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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Your Role: Quality Control Technician
The position will include routine testing of in process antigens and final product samples for the release of veterinary vaccines. The individual will be responsible for ensuring all methods are performed as written and filed with regulatory agencies and standard operating procedures.
Your Responsibilities:
* Perform required tests for bulk antigens, final products, and raw materials, as well as other procedures necessary to support company and laboratory objectives to meet specified timelines.
* Maintain aseptic laboratory technique at all times and ensure accuracy of test results through precision and attention to detail.
* Maintain accurate and concurrent testing records and ensure compliance with Company SOPs and specifications, USDA, and cGMP regulations. Assist with updating, writing, and maintaining SOP’s, bench records and data entry for the department.
* Environmental monitoring of clean rooms and personnel: assisting in and/or performing microbial and particulate tests (air sampling).
* Provide effective training as requested, confirming that individuals are trained on the procedure at hand and all required training documentation has been completed.
What you need to succeed (minimum qualifications):
* High School Diploma or equivalent required.
* Experience in working in a team environment and handling multiple tasks simultaneously.
* Proficient in Microsoft Word and Excel, capable of using a controlled informatics system.
What will give you the competitive edge (additional preferences):
* Bachelor of Science degree in Microbiology, Virology, Bacteriology, Biology, or related field
* Laboratory experience including cell culture, viral and/or bacterial propagation.
* Experience in biotechnology and aseptic technique.
Other Information:
* Location: Winslow, ME (Onsite)
* Shift: Monday-Friday, 7am-3:30pm (evening, weekend, and holiday hours may be required)
* Must be able to pass a background check and gain Select Age...
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Type: Permanent Location: Winslow, US-ME
Salary / Rate: 25
Posted: 2025-10-22 08:57:19
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a Senior Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The Senior Chemist will be responsible for performing laboratory analysis of intermediate and finished products for the quality department and any production requests.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Perform hands on training for new analysts.
* Revise and update training modules as needed.
* Perform duties as a subject matter expert for the department.
* Coordinate scheduling of training activities with new analysts.
* Maintain training records and documentation in Veeva.
* Work cross functionally with other department training admins to ensure site training compliance.
* Support new hires and cross-train team members as needed in laboratory duties.
* Troubleshoot training errors/failures and mentor growth in new analysts.
* Follow good manufacturing practices (GMP) and use good documentation practices (GDP).
* Ensure documentation is accurate and up to date and communicate revisions as needed.
* Maintains confidentiality, will provide feedback to department manager on employee performance.
* Excellent communication skills to work across all departments in the facility.
* Ability to troubleshoot equipment used in the quality department.
* Excellent in technical skill related to analytical testing.
* Perform other duties as assigned.
REQUIRED SKILLS AND QUALIFICATIONS
* A bachelor’s degree in a natural science; 5 years’ experience working in the pharmaceutical industry or equivalent.
* Working knowledge of HPLC, GC, IC, Karl Fischer, IR, UV, Dissolution, Microscope, Sampling thieves, and Production gowning.
* Working knowledge of current good manufacturing practices (cGMP’s).
* Proficiency in Microsoft Office Suite applications.
* Basic knowledge of the pharmaceutic...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-10-22 08:34:56
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Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!
Join our mission at Adare!
What can Adare offer you?
* Medical/dental/vision/life – low employee premiums
* 401k with a highly competitive match
* Generous PTO, including floating holidays
* Career growth and internal opportunities
* Tuition reimbursement
* Relocation assistance
* Performance-based bonus
* Employee Recognition Programs
We are seeking to hire a QC Chemist to join our Quality Control team…
If any of the below describes you, we would love to meet you!
JOB SUMMARY
The QC Chemist performs moderately complex physical and chemical testing of intermediate and finished products according to written procedures and trains less experienced Chemists as required.
Also responsible for testing of cleaning samples for more complex systems and more advanced instrument maintenance.
Responsible for timely analytical data reporting based on project timelines.
RESPONSIBILITIES AND LEARNING OPPORTUNITIES
* Demonstrate a more advanced knowledge of various test methods and instrument analysis techniques and be proficient with all sample types and test methods.
Perform more advanced troubleshooting/maintenance of the instrumentation.
* Responsible for more complex physical and chemical testing of raw material, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols.
* Demonstrate proficient ability to operate the instrument software applications, set up advanced sequences, troubleshoot software and report data while executing the higher complexity test methods that utilize instruments such as UV, FTIR, GC, and HPLC, and IC.
* As required, perform swabbing and analysis of more complex manufacturing equipment with no supervision in accordance with cGMP guidelines.
Provide input on cleaning related issues and investigations.
* Evaluate and maintain assigned calibrations for equipment in the laboratory as required and review the required documentation for compliance.
Review instrument qualification documents to support system change control actions and assist vendors during installation and PM’s.
* Investigate Out of Specification results, Out of Trend results and deviations in accordance with cGMP guidelines.
* Assist Management with writing and completion of inv...
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Type: Permanent Location: Vandalia, US-OH
Salary / Rate: Not Specified
Posted: 2025-10-22 08:30:27
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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:
Scientific/Technology
All Job Posting Locations:
Cornellà de Llobregat, Barcelona, Spain, Madrid, Spain
Job Description:
J&J IM develops treatments that improve the health and well-being of people worldwide.
Research and development areas encompass oncology, cardiovascular and retina disorders, immunology, and neuroscience.
Our goal is to help people live longer and healthier lives.
We have produced and marketed many first-in-class prescription medications and are poised to serve the broad needs of the healthcare market – from patients to practitioners and from clinics to hospitals.
To learn more about J&J IM, please visit https://www.jnj.com/.
Johnson & Johnson Innovative Medicine (J&J IM) is recruiting for the role of Senior Scientist – AI Agent Systems for Drug Discovery.
This position has a primary location of Barcelona, Spain.
The secondary location is Madrid.
This is a hybrid role.
The Machine Intelligence (MI) team within Data Science and Digital Health (DSDH) AI/ML is looking for a mission-driven Senior Scientist to help shape the future of autonomous AI in drug discovery and development.
You'll work with Large Language Models (LLMs) and advanced data science techniques, harnessing massive datasets spanning scientific literature, omics, and biomolecular knowledge.
Your work will directly accelerate how we discover therapeutics and advance them to clinical trials - making reasoning agents faster, more accurate, and more reliable.
Key focus areas include multimodal reasoning, agent robustness and uncertainty, agent memory architecture, and agent motivation frameworks.
Key Responsibilities:
* Develop and optimize multimodal reasoning systems that integrate scientific literature, omics data, chemical information, and structured data to derive actionable conclusions
* Build novel agent memory architectures to enable persistent knowledge retention and context-aware decision-making across extended discovery workflows
* Prototype and evaluate new approaches for uncertainty quantification and reliability assessment in AI-driven scientific reasoning
* Serve as a domain expert within the field by articulating to team members emerging approaches and methodologies within the AI/ML with a clear understanding of their practical applications
* Benchmark agent performance against hu...
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Type: Permanent Location: Cornellà de Llobregat, ES-B
Salary / Rate: Not Specified
Posted: 2025-10-22 08:23:41
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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:
Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson Innovative Medicine (J&J IM), a pharmaceutical company of Johnson & Johnson is recruiting for a Director, R&D Data Science, Data Products – Global Development.
This position has a primary location of Titusville, NJ but is also open to Spring House, PA or Cambridge, MA. This position requires up to 25% travel.
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
Position Summary
The Director, Data Products – Global Development is responsible for leading the strategy, design, and delivery of user-centric, reusable data products that enable advanced analytics, data science, and AI/ML solutions across the Global Development organization.
This role ensures that high-value internal and external development data assets—including protocol, study design, operational, regulatory, disclosure, and real-world data (RWD/RWE)—are standardized, productized, and integrated into Janssen’s enterprise R&D data ecosystem.
Working closely with Global Development Data Science teams, Clinical Development, Operations, and Regulatory stakeholders, as well as the broader Data Strategy & Products organization, this leader ensures that Global Development data products are AI-ready, semantically consistent, and interoperable, enabling trial efficiency, regulatory readiness, and improved compliance outcomes.
Key Responsibilities:
Data Product Strategy & Execution
* Lead a team to define and deliver data products addressing critical Global Development use cases (e.g., study startup, TMF metadata, operational KPIs, submission readiness).
* Define and maintain a roadmap for Global Development data products, spanning protocol development through clinical trial disclosure.
* Develop data products through agile delivery and FAIR data principles, ensuring scalability, interoperability, an...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-22 08:23:04
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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:
Titusville, New Jersey, United States of America
Job Description:
Johnson and Johnson Innovative Medicine (J&J IM), a pharmaceutical company of Johnson & Johnson is recruiting for a Director, R&D Data Science, MDM Products
This position has a primary location of Titusville, NJ but is also open to Spring House, PA or Cambridge, MA. This position requires up to 25% travel.
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
Position Summary
The Director, Product Mastering is responsible for establishing and governing an end-to-end mastering capability for product-related data, beginning with compounds in Therapeutic Discovery (TD), continuing through Preclinical Sciences & Translational Safety (PSTS), extending into Pharmaceutical Therapeutics Development & Supply (PTDS), and connecting seamlessly with clinical trial and regulatory data.
This lifecycle mastering ensures continuity into commercial brand naming and labeling.
This role ensures that product master data—including compounds, formulations, investigational products, clinical identifiers, regulatory submissions, and commercial brand hierarchies—is trusted, harmonized, and semantically consistent across the entire R&D to Commercial continuum.
The Director will leverage ontologies and knowledge graphs to connect and contextualize product information across silos, enabling advanced analytics, AI/ML, regulatory compliance, and global interoperability.
Key Responsibilities
End-to-End Product Mastering Strategy
* Define and execute a mastering strategy covering the full product lifecycle: from discovery compounds → preclinical entities → development products (PTDS) → clinical trial identifiers → regulatory designations → commercial brand names.
* Ensure a single, authoritative source of truth for all product-related master data, harmonized across functions and systems.
* Identify ga...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-22 08:23:03
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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:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Beijing, China
Job Description:
PRINCIPAL RESPONSIBILITIES
External Customer Engagement and Partnering
• Actively identify, develop, and engage key KOLs at regional level.
• Proactive and reactive communication/interpretation of medical/scientific data/information to KOLs.
• Through scientific interactions with KOLs, champion medical benefits of products and contribute to foster innovative therapeutic approaches to benefit patients
• Utilizes effective customer engagement strategies, skills, and technology to uncover deep actionable insights on treatment strategies, needs, and priorities that are relevant and important for mutually beneficial value to the customer and Janssen.
• Proactively builds a scientific informational resource network
Effectively Scientific Communication with internal/external customers
• To help customers and business partners stay abreast of significant advancements through timely identification and dissemination of emerging scientific and medical information from a multitude of sources.
• To respond to scientific queries of customers for approved products and products/indications in development, based on Medical Information documents e.g.
literatures, safety records, scientific FAQs etc.
• To organize and moderate advisory boards in cooperation with TA groups.
• To provide medical and product training and scientific support to Sales Representatives in coordination with Marketing team as appropriate.
• To collect insights from external customers and feedback timely to shape Brand/medical strategy
Scientific Communication Effectiveness with external/internal customers
• To organize local or regional medical education activities including program development, speaker selection and support in collaboration with ME&MA as appropriate.
• To support national and regional medical educational events including material development, speaker selection and support in collaboration with ME&MAs.
• Support medical affairs program and activities at local and regional level.
• Ensure program implementation 100% in compliance.
Stra...
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Type: Permanent Location: Beijing, CN-11
Salary / Rate: Not Specified
Posted: 2025-10-22 08:22:43
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ERM is seeking a Managing Consultant, Environmental Permitting in our Denver, Colorado office to manage, oversee, and conduct environmental impact assessment and regulatory compliance for energy facilities and energy-related development projects across North America. Focus primarily on new energy-related capital development, including oil and gas projects, electric transmission lines, and renewable energy projects. Projects may be regulated by the Federal Energy Regulatory Commission (FERC) or state and adjacent state siting agencies (e.g., Colorado Public Utilities Commission, New Mexico Public Service Commission).
Projects are often fast-paced, multi-faceted, and geographically diverse - allowing a talented person to apply their technical expertise in support of compliance with federal, state, and local regulations related to siting, water, waste, and National Environmental Policy Act (NEPA).
The position will require a candidate to work independently and manage projects and project teams, with the capacity to handle varying priorities and multiple tasks. The successful candidate will have demonstrated experience in overseeing environmental permitting and compliance for capital development projects, managing staff in a project setting, assessing environmental conditions and impacts, and possessing strong technical writing and communication skills.
RESPONSIBILITIES:
* Manage projects, either single or multi-site, on time and to budget, including elements such as scope and delivery requirements, budgeting, resourcing, planning, coordinating field and other technical work, and managing health and safety and risk aspects.
* Generate technical proposals and participate in business development with existing clients and identify new leads. Maintain client relationships to support repeat business.
* Review and comprehend project plans to assess environmental impact and scope of regulatory requirements.
* Prepare siting and permit applications required by federal, state, or local environmental regulatory authorities for facility development, expansion, maintenance, or decommissioning.
* Assist with the preparation of technical project documents, including, but not limited to writing, word processing, building tables and spreadsheets, tabulating and manipulating data, producing hard copy documents commensurate with the candidate’s technical background.
* Collaborate with other ERM practitioners to execute impact assessment and capital project permitting (ERM services broadly include baseline studies, environmental impact assessment, routing studies, land planning, and facility siting & permitting).
* Prepare environmental plans such as erosion control plans, storm water pollution prevention plans, site restoration plans, and spill prevention, control, and countermeasures plans.
* Assist in planning for, communicating, and ensuring compliance with project-specific federal, state and local environmen...
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Type: Permanent Location: Denver, US-CO
Salary / Rate: Not Specified
Posted: 2025-10-22 08:19:17
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General Purpose
Responsible for the regulatory oversight of multiple facility clinical programs located in different states.
This position provides support and education for nursing clinical programs.
The primary purpose is to assist with the design and implementation of clinical audits in vital areas requiring clinical improvement and then providing support and education that ensures regulatory compliance.
The position requires collaboration between Compliance Team members and Regional Teams (RDCS, ARDCS, RAI Specialists, IP Nurses).
This includes but is not limited to training of nurses in proper daily skilled documentation, wound documentation, and risk reduction.
Recommendations will strictly adhere to Medicare guidelines and PACS Best Practices.
Essential Duties
* Supports State and Federal Regulatory Compliance with monitoring, education, and implementation of
* clinical programs while collaborating with other members of the PACS Compliance Team and local PACS Regional Team members.
* Provides Facility Trainings as needed to support local facility clinical operations
* Educates and Mentors Registered and Licensed Nursing staff as necessary for proper daily skilled
* documentation and special focus areas including PDPM active diagnosis, fall management, wound treatment, and care planning in the EMR.
* Reviews EMR and Point Right to ensure strict compliance with Medicare guidelines
* Collaborates with Legal Team to monitor high risk liability areas and assist facilities to alleviate liability risk
* Tracks and trends clinical metrics for identified risk areas
* Participates in Facility CSR, Triple Check, and other meetings as directed
* Supports administrators in achieving clinical outcomes which adhere to industry standards of care and regulatory requirements.
* Intensive auditing responsibility of pertinent clinical topics.
* Monitors for trends affecting workflow, facility liability, and risk management
* Interface with other regional personnel to promote standardization across region
* Identifies opportunities within facilities for new programs (i.e.
Certified wound treatment)
* Supports facility with clinical reviews for probes, CERTs, ADR's, and ALJ's
* Reports to Vice President of Compliance Support any concerns with compliance or lack of adherence to company best practices
* Assists with Wound Module Training in the EMR
* Provides recommendations to supervisor for opportunities to improve company
* Must be able to travel by car and/or plane when necessary to reach assigned destination in a reasonable time frame
* Must maintain confidentiality of company and patient information
* Promotes positive attitude to coworkers and to company regarding the company, its mission statement, philosophies, and goals
* Inspire others to elevate their level of commitment
* Complete ongoing education with follow up in-service to appro...
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Type: Permanent Location: Farmington, US-UT
Salary / Rate: Not Specified
Posted: 2025-10-21 08:32:42
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Company
Federal Reserve Bank of Boston
As an employee of the Boston Fed, you will work to promote sound growth and financial stability in New England and the nation.
You will contribute to communities, the region, and the nation by conducting economic research, participating in monetary policy-making, supervising certain financial institutions, providing financial services and payments, playing a leadership role in the payments industry, and supporting economic well-being in communities through a variety of efforts.
The Boston Fed is one of 12 Reserve Banks and we serve all or parts of Connecticut, Maine, Massachusetts, New Hampshire, Rhode Island, and Vermont.
This role requires an in-person schedule with onsite work expected for intentional collaboration.
Candidates must reside in First District.
The Research Assistant (RA) program at the Boston Fed is a two-year program designed for recent college graduates with a background in economics, math, statistics, or related fields.
RAs work with economists on a variety of research projects and provide support for ongoing analysis of the New England, U.S., and global economies and monetary policy, as well as bank regulation, the payments system and financial markets.
Positions are available in our Research Department starting in June 2026. The Research Department provides current economic analysis and policy advice to Federal Reserve decision makers and conducts innovative research with the aim of improving our understanding of the regional, U.S.
and global economies and encouraging better policy outcomes.
The Boston Fed is an equal opportunity employer and is committed to supporting and fostering diversity within the broader economics research community.
If you are interested in gaining meaningful work experience, expanding your career options, and serving the public, we encourage you to apply for our Research Assistant Program.
RA Responsibilities
* Review, organize, and analyze economic and financial data.
* Write programs using statistical software such as STATA, MATLAB, R, SAS or Python
* Conduct literature reviews, perform thorough data analysis, and prepare written summaries of results for economists.
* Prepare charts and tables using spreadsheet and data visualization software packages.
* Conduct economic research for policy memos and for articles intended for publication by The Boston Fed, academic journals, and business periodicals.
* Design programs to clean data, perform statistical tests, and run regressions.
Update and maintain data series regularly used by economists.
* Proofread, edit, and fact-check articles and papers.
Qualifications
* A bachelor’s degree in economics, math, statistics, computer science, international relations, or related field with concentration in economics.
* Strong analytical, communications, and organization skills.
* Familiarity with programming languages and statistical software pa...
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Type: Permanent Location: Boston, US-MA
Salary / Rate: 77000
Posted: 2025-10-21 08:30:09
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A division of Harris, Aumentum is seeking a Support Services Manager.
This role is for a Support Services Manager who will lead a team of up to 10 people in our Support Department.
Your main goal will be to ensure our customers receive excellent technical software support.
This remote role welcomes candidates anywhere in the US.
Beyond leading your team, you will:
* Improve processes: Define and implement ways to resolve customer issues quickly and effectively, aiming to keep customers happy and encourage them to recommend us.
* Work with other teams: Collaborate with colleagues across departments to deliver successful software, provide high-quality technical solutions, and boost overall customer satisfaction.
* Be a key contact: Serve as a main point of contact for customers and handle escalated issues, building strong relationships.
Key Responsibilities:
* Help grow our maintenance revenue each year.
* Proactively follow up with customers, communicate clearly, and manage issues to meet our agreements and keep customers satisfied.
* Set clear goals for your team, track their progress, and coach them to perform at their best.
* Focus on the value of customer relationships, including their willingness to be a reference, and find ways to increase revenue from existing customers.
* Regularly review and improve our processes to make them more efficient.
* Resolve customer service issues and help improve our overall service.
* Understand maintenance contract details and explain them to customers to help meet monthly revenue targets.
* Handle HR tasks within the Support Department.
* Travel occasionally for customer visits, user group meetings, customer conferences, or process improvement trips.
* Improve operations to reduce customer calls and fix software issues.
* Monitor department performance by tracking trends and statistics, then report these findings to senior management.
* Act as a manager-level contact for customer issue escalations.
* Monitor customer satisfaction.
* Help create and implement support initiatives, such as knowledge bases, technical guides, and documentation.
* Work closely with other departments (R&D, Sales, Professional Services, Client Management) to resolve customer and internal issues promptly.
What we're looking for:
* A Bachelor's Degree (preferred).
* 5-7 years of experience in customer support or a similar role.
* A proven history of building or leading diverse and effective teams.
* Previous experience in a management, supervisory, or leadership position.
* Strong analytical and problem-solving skills.
* Excellent written, verbal, and interpersonal communication skills.
* The ability to work independently and lead a team, including remotely.
* The capacity to manage multiple teams and initiatives at once.
* Experience with ticket tracking software (e.g., Salesforce, TeamSupp...
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Type: Permanent Location: Tallahassee, US-FL
Salary / Rate: 90000
Posted: 2025-10-21 08:21:23
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Harris Computer, the largest operating group of Constellation Software Inc.
(TSX:CSU), is looking for a Business Development professional, based in the USA or Canada, to join our expanding team on the mergers and acquisitions (M&A) team.
This team works closely with Harris’ senior management in continuing the company’s success in acquiring software businesses.
This role is a full-time, remote, work from home position.
We will consider candidates from anywhere in North America.
As a member of the Harris Business Development team, you will report to the Manager of Business Development.
This role requires travel of up to 10% in North America, and a valid passport is required.
In this role you will be responsible for sourcing new acquisitions, developing relationships with key decision makers, and performing investment opportunity origination activities related to vertical market software businesses. You will be successful in this role if you are a people-person, have solid business acumen, love to continuously learn, experiment, and have a passion for creating and maintaining relationships.
Prior business development experience is helpful but not necessary.
Financial literacy, solid interpersonal abilities, and understanding of software and technology businesses are considered assets.
What your impact will be:
* Directly engage with the decision makers of software businesses in specifically identified vertical markets to identify, maintain, and nurture acquisition opportunities for Harris by using a suite of communication and customer relationship management tools.
* Continue relationships with our existing network of acquisition targets.
* Become the senior account manager for Harris’ M&A relationships in your area of coverage.
* Effectively communicate Harris’ investment strategy, while ensuring that the investment process is handled with care and professionalism.
* Support the M&A team in qualifying potential company targets.
* Track activities and maintain relevant information in Salesforce.
* Generate and report on leads, set up qualified investment opportunities, and move opportunities through the M&A pipeline to our M&A transactions team.
What we are looking for:
* 5+ years of related business experience.
Sales, business development, consulting, banking, investing, M&A sourcing, technology/software, investor relations or entrepreneurship/start-up experience are all considered valuable experience and will be highly considered.
* Aptitude and passion for business development and relationship management.
* Exceptional people skills, organizational, written and verbal communication skills.
* Self-starter with excellent prioritization and multi-tasking abilities who thrives on new challenges and takes initiative.
* Experimentation is part of what we do at Harris.
All candidates will be considered, if you think you may be a good fit for the rol...
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Type: Permanent Location: Tallahassee, US-FL
Salary / Rate: 90000
Posted: 2025-10-21 08:21:18
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
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Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-21 08:10:42
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POSITION SUMMARY:
This is position that is responsible for the operation and supporting activities surrounding a particular coating process. The primary equipment will be operated through HMIs (Human-Machine Interfaces) and a series of switches, pushbuttons, and other interactive control points. Successful Operators will be capable to produce the required amount of product in a defined period while ensuring all (Environment, Health and Safety (EHS) and Quality requirements are continuously satisfied. The Operator will be required to work as part of a team with Operations Support, Engineering, Maintenance, and Management personnel. Some overtime will be required on occasion to meet production and project schedules. Limited travel may be required in support of training program. Operators will be provided the opportunity to progress within the role as defined below.
DUTIES AND RESPONSIBILITIES:
* Perform complex and multi-level tasks from procedures and work instructions defining the tasks.
* Maintain timely and accurate record keeping using provided tools including digital and handwritten data entry and notes.
* Maintain 100% compliance with personal protective equipment (PPE) requirements while operating equipment and/or performing supporting operations, includes ensuring your personal protective equipment is functioning properly prior to starting a task.
* Effectively identify and communicate non-standard situations including (EHS) and Product Integrity concerns.
* Operate support equipment (pre/post coating) and support Coater Operators
* Maintaining metal coating fixtures for use in coater which including visually verifying condition, removing residual coatings, and removing any contamination that may have affected the fixtures.
* Cross training in other coating process areas as needed to support production requirements. Will be required to complete the training program for each process prior to performed assignments in that area.
QUALIFICATIONS:
* High school diploma or general education degree (GED).
* At least 2 years’ experience working in a production manufacturing environment
* Additional Education, Training, Certifications, or Licenses that are applicable will be considered and may be used to supersede either of the other two requirements.
* Must be able to read, write, and communicate in English.
* Read and interpret documents such as safety rules, operating instructions, and procedure manuals.
* Write routine reports and correspondence either in digital or handwritten formats.
* Good mathematical skills, scientific principles and reasoning ability
* Mechanically inclined individual that thrives in a hands-on, demanding environment with little direct supervision once assignments are handed out.
* May be required to operate of forklift (training provided).
PHYSICAL DEMANDS: Reasonable accommodat...
....Read more...
Type: Permanent Location: Oldsmar, US-FL
Salary / Rate: Not Specified
Posted: 2025-10-21 08:10:35
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
We’re driven by our vision of ‘Food and Companionship Enriching Life’ and our approach to sustainability – the Elanco Healthy Purpose™ – to advance the health of animals, people, the planet and our enterprise.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.
We believe that diversity is the driving force behind innovation, creativity, and overall business success.
Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
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)
+ This role currently operates on an 8-hour shift schedule.
Starting in July 2025, the position will transition to the 12-hour shift schedule stated above.
+ Please note that weekend work will have a 4% premium and work outside of your shift hours will have 10% premium.
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 ...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 30
Posted: 2025-10-20 08:21:20
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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!
$2,500 Sign-On Bonus! Apply Today!
Relocation Assistance Available
Your Role: Sr.
Specialist - Downstream Operations Technician (Night Shift)
The Downstream OpTech is technical process leader on the Downstream operations team responsible for manufacturing execution, changeover, and production control.
The role is dedicated to the execution and oversight of the Clarification, Chromatography, and Tangential Flow Filtration operations.
Your Responsibilities:
* Executes the operation with team serving as process leader, coach, trainer, and responsible party
* Performs and verifies Maintenance, process setup, troubleshooting, change over, process intervention.
* Operations representative for cross-functional process support team, engaging in process
* Real-time problem solving, process intervention, and technical experiment delivery
* Ensures process documentation is prepared and completed with accuracy and concurrence
What You Need to Succeed (minimum qualifications):
* Education: High School Diploma / GED
* Experience: A minimum of 3 years of experience in Liquid Protein A Chromatography at manufacturing scale
What will give you a competitive edge (preferred qualifications):
* Production scale filtration
* Formal Root Cause Investigation training
* Proficiency with SAP
* GMP manufacturing
* Tangential Flow Filtration
Additional Information:
* Travel: Minimal
* Location: Elanco Animal Health Elwood, KS
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 package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our pur...
....Read more...
Type: Permanent Location: Elwood, US-KS
Salary / Rate: 37.55
Posted: 2025-10-20 08:21:18
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
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: Animal Study Support Associate
As an Animal Study Support Associate, you will be an integral part of our team, providing professional veterinary technical support and hands-on care to animals involved in R&D studies and QC tests.
Your role will involve ensuring compliance with USDA Animal Welfare Act standards and AAALAC-accepted practices.
Your Responsibilities:
* Animal Care and Wellbeing: Provide primary veterinary technical and nursing care, including health monitoring, medication administration, and implementation of environmental enrichment and socialization programs.
* Study Support: Assist veterinarians with pre-, intra-, and post-study animal procedures, sample collection, and product administration.
* Sample and Supply Logistics: Coordinate receipt, processing, and shipment of diagnostic samples and test articles, adhering to relevant regulations.
Manage pharmacy and veterinary supply inventories, ordering, and researcher requests.
* Health Maintenance Program: Maintain routine health schedules for animal colonies, including vaccinations, deworming, and dental procedures, under veterinary guidance.
* Record Keeping and Compliance: Maintain accurate medical records and controlled substance logs, ensuring compliance with DEA regulations.
What You Need to Succeed (minimum qualifications):
* Minimum of Associates Degree in Veterinary Science or related field required.
What You Need to Succeed (preferred qualifications):
* Certified Veterinary Technician (CVT, RVT, or LCT).
* Experience in a Veterinary Technician position with various species is preferred.
Additional Information:
* Location: Fort Dodge, IA
* Opportunities: Elanco will support obtaining an AALAS certification at the ALAT level upon joining us in this role! You will also have the opportunity to have overtime if you are interested!
Don’t meet every single requirement? Studies have shown underrepresented 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...
....Read more...
Type: Permanent Location: Fort Dodge, US-IA
Salary / Rate: 27.12
Posted: 2025-10-20 08:21:18
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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 Trial Project Management
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium
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
Johnson & Johnson is currently seeking a Lead Local Trial Manager to join our Global Clinical Operations located in Beerse, Belgium.
A Lead, Local Trial Manager is considered as a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience.
This role is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries.
The Lead, Local Trial Manager is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents.
The Lead, Local Trial Manager is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
The Lead, Local Trial Manager actively leads or contributes to process improvement; training and mentoring of other LTMs and Site Managers (SM).
Compared to Associate, Local Trial Manager and Senior, Local Trial Manager roles, a Lead, Local Trial Manager is often assigned to more complex protocols and can work across Phase 1 – 3 studies in multiple therapeutic areas as needed to drive business needs.
The Lead, Local Trial Manager may also perform the role of Trial Delivery Manager (TDM)/Trial Delivery Leader (TDL) for single country as described in GCO procedural documents.
Principal Responsibilities:
* May be delegated by Functional Manager (FM)/Clinical Research Manager (CRM) to lead country protocol feasibility (if applicable) and site feasibility assessment in conjun...
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Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-10-20 08:11:17
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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:
Spring House, Pennsylvania, United States of America
Job Description:
Synthetic Organic Chemistry Summer Intern, Johnson & Johnson Spring House (Undergraduate Student)
Johnson & Johnson is currently seeking an undergraduate student for a synthetic organic chemistry intern position, located in Spring House, PA.
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 www.jnj.com.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
We are currently seeking an outstanding and motivated individual to work in the Discovery Chemistry group located in Spring House, PA, as a summer intern.
The internship program is focused on providing an undergraduate college student the opportunity to learn about the role of organic chemistry in drug discovery research.
The position offers real-life training in the skills and tools relevant to perform as a drug discovery chemist.
The synthetic organic chemistry intern will:
* Work collaboratively with a Johnson & Johnson scientist
* Synthesize, purify, and characterize novel drug-like compounds
* Enable reaction discovery to address key synthetic challenges
* Participate and present at project team meetings
* Be exposed to various other functions within the drug discovery teams at Johnson & Johnson
* Participate in campus-wide activities across the Spring House summer intern community
* Be based in Spring House, PA (suburban Philadelphia area)
Qualifications
* Candidates must be a sophomore, junior, or senior student en...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-20 08:11:13
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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:
Post Doc – Data Analytics & Computational Sciences
Job Category:
Career Program
All Job Posting Locations:
Cambridge, Massachusetts, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is recruiting for Postdoctoral Scientist, R&D Data Science and Digital Health, Real-World Evidence (RWE) Oncology
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
The Real-World Evidence (RWE) Oncology team within Johnson and Johnson Innovative Medicines is looking for outstanding postdoctoral scientist whose responsibilities include:
* Analyze observational databases and historical trial data to generate real-world insight to support regulatory agency interactions
* Develop study protocols, statistical analysis plans, and programming specifications.
Deliver high-quality outputs including analysis-ready datasets, tables and figures.
* Perform comprehensive reviews of scientific literature to contextualize findings and support study design and interpretation.
* Communicate research findings effectively through technical reports, presentations, and contributions to peer-reviewed publications
Required qualifications:
* A Ph.D.
degree in epidemiology or biostatistics
* Expert coding skills using R
* Strong expertise in conducting epidemiological research including research questions, designing studies, conducting analyses, and interpreting results
* Hands-on experience with data extraction, cleaning, and analysis, as well as statistical methods to mitigate confounding and selection biases
* Excellent interpersonal, communication and presentation skills
Preferred qualifications:
* Experience with real-world data sources (EHR, insurance claims, registry data)
* Familiarity with clinical trial design and data structure
* Subject matter knowledge in o...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-20 08:11:03
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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:
Strategy & Corporate Development
Job Sub Function:
Mergers, Acquisitions & Divestitures
Job Category:
People Leader
All Job Posting Locations:
New Brunswick, New Jersey, United States of America
Job Description:
Senior Director, Business Development, Neuroscience Acquisitions
Johnson & Johnson is currently seeking a Senior Director, Neuroscience Acquisitions to join our Innovative Medicine Business Development team, located in New Brunswick, NJ.
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/.
The Senior Director, Neuroscience Acquisitions, will be a key member of the J&J Innovative Medicine Business Development team, partnering closely with the Neuroscience Therapeutic Area to identify and deliver robust M&A analysis and execution. Specifically, this role will lead Neuroscience M&A efforts, functioning as our Neuroscience landscape expert, including conducting competitive analysis, identifying strategic M&A targets, and leading assessment and ultimately execution of critical acquisitions.
J&J Innovative Medicine Business Development is a part of Johnson & Johnson Innovation LLC, which is working to accelerate scientific innovation at all stages of development worldwide to deliver cutting-edge solutions that solve unmet needs for patients.
Johnson & Johnson Innovation provides scientists, entrepreneurs, and emerging companies with one-stop access to the broad resources of the Johnson & Johnson Family of Companies.
This includes access to dealmakers, through the innovation centers located in global life science hot spots and Johnson & Johnson Innovation – J&J Innovative Medicine Business Development; venture investment, through Johnson & Johnson Innovation – JJDC; company incubation, through Johnson & Johnson Innovation, JLABS; as well as R&D, manufacturing, and commercialization expertise.
We are J&J Innovative Medicine.
Our mission drives us.
Our patients inspire us.
We collaborate with the world for the health o...
....Read more...
Type: Permanent Location: New Brunswick, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-20 08:10:53
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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:
Titusville, New Jersey, United States of America
Job Description:
The EP IM/ID Co-Op position supports the Therapeutic Area Portfolio Clinical Team and is dedicated to maximizing the value of this portfolio through the execution of all phases of clinical development and in particular, provides active medical and scientific contribution to cross-functional clinical teams to support successful completion of clinical projects and deliverables that enable worldwide registrations for new indications, enhancements to the label and compliance with regulatory commitments for products in the market and in development.
The EP IMID Co-Op will:
* Work with the Clinical and overall EP IM/ID compound development teams (CDT) and their internal and external partners in the execution of specific tasks and projects specifically related to clinical studies and other tactical strategic activities conducted for the support of this portfolio.
* Work in concert with the Clinical Leaders on clinical trial concept and protocol development, execute clinical studies for new formulations, post-approval commitments, and new indications.
* Be actively involved in creation of Clinical Study Reports (CSRs), publication of clinical research findings and presentations to relevant FDA, EMA, or other Health Authorities, advisory committees, and review meetings.
* Participate in cross-functional teams for evaluation of new product ideas and related new technologies; review medical literature, clinical, medical and market access plans.
Qualifications
* Candidates must be enrolled in an accredited college/university pursuing MD, PhD, Pharm D or any other health care related advanced degree, with emphasis in Biological sciences and Public Health.
* Bachelor’s degree in the Biological Sciences with strong clinical experience or preferably possessing or enrolled in a Master’s degree in a Clinical Science or a related field or Paramedical (Allied Health care) professionals (including nurse practitioners, physician's assistants and midwifes) with strong clinical/research background would be considered.
* Candidates must be enrolled in an accredited college/university pursuing MD, PhD, Pharm D or any other health care related advanced degree, with emphasis in Biological sciences an...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-20 08:10:43
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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:
Malvern, Pennsylvania, United States of America
Job Description:
Join our innovative team at Johnson & Johnson to work on optimizing and stabilizing therapeutic antibody solutions.
Therapeutic antibodies are essential in modern medicine for their specificity and efficacy in treating various diseases.
This project seeks to address the challenges of maintaining antibody stability during storage and administration through cutting-edge research and technology.
Key Responsibilities:
* Engage and enhance experimental methods to explore stabilizing solutions for therapeutic antibodies within the J&J portfolio.
* Utilize cutting edge techniques to analyze and compare different protein aggregation mechanisms, aiming to better stabilize therapeutic antibodies against particle formation.
* Shadow scientists performing high-throughput screening (HTS) of solution variations in the lab to assess antibody stabilization.
* Generate and analyze datasets that aid in the prediction of particle formation across stability campaigns.
What You Will Gain:
* Hands-on experience in biological formulation and data analysis techniques.
* Insight into the methodologies for enhancing the stability of therapeutic antibodies.
* Exposure to cutting-edge research in the pharmaceutical industry and experience contributing to Johnson & Johnson's innovative solutions.
* Opportunity to collaborate with industry leaders and gain knowledge applicable to future scientific careers.
Qualifications:
* Currently enrolled in a Bachelor’s, Master’s, or PhD degree program in Biology, Chemistry, Bioengineering, Biophysics, or a related field.
* Basic knowledge of working in a laboratory setting is preferred but not required.
* Basic knowledge of data analysis techniques required, knowledge of advanced data analysis techniques preferred.
Permanently authorized to work in the U.S., must not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually requires future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship.
Johnson & Johnson is...
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Type: Permanent Location: Malvern, US-PA
Salary / Rate: Not Specified
Posted: 2025-10-20 08:10:40
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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:
Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America
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
Johnson & Johnson is currently recruiting Summer Interns for our Integrated Data Analytics and Reporting (IDAR) Summer Intern Training Academy! We are recruiting for the following department: Regulatory Medical Writing (RMW).
The positions are for university undergraduate students who will be entering their junior or senior year, or graduate students who will continue their postgraduate program after the internship.
We are seeking highly motivated candidates to join our Summer Intern Training Academy.
The Academy is a premier training program focused on developing and inspiring talent considering a career in pharmaceutical research and development.
You can gain hands-on experience and help advance our medicines in development at Johnson & Johnson.
Remote work options may be considered on a case-by-case basis and if approved by the Company.
As an intern in the RMW department, you have the opportunity to learn how to write high quality clinical documents to support the development, regulatory approval, and maintenance of our products.
These documents include investigator’s brochures, clinical trial protocols, and clinical study reports, as well as summaries of efficacy and safety and responses to health authority questions.
How you can make a difference: Apply your excellent writing skills, ability to interpret and summarize statistical and medical information and attention to detail to the design of our clinical trials and reporting of our data.
Qualifications:
* Candidates must be legally authorized to work in the U.S.
and must not require sponsorship for employment visa status now, or in the future (e.g., H1‑B).
* Candidate must be actively enrolled in an accredited University for the durati...
....Read more...
Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-10-20 08:10:35
-
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:
Business Intelligence
Job Category:
Professional
All Job Posting Locations:
Santa Clara, California, United States of America
Job Description:
Johnson & Johnson is hiring for a Business Intelligence Analyst – Shockwave Medical to join our team.
The position is FULLY REMOTE and can sit anywhere in the US.
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.
Ready to join a team that’s pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.
We are seeking a proactive and curious Business Intelligence Analyst to support the development and maintenance of Power BI solutions within the Shockwave Medical business unit, now part of Johnson & Johnson MedTech.
This role will contribute to our reporting capabilities and collaborate closely with US Sales Operations and other stakeholders to deliver impactful insights.
Key Responsibilities:
· Power BI Development: Design, build, and maintain Power BI reports and dashboards, ensuring accuracy and usability for business stakeholders.
· Semantic Model Development: Assist in creating and optimizing Power BI semantic models to support scalable analytics solutions.
· Collaboration: Work closely with US Sales Operations and cross-functional teams to understand reporting needs and deliver actionable insights.
· Data Quality & Integration: Support data integrat...
....Read more...
Type: Permanent Location: Santa Clara, US-CA
Salary / Rate: Not Specified
Posted: 2025-10-20 08:10:06
