-
ERM is looking for a hands-on Consulting Associate, Environmental Engineering, Geology, or Science to join our growing team.
Working under the direction of project managers and partners, the successful candidate will work on a wide variety of site investigation, remediation, compliance, and hazardous waste management projects throughout office service area; however, opportunities for travel throughout the United States and globally may also occur.
This is a great opportunity to work with ERM's technical experts to implement the latest investigation and remediation technologies as well as more sustainable approaches, while building the required experience to obtain your professional registration.
RESPONSIBILITIES:
* Conduct field work, including soil, sediment, groundwater, surface water, soil vapor, and indoor air sampling, aquifer testing, drilling oversight and soil logging, soil boring and monitoring well installation, well development, purging and sampling, remedial and wastewater treatment pilot tests, and remedial system operation and maintenance.
* Assist in groundwater and wastewater system performance monitoring.
* Perform Phase I and II environmental assessments to support property transfer transactions.
* Compile and evaluate data and assist in report preparation.
* Prepare environmental compliance work plans, permits, and reports for air quality, hazardous waste, spill prevention, storm water, and wastewater.
* Assist in ensuring compliance with all federal, state and local regulations.
* Work within quality/budget/schedule expectations and scope-specific assignments.
* Communicate with subcontractors, regulatory agents, tenants, and clients during field activities.
REQUIREMENTS:
* Bachelors in geology, hydrogeology, engineering, environmental science or related environmental discipline; Masters a plus.
Minimum 3.0 GPA.
Or equivalent experience.
* Recent graduate to 2 years of experience.
* Willingness/interest in field assignments; ability to perform field work standing or walking for full field days.
* Strong commitment to safety, including following established Health and Safety protocols.
* Effective written/verbal communication and organization/analytical skills; experience recording/writing detailed technical data and reports a plus.
* Ability to work independently and as part of a team.
* Detail-oriented with solutions and results-oriented aptitude and hands-on troubleshooting/problem-solving skills.
* Ability to multi-task, maintain flexibility, travel, and work independently with minimal supervision.
* Ability to lift at least 40 pounds.
* Driver's License Required: This position requires a valid driver's license and/or the ability to operate a company vehicle due to the nature of job duties, which include frequent travel to various client locations across a large geographical area.
* 40-hour OSHA HAZWOPER certification a ...
....Read more...
Type: Permanent Location: Raleigh, US-NC
Salary / Rate: Not Specified
Posted: 2025-04-11 08:06:48
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Position Description:
This role will focus on delivery of Remote Account Manager (RAM) sales activities.
The RAM team works in conjunction with the field sales team, increasing the reach, frequency and value of our customers.
They will demonstrate the value of Elanco products to enhance customer adoption of our brands, with timely account follow-up and tool selection to meet sales objectives.
They must deal with all aspects of the commercial relationship: carry out prospecting actions, promote products and services, order taking, management of customer questions on Elanco products or services, and forwarding those to the appropriate Elanco team when needed.
The RAM team generate sales directly or indirectly through remote calls and/or other virtual channels to our veterinary customers.
RAM is a key pillar of our omnichannel strategy and must collaborate closely with marketing to enhance the customer experience.
RAM is held accountable for delivering sales results through the application of our Customer Value Selling (CVS) model, implementing agreed tactics and meeting identified KPI’s.
Key responsibilities:
Remote Sales Competences:
* Meets expectations of S3/S4 sales competencies.
* Generates demand with identified accounts and influencers.
* Conducts remote customer meetings, implementing and executing marketing programs and value add customer initiatives.
* Utilizes Elanco CRM to identify customer opportunities to bring value and increase touchpoints.
* Masters the virtual communication platform of MS Teams/Zoom, phone, etc., to ensure effective sales interactions, meeting customers’ needs, virtual learning, communication, and purchasing preferences.
* Disciplined reporting of all call reports, territory intelligence and detail customer information within designed CRM respecting defined KPIs.
* Develops and manages long term relationships with key target customers to uncover needs, identify opportunities and generate recommendations to achieve sales targets.
* Leverages omni-channel approach to remote...
....Read more...
Type: Permanent Location: Hook, GB-HAM
Salary / Rate: Not Specified
Posted: 2025-04-10 08:30:19
-
Your Job
Georgia-Pacific is seeking a Product Developer - Retail Tissue, Towel, & Napkin for our Technical Center in Neenah, WI.
This is a position within the Retail TTN team where you will drive product design and new product innovation.
This opportunity will allow you to combine your technical expertise, leadership skills, creativity, and entrepreneurship to have a direct impact on business performance.
If you have a passion for connecting technical solutions with business and consumer needs, this could be the right opportunity for you!
What You Will Do
* Designing, experimenting, evaluating, and executing alternative solutions based on understanding of technical capabilities, consumer/customer unmet needs and market trends
* Connecting market and consumer needs to product design, performance, alternatives, and setting technical specifications/limits on final product design
* Work with business stakeholders, consumer research and technology platform to collaborate on successful execution of experimental development or commercialization projects
* Mitigating technical risk by designing and analyzing experiments, coordinating, and conducting mill trials, and collecting consumer/market feedback on product designs
* Developing Intellectual Property through the creation of invention disclosures, patent applications and trade secrets by partnering with the Legal team
* Solving complex problems, by exercising critical thought and approaching data analysis and potential recommended paths forward with a creative and open-minded approach
* Providing technical advice on claims, data substantiation, and overall product points of view to our business leaders, operations, manufacturing, sales, and marketing teams
Who You Are (Basic Qualifications)
* Bachelor's Degree or higher in Paper Science, Engineering or at least 3 years of product development experience in paper products
* Willing and able to travel an average of 25%
* Experience working in an R&D environment with demonstrated results independently leading projects or experiment, product development activities, and scaling up to commercial feasibility
* Technical knowledge of papermaking and converting
What Will Put You Ahead
* Advanced Engineering Degree (M.S.) in Engineering, Paper Science, or business
* Experience in Project Management
* Experience in tissue/towel/napkin product development or converting
* Experience with SAP (PLM/MDG)
* 5 plus years of experience in product development
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions...
....Read more...
Type: Permanent Location: Neenah, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-10 08:22:22
-
We are seeking a Supply Chain Analyst to oversee all aspects of supply planning and act as the key liaison between sales, marketing, production planning, and distribution on inventory-related matters.
This role ensures that the right inventory is in the right place at the right time to support business objectives and inventory targets.
Key Responsibilities:
* Supply Planning: Develop and manage supply plans based on demand forecasts and inventory levels.
* Purchase Order Management: Ensure accurate and timely PO releases with vendors.
* Risk Management: Monitor stock levels, preventing shortages or excess inventory, including new product launches, transitions, and end-of-life cycles.
* Inventory Management: Optimize inventory to support business goals.
* KPI Reporting: Track and report on key performance indicators for supply chain efficiency.
* Forecasting & Data Analysis: Analyze historical data and market trends to anticipate demand fluctuations.
* Process Improvement: Identify opportunities to enhance supply chain operations.
* Collaboration: Work closely with vendors, suppliers, logistics, and internal teams to resolve supply issues and optimize distribution.
* Continuous Training & Development: Stay updated on best practices and perform additional duties as assigned by management.
If you're a detail-oriented, analytical thinker with a passion for supply chain optimization, we encourage you to apply and join our team!
Work Experience:
* 1 to 3 years of experience in supply chain operations or a related industry.
Education & Training:
* Bachelor’s degree in Supply Chain Management, Business Management, Operations Management, or a related field.
* Supply chain-related certifications are preferred.
* Equivalent combinations of education and experience will be considered.
Skills & Competencies:
* Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
* Basic knowledge of database programs, preferably Oracle, is a plus.
* Strong understanding of supply chain processes, forecasting, and inventory management.
* Familiarity with Business Intelligence reporting software is a plus.
* Highly organized, detail-oriented, and deadline-driven with excellent time management skills.
* Strong analytical, problem-solving, and communication skills.
* Ability to multi-task and work effectively in a fast-paced, team-oriented environment.
Physical Demands:
* Ability to stand, sit, and move for extended periods.
* Frequent use of hands and fingers for tasks.
* May require walking, reaching above shoulder height, and lifting up to 25 pounds.
....Read more...
Type: Permanent Location: Rancho Cucamonga, US-CA
Salary / Rate: 85893
Posted: 2025-04-10 08:21:15
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Daten sind Deine Leidenschaft? Dann bewirb Dich als Trainee (m/w/d) für unser 360° Programm Biostatistik!
Begeistert Dich die Vorstellung, mit statistischer Expertise große Daten zu zähmen und aus ihnen lebensverändernde Erkenntnisse zu gewinnen? Bei uns im 360° Trainee-Programm im Bereich Biostatistik kannst Du genau das tun! Als Trainee (m/w/d) hast du die einzigartige Möglichkeit, Deine individuellen Stärken gezielt einzusetzen und dabei gleichzeitig den größten Mehrwert für Roche zu schaffen.
Wir suchen jemanden wie Dich, der bereit ist, die Welt der Gesundheit mit uns neu zu definieren und einen erstklassigen Karrierestart hinzulegen.
Beginne Deine Reise bei uns und gestalte die Zukunft mit!
Was Dich erwartet:
* Onboarding & Getting to know the Business bei Roche Pharma AG in Grenzach und Start im Bereich Biometrics & Epidemiology (ca.
12 Monate).
* Optionale Schwerpunkt-Phase, in der Du deine Stärken im Biostatistik Bereich gezielt ausbauen und Dich in einem Gebiet spezialisieren kannst (bis zu 3 Monate).
* Mind.
zwei Phasen in einer unserer Disease Area (z.B.
Neuroscience, Ophthalmologie), um ein ganzheitliches Verständnis der Roche Pharma AG als Vertriebsgesellschaft zu bekommen.
* Erfahrungen in globalen Projekten mit der eventuellen Möglichkeit eines Austausches vor Ort.
Wer Du bist:
* Abgeschlossenes Hochschulstudium (mind.
Master) in (Bio-)Statistik oder Mathematik, Physik, Psychologie, Data Science, Bioinformatik oder einem vergleichbaren Studiengang.
* Erste praktische Erfahrungen im Biostatistik, Data Science Bereich, z.B.
durch Praktika, Nebenjobs oder Selbstständigkeit.
* Analytisches, strategisches und unternehmerisches Denken zählt zu Deinen Stärken.
* Starke Kommunikations- und Präsentationsfähigkeiten in Deutsch und Englisch.
* Mutiges und offenes Auftreten sowie die Fähigkeit, andere Menschen für Deine Ideen zu begeistern.
* Fähigkeit, im Team zu arbeiten und andere zu inspirieren.
* Ein echtes Interesse daran, die Patient:innen in den Mittelpunkt Deiner Arbeit zu stellen.
Werde Teil unseres Teams und profitiere von:
* Teilnahme an unterschiedlichen Weiterbildungsangeboten und speziell für die Trainee-Community entwickelten Trainings.
* Aktives Trainee-Netzwerk mit regelmäßigen Events und Networking-Möglichkeiten.
* Flexible Arbeitszeiten und Home-Office-Möglichkeiten.
* Umfangreiches Benefit Angebot z.B.
Sport- und Vorsorgeangebote, Job-Rad-Lea...
....Read more...
Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2025-04-10 08:16:56
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Finanz Pionier:innen als Trainees (m/w/d) für unser StartUp 360° Traineeprogramm im Bereich Business Finance gesucht
Dein Herz schlägt für Zahlen? Du möchtest mitgestalten? Für Transparenz, gute Entscheidungsgrundlagen und für das Monitoring unseres Geschäfts zu sorgen, ist dein Ziel? Dann starte bei uns durch! Als Trainee (m/w/d) in unserem StartUp 360° Programm mit Schwerpunkt Business Finance hast Du die einzigartige Möglichkeit, Deine individuellen Stärken gezielt einzusetzen, einen erstklassigen Karrierestart hinzulegen und dabei gleichzeitig den größten Mehrwert für Roche zu schaffen.
Was Dich erwartet:
* Onboarding & Getting to know the Business bei Roche Pharma AG in Grenzach und Start im Business Finance Bereich (ca.
12 Monate).
* Optionale Schwerpunkt-Phase, in der Du deine Stärken im Finance Bereich gezielt ausbauen und Dich in einem Gebiet spezialisieren kannst (bis zu 6 Monate).
* Mind.
zwei Phasen in einer unserer Disease Area (z.B.
Neuroscience, Ophthalmologie), um ein ganzheitliches Verständnis der Roche Pharma AG als Vertriebsgesellschaft zu bekommen.
* Die Möglichkeit, sich aktiv einzubringen in die Optimierung und Weiterentwicklung unserer Controlling-Prozesse.
* Erfahrungen in globalen Projekten und Netzwerken mit der eventuellen Möglichkeit eines Austausches vor Ort.
Wer Du bist:
* Abgeschlossenes Hochschulstudium (mind.
Master) in Wirtschaftswissenschaften und/oder Wirtschaftsingenieurwesen mit dem Schwerpunkten Finanzen, Controlling, Rechnungswesen oder vergleichbarem.
* Idealerweise hast Du erste praktische Erfahrungen im Finanzbereich, z.B.
durch Werkstudententätigkeit, Praktika, Nebenjobs oder Selbstständigkeit sammeln können.
* Analytisches, strategisches und unternehmerisches Denken und die Freude, Innovation voranzutreiben, zählen zu Deinen Stärken.
* Ein globales Mindset und die Fähigkeit, über Grenzen hinweg zu denken, mit Interesse daran, Deine persönliche Weiterentwicklung auch global weiterzuverfolgen.
* Fähigkeit, in selbstorganisierten und crossfunktionalen Teams zusammenzuarbeiten und andere zu inspirieren.
* Starke Kommunikations- und Präsentationsfähigkeiten in Deutsch und Englisch.
Werde Teil unseres Teams und profitiere von:
* Teilnahme an unterschiedlichen Weiterbildungsangeboten und speziell für die Trainee-Community entwickelten Trainings.
* Aktives Trainee-Netzwerk mit regelmäßigen Events und Networking-Möglichkeiten.
...
....Read more...
Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2025-04-10 08:16:49
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
StartUp 360° Trainee Programm bei Roche für Absolventen (m/w/d) der BWL, Gesundheitsökonomie oder einer Naturwissenschaft.
Mache den Unterschied im Leben von Patient:innen!
Bist Du bereit, die Healthcare-Industrie zu revolutionieren? Suchst Du nach einer Plattform, um Deine Talente zu zeigen und aktiv an der Zukunft von Roche mitzuwirken? Dann ist unser StartUp 360° Programm genau das Richtige für Dich! Als Trainee (m/w/d) bieten wir Dir die einzigartige Möglichkeit, Deine individuellen Stärken gezielt einzusetzen und gleichzeitig den größten Mehrwert für Roche zu schaffen.
Starte Deine Karriere bei uns und lege einen erstklassigen Karrierestart hin, während Du die Welt der Gesundheit neu gestaltest!
Was Dich erwartet:
* Onboarding & Getting to know the Business bei Roche Pharma AG in Grenzach und Start in einer Disease Area (ca.
12 Monate).
* Optionale Schwerpunkt-Phase, in der Du deine Stärken gezielt ausbauen und Dich in einem Gebiet spezialisieren kannst (bis zu 6 Monate).
* Kundenkontakt-Phase, z.B.
als Fachreferent:in im Außendienst oder als Ansprechpartner:in für Ärzte und Patienten bei medizinischen Fragestellungen in Medical Information (flexibel 3-12 Monate).
* Erfahrungen in globalen Projekten mit der eventuellen Möglichkeit eines Austausches vor Ort.
Wer Du bist:
* Abgeschlossenes Hochschulstudium (mind.
Master) in Naturwissenschaften, Medizin, Pharmazie, BWL, VWL, Gesundheitsökonomie, Digital Management, Entrepreneurship, Psychologie oder vergleichbaren Studienrichtungen.
* Erste praktische Erfahrungen, z.B.
durch Praktika, Vereinsaktivitäten, Nebenjobs oder Selbstständigkeit.
* Analytisches, strategisches und unternehmerisches Denken zählen zu Deinen Stärken.
* Starke Kommunikations- und Präsentationsfähigkeiten in Deutsch und Englisch.
* Mutiges und offenes Auftreten sowie die Fähigkeit, andere Menschen für Deine Ideen zu begeistern.
* Fähigkeit, im Team zu arbeiten und andere zu inspirieren.
* Ein echtes Interesse daran, die Patient:innen in den Mittelpunkt Deiner Arbeit zu stellen.
Werde Teil unseres Teams und profitiere von:
* Teilnahme an unterschiedlichen Weiterbildungsangeboten und speziell für die Trainee-Community entwickelten Trainings.
* Aktives Trainee-Netzwerk mit regelmäßigen Events und Networking-Möglichkeiten.
* Flexible Arbeitszeiten und Home-Office-Möglichkeiten.
* Einem umfangreichen Benefit Angebot z.B.
Sport- und Vorsorgeang...
....Read more...
Type: Permanent Location: Grenzach, DE-BW
Salary / Rate: Not Specified
Posted: 2025-04-10 08:16:41
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
R&D Operations
Job Sub Function:
Clinical Supply Operations
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Job Description
About Innovative Medicine:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for an Associate Director, Trial Supply Lead to be located in Titusville, NJ, Horsham, PA or Beerse, Belgium.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):
Titusville, PA or Horsham, PA - Requisition Number: R-005771
Purpose:
Clinical Supply Chain (CSC) holds the responsibility of global clinical supplies of the Innovative Medicine Research & Development portfolio and the Global Medical Affairs portfolio.
Our activities include all in-house and outsourced manufacturing of clinical supplies (API, Drug Product, Packaged and Labeled Clinical Supplies), demand forecasting, supply planning, and global distribution of supplies.
Through a global network and organization we are responsible for the clinical supplies of Synthetics, Molecules and Bio Therapeutics and Advanced Therapies products in development and low volume commercial supply and secure the supply to more than 60.000 patients in more than 330 clinical trials every year.
You will be responsible for:
* Supervising a group of individuals responsible for:
Studying drug management for pharma R&D clinical trials.
Ensures 99.5% Successful Dose, optimized inventory levels, optimized campaigns and minimized waste for the trial.
Monthly demand planning with clinical teams and within CSC kit demand planning tools
Studying drug budgets (OOP$ and FTEs)
* Ensuring monthly cS&OP cycle adherence and takes leadership over the escalation and (where applicable) resolution of critical risks and issues.
Leads S&OP escalation topics with ...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-04-10 08:13:48
-
About the Company:
Merz is a family-owned medical device and pharmaceutical company with headquarters in Germany.
Our Global Technical Operations based in WI manufactures, packages, and ships several innovative products so that people all over the world can look better, feel better and live better.
Key Responsibilities:
Microbiological SME / Process Leader:
* Operate as site Microbiological Subject Matter Expert (SME), maintaining high level of expertise in current global regulatory requirements for the manufacture of sterile medical devices, assuring adherence to “state of the art” requirements.
* Own site level Microbiology Testing program, including development, validation and implementation of Test Methods and Equipment.
* Evaluate and implement new microbiology technologies per Quality System Standards, Quality System Regulations, and other company procedures around which the Quality System is developed.
* Proactively Write, revise and review related Standard Operating Procedures (SOPs) and Department related Protocols.
* Establish and Maintain site microbiological and contamination control program(s) including associated employee training.
Microbiological Testing:
* Establish and Maintain Site Programs for:
* a.
Endotoxin and Bioburden testing
* b.
Environmental Monitoring (EM) of the Cleanrooms
* c.
Quality analysis of the water systems
* Coordinate daily operations for a team of microbiologists
Sterilization:
* Responsible for qualifying and maintaining the qualification of quality assurance activities associated with the sterilization of site’s products.
* Maintain risk assessments required for parametric release.
Data Analysis:
* Perform quality review for microbiological testing/EM monitoring data.
* Responsible for the identification and communication of adverse trends in routine microbiological monitoring.
Root Cause Analysis and Corrective Action:
* Lead laboratory root cause analysis investigations and implement corrective and preventive actions, reduce finished product average cycle time, and reduce laboratory related errors through method improvements, and effective training.
Audit Activities:
* Operate as site Microbiological SME in scope of internal and external audits.
* Participate in and/or perform internal and supplier audits as needed.
Operational Support:
* Support site facilities and manufacturing teams to assure compliance to sterilization, product, process, environmental and cleaning requirements to ensure product quality and Quality System requirements are met.
Education:
BS/BA in Microbiology, Biology, or Physical Science.
Required
Masters Degree in Microbiology or equivalent.
Preferred
Experience:
* 8 years Pharmaceutical/ Medical Device Microbiological Quality / Sterility Assurance experience.
Required
* GLP/GMP experience.
Required
Knowledge, Skills and Abilities:
* Strong t...
....Read more...
Type: Permanent Location: Racine, US-WI
Salary / Rate: Not Specified
Posted: 2025-04-09 08:58:44
-
Company
Federal Reserve Bank of New York
Federal Reserve Bank of New York
Working at the Federal Reserve Bank of New York positions you at the center of the financial world with a unique perspective on national and international markets and economies.
You will work in an environment with a diverse group of experienced professionals to foster and support the safety, soundness, and vitality of our economic and financial systems.
The Bank believes in work flexibility to balance the demands of work and life while also connecting and collaborating with our colleagues in person.
Employees can expect to be in the office a couple of days per week as needed for meetings and team collaboration and should live within a commutable distance.
What we do:
Economists provide analytic support for the New York Fed's core missions and engage in scholarly research on a broad range of topics.
They contribute to the formulation and implementation of monetary policy, the supervision of financial institutions, the smooth operations of the payments system, the analysis of the impact of policies on consumers and communities and the way in which the financial system supports economic growth using insights from macroeconomics, microeconomics asset pricing and corporate finance.
Areas of research include financial intermediation, monetary policy, household and public policy and financial stability.
As an Economist, you will:
* Conduct scholarly research for publication in high-quality, peer-reviewed academic journals.
* Provide rigorous analysis of policy issues related to the Bank’s mandate using advanced modeling and econometric techniques.
* Contribute analytical work and prepare technical memoranda and briefings for senior bank leaders in support of policy decisions.
* Collaborate with subject matter experts on model development, forecasts, and analysis.
* Engage in outreach to the academic and official sector research communities through participation in seminars and conferences, as well as technical working groups.
* Perform in accord with the Bank’s touchstone behaviors, as described below.
What we are looking for:
* PhD in Economics, Finance, or a related field preferred
Please visit our website to learn more and review the FAQs prior to submitting your application.
Please indicate your area of interest in your cover letter and/or application: Fields of interest:
C – Mathematical and Quantitative Methods
D – Microeconomics
E – Macroeconomics and Monetary Economics
F – International Economics
G – Financial Economics
H – Public Economics
J – Labor and Demographic Economics
L – Industrial Organization
R – Regional, Real Estate, and Transportation Economics
Salary Range: 160,000-217,600-275,200 / year
Touchstone Behaviors set clear expectations for leading with impact at every stage of our careers and aspire to achieve in our continued growth and development.
* Communicate Authentically...
....Read more...
Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2025-04-09 08:49:36
-
Shape Your World
At Alcoa, you will become an essential part of our purpose: to turn raw potential into real progress.
The way we see it, every Alcoan is a work-shaper, team-shaper, idea-shaper, world-shaper.
This is your opportunity to help share the future of sustainability with world-changing innovations and low-carbon technologies.
Become a valued part of the team that’s shaping the future of aluminium, revolutionising the way the world lives, builds, moves and flies.
Be part of it and shape your world.
About the Role:
Our Wagerup Refinery are seeking applications for a permanent fulltime Environmental Scientist Working Monday to Friday.
Our Environmental Scientists support and achieve high standards in all environmental expectations on site.
In this position we see you as vital to our business to:
* Support environmental targets being met via collaboration within our operations to achieve compliance with licenses and regulations,
* Drive efficiency initiatives, increase environmental awareness, and improve current and future environmental performance,
* Assist our operating, maintenance, and functional personnel in the implementation of Alcoa Corporate and site-specific environmental activities, as well as contribute to training of our personnel in environmental monitoring, responsibility and general awareness.
* Prepare reports for internal purposes, and statutory authorities
* Manage environmental contractors and consultants to deliver monitoring and reporting outcomes.
* Provide technical advice to the Environmental Manager on assigned environmental aspects
What’s on offer:
* Career development opportunities to pursue your passion
* Benefits allowance
* Performance related bonus (variable)
* 16 weeks paid parental leave scheme
* Paid annual volunteer hours
* Social and diversity focused engagement opportunities
What you can bring to the role:
To play a part in our ongoing success we are seeking someone with:
* Tertiary qualifications in Environmental Sciences or related degree coupled with relevant working experience
* Effective communication and influencing skills to bring people along the journey.
* Comprehensive report writing and analytical skills.
* Passion for environmental awareness and a forward-thinking attitude.
* Experience with environmental aspects including incident investigation, dust, stack air, water, contaminated sites and land management would be highly desirable.
Additional information
* Interviews may progress prior to the closing date, although all applications will be considered.
* You will only be contacted if you are shortlisted for an interview, this process can take up to four weeks from the closing date.
#LI-SV1
About the Location
Alcoa's Wagerup Refinery is one of the world's most environmentally and technologically advanced alumina refineries, and produces approximately 2.9 million metric tons of a...
....Read more...
Type: Permanent Location: WAROONA, AU-WA
Salary / Rate: Not Specified
Posted: 2025-04-09 08:23:03
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Als Medical Science Partner (m/w/d) im Indikationsgebiet Gynäkologische Onkologie bist Du für die Umsetzung klinischer Studienprojekte der Firma Roche Pharma AG in den Studienzentren Deines Gebietes mitverantwortlich.
Zunächst arbeitest Du als Teil interner Teams überwiegend an klinischen Studien der Phasen 1-3 sowie einem Register mit.
Für die Studienärzt:innen und ihre Studienkoordinator:innen bist Du erste/r Ansprechpartner:in direkt vor Ort.
Im Verlauf rückt die medizinisch-wissenschaftliche Begleitung der Ideen Deiner Studienärzt:innen für Investor Initiated Studies (IIS) sowie die Umsetzung von Real World Projekten zur Schließung strategisch relevanter Datenlücken zunehmend in Ihren Fokus.
Deine Aufgaben
Du kennst oder erkennst die für die erfolgreiche Studiendurchführung relevanten Interessengruppen, deren Interaktionen und trägst zur umfassenden Kenntnis des gesamten Studienumfelds in Deiner Indikation bei.
Für die Therapeutic Area Experts (TAE) bist Du unabhängig von laufenden Studien die direkte Verbindung zu Forschung und Entwicklung bei Roche und trägst durch vertiefte wissenschaftliche Diskussionen und durch aktives Netzwerken zum Erkenntnisgewinn bei.
Du stellst das Bindeglied zu medizinischen und nicht-medizinischen internen Stakeholdern - lokal wie global - dar.
Durch Deine gewonnenen Insights nimmst Du Einfluss auf die Forschungs- und Produktstrategie, die in Deiner Disease-Area entschieden wird.
Innerhalb Deines Gebietes bist Du gemeinsam mit den weiteren Feldfunktionen in enger Kooperation tätig.
Mit Deinem Wissen vertiefst Du unser Verständnis für den Weg der Patient:innen innerhalb der Indikation von der Diagnose über deren Management und Behandlung bis hin zur Nachsorge (Patient Journey).
Deine Hauptaufgaben als Medical Science Partner (m/w/d) sind:
* Primary Point of Contact (PPoC) für die auf die Umsetzung von klinischen Studien fokussierten Ärzt:innen; wissenschaftliche Diskussion, Gedankenaustausch und CoCreation
* In Zusammenarbeit mit den Abteilungen der Klinische Forschung (lokal und global) Unterstützung in Vorbereitung und Rekrutierung der von der Roche Pharma AG in Deutschland initiierten Studien
* Mapping national / international agierender forschender Ärzt:innen
* Unterstützung der Optimierung von Studienmanagementprozessen
* Generierung von Insights zur Studien- und Therapielandschaft
Wer Du bist:
Für die Funktion als Medical Science Partner (m/w/d) has...
....Read more...
Type: Permanent Location: North Rhine-Westphalia, DE-NW
Salary / Rate: Not Specified
Posted: 2025-04-09 08:16:13
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Senior Specialist - Upstream Operations Technician
The Upstream OpTech is technical process leader on the Upstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of cellular expansion from benchtop through production bioreactor processes.
Your Responsibilities:
* Executes the operation with team serving as process lead, coach, trainer, and responsible party.
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Serve as the operations representative and subject matter expert for cross-functional process support team.
* Real-time problem solving, process intervention, and technical experiment delivery, and continuous improvement.
* Ensure process documentation is prepared and completed with accuracy and concurrence.
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: minimum of 3 years experience with cellular growth/expansion processes.
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Fermentation
* Proficiency with SAP
* GMP manufacturing
* Aseptic experience
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
* Shift: 12 hour Day shift 5a-5:15p 2 week rotation (M,T,F,Sa,Su,W,R)
+ Shift premiums available for night and weekend work
Don’t meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification.
At Elanco we are dedicated to building a diverse and inclusive work environment.
If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply.
You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: Not Specified
Posted: 2025-04-08 08:12:37
-
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Job Description
Your Role: Global Research Project Leader (RPL)
As a Global Research Project Leader (RPL), you will be at the forefront of indication research and drug development in animal health.
You’ll lead the creation and management of a cutting-edge portfolio that bridges commercial needs with scientific research strategies.
In this role, you will deliver value-driven projects from concept through pipeline entry, ensuring technical feasibility, regulatory compliance, and commercial viability.
Your Responsibilities:
* Define the competitive landscape and lead the research strategy for indication projects in key animal health areas.
* Evaluate both internal ideas and external technologies to assess technical merit, strategic fit, and potential value for the company.
* Drive Proof-of-Concept-validated projects from discovery through pipeline entry, managing timelines, resources, risks, and regulatory challenges.
* Lead multi-disciplinary research teams, fostering cross-functional collaboration to solve complex technical and commercial challenges.
* Ensure customer insights are integrated into research projects by collaborating with marketing and commercial teams to shape business strategies.
What You Need to Succeed (minimum qualifications):
* Education: DVM and/or PhD with a minimum of 6 years of discovery, indication research, and/or pre-clinical research experience, with at least 2 years as a regular Project Team Member at a pharmaceutical/biotech organization.
* Top Skills: Proven expertise in project management, strategic thinking, and complex problem-solving within scientific and regulatory environments.
What Will Give You a Competitive Edge (preferred qualifications):
* Proven track record of leading research projects through discovery and pipeline entry, delivering validated technical and business cases.
* Strong business acumen with the ability to connect scientific research to commercial goals.
* Expertise navigating technical feasibility, regulatory hurdles (FD...
....Read more...
Type: Permanent Location: Greenfield, US-IN
Salary / Rate: Not Specified
Posted: 2025-04-08 08:12:33
-
Looking for a chance to make a meaningful 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 highly value our employees, who work relentlessly to help 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 patients, the global healthcare community, collaborators and partners, and each other.
Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.
It’s our work, our passion, and our legacy.
We invite you to join us.
Hybrid
Employee Value Proposition:
At Taiho Oncology, we are dedicated to transforming the landscape of cancer treatment and improving patients' lives.
As a Senior Manager, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging your expertise to drive innovative clinical research and contribute to groundbreaking therapies.
We offer a collaborative and inclusive work environment where your ideas and contributions are valued.
Join us to advance your career, work with passionate and skilled professionals, and make a meaningful impact on the fight against cancer.
At Taiho Oncology, you will find purpose, growth, and the opportunity to be at the forefront of cancer research.
Position Summary:
The Senior Manager, Clinical Research Scientist has responsibility assisting in design, execution and reporting of current and future clinical oncology trials ranging from phase 1 - 3.
Additionally, this role position supports the responsible medical monitor in the execution of key tasks involved in the design, conduct, monitoring and review of study data, analysis and reporting of clinical trials.
Performance Objectives:
* Collaborates with other key team members (Medical monitor, Project Manager, Clinical Operations, Data Management, Biostatistics, PV, PK, Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results.
* Use scientific expertise to support the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs), investigator brochures, DSUR, NDA/MAA registration documents and publications.
* Reviews and summarizes ongoing clinical data (from EDC and listings) to monitor the quality of the study, ensure clean data flow into the study database and compliance with the protocol.
* Keeps the latest knowledge in clinical development through publications and scientific conferences and leverages the knowledge for designin...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2025-04-08 08:08:38
-
At MTM, we are not just colleagues; we are collaborators on a shared mission; communities without barriers.
We have exciting opportunities to join our growing team where your work has a direct impact on the communities we serve.
Our company culture is one of innovation, collaboration, and growth.
If you are passionate, driven, and ready to join a team where your work will directly transform and shape our industry, then we want to talk to you!
What Will Your Job Look Like?
The Safety and Facility Monitor is responsible for ensuring transportation providers who contract with MTM meet and exceed the compliance requirements contained in our contract.
This includes performing random and/or schedule site visits, inspections and provide street level monitoring.
The Safety and Facility Monitor performs semi-annual vehicle inspections to ensure vehicle compliance with all ADA and other Federal, State and Local regulatory standards.
This position will primarily be Monday-Friday 9am-5:30pm.
The office is located at 4100 Garden City Drive, Hyattsville, MD 20785.
What You’ll Do:
* Conduct periodic inspections of vehicles and equipment being used for service throughout the term of the contract.
Such inspections may be conducted at the paratransit operating facility, MetroAccess main facility, during the provision of service, or at another time and location as stipulated by MetroAccess
* Will review vehicle files for inspection to ensure that required maintenance activities are being completed appropriately
* Performs scheduled and random visits (local travel) to required facilities to verify level of service and provider adherence to contract standards
* Perform onsite visits and street observations of current MetroAccess customers in the DMV
* Perform on street observations of providers’ vehicles, drivers and services Document on street observations and provide input to MetroAccess on both positive and negative findings
* Schedule facility and maintenance inspections
* Meet with the service provider to audit files and records, educate the contractor, and review any areas of deficiency
* Perform random and/or scheduled site visits and inspections
* Monitor pick-ups and drop-offs at major trip generators for safety and efficiency
* Ensure safety and comfort features are in good working order (i.e.
brakes, tire tread, signals, etc.)
* Conduct location reviews to evaluate accessibility and locate any unsafe stops or conditions
* Prepare and present comprehensive reports and briefings
* Maintain extensive knowledge and understanding of MetroAccess operating policies and procedures
* Observe operator behavior, driving records, handling of customers and timeliness of transports
* Respond to MetroAccess on all inquiries in a timely manner and attend meetings
* Plan and document deficiencies and provide follow up reports to management on a regular basis
* Investigate qu...
....Read more...
Type: Permanent Location: Hyattsville, US-MD
Salary / Rate: Not Specified
Posted: 2025-04-08 08:08:24
-
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following:
* Maintain a clean, orderly, and safe work area
* Wear all required personal protective equipment
* Must complete Chromalloy fork lift training
* Must complete overhead crane training
* Build, repair, and tear out a crucible assembly
* Build, repair, and tear out a tundish assembly
* Prepare ingot molds for cast
* Weigh-up and organize elemental raw materials & revert for melt campaigns
* Safe operation and preventive maintenance of the ingot stripping press
* Safe operation and preventive maintenance of the crop saw
* Safe operation and preventive maintenance of the robotic mold cleaning cell
* Safe operation and preventive maintenance of the ingot blast unit
* Safe operation and preventive maintenance of the abrasive saw and band saw
* Safe operation and preventive maintenance of the laser marker
* Other duties may be assigned as appropriate
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed are representative of the knowledge, skill, and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
....Read more...
Type: Permanent Location: Tampa, US-FL
Salary / Rate: Not Specified
Posted: 2025-04-08 08:07:57
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Was macht unseren Bereich aus:
Die Hauptabteilung „Diagnostic Operations Mannheim“ am Standort Penzberg steht für Zuverlässigkeit, Qualität und Wachstum und sieht sich in der Verantwortung, Patienten medizinisch-diagnostische Resultate bereitzustellen.
Dafür beliefern wir nicht nur Patienten selbst, sondern versorgen auch Krankenhäuser und Labore mit diagnostischen Reagenzien und Teststreifen.
Dein Team:
Wir sind ein 15-köpfiges gut organisiertes Team, und erfüllen gemeinsam die eingehenden Aufträge zeitnah nach bestehenden Vorgaben.
Gegenseitige Unterstützung, selbstständiges und zielorientiertes Arbeiten, sowie ein hohes Maß an Kommunikationsfähigkeit und ein respektvoller Umgang mit den Kollegen ist für uns selbstverständlich.
Die Arbeit in unserem Team innerhalb der Abteilung „Standardization & Quality Control“ ist sehr vielschichtig.
Für die Standardisierungen von Elecsys® Tests und die Sollwertermittlungen der testspezifischen Kalibratoren und Kontrollen arbeiten wir an allen cobas® Analyzern, von kleinem Tischgerät bis hin zu großen Hochdurchsatzgeräten.
Unterstütze uns mit Deinem Wissen bei folgenden Aufgaben:
* Die selbstständige Konzeption und Durchführung von Messungen an cobas® Analyzern zu Sollwertermittlungen und Standardisierungen legen wir vertrauensvoll in deine Hände
* Prüfung sowie Dokumentation der Messergebnisse werden von dir nach bestehenden Vorgaben durchgeführt
* Du übernimmst Verantwortung für unsere Geräte und organisierst in Abstimmung alle notwendigen Instandhaltungsmassnahmen
Diese Position erfordert deine Bereitschaft zum Umgang mit Humanmaterial
Für diese verantwortungsvolle und spannende Position suchen wir genau dich:
* Du bringst eine erfolgreich abgeschlossene Ausbildung, optimalerweise als Chemielaborant (m/w/d), CTA, BTA, LTA, MTLA oder MFA mit
* Zudem konntest Du idealerweise bereits Erfahrung in einem analytischen Labor sammeln
* Du hast sehr gute Kenntnisse im Umgang mit unterschiedlichen Software-Programmen wie Excel, Word und hast Freude daran dich in neue Programme einzuarbeiten
* Das Umfeld von Analyseautomaten / Immunoanalyzern sowie gültige GMP-Regeln sind dir bestenfalls bereits bekannt
* Du zeichnest dich durch eine selbstständige, genaue und zuverlässige Arbeitsweise aus und bist geschickt im Umgang mit komplexer Technik und hast Freude daran Neues zu lernen
* Du besitzt ein ausgeprägtes Organisationstalent, Zuverlässigkeit, ...
....Read more...
Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-08 08:04:09
-
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
Join Roche, where every voice matters.
The Position
Roche in 50 Worten
Eine gesündere Zukunft.
Das treibt uns an, innovativ zu sein. Wir bringen die Wissenschaft voran, damit alle die Gesundheitsversorgung erhalten, die benötigt wird.
Wir schaffen eine Welt, in der wir alle mehr Zeit mit den Menschen verbringen können, die wir lieben.
Das macht uns zu Roche.
Wer sind wir und was machen wir
Wir stellen durch unseren Einsatz, unsere Erfahrung und unsere Leidenschaft für In-vitro-Diagnostika sicher, dass Patienten weltweit zuverlässige medizinische Diagnoseergebnisse erhalten.
Zu diesem Zweck versorgen wir Kunden auf der ganzen Welt, d.
h.
Labors, Krankenhäuser, Apotheken, Arztpraxen und Patienten, mit diagnostischen Tests und Teststreifen.
Unsere oberste Maxime ist, dass sich alle Kunden zu 100 Prozent auf die Qualität unserer Produkte verlassen können.
Mit über 1.700 Mitarbeitern ist Diagnostics Global Operations Core Lab (DOM), vertreten an den Roche Standorten in Mannheim und Penzberg, einer der größten Partner im Diagnostika Global Operations Netzwerk.
Als enger Partner der Forschung und Entwicklung für die Einführung immunologischer, klinisch-chemischer und Point-of-Care In-vitro-Diagnostik richten wir unseren Fokus darauf, unseren Kunden kontinuierlich Produktinnovationen zu liefern und damit unsere Position als ein wesentlicher Leistungsträger für Global Operations und die Diagnostics Division weiter auszubauen.
Wer bist Du
* Du hast eine naturwissenschaftliche Ausbildung erfolgreich abgeschlossen.
* Du bringst mehrjährige Berufserfahrung in Labortätigkeiten und im Umgang mit DV Systemen mit
* Du bist gewohnt genau und zuverlässig zu arbeiten
* Du kennst Dich aus mit mathematisch-naturwissenschaftlichen Methoden, wie Mittelwert, Median, Varianz und Standardabweichung
* In Deiner bisherigen Tätigkeit hast Du bereits erste Erfahrungen im Elecsys Umfeld bekommen
* Die regulatorischen und gesetzlichen Vorgaben sind Dir bekannt.
* Du zeichnest dich durch eine proaktive Arbeitsweise aus und gestaltest deinen Arbeitsalltag agil und flexibel
* Hohe Teamfähigkeit, gute Kommunikation und wertschätzender Umgang sind Dir wichtig.
* Du brennst dafür, etwas Gutes zum Wohle unserer Patienten zu tun
Was erwartet Dich
Die Abteilung ‘DOM Standardization and Quality Control” ist verantwortlich für die Qualität unserer immunologischen und klinisch-chemischen in-vitro Diagnostik Produkte.
In der Prozesskette der Herstellung von Reagenzien für die immun...
....Read more...
Type: Permanent Location: Penzberg, DE-BY
Salary / Rate: Not Specified
Posted: 2025-04-08 08:03:41
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Pharmacokinetics & Pharmacometrics
Job Category:
Scientific/Technology
All Job Posting Locations:
Spring House, Pennsylvania, United States of America
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Principal Scientist, Clinical Operations to be in Spring House, PA.
Purpose:
This is a clinical operations support position within the Bioanalytical Discovery and Development Sciences (BDDS).
We work with internal bioanalytical groups and external partners to ensure the completion of all activities related to clinical study data deliveries and sample management.
We work to support all therapeutic areas within Johnson & Johnson, spanning nonclinical studies to post-market clinical development.
You will be responsible for:
* Serve as a point of contact within the Trial & Laboratory Operations group, serving as primary liaison to partnering groups, as well as a representative on project teams as required.
* Ensure accurate receipt, shipment, handling and storage of frozen biological specimen samples in support of non-clinical and clinical studies.
* Lead a team to support all aspects of the receipt and inventory of frozen laboratory samples sent from central laboratory or contract laboratory into freezers using Laboratory Information Management Systems (LIMS) to track sample chain of custody.
* Ensure samples are provided to scientists for analysis using LIMS to meet study timelines.
* Support management of the sample storage assets (freezers, chart recorders, handheld scanners, etc.), as well as the freezer inventory system and other sample management activities with contractors.
* Review and provide comments on the technical documents (protocols, statement of works and lab manuals) from internal groups, Central Laboratories, and outsourced bioanalytical laboratories for studies where the department conducts analyses, receives results, or has oversight of an ex...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-07 08:02:47
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Discovery & Pre-Clinical/Clinical Development
Job Sub Function:
Biotherapeutics R&D
Job Category:
Scientific/Technology
All Job Posting Locations:
US026 PA Spring House - 1400 McKean Rd
Job Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are seeking a highly motivated and experienced scientist to join our Lentivirus Small Scale PD team as a Principal Scientist.
You will be responsible for:
* You will integrate into the upstream process development team and lead, contribute, and advance process development of lentiviral vector-based products for CGT within DPDS, API.
* You will have a meaningful role in the planning, prioritization, innovation, and execution of early or late phase lentiviral projects.
* You will identify and conceptualize new ideas, designing, planning and leading experiments, prioritizing areas of focus based on business objectives, and analyzing complex issues by problem-solving and turning solutions into reality.
* You will be responsible for interpreting experimental data, and then summarizing and reporting the findings to the project team, generating technical documents, and when applicable, presenting to senior management.
* Along with cell therapy process subject matter experiments, you will interact and work with internal or external GMP clinical or commercial manufacturing sites.
Qualifications:
Required:
* BS or MS degree in Chemical Engineering, Biomedical Engineering, Biological Sciences, Chemistry, Biochemistry, or other equivalent and background with 6-8 years of experience is required; or a PhD with 4+ years of post-doctoral and/or relevant industry experience is highly preferred.
* Broad knowledge in viral vector process development, preferably upstream process development, and good understanding of cell culture parameters.
* Hands-on experience with aseptic techniques, cell culture in shake flasks, Wave bioreactors, and bioreactor systems, and cell counting/monitoring methods.
* Highly organized, meticulous, and ...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-07 08:02:11
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Data Analytics & Computational Sciences
Job Sub Function:
Data Science
Job Category:
People Leader
All Job Posting Locations:
US026 PA Spring House - 1400 McKean Rd, US064 CA San Diego - 3210 Merryfield Row, US258 MA Cambridge - 255 Main St
Job Description:
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
We are searching for the best talent for a Senior Director, Computationally Driven Drug Discovery with the primary and preferred location for this position in Spring House, PA. Consideration may be given for candidates who can be based in Cambridge, MA or San Diego, CA.
Johnson & Johnson Innovative Medicine (JJIM) is on a mission to improve human health with a focus in Oncology, Neuroscience, and Immunology.
We are searching for a Senior Director to join the In Silico Discovery team to help drive this mission forward with the application and development of cutting-edge molecular design strategies and AI/ML (Artificial Intelligence/Machine Learning) tools with direct impact on portfolio projects and team.
The In Silico Discovery Unit is a computational discovery team embedded in the Therapeutics Discovery organization, a modality agnostic discovery engine within JJIM responsible for driving all aspects of computational drug discovery across J&J’s Therapeutic Areas.
As a member of the In Silico Discovery Leadership Team and the Extended Leadership Team of Therapeutics Discovery, this role will play an influential part in transforming the organization into a computationally driven and prediction-first discovery engine.
This is an opportunity for an experienced leader with machine learning and structure-based drug design expertise to contribute to the most impactful and transformative projects at J&J.
Key Responsibilities:
* Drive our drug discovery transformation with a core responsibility to develop and apply our ambitious AI/ML strategy to bring computational methods to the forefront of drug design
* Foster scientific excellence by integrating cutting-edge technologies in structure-based drug design w...
....Read more...
Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-04-07 08:01:51
-
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Career Programs
Job Sub Function:
Non-LDP Intern/Co-Op
Job Category:
Career Program
All Job Posting Locations:
US052 OH Cincinnati - 4545 Creek Rd
Job Description:
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness.
Learn more at https://www.jnj.com/medtech
Johnson & Johnson is recruiting for R&D Quality Engineering Co-ops for the Summer 2025 term within our MedTech sector, located in Cincinnati, OH.
The Summer 2025 term dates are from 5/5/2025 - 8/15/2025
You will be responsible for:
* Collaborate with teams across J&J MedTech on Quality Engineering projects.
* Support and/or perform risk management activities.
* Learn and apply various statistical techniques to analyze data.
* Develop and contribute to training materials including procedures and work instructions.
* Strengthen presentation, communication, and leadership skills.
* Work with a diverse team of quality, development, test, and design engineers.
* Take advantage of training courses offered at J&J.
* Support project teams in ensuring the product being developed is safe and effective for patient use.
* Have the opportunity to work at and support J&J MedTech in Cincinnati, Ohio
* Work in MT Quality Engineering with the chance to support various project teams.
* Report directly to and receive assignments from their assignment manager while also working with the broader team for additional assignments.
* Participate in and/or lead on-campus activities such as learning committees, volunteer events, and meet and greet luncheons with full time associates.
Qualifications
* Enrolled in an accredited College/University pursuing a Bachelor’s or Master’s degree in Mech...
....Read more...
Type: Permanent Location: Cincinnati, US-OH
Salary / Rate: Not Specified
Posted: 2025-04-07 08:01:42
-
Join a great place to work with MissionSquare, a financial services corporation with approximately $79 billion in assets under management and administration and over 600 employees.
Founded in 1972, MissionSquare is dedicated exclusively to the retirement needs of public sector employees.
We focus on delivering results-oriented retirement and retiree health savings plans, education, investment options, personalized guidance, and related services to public sector participants in more than 9,200 plans and nearly 2 million participant accounts.
We strive to make the administration of retirement programs as easy and cost-effective as possible.
We have an extraordinary talent base and invite you to consider joining MissionSquare's Revenue & Sales team.
The Relationship Management Director is responsible for overall relationship and retention of MissionSquare’s largest clients.
They will deliver face-to-face proactive account management by serving as the primary liaison between clients and MissionSquare.
This requires the ability to expand and deepen broad plan sponsor relationships and maintain strong client satisfaction and reference ability.
The Relationship Management Director (RM) is required to assist plan sponsors in managing plan risks and their fiduciary responsibilities by discovering client goals and objectives, proposing new business solutions, and implementing services and products to fulfill the clients’ needs and objectives.
Requires residency in the Southern, CA area
Essential Functions for this role include:
* Deliver proactive account management and direct the overall retention strategy of MissionSquare’s Tier 1 clients.
* Direct the corporate service delivery for assigned cases. Work collaboratively with both the local service team and home office staff to ensure clients’ needs are met including individual meetings with participants and key influencers when possible.
* Build and broaden client relationships across all key influencers
* Determine client goals and objectives and develop and manage a strategic business plan towards those objectives.
* Lead periodic relationship oversight reporting, including but not limited to delivery of Visual Analytics, Plan Investment and Plan Service Reports.
* Assist clients with adding products and services to fulfill their needs and meet their plan and fiduciary responsibilities.
* Regularly support and implement corporate initiatives.
* Ensure long-term client satisfaction and reference ability.
* Identify new business and service/product expansion opportunities for MissionSquare.
If you have the following skills, we encourage you to apply:
* BA/BS or equivalent experience
* 10 or more years of experience
* Series 7 and 63, as well as Life, Health & Variable Annuity Licenses
* Senior-level relationship management experience in a financial serv...
....Read more...
Type: Permanent Location: Los Angeles, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-06 08:03:21
-
Join a great place to work with MissionSquare, a financial services corporation with approximately $79 billion in assets under management and administration and over 600 employees.
Founded in 1972, MissionSquare is dedicated exclusively to the retirement needs of public sector employees.
We focus on delivering results-oriented retirement and retiree health savings plans, education, investment options, personalized guidance, and related services to public sector participants in more than 9,200 plans and nearly 2 million participant accounts.
We strive to make the administration of retirement programs as easy and cost-effective as possible.
We have an extraordinary talent base and invite you to consider joining MissionSquare's Revenue & Sales team.
This position manages, mentors, and motivates assigned Retirement Plan Specialists to meet and exceed sales and client retention goals.
Also responsible for mentoring, training, and coaching new Regional Managers.
Manage the market development of the assigned region, which includes assisting with MVP in regional profitability, placing new products and services, retaining business, and serving as the relationship manager for assigned clients.
Significant travel within the assigned territory is required.
Requires residency in Northern, CA (Bay Area)
Essential Functions for this role include:
* Develop and implement business, operating, market, and strategic plans for geographic markets.
* Ensure the retention and expansion of the existing client base.
* Personally responsible for selected major relationships within the territory.
* Act as the focal point for communicating essential product/business information from the Corporate Headquarters and the Marketing Division to the assigned RPS.
* Mentor, train, and coach new Regional Managers.
* Handle SMARSH reviews for new Regional Managers who do not have the Series 26 license.
* Instill a high level of sales motivation in the territorial team and serve as coach and on-the- job trainer as appropriate.
* Other duties as assigned.
If you have the following skills, we encourage you to apply:
* BA/BS or equivalent experience.
* Five to seven years of experience.
* FINRA Series 6 (or 7), 63, 65 (or 66 in lieu of 63 & 65) required
* FINRA Series 26 (or 24 in lieu of 26)
* State life insurance license
* Proven field sales record with large multi-million-dollar financial services/retirement accounts.
* Two to four years of Regional Manager experience.
* Significant knowledge of investment products, with an emphasis on deferred compensation, defined benefits, and defined contribution plans.
Good understanding of specific plan provisions and legislative regulations and compliance issues.
* Sales management experience in financial services and/or public sector financial services is highly desirable.
* Strong r...
....Read more...
Type: Permanent Location: San Francisco, US-CA
Salary / Rate: Not Specified
Posted: 2025-04-06 08:03:20
