resolve them quickly.
* Maintains professional demeanor at all times.
* Uses exceptional multitasking skills to streamline processes and effectively manage daily tasks.
* Performs clerical tasks such as filing, typing, telephone and computer input
* Completes apartment inspections before tenant occupancy and after apartments are vacated.
* Works with the management team to ensure apartments are ready for occupancy.
Minimum Qualifications
Bachelor’s degree required. Certified Occupancy Specialist Certification preferred.
New hire without COS Certification will attend company paid training and must pass COS exam within 6 months of hire. Proficiency with Microsoft Office products and strong verbal and written communication skills required.
Interested candidates may select the following link to apply on-line.
https://recruiting.ultipro.com/WES1010/JobBoard/dc686796-57ca-4fa7-a2d7-68f4e5612bd8/OpportunityDetail?opportunityId=1bba1a5b-bfeb-4e8d-9e7e-042e3db97fb9
Salary starts at $20.84/hour
See job description
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Type: Permanent Location: Jacksonville, US-FL
Salary / Rate: 20.84
Posted: 2024-03-21 07:04:17