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The Support Specialist will be responsible for providing technical support for our Tricentis catalog with a concentration in our Tricentis Tosca product.
Responsibilities
* Responsible for the technical analysis and processing of requests from all customer segments.
* Responding to issues, requests and inquiries via self-service cases, live chat, phone and video.
* Identify & organize cases according to priority and escalate cases to engineers when necessary.
* Make suggestions and help improve with internal documentation and knowledge base content.
* Collaborate with customers to deliver a superior customer experience, leveraging effective communication and problem-solving skills to ensure their needs are met with satisfaction.
Qualifications
* Have strong analytical, organizational, written, and verbal communication skills.
* Have a broad spectrum of basic technical knowledge in the areas of databases, programming, network technology.
* Ability to easily familiarize yourself with complex software applications.
* Approach problems in an analytical and solution-oriented manner.
* Proven track record in a strong customer facing support role.
* Previous experience with QA/automation testing tools is a plus (but not required).
Why Tricentis?
Tricentis Core Values:
At Tricentis, we strive for success while inspiring those around us by knowing what we need to achieve and how we’ll achieve it.
Our core values serve as our guiding light to drive our every action and define our ways of working so that we can create and enjoy a successful journey and reach higher heights together.
* Demonstrate Self-Awareness: Own your strengths and limitations.
* Finish What We Start: Do what we say we are going to do.
* Move Fast: Create momentum and efficiency.
* Run Towards Change: Challenge the status quo.
* Serve Our Customers & Communities: Create a positive experience with each interaction.
* Solve Problems Together: We win or lose as one team.
* Think Big & Believe: Set extraordinary goals and believe you can achieve them.
We offer:
* Market competitive salary + success-oriented commission / bonus
* Supportive and engaged leadership team.
* Career path and professional & personal development.
* 401(k) / pension plan, full benefits package available.
* Hybrid work environment.
* Personal and professional development.
* And more!
Tricentis is proud to be an equal opportunity workplace.
Qualified applicants will receive consideration for employment without regard to race, color, ethnicity, gender, religious affiliation, age, sexual orientation, socioeconomic status, or physical and mental disability and other statuses protected by law.
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Type: Permanent Location: Atlanta, US-GA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:25:51
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Job Title: Customs Brokerage Agent
Job Location: Port Huron, MI
DHL Global Forwarding (DGF) manages the flow of goods and information across a customer's global supply chain utilizing air/ocean/ground transportation, customs brokerage services, and dedicated warehousing/distribution centers.
As part of DHL Group, the world’s leading logistics provider operating in over 220 countries, we invite you to join our dynamic team.
Explore more about our vibrant career opportunities at DHL Careers.
Your Adventure Awaits!
We are thrilled to announce an exciting opportunity for a CUSTOMS BROKERAGE AGENT! In this pivotal role, you will orchestrate the movement of traffic from foreign destinations, ensuring a smooth and compliant process every step of the way.
Key Responsibilities:
* Assist in the customs and trade compliance processes to help ensure smooth and cost-effective customs clearance.
* Learn to classify dutiable import/export shipments, ensuring they comply with all government regulations.
* Support the import/export documentation process by receiving, reconciling, consolidating, and summarizing necessary documents and information.
* Participate in data entry activities, inputting information into the customs operating system and assisting in setting up master data for transactions.
* Help screen and update documentation to ensure compliance with federal regulations while supporting the archiving of important documents.
* Aid in filing customs entries and managing post-entry transactions efficiently.
* Maintain customer part lists and regularly update shipment information and physical status to keep records accurate.
* Collect necessary information to assist team members with duty, tax, and billing discrepancies.
* Follow established processes and systems for completing assigned tasks, reporting any recurring issues to supervisors for guidance.
* Research and help obtain the permits, licenses, and certificates needed for customs clearance and other formalities.
* Provide basic advice to customers on legal and customs topics, including trade compliance for shipments to sanctioned countries.
* Communicate with customs authorities to inquire about shipment status and any special handling needs.
Skills / Requirements:
* High School diploma or GED required.
* Exceptional oral and written communication skills.
* Strong customer service orientation.
* Proficiency in Microsoft Office products (Outlook, Word, and Excel).
* Experience in Customs Brokerage preferred but not required.
Pay Rate: $15.86 - $21.15/hr.
(Based on Experience)
Benefits (All Non-Union Employees)
* Compensation: Competitive base salary plus role dependent performance-based incentives.
* 401(k) Match: $1-for-$1 match up to 4% quarterly + 2% annual base contribution.
* Stock Purchase Plan: Ability to purchase Deutsche Post AG shares at a discounted rate.
* Medical: ...
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Type: Contract Location: Port Huron, US-MI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:25:28
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Summary
The Quality CMM Operators role is to create inspection programs for coordinate measuring machines and to ensure the machine is properly working throughout programming scripts and tests.
The incumbent is responsible for Gauge control and Gauge calibration.
Core Competencies
* Communication
* Energy and Stress
* Technical Capacity
* Database Concepts
* GD&T and Blue print reading
* Problem Solving
* Accountability and Dependability
* Performance Management
* Ethics and Integrity
* Analytical
Job Duties
* Calibrations of all equipment and record keeping of such equipment.
* Calibration, maintenance and repair of all CMM fixtures.
* Annual layouts
* Responsible for the dimensional part of doing a PPAP on a new product.
* R&R studies
* Capability studies
* Statistical analysis
* Customer relations
Requirements
* High School Diploma or equivalent
* 2-4 years’ work experience in related field
* Extensive mathematical knowledge
* Knowledge of basic computer hardware and applications software.
* Strong organizational skills.
* Strong communication skills (both verbal and written).
* Proficiency with database applications and administration systems, specifically Microsoft Office.
* Ability to work effectively alone and prioritize.
* Must be a highly motivated, service and team-oriented individual with an attention to detail.
* Enthusiasm for challenge and new initiatives are prerequisites.
* Strong analytical ability
* Troubleshooting ability is required
* Strong decision making and problem solving skills
* Demonstrated good internal customer service skills
* Proven good presentation skills.
* Good presentation skills
* Ability to manage multiple projects.
* Detail oriented
Requirements
* High School Diploma or equivalent
* 2-4 years’ work experience in related field
* Extensive mathematical knowledge
* Knowledge of basic computer hardware and applications software.
* Strong organizational skills.
* Strong communication skills (both verbal and written).
* Proficiency with database applications and administration systems, specifically Microsoft Office.
* Ability to work effectively alone and prioritize.
* Must be a highly motivated, service and team-oriented individual with an attention to detail.
* Enthusiasm for challenge and new initiatives are prerequisites.
* Strong analytical ability
* Troubleshooting ability is required
* Strong decision making and problem solving skills
* Demonstrated good internal customer service skills
* Proven good presentation skills.
* Good presentation skills
* Ability to manage multiple projects.
* Detail oriented
....Read more...
Type: Permanent Location: Battle Creek, US-MI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:22:26
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Your Job
Phillips-Medisize, a Molex Company, is seeking a Quality Engineer to join our teams in Wisconsin.
We have opportunities available at our New Richmond, Menomonie, and Hudson facilities.
This role will support, organize, and coordinate activities of the quality function with the goal of providing products/services that meet customer expectations.
Devise and implement continuous improvement methodology supporting manufacturing, support groups and ensure customer satisfaction is maintained.
Our Team
Phillips-Medisize, LLC, a Molex company, is a leading global provider of medical molding and assembly services.
What You Will Do
* Ensure compliance with FDA 21 CFR 820 210:211, ISO 13485, and ISO 14971.
* Review specifications and ensure adherence to material and process requirements.
* Oversee validation and verification of manufacturing processes and equipment.
* Manage documentation for change management and non-conformance reports.
* Lead investigations and root cause analysis of non-conformances.
* Author tech reports, CAPAs, compliant investigations, and validations.
* Work with suppliers to meet quality requirements.
* Support customer complaint management.
* Troubleshoot manufacturing and field issues.
* Analyze quality data and trends; identify improvement areas.
* Champion continuous improvement initiatives.
* Mentor junior quality engineers.
* Collaborate with cross-functional teams.
Who You Are (Basic Qualifications):
* Bachelor's degree or equivalent experience
* Minimum of 4 years of quality-related experience in a medical manufacturing environment
* Experience working in a regulated environment
* Knowledge of automated assembly and test procedures
* Working knowledge of regulatory requirements including FDA 21 CFR 820, ISO 13485
* Experience working with an ERP system (SAP)
* Strong data analysis skills
* Strong technical writing and problem-solving skills
* Experience in packaging, serialization, sterilization, and complaint handling
* Experience with updating the test procedures in testing equipment
What Will Put You Ahead:
* Experience in supplier quality management
* Pharmaceutical experience
LI-SD5
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
L...
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Type: Permanent Location: New Richmond, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:54
-
Your Job
Phillips-Medisize, a Molex Company, is seeking a Quality Engineer to join our teams in Wisconsin.
We have opportunities available at our New Richmond, Menomonie, and Hudson facilities.
This role will support, organize, and coordinate activities of the quality function with the goal of providing products/services that meet customer expectations.
Devise and implement continuous improvement methodology supporting manufacturing, support groups and ensure customer satisfaction is maintained.
Our Team
Phillips-Medisize, LLC, a Molex company, is a leading global provider of medical molding and assembly services.
What You Will Do
* Ensure compliance with FDA 21 CFR 820 210:211, ISO 13485, and ISO 14971.
* Review specifications and ensure adherence to material and process requirements.
* Oversee validation and verification of manufacturing processes and equipment.
* Manage documentation for change management and non-conformance reports.
* Lead investigations and root cause analysis of non-conformances.
* Author tech reports, CAPAs, compliant investigations, and validations.
* Work with suppliers to meet quality requirements.
* Support customer complaint management.
* Troubleshoot manufacturing and field issues.
* Analyze quality data and trends; identify improvement areas.
* Champion continuous improvement initiatives.
* Mentor junior quality engineers.
* Collaborate with cross-functional teams.
Who You Are (Basic Qualifications):
* Bachelor's degree or equivalent experience
* Minimum of 4 years of quality-related experience in a medical manufacturing environment
* Experience working in a regulated environment
* Knowledge of automated assembly and test procedures
* Working knowledge of regulatory requirements including FDA 21 CFR 820, ISO 13485
* Experience working with an ERP system (SAP)
* Strong data analysis skills
* Strong technical writing and problem-solving skills
* Experience in packaging, serialization, sterilization, and complaint handling
* Experience with updating the test procedures in testing equipment
What Will Put You Ahead:
* Experience in supplier quality management
* Pharmaceutical experience
LI-SD5
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
L...
....Read more...
Type: Permanent Location: Hudson, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:54
-
Your Job
Phillips-Medisize, a Molex Company, is seeking a Quality Engineer to join our teams in Wisconsin.
We have opportunities available at our New Richmond, Menomonie, and Hudson facilities.
This role will support, organize, and coordinate activities of the quality function with the goal of providing products/services that meet customer expectations.
Devise and implement continuous improvement methodology supporting manufacturing, support groups and ensure customer satisfaction is maintained.
Our Team
Phillips-Medisize, LLC, a Molex company, is a leading global provider of medical molding and assembly services.
What You Will Do
* Ensure compliance with FDA 21 CFR 820 210:211, ISO 13485, and ISO 14971.
* Review specifications and ensure adherence to material and process requirements.
* Oversee validation and verification of manufacturing processes and equipment.
* Manage documentation for change management and non-conformance reports.
* Lead investigations and root cause analysis of non-conformances.
* Author tech reports, CAPAs, compliant investigations, and validations.
* Work with suppliers to meet quality requirements.
* Support customer complaint management.
* Troubleshoot manufacturing and field issues.
* Analyze quality data and trends; identify improvement areas.
* Champion continuous improvement initiatives.
* Mentor junior quality engineers.
* Collaborate with cross-functional teams.
Who You Are (Basic Qualifications):
* Bachelor's degree or equivalent experience
* Minimum of 4 years of quality-related experience in a medical manufacturing environment
* Experience working in a regulated environment
* Knowledge of automated assembly and test procedures
* Working knowledge of regulatory requirements including FDA 21 CFR 820, ISO 13485
* Experience working with an ERP system (SAP)
* Strong data analysis skills
* Strong technical writing and problem-solving skills
* Experience in packaging, serialization, sterilization, and complaint handling
* Experience with updating the test procedures in testing equipment
What Will Put You Ahead:
* Experience in supplier quality management
* Pharmaceutical experience
LI-SD5
At Koch companies, we are entrepreneurs.
This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions.
Any compensation range provided for a role is an estimate determined by available market data.
The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.
Hiring Philosophy
All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds.
We are Military Ready and Second Chance employers.
L...
....Read more...
Type: Permanent Location: Menomonie, US-WI
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:53
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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:
Supply Chain Planning
Job Sub Function:
Planning Strategy & Capabilities
Job Category:
Professional
All Job Posting Locations:
Zug, Switzerland
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.
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):
United States - Requisition Number: R-030476
Switzerland - Requisition Number: R-032827
Ireland and Belgium - Requisition Number: R-032829
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for a Director, Digital Capability Lead! This hybrid position will be located in Titusville, New Jersey (USA).
Alternate hybrid locations may be considered at other Innovative Medicine Supply Chain hubs such as Horsham, Pennsylvania (USA); Zug, Switzerland; Cork, Ireland; or Beerse, Belgium.
As a member of the Value Chain Management (VCM) organization, the Director, Digital Capability Lead is a strategically critical leadership role within J&J IMSC.
This position is designed for a techno-functional leader with a great foundation in global digital product lifecycle management, end-to-end pharmaceutical supply chain operations, and deep experience leading transformation in sophisticated environments.
This position will have 3-4 direct team members and a group of approximately 20 people/contractors.
KEY RESPONSIBILITIES:
Strategic Digital Capability Leadership for VCM
* Shape the vision and strategy for digital capabilities in VCM, ensuring effective execution and measurable impact.
* Govern the entire product lifecycle, from discovery to scaling, fostering business adoption.
* Act as a liaison to interpret the technology and strategic priorities while handling budgets and key ...
....Read more...
Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:08
-
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:
Supply Chain Planning
Job Sub Function:
Planning Strategy & Capabilities
Job Category:
Professional
All Job Posting Locations:
Beerse, Antwerp, Belgium, Cork, Cork, Ireland, Ringaskiddy, Cork, Ireland
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.
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):
United States - Requisition Number: R-030476
Switzerland - Requisition Number: R-032827
Ireland and Belgium - Requisition Number: R-032829
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for a Director, Digital Capability Lead! This hybrid position will be located in Titusville, New Jersey (USA).
Alternate hybrid locations may be considered at other Innovative Medicine Supply Chain hubs such as Horsham, Pennsylvania (USA); Zug, Switzerland; Cork, Ireland; or Beerse, Belgium.
As a member of the Value Chain Management (VCM) organization, the Director, Digital Capability Lead is a strategically critical leadership role within J&J IMSC.
This position is designed for a techno-functional leader with a great foundation in global digital product lifecycle management, end-to-end pharmaceutical supply chain operations, and deep experience leading transformation in sophisticated environments.
This position will have 3-4 direct team members and a group of approximately 20 people/contractors.
KEY RESPONSIBILITIES:
Strategic Digital Capability Leadership for VCM
* Shape the vision and strategy for digital capabilities in VCM, ensuring effective execution and measurable impact.
* Govern the entire product lifecycle, from discovery to scaling, fostering business adoption.
* Act as a liaison to interpret the technology...
....Read more...
Type: Permanent Location: Ringaskiddy, IE-CO
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:06
-
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:
Beerse, Antwerp, Belgium
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 Innovative Medicine is hiring a Principal Scientist, Cheminformatics to join our team. The US location options for this position are Spring House, PA, Cambridge, MA, and San Diego, CA. Consideration may also be given for this position to be located in 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 that aligns with your preferred location:
USA - Requisition Number: R-026889
Belgium - Requisition Number: R-027978
We are seeking a highly skilled and innovative Principal Scientist in Cheminformatics to join our team.
While strong emphasis will be put on informatics support for our DNA Encoded Library (DEL) platform, the successful candidate will also play a broader role in establishing industry-leading small molecule informatics capabilities, supporting bench scientists in every step of the DMTA cycle and guiding them in analysis and decision-making.
This role will collaborate closely with project and platform teams to understand their ways of working and participate in the development of a future-looking informatics strategy for small molecules, including data provisioning, analytics, and visualization for hit identification and compound optimization.
Key Responsibilities:
* Lead the development and implementation of advanced cheminformatics tools for small molecule analysis and DEL informatics.
* Implement statistical approaches to improve selection of compounds for off-DNA synthesis and accelerate workups of DEL screens.
* Enhance our internal DEL ML virtual screening capabilities and apply to key projects.
* Collaborate with inter...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-11 08:19:00
-
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:
Supply Chain Deliver
Job Sub Function:
Warehouse & Distribution
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
We are searching for the best talent for a European Distribution Network Business Support Specialist to be in Beerse, Belgium!
This is a fixed term position for 12 months.
In this role, you'll collaborate across the operational distribution network of JJIM in the EMEA region - from manufacturing to European hubs in Belgium, and worldwide distribution centers - supporting the entire supply chain process.
The Business Support Specialists are responsible to ensure smooth inbound processes from system point of view (EU2) and inventory management for the European Hubs: DC Beerse & DC La Louvière.
As a Business support specialist, you will:
* Ensure smooth replenishment of Hubs and worldwide DCs by proactively supervising system flows.
* Support inventory management and resolve system issues disrupting distribution.
* Coordinate returns and sample requests within the European network.
* Drive monthly SLOB analysis and follow-up on destruction processes with stakeholders.
* Perform ad hoc inventory reconciliations and recall management.
* Optimize network efficiency and compliance through system configurations and master data updates.
* Participate in UAT and Business Testing for process changes or troubleshooting.
* Manage inbound and inventory metrics, driving performance improvements.
* Lead process improvements and lean initiatives with partners (Transportation, Operations, QA, IT).
* Support distribution readiness for New Products, Divestitures, Serialization, & End-of-Life planning.
* Maintain quality and safety compliance through SOPs, WIs, and audit readiness.
Qualifications
* Bachelor's Degree or equivalent; advanced degree or Supply Chain Certification (APICS) preferred.
* 2+ years’ experience in a complex, international environme...
....Read more...
Type: Permanent Location: Beerse, BE-VAN
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:39
-
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:
Quality
Job Sub Function:
R&D/Scientific Quality
Job Category:
Professional
All Job Posting Locations:
Danvers, Massachusetts, United States of America
Job Description:
About MedTech
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
We are searching for the best talent for Software Design Quality Engineer role to be located at Danvers, MA.
The ideal candidate for the Software Design Quality Engineer position will support various New Product Development and sustaining activities as well as play a role in product risk management, cybersecurity, change controls, and design controls.
This engineer should excel in an environment that embraces teamwork, change, risk-based decision-making and flexibility.
Be ready to make a significant contribution to a dynamic, fun, multi-disciplinary team, where a self-motivated engineer with excellent written and verbal communication skills stands ready to succeed.
Seize the opportunity today to join this collaborative, high performing team within the fastest growing business in MedTech. Come join our Abiomed team today!
Key Responsibilities:
* Support design and development activities within the software development lifecycle for Software as a Medical Device (SaMD) and Software in a Medical Device (SiMD) products.
* Use technical expertise, knowledge, and experience to rapidly innovate the companies’ medical devices for use in chronic heart failure patients.
* Facilitate and conduct risk management activities including development of Risk Management Plans, Hazard Analyses, Software Failure Modes and Effects Analysis (SFMEA) and Risk Management Reports.
* Evaluate end user needs, standards requirements, and risk evaluations to generate design requirements and engineering targets which include but are not limited to software detailed designs, software architecture and specifications.
* Participate in software development sprint cycles by supporting the software development team through attending SCRUMs, design reviews, code reviews and providing feedback of software verification and validation deliverables.
* Develop and/or review test protocols, reports, and engineering summaries
* Participate in prod...
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Type: Permanent Location: Danvers, US-MA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:25
-
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:
Quality
Job Sub Function:
Quality Assurance
Job Category:
Professional
All Job Posting Locations:
Gent, East Flanders, 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
We are looking for the best talent for a QA Associate for the CAR-T hub to be in Ghent Belgium!
Purpose: CAR-T (chimeric antigen receptor T-cell therapy) is an innovative approach to eliminate cancer cells, which work by harnessing the power of a patient’s own immune system.
They are created from the patients’ own T cells and are engineered to eliminate cancer cells expressing a specific antigen.
To support the CAR-T program in EMEA, J&J has built two CAR-T manufacturing centers in the Ghent area (Belgium).
The QC laboratories are operating from the existing J&J Beerse site.
CAR-T investigational medicinal and commercial CAR-T products are manufactured in the Ghent facilities.
In this role, you are reporting in the J&J QA CAR-T organization and work closely with your peers from Material Science and Technology, Operations and Quality Control.
The QA Associate, CAR-T Europe is responsible that product and process related investigations, complaints, batch review and release activities are accurately handled on time and in line with all ATMP/GMP requirements.
As a QA Associate, you will:
* Review and approve batch documentation to verify compliance with regulatory and company standards.
Release of incoming raw and starting materials and Final Drug Product release.
* Investigation Support: Provide technical, quality, and compliance expertise to support in-depth investigations related to deviations, complaints, and other quality issues to ensure timely resolution.
* Ensure that deviations and complaints are promptly and thoroughly investigated, with particular attention to those that may affect patient safety or product supply.
Raise issues that could have significant impacts on quality.
* Ensure that appropriate corrective and preventive actions (CAPAs) are identified and implemented in...
....Read more...
Type: Permanent Location: Gent, BE-VOV
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:23
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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:
Supply Chain Deliver
Job Sub Function:
Warehouse & Distribution
Job Category:
Business Enablement/Support
All Job Posting Locations:
Schiphol, North Holland, Netherlands
Job Description:
We are searching for the best talent for Expert Warehouse Operator to be based in Schiphol.
In this vital role, you'll ensure smooth daily operations within our Warehouse department or Distribution Center, supporting the receipt, handling, storage, and shipment of goods.
Your work will have a direct impact on our ability to deliver quality products efficiently and safely, supporting a collaborative and dynamic team that values continuous improvement.
This position offers a rewarding opportunity to contribute to a fast-paced, safe, and sustainable work environment.
If you're passionate about operational excellence and eager to grow your skills in an encouraging setting, we’d love to hear from you!
As an Expert Warehouse Operator, you will be responsible for:
* Handling, labeling, and storing materials accurately according to procedures to ensure quality and compliance.
* Receiving goods, sampling, weighing, and dispensing raw materials to support production needs.
* Managing internal and external shipments, coordinating transport, and ensuring timely delivery.
* Maintaining inventory accuracy through cycle counting and managing administrative documentation.
* Keeping workspaces and equipment clean, organized, and in excellent condition using Lean tools like visual management.
* Actively participating in continuous process improvements and sharing knowledge to enhance team performance.
Required qualifications:
* Relevant MBO diploma or equivalent education.
* 2-4 years of experience in warehouse operations or logistics.
* Proficiency in computer systems and software used for warehouse management.
* Good understanding of cGMP, EHSS, and Lean principles tailored to warehouse environments.
* Fluent in English; Dutch language skills are a plus, but not required.
Additional Details:
* This position is offered on a 12-month contract basis.
* The role involves rotating shift work, operating 7 days a week from 07:30 to 16:00.
* You'll work 2 weekends every 6 weeks, supporting a flexible and collaborative work schedule.
The anticipated base pay range for this position is 31,700 to 47.000 on an annual basis and includes 8% holiday allowa...
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Type: Permanent Location: Schiphol, NL-NH
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:22
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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:
Supply Chain Planning
Job Sub Function:
Planning Strategy & Capabilities
Job Category:
Professional
All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Titusville, New Jersey, 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.
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):
United States - Requisition Number: R-030476
Switzerland - Requisition Number: R-032827
Ireland and Belgium - Requisition Number: R-032829
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
We are searching for the best talent for a Director, Digital Capability Lead! This hybrid position will be located in Titusville, New Jersey (USA).
Alternate hybrid locations may be considered at other Innovative Medicine Supply Chain hubs such as Horsham, Pennsylvania (USA); Zug, Switzerland; Cork, Ireland; or Beerse, Belgium.
As a member of the Value Chain Management (VCM) organization, the Director, Digital Capability Lead is a strategically critical leadership role within J&J IMSC.
This position is designed for a techno-functional leader with a great foundation in global digital product lifecycle management, end-to-end pharmaceutical supply chain operations, and deep experience leading transformation in sophisticated environments.
This position will have 3-4 direct team members and a group of approximately 20 people/contractors.
KEY RESPONSIBILITIES:
Strategic Digital Capability Leadership for VCM
* Shape the vision and strategy for digital capabilities in VCM, ensuring effective execution and measurable impact.
* Govern the entire product lifecycle, from discovery to scaling, fostering business adoption.
* Act as a liaison to ...
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Type: Permanent Location: Titusville, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:18:00
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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:
Finance
Job Sub Function:
Finance Business Partners
Job Category:
People Leader
All Job Posting Locations:
Beerse, Antwerp, Belgium, Bogotá, Distrito Capital, Colombia, Cork, Cork, Ireland, Maidenhead, Berkshire, United Kingdom, Manila, National Capital, Philippines, New Brunswick, New Jersey, United States of America, Prague, Czechia, Zug, Switzerland
Job Description:
Job Title - Technology & Data Solutions Lead, IMFT
Reporting to - Head of Technology & Data Solutions, IMFT
# direct / indirect reports – 3 / 6
Location: Global role, location could be within EMEA, NA, APAC or LATAM
Position Description Summary
We are seeking a Director, IM Technology & Data Solutions to play a pivotal role in transforming our finance operations and enabling next-level digital innovation.
This senior leadership role is integral to the Innovative Medicine Finance Transformation (IMFT) program, and you will be responsible for ensuring seamless integration of technology solutions and data governance across our finance functions.
As the Technology & Data Solutions Lead for integrated technologies, you will oversee and manage the implementation of technical solutions while ensuring that our data governance frameworks, digital transformation efforts, and analytical capabilities are aligned with business goals.
You will drive the integration of solutions that enable data-driven decision-making, streamline operations, and enhance overall patient-centric value creation. You will work closely with our Global Process Owners in our Value Stream teams, understanding business process requirements, as well as with our J&J Technology team, Finance Technology team, and third-parties to build the technology solutions.
This is an exciting opportunity to be at the forefront of a finance transformation in the Innovative Medicine space, shaping the future of finance operations and contributing to patient-centric outcomes.
Key interactions
Collaborative Leader: Ability to engage and lead cross-functional teams, including finance, technology, and business partners, to drive successful technology deployments.
Close collaboration and joint decision-making with value stream leaders will be an essential success factor in ensuring that designed approaches are reflected and supported by future technology solutions.
Within IM FIN: Value Stream Leads, Global Process Owners, PMO, Strategy & Value Management, Tax, Compliance, Transcen...
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Type: Permanent Location: Zug, CH-ZG
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:55
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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:
Cambridge, Massachusetts, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, 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 Innovative Medicine is hiring a Principal Scientist, Cheminformatics to join our team. The US location options for this position are Spring House, PA, Cambridge, MA, and San Diego, CA. Consideration may also be given for this position to be located in 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 that aligns with your preferred location:
USA - Requisition Number: R-026889
Belgium - Requisition Number: R-027978
We are seeking a highly skilled and innovative Principal Scientist in Cheminformatics to join our team.
While strong emphasis will be put on informatics support for our DNA Encoded Library (DEL) platform, the successful candidate will also play a broader role in establishing industry-leading small molecule informatics capabilities, supporting bench scientists in every step of the DMTA cycle and guiding them in analysis and decision-making.
This role will collaborate closely with project and platform teams to understand their ways of working and participate in the development of a future-looking informatics strategy for small molecules, including data provisioning, analytics, and visualization for hit identification and compound optimization.
Key Responsibilities:
* Lead the development and implementation of advanced cheminformatics tools for small molecule analysis and DEL informatics.
* Implement statistical approaches to improve selection of compounds for off-DNA synthesis and accelerate workups of ...
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Type: Permanent Location: Spring House, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:37
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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:
Strategic Planning
Job Category:
Professional
All Job Posting Locations:
Raritan, New Jersey, United States of America
Job Description:
Johnson & Johnson Innovative Medicine is currently recruiting for a Director, Global Portfolio Strategy & Operations, Global Commercial Strategy Organization, Global Commercial Strategy Organization to be located in Raritan, NJ.
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
Purpose: The Director, Global Portfolio Strategy & Operations reports to the Senior Director, Global Portfolio & New Business Development.
In this role, the Director will support the WW Chairman for Innovative Medicine and Company Group Chairman, Global Commercial Strategy Organization, by leading transformational cross-functional strategic initiatives including the strategic plan for the pharmaceutical sector, as well as developing perspectives on key topics for internal and external communications and overall J&J IM Communication Branding.
The Director will also drive process, content and business impact for large, complex, and highly visible projects.
Key Responsibilities
* Provide a range of strategy and operations leadership for the Group Operating Committee and/or the Global Commercial Strategy organization
* Design, structure and lead critical and highly visible strategic projects across J&J Innovative Medicine
* Execute stakeholder engagement plans to drive alignment with senior leaders and develop pragmatic strategies and implementation plans
* Take full accountability for successful project delivery and demonstrated business impact
* Formulate points of view on a range of topics pertinent to Johnson & Johnson, through primary and secondary research and analysis
* Lead the process to identify, gather and prioritize key goals and objectives at different levels of the organization and establish key metrics to measure performance
* Support the Worldwide Chairman and/or Company Group Chairman, Global Commercial...
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Type: Permanent Location: Raritan, US-NJ
Salary / Rate: Not Specified
Posted: 2025-09-11 08:17:34
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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:
Technology Product & Platform Management
Job Sub Function:
Technical Product Management
Job Category:
People Leader
All Job Posting Locations:
Wilson, North Carolina, United States of America
Job Description:
Johnson & Johnson is recruiting for an IT Manager, Technical Product Owner located in Wilson, North Carolina, USA.
J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients.
The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience.
J&J’s significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.
As an integral member of a high-performance team, the IT Manager and Technical Product Owner will be responsible for developing and owning the strategic vision, prioritization, and deployment of IT infrastructure and digital products to support new manufacturing site-specific business capabilities.
This role will serve as the product owner for all technology products specific to the site, driving the product vision and setting priorities.
Furthermore, the individual will establish a robust end-to-end IT operational support framework in collaboration with the IT Site Leadership Team and business partners.
This includes providing ongoing support to continuously enhance process efficiencies, reliability, and cybersecurity.
Key Responsibilities
Product Ownership
* Product owner for Site Operational Excellence services and Site-Specific Digital Products.
Includes end to end digital eco-system and integration within the site.
* Lead digital enablement initiatives for new site launches and expansion projects.
Product Vision and Strategy
* Develop and communicate the product vision, strategy, and roadmap based on business needs, aligning with global MAKE IT objectives and ensuring effective stakeholder communication.
* Ensure site digital products align with global product categories to maximize business value and facilitate standardization across sites.
* Support business stakeholders and IT leaders in crafting robust business cases.
Product Management
* Collaborate with cross-functional site stakeholders (MTO, R&D, TO&R, enterpr...
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Type: Permanent Location: Wilson, US-NC
Salary / Rate: Not Specified
Posted: 2025-09-11 08:16:51
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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:
Supply Chain Deliver
Job Sub Function:
Warehouse & Distribution
Job Category:
Business Enablement/Support
All Job Posting Locations:
CN038 Suzhou Changyang Rd
Job Description:
Communicates technical project plans and delegation of key assignments within the department for customer-specific warehouse and distribution needs and requirements.
Inspects and monitors warehouse delivery scheduling and flow into the warehouse database to ensure smooth product processing and movement.
Loads procedures for warehousing pick and pull into department database, including wave picking, batch picking, and zone picking, to ensure efficient product out-the-door movement and quick cycle times.
Applies technical expertise to support product forecasting into the warehouse by analyzing data-driven customer product history and recommending future product ordering processes to management.
Acts as a subject matter expert in the technical aspects of warehousing and distribution solutions and develops new ideas for continuous improvement, tailored to specific customer’s supply chain delivery needs.
Assists with the stringent monitoring of product availability on an ongoing basis, reviewing key performance measures established by management to help ensure core targets and objectives are being met.
Demonstrates Johnson & Johnson’s Leadership Imperatives and Credo.
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Type: Permanent Location: Suzhou, CN-32
Salary / Rate: Not Specified
Posted: 2025-09-11 08:16:19
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Darby, PA - Seeking Emergency Medicine Practice Administrator
Everybody Has A Role to Play in Transforming Healthcare
As a Practice Administrator, you play a vital role in our mission to improve lives.
Provide direct, business operations support to our medical directors, site physician partners, advanced providers and scribe (when applicable) employees.
At Vituity we know the impact you can have.
Join the Vituity Team.
At Vituity we've cultivated an environment where passion thrives, and success comes through shared purpose.
We were founded in a culture that values team accomplishments more than individual achievements, an approach we call "culture of brilliance." Together, we leverage our strengths and experiences to make a positive impact in our local communities.
We foster this through shared goals and helping our colleagues succeed, and we also understand the importance of recognition, taking the time to show appreciation and gratitude for a job well done.
Vituity Locations: Vituity has opportunities at 475 sites across the country, serving 9 million patients a year.
With Vituity, if you ever need to move, you can take your job with you.
The Opportunity
* Act as the operational administrator for the site Vituity leadership and as the interface for the practice to the hospital and community.
* Act as the front-line liaison for the provider team with hospital C-Suite, nursing leadership, nursing staff, and Vituity support team.
* Provide executive support to the site medical director and site management team to meet contract expectations.
* Provide support for all site financials to include, but not limited to, contract stipends, expense reimbursements, and site payroll timecards.
* Act as the super user for all Vituity software applications and as a point person for hospital software and hardware systems.
* As appropriate to site practice, provide support to Vituity providers acting as a percipient witness in criminal or civil disputes including, but not limited to, receiving and routing subpoenas, scheduling depositions and trial testimony as applicable, development of a provider fee schedule, and including malpractice carrier as appropriate.
* Provide office management to include, but not limited to, all aspects of meeting management, office systems, supplies, site events, and customer service.
* As applicable to the practice line, facilitate all aspects of the daily patient census and attend daily multi-disciplinary rounds.
* As applicable to the site practice, responsible for all aspects of the site clinical schedules to ensure adequate coverage with no disruption to patient care.
* Collect, track, and analyze all site financial and operational data.
* Project management as needed of the site operational programs to include, but not limited to, Operations Meetings, Patient Experience Program, Quality/Performance Improvement Program, Advanced Provider and/or Scribe Programs, and...
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Type: Permanent Location: Darby, US-PA
Salary / Rate: Not Specified
Posted: 2025-09-11 08:14:00
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Wilmington, DE - Seeking Emergency Medicine Practice Administrator
Everybody Has A Role to Play in Transforming Healthcare
As a Practice Administrator, you play a vital role in our mission to improve lives.
Provide direct, business operations support to our medical directors, site physician partners, advanced providers and scribe (when applicable) employees.
At Vituity we know the impact you can have.
Join the Vituity Team.
At Vituity we've cultivated an environment where passion thrives, and success comes through shared purpose.
We were founded in a culture that values team accomplishments more than individual achievements, an approach we call "culture of brilliance." Together, we leverage our strengths and experiences to make a positive impact in our local communities.
We foster this through shared goals and helping our colleagues succeed, and we also understand the importance of recognition, taking the time to show appreciation and gratitude for a job well done.
Vituity Locations: Vituity has opportunities at 475 sites across the country, serving 9 million patients a year.
With Vituity, if you ever need to move, you can take your job with you.
The Opportunity
* Act as the operational administrator for the site Vituity leadership and as the interface for the practice to the hospital and community.
* Act as the front-line liaison for the provider team with hospital C-Suite, nursing leadership, nursing staff, and Vituity support team.
* Provide executive support to the site medical director and site management team to meet contract expectations.
* Provide support for all site financials to include, but not limited to, contract stipends, expense reimbursements, and site payroll timecards.
* Act as the super user for all Vituity software applications and as a point person for hospital software and hardware systems.
* As appropriate to site practice, provide support to Vituity providers acting as a percipient witness in criminal or civil disputes including, but not limited to, receiving and routing subpoenas, scheduling depositions and trial testimony as applicable, development of a provider fee schedule, and including malpractice carrier as appropriate.
* Provide office management to include, but not limited to, all aspects of meeting management, office systems, supplies, site events, and customer service.
* As applicable to the practice line, facilitate all aspects of the daily patient census and attend daily multi-disciplinary rounds.
* As applicable to the site practice, responsible for all aspects of the site clinical schedules to ensure adequate coverage with no disruption to patient care.
* Collect, track, and analyze all site financial and operational data.
* Project management as needed of the site operational programs to include, but not limited to, Operations Meetings, Patient Experience Program, Quality/Performance Improvement Program, Advanced Provider and/or Scribe Programs...
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Type: Permanent Location: Wilmington, US-DE
Salary / Rate: Not Specified
Posted: 2025-09-11 08:13:55
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Ardurra Company is seeking an experienced Professional Engineer to join our team as a Land Development Project Manager in Coeur d'Alene, ID or Spokane, WA!
Required Qualifications
* Bachelor’s Degree in Civil Engineering
* PE License for Idaho or Washington
* 8+ years of related experience within specific region in site design and permitting with notable experience managing clients and employees
* Business Development/Network within region, highly preferred
* Strong communication skills both written and verbal
* Strong organizational, analytical, and problem-solving skills
* Proficient working knowledge of Microsoft Office Suites
* Highly self-motivated self-starter, able to forecast and initiate project management tasks
Key Responsibilities
* Oversee projects, staff, and client relations
* Work directly with governmental agencies
* Responsible for land development projects with a strong background in:
* Grading
* Drainage
* Wet and Dry Utilities
* Roadway design
* Overseeing/preparing lotting layouts
Identify, analyze, and execute business development opportunities within specific network region
Prepare scope and fee estimates
Prepare invoicing
Work within a multi-disciplinary engineering environment
Strong background in construction practices
Physical Requirements
* Prolonged periods sitting at a desk and working on a computer
* Ability to navigate various locations and settings of the company
* Occasionally lift and/or move up to 25 pounds
* Must possess a valid driver’s license and be able to safely operate a vehicle
Salary
$130,000 - $160,000
Why Ardurra?
While Ardurra offers competitive compensation and rich benefits programs, it is our culture that truly sets us apart from our peers.
We nurture a family-like culture, striving to create a work environment that is enjoyable, challenging and rewarding but also fun.
We are acutely focused on developing our staff, whether through our internal Ardurra Academy or through our industry-leading Leadership program.
We have made a deliberate and focused commitment to nurture a people-centric culture where people are: valued as individuals; supported in their professional and career development with multiple, varied career paths; provided the tools and resources to be successful, engaged, and satisfied in their work; and positive benefits, time-off programs, and flexibility to help maintain a healthy balance between work and home.
Ardurra is an Equal Opportunity/ Affirmative Action Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, gender identity or sexual orientation.
NOTICE TO THIRD PARTY AGENCIES:
Ardurra does not accept unsolicited resumes from recruiters or employment agencies.
In the absence of a ...
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Type: Permanent Location: Coeur d Alene, US-ID
Salary / Rate: Not Specified
Posted: 2025-09-11 08:12:41
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Long Beach, CA - Seeking Anesthesiology Practice Administrator
Everybody Has A Role to Play in Transforming Healthcare
As a Practice Administrator, you play a vital role in our mission to improve lives.
Provide direct, business operations support to our medical directors, site physician partners, advanced providers and scribe (when applicable) employees.
At Vituity we know the impact you can have.
Join the Vituity Team.
At Vituity we've cultivated an environment where passion thrives, and success comes through shared purpose.
We were founded in a culture that values team accomplishments more than individual achievements, an approach we call "culture of brilliance." Together, we leverage our strengths and experiences to make a positive impact in our local communities.
We foster this through shared goals and helping our colleagues succeed, and we also understand the importance of recognition, taking the time to show appreciation and gratitude for a job well done.
Vituity Locations: Vituity has opportunities at 475 sites across the country, serving 9 million patients a year.
With Vituity, if you ever need to move, you can take your job with you.
The Opportunity
* Act as the operational administrator for the site Vituity leadership and as the interface for the practice to the hospital and community.
* Act as the front-line liaison for the provider team with hospital C-Suite, nursing leadership, nursing staff, and Vituity support team.
* Provide executive support to the site medical director and site management team to meet contract expectations.
* Provide support for all site financials to include, but not limited to, contract stipends, expense reimbursements, and site payroll timecards.
* Act as the super user for all Vituity software applications and as a point person for hospital software and hardware systems.
* As appropriate to site practice, provide support to Vituity providers acting as a percipient witness in criminal or civil disputes including, but not limited to, receiving and routing subpoenas, scheduling depositions and trial testimony as applicable, development of a provider fee schedule, and including malpractice carrier as appropriate.
* Provide office management to include, but not limited to, all aspects of meeting management, office systems, supplies, site events, and customer service.
* As applicable to the practice line, facilitate all aspects of the daily patient census and attend daily multi-disciplinary rounds.
* As applicable to the site practice, responsible for all aspects of the site clinical schedules to ensure adequate coverage with no disruption to patient care.
* Collect, track, and analyze all site financial and operational data.
* Project management as needed of the site operational programs to include, but not limited to, Operations Meetings, Patient Experience Program, Quality/Performance Improvement Program, Advanced Provider and/or Scribe Programs, an...
....Read more...
Type: Permanent Location: Laguna Hills, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:46:04
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Long Beach, CA - Seeking Anesthesiology Practice Administrator
Everybody Has A Role to Play in Transforming Healthcare
As a Practice Administrator, you play a vital role in our mission to improve lives.
Provide direct, business operations support to our medical directors, site physician partners, advanced providers and scribe (when applicable) employees.
At Vituity we know the impact you can have.
Join the Vituity Team.
At Vituity we've cultivated an environment where passion thrives, and success comes through shared purpose.
We were founded in a culture that values team accomplishments more than individual achievements, an approach we call "culture of brilliance." Together, we leverage our strengths and experiences to make a positive impact in our local communities.
We foster this through shared goals and helping our colleagues succeed, and we also understand the importance of recognition, taking the time to show appreciation and gratitude for a job well done.
Vituity Locations: Vituity has opportunities at 475 sites across the country, serving 9 million patients a year.
With Vituity, if you ever need to move, you can take your job with you.
The Opportunity
* Act as the operational administrator for the site Vituity leadership and as the interface for the practice to the hospital and community.
* Act as the front-line liaison for the provider team with hospital C-Suite, nursing leadership, nursing staff, and Vituity support team.
* Provide executive support to the site medical director and site management team to meet contract expectations.
* Provide support for all site financials to include, but not limited to, contract stipends, expense reimbursements, and site payroll timecards.
* Act as the super user for all Vituity software applications and as a point person for hospital software and hardware systems.
* As appropriate to site practice, provide support to Vituity providers acting as a percipient witness in criminal or civil disputes including, but not limited to, receiving and routing subpoenas, scheduling depositions and trial testimony as applicable, development of a provider fee schedule, and including malpractice carrier as appropriate.
* Provide office management to include, but not limited to, all aspects of meeting management, office systems, supplies, site events, and customer service.
* As applicable to the practice line, facilitate all aspects of the daily patient census and attend daily multi-disciplinary rounds.
* As applicable to the site practice, responsible for all aspects of the site clinical schedules to ensure adequate coverage with no disruption to patient care.
* Collect, track, and analyze all site financial and operational data.
* Project management as needed of the site operational programs to include, but not limited to, Operations Meetings, Patient Experience Program, Quality/Performance Improvement Program, Advanced Provider and/or Scribe Programs, an...
....Read more...
Type: Permanent Location: Long Beach, US-CA
Salary / Rate: Not Specified
Posted: 2025-09-10 08:45:55
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Cayenta is seeking a forward-thinking AI Engineer to join our R&D team and bring practical Artificial Intelligence capabilities to our Enterprise Resource Planning (ERP) and Customer Information System (CIS) platforms.
This role is focused on leveraging existing AI tools, frameworks, and orchestration platforms—not building foundational AI models from scratch.
You’ll be applying AI technologies like LangChain, Langflow, Azure AI Studio, Hugging Face, and OpenAI APIs, as well as orchestration protocols like A2A or MCP, to deliver real features such as AI-powered customer service agents, ERP copilots, and semantic document search tools.
You’ll work collaboratively across teams to experiment, prototype, and deliver production-ready AI functionality that improves user experiences and business outcomes.
The AI Engineer reports to the Director of Research & Development, with a preference for candidates based in Canada.
What Will Be Your New Role:
* Develop AI-augmented functionality embedded in Cayenta’s ERP and CIS applications to support user efficiency and intelligent automation.
* Design and build intelligent CSR-facing agents, RAG-enabled copilots, and context-aware assistants for operations and customer service teams.
* Utilize AI orchestration tools like LangChain, Langflow, and cloud-based AI platforms (e.g., Azure OpenAI, OpenAI, Hugging Face) to quickly prototype and refine solutions.
* Integrate AI solutions into our Go/.Net/C#/React/Python based architecture, working closely with frontend/backend developers to ensure seamless user experiences.
* Implement semantic search, prompt engineering, vector-based retrieval, and agent chaining using modern LLM techniques.
* Process unstructured content (e.g., PDFs, emails, knowledge bases) to enable intelligent AI interactions within enterprise workflows.
* Iterate rapidly on prototypes using internal feedback, balancing feasibility, performance, and value.
* Ensure all AI solutions are aligned with Cayenta’s data governance, security, and responsible AI practices.
What Are We Looking For:
* 2–5 years of relevant experience in software development, AI tooling, or AI feature integration.
* Bachelor’s degree in Computer Science, Software Engineering, Data Science, or a related field.
* Strong working knowledge of AI application development using platforms such as:
+ LangChain, Langflow, OpenAI APIs
+ Azure AI Studio, Hugging Face, or similar GenAI tools
* Solid grasp of key AI/LLM concepts, including:
+ Retrieval-Augmented Generation (RAG)
+ Prompt engineering
+ Semantic search and vector embeddings
+ Agent orchestration and task chaining
* Proficiency with Python, or other backend frameworks, and experience integrating APIs or services into enterprise systems.
* Familiarity with low-code/no-code AI platforms, and comfort working across different layers ...
....Read more...
Type: Permanent Location: Ottawa, CA-ON
Salary / Rate: 140000
Posted: 2025-09-10 08:38:40
