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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
At Bristol Myers Squibb we are reimagining the future of cell therapy.
With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.
If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
Position Summary:
The Lead Manufacturing Associate, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs.
The Lead Manufacturing Associate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind, with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy.
Shifts Available:
6am – 6pm, rotating schedule including holidays and weekends
Responsibilities:
* Performing patient process unit operations and support operations described in standard operating procedures and batch records.
* Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
* Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements.
* Completing training assignments to ensure the necessary technical skills and knowledge.
* Working in a cleanroom environment and performing aseptic processing; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements.
* Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations.
* Demonstrating strong practical and theoretical knowledge of work.
* Solving complex problems; taking new perspectives using existing solutions
* Identifying innovation solutions
* Setting up manufacturing areas and equipment/fixtures; performing facility and equipment commissioning activities.
* Working closely with Manufacturing Managers to ensure seamless pass down and communication of operational status.
* Working with production planning and leadership to execute daily unit...
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Type: Permanent Location: Devens, US-MA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:44
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
This territory includes: All of New York State- The major cities are Buffalo, Syracuse, Albany, and Binghamton
As part of the commercial organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology products in a defined geography.
* The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.
* The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment. CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations. CNC interactions are aligned with on-label commercial strategies and the needs expressed by customers.
* CNCs may develop relationships with oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.
* CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.
Product responsibilities may change based on franchise and business needs.
Customer Focus
* Develop and maintain relationships with academic and community HCPs within assigned geography to provide on-label clinical and product education for BMS hematology and oncology products.
The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing on-label approved marketing materials.
* Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
* Demonstrate proficiency in using available on-label CNC resources and presentations.
Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal-guidelines and directives.
* Consistently evaluate the impact of CNC activities in an account a...
....Read more...
Type: Permanent Location: Buffalo, US-NY
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:43
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Working with Us
Challenging.
Meaningful.
Life-changing.
Those aren’t words that are usually associated with a job.
But working at Bristol Myers Squibb is anything but usual.
Here, uniquely interesting work happens every day, in every department.
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.
You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams.
Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Read more: careers.bms.com/working-with-us.
Position Summary:
We are seeking a strong Full Stack Developer to serve in an AI‑first, agile product team supporting Global Development Operations (GDO).
This role is responsible for developing and operating AI-native products where large language models, agentic workflows, and data‑driven intelligence are the default approach to solving business problems—not an add‑on.
The ideal candidate will bring deep hands-on programming experience delivering Generative and Agentic AI solutions in a regulated environment.
Specific Responsibilities:
* Develop and maintain LLM-native and agentic applications as long-lived products, incorporating human in the loop patterns, continuous learning, monitoring, and governance as part of the standard operating model.
Frameworks include Claude, OpenAI, AWS Bedrock, and LangChain.
* Develop and maintain scalable, stable, reliable, and secure applications using Python/Java and modern frontend frameworks like React JS.
Leverage vibe coding best practices to build production-grade applications and prototypes faster.
* Responsible for the support, maintenance, and continuous improvement of a portfolio of SaaS and in-house applications, ensuring high availability, performance, and operational stability.
* Partner with business and technology stakeholders to manage application support, incident resolution, enhancements, and lifecycle activities across multiple enterprise platforms.
* Implement microservices-based solutions on AWS cloud platform.
* Incorporate microservices, APIs, MCPs and event-driven processes.
* Implement CI/CD practices for software applications.
* Monitor model performance in production and manage model drift, retraining, and rollback strategies.
* Use critical thinking to investigate issues with systems and data, and identify solutions for short-term remediation and long-term strategy.
Requirements:
* Must have a minimum of 2 years of related work experience in software development; Pharma/Life Sciences experience is a plus.
* B...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:43
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
As we continue to evolve our People capabilities, we are seeking a Director, Talent Acquisition Innovation to support the strategic reimagining and modernization of our talent acquisition function.
This role will serve as a key contributor to multiple TA transformation initiatives, including but not limited to driving process redesign, technology enablement, workforce planning integration, and capability building to create a scalable, data-driven, and client-centric recruiting model.
The Director will partner closely with HR leadership, business stakeholders, TA operations, and the TA Leadership team to ensure the function is positioned to attract world-class talent in support of BMS's patient-focused mission.
Key Responsibilities
Strategy & Transformation Leadership
* Lead the design and execution of a multi-year Talent Acquisition transformation roadmap, including process redesign, operating model evolution, and technology modernization
* Identify and prioritize opportunities to improve recruiter effectiveness, candidate experience, hiring manager partnership, time-to-fill, and NPS across all talent segments
* Drive alignment between TA transformation initiatives and BMS enterprise HR strategy, workforce planning, and organizational goals
* Develop change management strategies and communication plans to ensure successful adoption of new tools, processes, and ways of working
Technology & Data
* Support the project governance and strategy stewardship of the TA technology stack including tech stack consolidation and AI-powered enhancements across the TA lifecycle.
* Establish and govern TA analytics frameworks in partnership with BMS’ Analytics, People Science, and People Services organizations — defining KPIs, dashboards, and reporting cadences that provide actionable insights to business and HR leaders.
Process Excellence & Operational Model
* Lead sub teams to redesign and standardize end-to-end recruiting processes globally, ensuring consistency, compliance, and scalability
* Partner with TA Operations, HR COEs, and external vendors to build a best-in-class, efficient delivery model
* Define and implement quality standards for interviews, selection, and offer processes in alignment with legal and regulatory requirements
Indirect Team Leadership + Project Support
* Lead and support multiple transformation teams t...
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Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:42
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
This territory includes: Memphis, TN, Baton Rouge, New Orleans, and Lafayette, LA and Jackson MS.
As part of the Oncology Field Medical organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology and oncology products in a defined geography.
* The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.
* The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment. CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations. CNC interactions are aligned with medical strategies and the needs expressed by customers.
* CNCs may develop relationships with hematology or oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.
* CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.
Product responsibilities may change based on franchise and business needs.
Customer Focus
* Develop and maintain relationships with academic and community HCPs within assigned geography to provide clinical and product education for BMS hematology and oncology products.
The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing approved education materials.
* Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
* Demonstrate proficiency in using available on-label CNC resources and presentations.
Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal guidelines and directives.
* Consistently evaluate the impact ...
....Read more...
Type: Permanent Location: Baton Rouge, US-LA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:41
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
The General Manager, Devens is the senior leader accountable for the end-to-end performance, compliance, and strategic direction of BMS’s large-scale commercial biologics Global Business Unit (GBU) operations at Devens, and serves as the Campus Lead for the full Devens site, spanning both the GBU Biologics organization and the Cell Therapy business unit.
This role oversees all GBU Biologics site operations at Devens – from cell culture and manufacturing sciences & technology (MS&T) to large-scale commercial drug substance production – with full accountability for talent development, safety, quality, regulatory compliance, supply reliability, and cost management across the Biologics organization.
As Campus Lead, the General Manager also owns end-to-end site services and shared infrastructure – Site Engineering, Environmental Health & Safety, Security, and Facilities – that support both the GBU Biologics and Cell Therapy business units operating on the Devens campus, ensuring both organizations have the capacity, capabilities, and infrastructure to deliver on their respective missions.
A defining focus of this role over the next several years is leading the transformation and integration of the GBU Biologics and Cell Therapy business units at Devens – building a single, unified campus operating model, governance structure, and culture that harmonizes site services, talent, and ways of working across both modalities.
This includes championing innovative, digitally enabled and AI-driven transformation – advanced analytics, automation, digital twins, and other Industry 4.0 capabilities – to reimagine site processes, accelerate integration, and establish Devens as a “smart campus” that delivers sustainable competitive advantage.
The General Manager also serves as the primary representative of the Devens campus both within the global manufacturing network (driving adoption of world-class standards and sharing best practices across BMS’s network of manufacturing sites) and externally (engaging with regulatory authorities, government officials, industry partners, and the local community to uphold the Company’s reputation and advance strategic initiatives).
This position is pivotal in ensuring that the Devens campus remains a world-class, innovative biologics and cell therapy manufacturing hub that reliably delivers life-saving medicin...
....Read more...
Type: Permanent Location: Devens, US-MA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:41
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary:
We are seeking a Manager, Full Stack Engineer to serve in an AI‑first, agile product team supporting Global Development Operations (GDO).
This role is accountable for designing, building, and operating AI‑native products where large language models, agentic workflows, and data‑driven intelligence are the default approach to solving business problems—not an add‑on.
The ideal candidate brings hands‑on engineering expertise and proven experience delivering production‑grade Generative and Agentic AI solutions in a regulated environment.
This individual will help shape how products are designed, developed, delivered, and continuously improved, embedding AI into core workflows to augment decision‑making, automate execution, and scale impact across GDO.
Specific Responsibilities:
* Design and maintain LLM‑native and agentic systems as long‑lived products, incorporating human‑in‑the‑loop patterns, continuous learning, monitoring, and governance as part of the standard operating model.
Frameworks include Claude, OpenAI, AWS Bedrock, and LangChain.
* Partner with product managers and GDO stakeholders to identify opportunities where AI can augment human decision‑making, automate execution, and create step‑change improvements in clinical and operational workflows.
* Design, develop, and maintain secure, scalable applications using Python/Java/Node JS/React JS.
* Responsible for the support, maintenance, and continuous improvement of a portfolio of SaaS and in-house applications, ensuring high availability, performance, and operational stability.
* Partner with business and technology stakeholders to manage application support, incident resolution, enhancements, and lifecycle activities across multiple enterprise platforms.
* Incorporate microservices, APIs, MCPs, event-driven processes, and middleware within enterprise systems.
* Use critical thinking to investigate issues with systems and data, and identify solutions for short-term remediation and long-term strategy.
* Implement CI/CD practices for software applications.
* Monitor model performance in production and manage model drift, retraining, and rollback strategies.
* Ensure compliance with data governance, privacy, and security standards.
Requirements:
* Must have a minimum of 5 years of strong experience in software engineering; Pharma/Life Sc...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:40
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Working with Us
Challenging.
Meaningful.
Life-changing.
Those aren’t words that are usually associated with a job.
But working at Bristol Myers Squibb is anything but usual.
Here, uniquely interesting work happens every day, in every department.
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it.
You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams.
Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Read more: careers.bms.com/working-with-us.
At Bristol Myers Squibb we are reimagining the future of cell therapy.
With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.
If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
BMS Cell Therapy Manufacturing is seeking a Senior Manufacturing Associate, Cell Therapy that brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs.
The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind.
We are searching for enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy.
Shifts Available:
6pm - 6am, rotating shift including holidays and weekends, onsite
Responsibilities:
* Execute operations described in standard operating procedures and batch records.
* Demonstrates strong practical and theoretical knowledge in their work.
* Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
* Solves simple problems; takes new perspectives using existing solutions.
* Performs tasks in a manner consistent with the safety policies, quality systems, and GMP requirements.
* Completing training assignments to ensure the necessary technical skills and knowledge.
* Training others on SOPs, Work Instructions to successfully complete manufacturing operations.
* Supports investigations.
* Identifies innovative solutions.
* Assisting in setting up manufacturing areas and equipment/fixtures.
Perform facility and equipment commissioning activities.
* Writing manufacturing operating procedures that are technically sound, promote effective and efficient operations, and comply...
....Read more...
Type: Permanent Location: Devens, US-MA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:39
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
Partners with the Global Program Lead (GPL) and Global Project Manager (GPM) to co-lead the strategic and operational planning and decision-making process with a BMS Global Program Team (GPT) in early and/or late development.
The Associate Director PM will provide content expertise to the timing, costs, and resources required for development programs and be able to successfully deliver their program(s) milestones and goals.
As the strategic partner and operational lead for development and lifecycle management programs, the Associate Director GPM works to ensure that cross-functional teams operate effectively, fostering positive team dynamics and championing BMS’ operating model.
Duties/Responsibilities
*
+ The PM partners closely with the Global Program Lead (GPL) and Global Project Manager (GPMT) to lead sub-teams of the Global Program Team (GPT) to drive the development of integrated, efficient, and cross-functional program execution plans.
+ Coordinates and plans the activities for the GPT, including milestone setting, budget forecasting, resource planning, scenario planning, and developing an integrated program plan based on cross-functional inputs and assumptions.
+ Facilitates team goal setting and tracking to ensure adherence to plan and strategy and in preparation for end of year team evaluation process.
+ Manages all associated GPT sub-teams and tracking integrated deliverables and preparing the GPT for governance interactions at program inflection points.
+ The PM is accountable for integrated cross-functional planning bringing together diverse functional plans and strategies, definition of the program operational strategy, management of timelines, budget, quality, and risk assessment and mitigation.
+ The PM works independently to provide best in class operations and project management expertise to drive the GPT and sub-teams toward execution excellence.
The PM provides an independent voice to shape the overall project strategy and drive optimal decisions for the broader portfolio value.
+ At the associate director level, the Project Manager (PM) is accountable for one or more GPTs and associates sub-teams of moderate complexity in the early/late development space and is expected to be autonomous in their day-to-day work.
The Project Manager may also serve as part of a...
....Read more...
Type: Permanent Location: Princeton, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:39
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
This territory includes: Indianapolis, Dayton, Columbus, Fort Wayne, Bloomington
As part of the Oncology Field Medical organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology and oncology products in a defined geography.
* The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.
* The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment. CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations. CNC interactions are aligned with medical strategies and the needs expressed by customers.
* CNCs may develop relationships with hematology or oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.
* CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.
Product responsibilities may change based on franchise and business needs.
Customer Focus
* Develop and maintain relationships with academic and community HCPs within assigned geography to provide clinical and product education for BMS hematology and oncology products.
The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing approved education materials.
* Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
* Demonstrate proficiency in using available on-label CNC resources and presentations.
Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal guidelines and directives.
* Consistently evaluate the impact of CNC activities i...
....Read more...
Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:38
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Life at BMS
At RayzeBio, every day is an opportunity to ignite meaningful change.
As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology.
Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.
Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do.
From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients.
Learn more about RayzeBio: https://careers.bms.com/rayzebio/
Job Title: Facilities Maintenance Supervisor
Department: Facilities Engineering
Location: Indianapolis, IN
FLSA Status: Exempt
Reports To: Associate Director, Facilities Engineering
Direct Reports: 3–5 (Facilities Technicians)
Summary
The Facilities Maintenance Supervisor leads the day-to-day operation, maintenance, and upkeep of building systems and infrastructure at RayzeBio's radiopharmaceutical manufacturing site in Indianapolis.
This role directly supervises a team of 3–5 Facilities Technicians, coordinating and prioritizing preventive and corrective maintenance activities across HVAC, electrical, plumbing, chilled water, compressed air, and emergency power systems in both cleanroom and non-cleanroom environments.
Acting as the primary point of contact for day-to-day contractor activity, the Supervisor manages vendor scheduling, work quality, and site access for calibration, repair, test and air balance (TAB), HEPA certification, and minor improvement projects, escalating larger capital or engineering initiatives to the Associate Director of Facilities Engineering.
This position bridges hands-on technical execution with first-line people leadership, ensuring the technician team is deployed effectively, trained, and held accountable to safety, quality, and GMP standards, while keeping site leadership informed on maintenance performance, backlog, compliance status, and contractor-related quality issues.
Job Responsibilities
Essential duties and responsibilities include the following.
Other duties may be assigned.
* Directly supervise, schedule, and coach a team of 3–5 Facilities Technicians, assigning daily work, reviewing performance, and supporting hiring, onboarding, and development.
* Plan and prioritize preventive and corrective maintenance work orders across HVAC, electrical, plumbing, chilled water, compressed air, backup generator, UPS, and lighting systems to minimize downtime and ensure continuity of operations.
* Serve as the primary day-to-day site contact for contractors and vendors performing maintenance, calibration, and minor improvement work, coordinating scheduling, site access, and scope confirmation, and verifying work quality and completion.
* Review...
....Read more...
Type: Permanent Location: Indianapolis, US-IN
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:38
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Role: Vice President and Assistant General Counsel, RayzeBio
Location: San Diego, CA
Background
RayzeBio is a dynamic biotechnology company headquartered in San Diego, CA.
Launched in late 2020 and acquired by Bristol Myers Squibb (BMS) in 2024 as a wholly owned subsidiary, the company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes.
RayzeBio operates as a standalone entity within the BMS organization, maintaining its biotech culture with the opportunity to leverage the best-in-class oncology capabilities of BMS.
RayzeBio is developing innovative drugs against targets of solid tumors.
The lead asset, RYZ101, is in Phase 3 testing for patients with gastroenteropancreatic neuroendocrine tumors (GEP-NETs). In addition, Rayzebio has the leading radiopharmaceuticals pipeline with novel assets targeting HCC, RCC, and Prostate cancer amongst others. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.
Summary
We are currently looking for a Vice President and Assistant General Counsel to lead the entirety of the legal function within RayzeBio and serve on the LT.
The Vice President and Assistant General Counsel will report into the BMS Law Department and is responsible for ensuring legal compliance, mitigating risks, and providing strategic guidance across various facets of our operations.
The Vice President and Assistant General Counsel plays a crucial role in navigating complex legal landscapes, while overseeing a diverse portfolio of responsibilities ranging from regulatory compliance to contractual negotiations.
Job Responsibilities
Essential duties and responsibilities include the following.
Other duties may be assigned.
* Advising the President and leadership team of key risks potentially impacting the functionality of the business.
* Near-term focus will be on leading the legal support for supply chain, clinical trials, regulatory issues and commercialization capabilities
* Assume a leadership role in the negotiation, drafting and review of a broad range of contracts, including
* clinical trial agreements, vendor and services agreements, licensing agreements, confidentiality agreements,
* partnership agreements, among others.
* Establish strong, collaborative relationships with the functional leads within the organization and the...
....Read more...
Type: Permanent Location: San Diego, US-CA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:37
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
This territory includes: Washington, DC and Baltimore, MD
As part of the commercial organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology products in a defined geography.
* The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.
* The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment. CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations. CNC interactions are aligned with on-label commercial strategies and the needs expressed by customers.
* CNCs may develop relationships with oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.
* CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.
Product responsibilities may change based on franchise and business needs.
Customer Focus
* Develop and maintain relationships with academic and community HCPs within assigned geography to provide on-label clinical and product education for BMS hematology and oncology products.
The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing on-label approved marketing materials.
* Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
* Demonstrate proficiency in using available on-label CNC resources and presentations.
Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal-guidelines and directives.
* Consistently evaluate the impact of CNC activities in an account and plan for follow-up or next steps.
* Respond a...
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Type: Permanent Location: Washington, US-DC
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:36
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
At Bristol Myers Squibb we are reimagining the future of cell therapy.
With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.
If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Manufacturing Associate manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management.
Manufacturing Associates adhere to regulatory requirements while performing job functions.
Job duties are performed within a team according to an assigned, production shift schedule.
Communication of production deviations and assistance with quality investigations are required, as applicable.
Shift Available:
* Quad 3 Wednesday - Saturday (with every other Wednesday off), Onsite Day Shift, 5 a.m.
- 5:30 p.m.
Responsibilities:
* Perform set-up and operation of equipment to support production of blood component lots through cell culture, harvest, and cryopreservation.
* Support deviation investigations and write ups as needed.
Support on time closure of any assigned CAPAs within the designated shift.
* Aseptic technique is required for tube most activities: welding, connections, and transfers, at minimum.
Aseptic qualification is required.
* Weighs and measures in-process materials to ensure proper quantities are added/removed.
* Adheres to the production schedule ensuring on-time, internal production logistics.
* Records production data and information in a clear, concise, format according to proper GDPs.
* Perform all tasks in a manner consistent with site safety policies, quality systems, and GMP requirements.
* Works in a team based, cross-functional environment to complete production tasks required by shift schedule.
* Motivated, team consciousness individuals are needed to fulfill job requirements.
* Become a SME and qualified trainer within a designated function of manufacturing.
Supervision will be managed by the shift Supervisor or designated Team Lead.
* Maintain on time completion of training assignments to maintain the necessary technical skills and process knowledge.
* Perfo...
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Type: Permanent Location: Summit, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:36
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Summary:
Bristol Myers Squibb is seeking a Software Engineer to join the AI Engineering and Enablement team at their New Jersey office.
This role will focus on developing, testing, maintaining, and enhancing software applications and components that support business and technology needs.
The ideal candidate will have strong software engineering fundamentals, hands-on programming experience, and familiarity with modern development practices.
The candidate should also be comfortable using AI-assisted development tools or AI agents to help write, test, debug, and improve code as part of day-to-day software development.
This role is best suited for someone with at least 2 years of software development experience and at least 1 year of exposure to AI-related development, AI-enabled applications, or AI-assisted software engineering.
Key Responsibilities:
* Develop, test, maintain, and enhance software applications and components using modern programming languages such as Python, JavaScript, Java, Go, or similar languages.
* Write clean, secure, maintainable, and efficient code following established software development standards and best practices.
* Collaborate with engineers, product owners, and business users to understand requirements and translate them into technical solutions.
* Troubleshoot, debug, and resolve application issues, escalating risks or complex problems when needed.
* Participate in code reviews and contribute to improvements in code quality, testing, and development practices.
* Support integration of applications with APIs, databases, cloud services, and software tools.
* Use AI-assisted development tools or AI agents to support coding, testing, debugging, and documentation.
* Contribute to continuous improvement of development processes, agile engineering practices, and secure application development.
Required Qualifications:
* Bachelor’s degree in Computer Science, Engineering, Information Technology, or a related field, or equivalent practical experience.
* Minimum of 2 years of professional software development experience.
* Minimum of 1 year of exposure to AI development, AI-enabled applications, automation, or AI-assisted software engineering.
* Experience with at least one modern programming language, preferably Python.
* Understanding of software development fundamentals, including applica...
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Type: Permanent Location: Seattle, US-WA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:35
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
The Medical Science Liaison (MSL) role embodies our medical mission to be recognized as the trusted partner for internal stakeholders and the healthcare community, driving scientific exchange to enhance medical education, data generation, insight generation and patients’ access to medicine.
The MSL is responsible for identifying disease and product related medical needs in a defined geography.
The primary role of the MSL is to develop and maintain relationships with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system.
The purpose of their interactions is to engage in meaningful scientific exchange that will ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer to peer discussions aligned with medical strategies and needs expressed by external stakeholders, and to facilitate research.
The MSL also serves as the medical resource for external stakeholders in the community.
Key Responsibilities
* External Environment and Customer Focus
* Develop and maintain relationships with academic and community research thought leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product, and HEOR related questions.
The MSL will use various channels for interactions (1:1, group presentations, remote, etc.)
* Demonstrate proficiency in using available scientific resources and presentations.
Effectively present information to TL/HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.
* Actively assess the medical landscape by meeting with TL/HCPs/Access Stakeholders to understand their needs and expertise.
Continuously update own knowledge in treatment strategies, products, unmet medical needs, clinical trials, health economics outcomes research and scientific activities.
Understand the competitive landscape and evolving healthcare models and actively prepare to address informational needs of customers
* Identify opportunities to partner with HCPs on disease state initiatives, collaborative research projects, and investigator sponsored research (ISR) of interest and in alignment with BMS strategic objectives
* Attend medical congresses and local/regional meetings.
Collect and provide meaningful medical insights...
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Type: Permanent Location: Lawrence Township, US-NJ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:35
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
At Bristol Myers Squibb we are reimagining the future of cell therapy.
With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure.
If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there’s no better place than here at BMS with our Cell Therapy team.
The Clinical Manufacturing Associate II, Cell Therapy brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs.
The Associate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind.
The Associate must be enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support Clinical Manufacturing Start Up activities, and direct manufacturing operations for Clinical Cell Therapy.
Shifts Available:
TBD
Responsibilities:
* Performing Clinical patient process unit operations and supporting operations described in standard operating procedures and batch records.
* Demonstrates strong practical and theoretical knowledge of work
* Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records.
* Solving simple problems; taking new perspectives using existing solutions
* Identifies innovative solutions
* Performing tasks in a manner consistent with the safety policies, quality systems, and cGMP requirements.
* Completing training assignments to ensure the necessary technical skills and knowledge.
* Referencing Batch Records, Standard Operating Procedures and Work Instructions to successfully complete manufacturing operations.
* Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts.
* Working in a cleanroom environment and performing aseptic processing; maintaining manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regiment as required to meet global Health Authority requirements.
* Collaborating with support groups on recommendations and solving technical and operational problems.
* Assisting in setting up manufacturing areas ...
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Type: Permanent Location: Devens, US-MA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:33
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At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
As part of the commercial organization, the Clinical Nurse Consultant (CNC) is a trusted clinical expert responsible for developing professional relationships and educating key Health Care Professionals (HCP) involved in the care of patients receiving BMS hematology products in a defined geography.
* The primary role of the CNC is to drive peer to peer interactions with customers that optimize patient outcomes by delivering end-to-end clinical exchanges that clarify the complexities of patient identification and management.
* The purpose of these interactions is to deliver a continuum of clinical education and support that address the needs of HCPs starting or continuing patients on BMS hematology and oncology medicines, optimizing patient management and duration of treatment. CNCs also educate on unmet disease needs and discuss the current treatment landscape for these patient populations. CNC interactions are aligned with on-label commercial strategies and the needs expressed by customers.
* CNCs may develop relationships with oncology focused Patient Support Groups for the purpose of presenting approved presentations that address specific patient education needs identified by the group leader.
* CNCs are viewed as clinical experts by their customers for the BMS hematology and oncology portfolio.
Product responsibilities may change based on franchise and business needs.
Customer Focus
* Develop and maintain relationships with academic and community HCPs within assigned geography to provide on-label clinical and product education for BMS hematology and oncology products.
The CNC will use various channels for interactions (1:1, group presentations, remote, etc.) while utilizing on-label approved marketing materials.
* Actively assess the treatment and patient management landscape by meeting with HCPs to understand their needs and current patient management processes/protocols.
* Demonstrate proficiency in using available on-label CNC resources and presentations.
Effectively utilize platform skills for presenting information to HCPs and be able to respond to questions, ensuring accuracy and compliance with local procedures, ethical and legal-guidelines and directives.
* Consistently evaluate the impact of CNC activities in an account and plan for follow-up or next steps.
* Respond and adapt quickly to support new and ongoing educational...
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Type: Permanent Location: Philadelphia, US-PA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:30
-
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work.
Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases.
We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
The RNA Purification Process Development function plays a central role in designing efficient, robust, and scalable manufacturing processes.
By combining deep scientific expertise with enabling technologies and strong cross-functional partnerships, RNA Process Development delivers transformative innovation across the pipeline.
The Scientist executes robust experiments for drug substance programs spanning early- to late-stage development across circular and linear mRNA modalities.
Reporting to the Principal Scientist, this role encompasses hands-on contributions, addressing critical challenges by driving sound experimental execution and manufacturing support.
The candidate should be driven by developing and characterizing chromatography and filtration steps for improving the yield, quality and robustness of purification process steps.
Key Responsibilities
* Design, execute, and analyze experiments for existing and novel process modes using DoE and statistical modeling
* Define the RNA drug substance purification process, the critical parameters, and the design space
* Experiment using high throughput/automated or data rich experimental setups
* Design experiments to confirm robust process performance across the control space
* Collaborate with analytical teams to enable deeper characterization of RNA properties and impurity profiles
* Collaborate closely with upstream PD to characterize IVT feed stream to maximize RNA yield and purity
* Prepare technical reports, and communicate findings internally and externally as appropriate
* Participate in tech transfer activities to GMP manufacturing sites for RNA programs
Qualifications & Experience
* Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field
+ BS with 6+ years’ experience in science related disciplines
+ MS with 4-6 years’ experience in science related disciplines
+ PhD with 0 - 2 years’ experience in science related disciplines
* Expertise in chromatography, filtration (TFF/UF-DF), and innovative separation unit operations
* Solid knowledge foundation of statistical design of experiments (DoE) and analysis of multivariate data
* Experience with performing process analytics and biophysical characterization techniques such as HPLC, CE, & gel electrophoresis
* Knowledge of cGMP, ICH, regulatory guide...
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Type: Permanent Location: Cambridge, US-MA
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:26
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About the role
SUMMARY:
The Recruiter is responsible for sourcing and recruiting candidates to fill temporary, temporary to hire and/or direct hire job orders for a variety of standard to moderately complex clients.
Assists with building and maintaining a comprehensive candidate pipeline that addresses client needs.
The Recruiter is expected to provide exceptional customer service to our clients and candidates.
This role is also responsible for developing new business, maintaining current relationships and sales techniques.
What you'll be doing
ESSENTIAL DUTIES & RESPONSIBILITIES:
Sourcing:
* Attend to all candidates that enter into contact with the branch, whether in person or online, ensuring that all candidates are provided with correct information about PDS, offers, job guidance and training and development programs in a clear and professional manner.
* Manage PDS website and all digital tools to monitor the selection process, creating processes based on target categories, searching for candidates, and registering the status of candidates.
* Develop and own local recruiting resource relationships and grass roots recruiting plans.
Coordinate logistics for recruiting events.
Recruiting:
* Establish a recruitment plan based on the number of workers necessary to achieve the goal
* Qualify candidates against pre-determined standard requirements.
* Conduct behavioral interviews to qualify candidates and determine best placement options.
* Assist candidates with resume and interview preparation, coaching for specific roles
* Enter and track assignment and/or candidate data in Applicant Tracking Systems (ATS).
Retention:
* Build and maintain relationships with candidates and clients.
* Responsible for retention of individual clients.
* Responsible for retention of candidates and clients along with manager.
* Ensure that clients and candidates receive excellent service.
* Identify a training plan for candidates and temporary employees to improve their employability with the branch's corporate clients.
* Respond to candidate and/or temporary employee inquiries and escalates as necessary.
* Field and address standard client requests.
* Provide coaching and counseling around job performance to associates as necessary.
Sales:
* General knowledge of the Adecco Group's service portfolio.
* Ability to price and sell services (conversions, temporary and perm placement business)
* With manager, build and maintain knowledge of target industries, clients, roles, market share and competition.
Financials:
* Knowledge and control of the main variables affecting the branch's gross margin (workers comp, pay rates, federal and state regulations, taxes, benefits etc.)
* General knowledge of the financial objectives and current status (revenues, average GM, costs, impact of DSO, workers comp etc.)
* Participate in special projects and performs other d...
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Type: Permanent Location: Mesa, US-AZ
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:26
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About this role
The Recruiter is responsible for sourcing and recruiting candidates to fill temporary, temporary-to-hire, and direct-hire job orders for a variety of moderately complex, complex, and specialized clients-partners with clients to define strategic objectives and hiring needs.
Analyzes hiring needs, determines best recruiting methods, and creates/deploys client-specific and role-specific recruiting strategies.
Builds and maintains a comprehensive candidate pipeline that addresses client needs.
Serves as subject matter expert on market trends, target industries, and roles.
Acts as a team leader in the absence of management.
What you'll be doing
Recruiting/Skill Marketing:
* Anticipate and understand the local talent market and implement a workforce planning strategy to ensure a continuous pipeline of quality talent; Develop candidate and community engagement programs to strengthen Adecco's footprint in the market.
* Builds and maintains relationships with both passive and active candidates.
* Redeploys temporary associates.
* Analyzes hiring needs, determines best-recruiting methods, and creates/deploys client-specific and role-specific recruiting strategies.
* Assist candidates with resumes, interview preparation, and coaching for specific roles.
* Assist with identifying, sourcing, and screening top-quality candidates for open opportunities within the client program, as needed.
* Analyzes candidates found through prescreening activities and evaluates skills and experience to determine match to inventory needs.
* Assesses candidates to ensure qualification match, cultural fit, and compatibility with client requirements.
* Achieve complete understanding and execute required recruitment, interview, and submission activity KPIs.
* Act as a subject matter expert (SME) related to Adecco's recruitment tools and processes.
* Attend to all candidates that contact the branch, whether in person or online, ensuring that all candidates are provided with correct information about Adecco, offers, job guidance, and training and development programs clearly and professionally.
* Conduct structured/behavioral interviews to qualify candidates and determine the best placement options.
* Conducts moderately complex searches leveraging Adecco and internet tools, analyzes results, and modifies as appropriate to meet needs inventory.
* Coordinates and consults with hiring managers to understand clients' specialized needs better, maximize service level and encourage relationship building.
* Maintains records of competitors in the area that display their respective shares of the market, locations, services, and benefits offered.
* Develops candidate executive summary for resume submittal.
* Develops long-term relationships with Associates while on assignment, striving for redeployment.
* Makes calls and visits to customers and prospects to discuss services and resol...
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Type: Permanent Location: Rochester, US-NY
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:25
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Schedule
* This will be your standing schedule. We are looking for a RT that can work the following schedule below consistently.
+ 4- 6 hours per shift; maybe up to 8 hours depending on caseload
+ Saturday and Sunday
Respiratory Therapist (RT)
Looking for a full time talented and motivated Respiratory Therapist to join our dynamic team.
The position is within a Skilled Nursing facility.
Candidate should possess passion for geriatric population, must contain a license in the state of practice, be able to evaluate and treat independently without direct supervision, and posses the desire to perform functional therapeutic activities to assist residents improve in their experience.
Job Description
* Completes assessments and implements respiratory techniques to maintain and progress the rehab patients with many different Respiratory illness/diseases and non respiratory illness.
* Initiate therapies, maintain patient records, operate, check, and assemble equipment
* Complete a variety of bedside treatments
* Complete in-services for nursing staff every quarter
* Responsible for completing daily, weekly and monthly documentation
* Attend applicable IDT meetings
* Experience with tracheotomy
* Experience is a long term care setting
* Follow procedure and protocol of facility
* Completes tracking, auditing and caseload management
* Performs related duties as required
* Described in the Departmental Policy and procedure Manual in these areas of skilled interventions:
* Oxygen weaning therapy
* Omniflow – Biofeed back
* Group respiratory therapy
* Standardized respiratory testing
* Aerosol therapy
* IPPB therapy
* Incentive Spirometry
* Chest physiotherapy
* Deep breathing and coughing
* Bronchial hygiene therapy
* PEP therapy
* Postal Drainage
* Positioning
* Oro/Naso-pharyngeal suctioning
* Airway clearance/management techniques
* Trachea-bronchial suctioning
* Tracheostomy care
* Spirometry Bedside Testing
* CPAP/BIPAP
* High-Flow Oxygen
* Cardiac Program
* Pulmonary Program
* Cardio-pulmonary resuscitation
QUALIFICATIONS/REQUIREMENTS:
* Graduate of COARC accredited AS or BS Respiratory program.
Licensed as RRT or CRT.
* Licensed in the state in which practicing BLS certification.
Background Screening Requirment:
This position is subjet to Florida background screening requirments.
For information please visit : https://info.flclearinghouse.com
An Equal Opportunity Employer
INDTHE
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Type: Permanent Location: Fort Lauderdale, US-FL
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:24
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Occupational Therapist
The Creekside Center for Rehabilitation and Healing is looking for a talented and hard-working Occupational Therapist to join our ever-growing team.
Responsibilities Include:
The Occupational Therapist is responsible for the assessment of referred patients that require rehabilitation services which includes: providing direct patient care to assess their medical condition, functional capabilities, limitations and restrictions and potential for rehabilitation.
Also, the Occupational Therapist will establish and administer a treatment program with specific goals determined according to the patients capacity and tolerance under the direction of the Physician.
As well, the Occupational Therapist must set realistic and achievable goals for their patients, document and record the patients condition and educate patients and families in an appropriate therapy method.
Qualifications/Requirements:
* Must have graduated from an accredited Occupational Therapist college or university.
* Must have a valid professional license and registration for state of practice.
* The Occupational Therapist is responsible for overseeing and supervising Occupational Therapy Assistants.
* Experience with long-term care and/or geriatric care is preferred but not limited to.
* Well versed with documentation writing
* Evaluations, weekly progress notes, re-certification and discharge documentations.
* Collaborates with all disciplines to provide best patient centered treatment and care.
* Exceptional patient service skills and ability to demonstrate clinical excellence
* Report to work on time, adhere to scheduled hours and demonstrate professionalism at all times.
* Perform all other duties assigned by Director of Rehabilitation
* Compliance with confidentiality, HIPPA and Federal Residents Rights.
Shift Needs: All positions are available.
An Equal Opportunity Employer
INDTHE
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Type: Permanent Location: Nashville, US-TN
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:23
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Riverside is a 520 bed facility in the Upper West Side in Manhattan with 220 short term beds, with an exceptional rehab gym and onboarding program.
Ideal for new grads as a stepping stone into their career and one block from the subway.
We are hiring a full time Occupational Therapist to join our rehabilitation team.
Hiring for this role is done on site by our Director of Rehab and facility leadership, not by an outside recruiter.
You will interview with the people you will actually work with.
We are part of a growing network of 35 skilled nursing facilities, which means real clinical support behind you and real places to go from here.
Why This OT Role Is Different
* Interdisciplinary by design.
OT, PT, SLP, nursing team, dietitian, respiratory, social work, and MDS work from the same plan and the same table.
You will not be treating in a silo.
* A training environment.
New graduates are welcome.
You get structured mentorship, hands on orientation, and ongoing clinical education from clinicians who want to teach.
* Leadership that is present.
Our Director of Rehab and facility administration are invested in where you want to be in five years and will talk with you about it regularly, not only once a year at review time.
* Growth you can actually reach.
A 35 facility network that is still expanding means specialty program development, mentorship roles, and leadership tracks, including:
+ Dementia clinical focus champions
+ Respiratory champions and step down
+ Adaptive equipment liaison specialists
+ Assistant director and lead or senior therapist ladder programs
* Work life balance is an operating priority.
Tell us the schedule you need, and we will work with you to build it.
Our residents come first, and happy therapists equal happy patients.
What You Will Do
* Evaluate referred residents to determine medical status, functional ability, limitations, precautions, and rehabilitation potential
* Build individualized treatment plans with measurable, achievable goals based on each resident’s capacity and tolerance, under physician direction
* Deliver skilled occupational therapy interventions focused on ADL performance, safety, and return to prior level of function
* Complete evaluations, weekly progress notes, recertifications, and discharge documentation accurately and on time
* Educate residents, families, and caregivers on therapy techniques, safety, and carryover strategies
* Collaborate with PT, SLP, nursing, dietitians, and social work to deliver patient centered care and support discharge readiness
* Recommend adaptive equipment, durable medical equipment, and environmental modifications
* Supervise Occupational Therapy Assistants and students in accordance with the state practice act
What You Will Need
* Degree in Occupational Therapy from an accredited program
* Valid Occupational Therapist license and registration ...
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Type: Permanent Location: New York, US-NY
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:22
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SPEECH LANGUAGE PATHOLOGIST (SLP) Full Time and PRN
Sign-on bonus!
Highly Competitive Rates!
Gallatin Center for Rehabilitation and Healing is seeking a Speech Language Pathologist (SLP) to join our team.
Speech Language Pathologist (SLP) Responsibilities Include:
The Speech Language Pathologist is responsible for the assessment of referred patients that require rehabilitation services which includes: providing direct patient care to assess their medical condition, functional capabilities, limitations and restrictions and potential for rehabilitation.
Also, the Speech Language Pathologist will establish and administer a treatment program with specific goals determined according to the patient's capacity and tolerance under the direction of the Physician.
As well, the Speech Language Pathologist must set realistic and achievable goals for their patients, document and record the patient's condition and educate patients and families in an appropriate therapy method.
Speech Language Pathologist (SLP) Qualifications/Requirements:
* Must have graduated from an accredited Speech Therapist college or university.
* Must have a valid professional license and registration for state of TN
* Experience with long-term care and/or geriatric care is preferred but not limited to.
* Well versed with documentation writing
* Evaluations, weekly progress notes, recertification and discharge documentations.
* Collaborates with all disciplines to provide best patient centered treatment and care.
* Exceptional patient service skills and ability to demonstrate clinical excellence
* Report to work on time, adhere to scheduled hours and demonstrate professionalism at all times.
* Perform all other duties assigned by Director of Rehabilitation
* Compliance with confidentiality, HIPPA and Federal Residents Rights.
An Equal Opportunity Employer
INDTHE
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Type: Permanent Location: Gallatin, US-TN
Salary / Rate: Not Specified
Posted: 2026-10-02 08:57:21
