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At NASCAR, you will find a community of passionate individuals who care about our sport and are united in seeing it grow.We are a company unlike any other. We want you to bring your experience, skills and passion to our close-knit, high-energy environment in which our employees thrive and where you can prosper. We know the key to our success is our employees and we offer highly competitive salaries, a solid benefits package focused on wellness, and opportunities for you to grow and develop both personally and professionally. It won’t take you long to find out that you are on the right track here at NASCAR!NASCAR seeks a talented professional to join in the position of Network Engineerbased in our Daytona Beach, Florida office. NASCAR Network Engineer will be required to provide enterprise-level assistance to our customers. You will diagnose and troubleshoot network and hardware problems and help maintain a highly available, flexible, and resilient network. Network Engineer responsibilities include resolving network issues, supporting existing network solutions, and ensuring our network is documented, available, and flexible to adapt to the demands from our customers. You will actively participate in group and individual training sessions to continue to learn and grow on the job and at industry events.Duties include but are not limited to: <ul><li>Follows core processes and procedures to ensure operational success&nbsp;</li><li>Monitor, track, benchmark, and analyze Voice/Data Network trends&nbsp;</li><li>Analyze performance of responsible technologies and documented solutions, identify problem areas, and resolve root cause.&nbsp;</li><li>Triage Service Incidents and Requests, and Problems reported by customers&nbsp;</li><li>Assess the need for system reconfiguration based on Incidents and make sound recommendations&nbsp;</li><li>Research emerging infrastructure solutions and other collaborative products, services, protocols, and standards</li><li>Ensure the availability, stability, and integrity of Data, Voice, Video, and Wireless networks across security, wireless, routing, and switching platforms</li><li>Support disaster recovery and business continuity programs</li><li>Provide prompt and accurate feedback to customers using tickets and all other appropriate mechanisms</li><li>Prioritize and manage multiple open issues simultaneously</li><li>Document technical knowledge in the form of notes, manuals, tickets, documents, designs, network architecture topologies and emails&nbsp;</li><li>Provide On-Call support on a schedule set forth by the Director, Network Engineering.</li></ul>Required skills / experience: <ul><li>Associate degree or equivalent Experience Required &nbsp;</li><li>5+ Years in a Network Engineering Role&nbsp;</li><li>CCNA Required (200-301)</li><li>CCNP Strongly Encouraged (350-401 ENCOR + Concentration Exam)</li></ul> Technical Skillsets:<ul><li>Competent with Network operations&nbsp;</li><li>Capable of performing onsite Event Support and Engineering&nbsp;</li><li>Experience in Cisco, Juniper, Extreme, Palo Alto and Ubiquiti infrastructure and applications &nbsp;</li><li>Extensive experience in networking products including routers, switches, firewalls, VPN, IPS/IDS, Load Balancing solutions&nbsp;</li><li>Experience in cloud networking. &nbsp;AWS and Azure.</li><li>Experience with Wide Area Networking, BGP, Telco tickets and interactions</li><li>Experience in network management tools and in packet capture analysis</li><li>Knowledgeable on Data Center infrastructure included but not limited to Networking, VXLAN, Server, Virtualization, DNS, Storage, and Environmental controls</li><li>Hands-on experience installing, configuring, managing and deploying Cisco Unified Communications Manager and Teams Voice</li><li>Experience with voice routing and troubleshooting to multiple phone systems.</li><li>Knowledgeable in programming skills using Python, REST, JSON, XML, and git.</li><li>Professional competencies in computer engineering or related field of work&nbsp;</li><li>Conscientious and efficient in meeting commitments, observing deadlines, and achieving results &nbsp;</li><li>Able to work independently with minimum supervision &nbsp;</li><li>Capable of preparing reports, designs, and papers on technical issues&nbsp;</li><li>Proven analytical skills to arrive at sound conclusions when dealing with complex issues&nbsp;</li><li>Ability to contribute to the development of policies and to optimize procedures and guidelines &nbsp;&nbsp;</li><li>Ability to contribute to cross-functional teams from Engineering, Applications, Technology, and others in the management of day-to-day operations, to resolve incidents, and improve the organization</li><li>Ability to Assist in leading a program of continuous improvement within the IT department&nbsp;</li><li>Seek opportunities to grow and become a better and established leader&nbsp;</li><li>Ability to plan and organize work consistent with the strategic goals of NASCAR &nbsp;</li><li>Identify priority activities and assignments and to ensure the effective monitoring and implementation of release plans</li><li>Experience with all phases of network projects including, design, test, deploy, validate, operate, optimize, and decom through established company process and peer review</li><li>Excellent skills in communicating with people from different backgrounds and technical abilities &nbsp;</li><li>Ability to communicate to Leadership effectively</li><li>Ability to communicate complex technical items to non-technical individuals succinctly</li><li>Naturally work with teammates to pass on critical information and to help prevent others from learning the hard way issues personally experienced</li><li>Collaborate openly and critically with the intent of improving the organization</li><li>Ability to keep abreast of developments and relevant technologies applicable to the profession &nbsp;</li><li>Skillful in identifying customer needs and establishing and maintaining effective relationships with internal and external stakeholders &nbsp;</li><li>Ability to make sound and timely decisions while handling pressure, at all times staying within process</li></ul>Apply Now!Learn more about this role and our team by applying at <a href="https://careers.nascar.com/&amp;nbsp" target="_blank">https://careers.nascar.com/&amp;nbsp</a>; for consideration.NASCAR is committed to fostering a diverse work environment where all employees feel valued and empowered. NASCAR is an Equal Opportunity Employer (EEO). We seek to attract and retain the best qualified people available. All qualified applicants will receive consideration for employment without regard to race, color, gender, gender identity and expression, age, national origin, disability, religion, sexual orientation, genetic information, pregnancy, veteran status or any basis that is protected by applicable law except where a bona fide occupational qualification exists.

NASCAR

Network Engineer

Job Summary / General Purpose:Provide regional project management and engineering oversight for Sprague’s operational assets in Connecticut and Rhode Island. Work with the Engineering Team, Operations Management, and terminal personnel to maintain Sprague’s assets and ensure sustained readiness and reliability in compliance with all federal, state, local and internal Sprague operating requirements. Work with Materials Handling and Refined Products business units to develop and execute project scopes for new growth opportunities.Major Duties / Responsibilities:• Coordinate with the Engineering Team to assess infrastructure and equipment requirements through formal and informal inspection programs and develop long-term capital and strategic recommendations to maintain assets in full compliance with federal, state and local regulations and within Sprague guidelines. • Provide engineering project management support for major expansion projects and to terminal managers during construction and repairs to facility tanks, pipelines, marine structures, electrical and mechanical systems. • Develop detailed cost estimates for maintenance and expansion projects. Work with contractors and engineers to establish work scopes and solicit bids. Review and approve engineering plans &amp; drawings and meet with contractors and engineers prior to startup to discuss the layout and expectations for projects. • Track progress of each project against goals, objectives, approved budgets and schedule. Reports status and variances. Develop detailed work plans, schedules, project estimates, resource plans and status reports. Works with contractors to assure adherence to schedule and budget. • Interface with project controls personnel to ensure completion within budget and on schedule. Provide monthly updates of capital project forecasts to ensure that costs remain within authorization limits. • Coordinate key asset inspections including storage tank, pipeline and dock inspections. Conduct, as necessary, Engineering analysis either in-house or through third party engineering firms. • Respond to emergencies by providing engineering support to Operations Management and terminal personnel. • Assist in the expansion of Sprague’s product line and support terminal acquisition and integration through due diligence, capital needs assessments, expense and personnel planning and environmental compliance program support. Provide support to marketing projects throughout all phases of design, development and implementation. • Greater than 25% travel required.Education / Experience / Skill Requirements:• Seven years of experience in engineering or construction management within the petroleum, energy, material handling, marine, or power generation industries required. • Specific experience in project management with direct responsibility for large-scale projects is preferred. • Bachelor’s degree in an Engineering discipline (Mechanical, Electrical, Marine, or Civil), construction management, or related field required. • Successful track record of project execution. Demonstrated ability to identify project risks, develop risk mitigation and contingency plans, and implement action plans to reduce or eliminate risks. • Ability to successfully assess capital requirements and implement long-term upgrades within a structured compliance program. • Demonstrated organizational and project management skills with the ability to handle multiple simultaneous projects. • Strong computer skills including Engineering Applications, MS Office Suite and Project Management software. • Strong analytical, communication and presentation skills. • Self-starter with demonstrated record of pro-active contributions and ability to successfully implement company goals. • Valid driver’s license. • Ability to pass a background check and obtain a TWIC (Transportation Worker Identification Credential)

Sprague

Sprague Resources GP LLC

Sr. Engineering Project Manager

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 rich in diversity. 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.Job Description: We are seeking a highly skilled and motivated MES Infrastructure and Platform Administrator to join our Manufacturing Execution System (MES) team. As the MES Infrastructure and Platform Administrator, you will be responsible for the administration, configuration, and support of our Emerson Syncade MES platform and infrastructure. You will execute platform and infrastructure upgrade projects, develop Quality Review Manager (QRM), labels, and reports, and provide training to new MES resources and end users. Additionally, you will be part of a rotational on-call support team for manufacturing operations.Responsibilities:<ul><li>Administer and maintain the Emerson Syncade MES platform and infrastructure, including user access management, system configurations, and security settings.</li><li>Execute Emerson Syncade MES platform and infrastructure upgrade projects, ensuring smooth transition and minimal disruption to manufacturing operations.</li><li>Develop a deep understanding of the Emerson Syncade MES technology platform to support investigations, upgrades, and troubleshooting.</li><li>Execute Quality Review Manager (QRM), labels, and reports development projects within the Emerson Syncade MES system.</li><li>Utilize tools such as Infobatch and Bartender application for labeling and reporting.</li><li>Create and maintain the MES Platform Administration framework, including standard operating procedures (SOPs) and work instructions.</li><li>Deliver training on the Emerson Syncade MES platform to new MES resources and end users, ensuring their proficiency in utilizing the system.</li><li>Collaborate with cross-functional teams to gather requirements and implement system enhancements.</li><li>Ensure compliance with regulatory requirements, such as FDA regulations and Good Manufacturing Practices (GMP) guidelines, during system changes and upgrades.</li><li>Troubleshoot and resolve issues related to Emerson Syncade MES system functionality and data integrity, working closely with IT and vendor support teams.</li><li>Provide rotational on-call support for manufacturing operations, addressing urgent system issues and ensuring minimal disruption to production.</li><li>Stay updated on industry trends and advancements in MES systems, providing recommendations for system optimization and process improvements.</li><li>Participate in cross-functional meetings and initiatives to drive continuous improvement and align MES system capabilities with business requirements.</li><li>Knowledge of industry standard integration protocols and programming applications such as OPC, ODBC, SQL, and Web API.</li><li>SQL Server Administration and SQL programming.</li></ul>Qualifications:<ul><li>Bachelor's degree in Computer Science, Engineering, or a related field.</li><li>8-10 years of experience in Emerson Syncade MES platform administration, preferably in the pharmaceutical or biotechnology industry.</li><li>Strong knowledge of Emerson Syncade MES system, including administration, configuration, and user access management.</li><li>Experience in executing Emerson Syncade MES platform and infrastructure upgrade projects.</li><li>Proficiency in Quality Review Manager (QRM), labels, and reports development within the Emerson Syncade MES system.</li><li>Experience with Infobatch and Bartender application for labeling and reporting.</li><li>Understanding of regulatory requirements, such as FDA regulations and GMP guidelines, in a manufacturing environment.</li><li>Excellent problem-solving and troubleshooting skills, with the ability to analyze complex issues and provide effective solutions.</li><li>Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.</li><li>Self-motivated and detail-oriented, with the ability to work independently and manage multiple priorities.</li><li>Knowledge of industry standard integration protocols and programming applications such as OPC, ODBC, SQL, and Web API.</li><li>SQL Server Administration and SQL programming.</li><li>Familiarity with software development principles and methodologies.</li><li>Knowledge of web application development technologies and frameworks.</li></ul>#LI-HybridIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb

Principal MES Engineer

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 rich in diversity. 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.When you join BMS, you are joining a diverse, high-achieving team united by a common mission.&nbsp;The Discovery Biotherapeutics team at BMS seeks to understand the structure and function of complex molecules such as bispecific antibodies, antibody drug conjugates and endogenous proteins in order to optimize their utility as therapeutic agents.&nbsp; We collaborate with biology and translational scientists imbedded in the Thematic Research Centers in order to prosecute Targets and Biological pathways with disease modifying potential. By using a blend of internal and external technologies and capabilities, we work to discover and deliver first-in-class as well as best-in-class molecules that warrant clinical evaluation for patient benefit. Here, you’ll get the chance to grow and thrive through opportunities that are uncommon in scale and scope. You’ll pursue innovative ideas while advancing professionally alongside some of the brightest minds in biopharma.We are seeking an enthusiastic, creative, and versatile Senior Scientist to join our collaborative Protein Engineering team to drive technological innovation, discover and engineer innovative biotherapeutic candidates. Our group acts on new ideas in the laboratory and thrives on the design-build-test cycle. You will solve complex protein engineering problems, develop new skills, and use them to implement robust platforms for protein therapeutic optimization. You will collaborate with talented colleagues and share what you learn. You will present at internal and external meetings, contribute to therapeutic pipeline projects, publications, and patents. Responsibilities include selection-based assays using protein display library technologies, binder engineering for antibody-target interaction, cross-function and cross-site collaboration and project management.Responsibilities<ul><li>Drive efforts to engineer antibodies, multispecifics, and alternative biologics formats for optimal therapeutic performance</li><li>Selections on yeast display libraries, routine operation and maintenance of a sorter</li><li>Library design in collaboration with AI/ML engineers, library construction, NGS</li><li>Independently perform routine molecular biology techniques, DNA assembly and cloning, design expression constructs for external synthesis, and coordinate construct and library orders with CROs</li><li>Analyze library NGS data using no-code or low-code bioinformatics platforms</li><li>Independently perform complex experiments, troubleshoot, expertly analyze and interpret experimental results with strong attention to detail and documentation practices</li><li>Present results internally and externally, attend industry conferences</li><li>Accomplish goals under project team timelines</li></ul>Basic Qualifications<ul><li>Bachelor’s Degree with 7+ years of academic or industry experience</li></ul>OR&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<ul><li>Master’s Degree with 5+ years of academic or industry experience or</li></ul>OR<ul><li>PhD in Biochemistry, Bioengineering, Molecular Biology, or related fields with 2+ years of academic or industry experience</li></ul>Preferred Qualifications<ul><li>PhD in Biochemistry, Bioengineering, Molecular Biology, or related fields with 2+ years of relevant post-graduate or biotech/biopharma industry experience</li><li>Experience with molecular and microbiology techniques underlying yeast display work</li><li>In-depth understanding and experience in antibody engineering is highly desirable</li><li>Demonstrated experience in working in a cross-functional organization is required</li><li>Experience in lead discovery and optimization is preferred</li><li>Fundamental understanding of proteins, antibodies, and structure-function relationships required. Familiarity with protein structure analysis (Pymol, Chimera, MOE).</li><li>DNA and RNA purification, cloning, PCR, Sanger sequencing, NGS library preparation</li><li>Flow cytometry and FACS</li><li>Familiarity with protein-protein interaction techniques and kinetics (BLI, SPR, on-cell binding)</li><li>Bioinformatics or data science experience is desirable (bash, Python, or R)</li><li>Proficiency with Microsoft Office suite, FlowJo, Prism, DNA cloning software</li><li>Excellent written and oral communication skills</li></ul>The starting compensation for this job is a range from $109,000 - $150,700 plus incentive cash and stock opportunities (based on eligibility). The starting pay rate takes into account characteristics of the job, such as required skills and where the job is performed. Final, individual compensation will be decided based on demonstrated experience.Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Career Site.Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Scientist - Protein Engineering

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 rich in diversity. 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.Job Profile:BMS is seeking an experienced directory services engineer who will be able to management directories across the entire company. The candidate needs to be a self-starter with high learning agility and the ability to translate complex requirements into working solutions. This is a technical role in a team with equally dedicated and passionate Engineers supporting our Cyber Identity and Directory services.Job Description &amp; Responsibilities: <ul><li>Advanced knowledge of LDAP directories based on ForgeRock Directory services, Oracle DSEE, Azure AD, Virtual Directory solutions as well as hands on experience with cloud infrastructure platforms (ex: AWS/Azure)</li><li>Ensure Directory Services platforms are secure, compliant, and highly available.</li><li>Work with the Architecture team to implement and integrate technical solutions.Proactively identify areas of improvements, opportunity for innovations and ways to enhance the directory services environment.</li><li>Effectively work directly with clients, team members, technical experts, professional staff, and management as needed to deliver new capabilities or provide operational support.</li><li>Have experience in Linux operating systems which would involve installing a few software, patching etc.</li><li>Have experience in application servers like Apache tomcat, JBoss, WebLogic, WebSphere etc.</li><li>Scripting experience (Bash, PowerShell, Python, Java Script etc.).</li><li>Software development experience, understanding of OOP principles, REST APIs, MVC architecture and Java frameworks (Spring).</li><li>Understanding of load balancers, proxies, and end-to-end encryption architecture.</li><li>Be self-directed, take the lead on technical escalations and drive incidents or problems until resolution. That involves automation, networking, cloud infrastructure security, and integration with 3rd party products.</li><li>Develop Architecture documents, requirements, network designs, roadmaps, technology/maintenance/upgrade lifecycle, execution plans, monitoring, and health checks validations, recovery plan, roll back plans, and DR Solutions.</li><li>Own Root Cause Analysis and Problem Management.</li><li>Direct the installation, configuration, and maintenance of the Directory platforms.</li><li>Take part in an after-hours on-call support rotation and implement solutions, patching and deployment activities after hours as needed.</li><li>Establish and maintain effective relationships with Internal Infrastructure, Application and Business partners to understand needs, use, and systems to facilitate effective IAM solutions. </li><li>Demonstrate a keen interest in acquiring knowledge of new technologies.</li></ul>Qualification:<ul><li>5+ years of experience in ForgeRock Directory or Oracle DSEE</li><li>This role requires an in-depth knowledge with ForgeRock Directory or Oracle DSEE as well as hands on experience with cloud infrastructure platforms (ex: AWS/Azure)</li><li>Possess expertise in Linux operating systems, including tasks such as software installation, patching, and more.</li><li>Possess expertise in utilizing application servers such as Apache Tomcat, JBoss, WebLogic, WebSphere, and others.</li><li>Proficient in one of the known programming and scripting language (Python, Java, JavaScript)</li><li>Self-directed with excellent communication and documentation skills</li><li>BS or equivalent in information technology, computer engineering, computer science, or related field</li></ul><h4>#HYDIT #LI-Hybrid</h4>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Engineer, Identity Access Management

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 rich in diversity. 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.RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.The Validation Engineer I will help support the Radiopharmaceutical facility and GMP operations in Indianapolis.&nbsp; The Validation Engineer I will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly specialized facility, utility, analytical, and process equipment.&nbsp; The position will utilize a wide range of engineering disciplines to support the advancement from construction to clinical development and subsequent GMP commercial operations.&nbsp; Additional responsibilities may include the onboarding of new technologies, process development, GMP operations support, deviation investigation, CAPA management, continuous improvement projects, and future facility expansion projects.Key Responsibilities:<ul><li>Work with the project team and/or General Contractor as required to support the commissioning and validation of a 60,000 sq. ft. office, warehouse, and GMP Radiopharmaceutical production facility</li><li>Develop and implement the CQV strategies for the GMP spaces including but not limited to office, warehouse, development, quality control, sterility/microbiology, and GMP production areas</li><li>Work with consultant(s) as required to support the implementation and execution of the CQV program&nbsp; </li><li>Support the engineering, QC, and Operations team as required to improve and implement new processes</li><li>Provide validation support for day-to-day development and GMP operations</li><li>Provide engineering and operational support as required</li><li>Develop expertise in areas of validation (process validation, QC assets, CSV, cleaning validation, etc)</li><li>Apply technical knowledge and abilities to investigate manufacturing deviations</li><li>Review data and documentation to support investigations</li><li>Participate and drive projects and continuous improvement efforts</li><li>Draft GMP documentation including but not limited to SOP’s, Forms, Protocols, Technical Documents, Reports, Deviations, CAPAs, Change Controls and reports.</li><li>Support Health Authority Inspections</li><li>Maintain department KPIs related to performance </li><li>Provide support executing equipment and process validations as necessary.</li></ul>Education &amp; Experience:<ul><li>BS or MS in scientific related field or equivalent work experience</li><li>2-5 years of experience in Radiopharmaceutical or injectable GMP manufacturing environment</li><li>2-5 years of validation experience within a GMP environment</li></ul>Skills &amp; Qualifications:<ul><li>Good technical writing skill set</li><li>Must possess an independent mindset and tenacity</li><li>Highly motivated and organized professional with strong interpersonal and communication skills.</li><li>Proven experience working with teams in a GMP environment.</li><li>Multi disciplined engineer with GMP experience</li><li>Excellent professional ethics, integrity, and ability to maintain confidential information.</li></ul>#LI-ONSITE #RAYZEBIOIf you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Validation Engineer I

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 rich in diversity. 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 SummaryThis is the Engineer-in-Training level where incumbents will initially perform a variety of routine Site/Facilities engineering tasks in a training status under close supervision. Incumbents will perform basic engineering tasks such as the review of less complex plans, performance of basic engineering calculations, the writing of permits, the performance of computer drafting, and the inspection of parts of an engineering project. Key Responsibilities<ul><li>Perform basic site/facilities capital project design modifications.</li><li>Develop basic detail drawings for construction.</li><li>Perform engineering change processes as necessary to support existing site operational functions.</li><li>Create or modify 2-D AUTOCAD drawings.</li><li>Generate and scan prints.</li><li>Develops, prepares and/or reviews engineering plans and designs for structures, facilities, and/or systems.</li><li>Develops, prepares and reviews reports and studies to identify and recommend engineering solutions.</li><li>Performs engineering inspections of systems operations and of structures and facilities during construction.</li><li>Reviews engineering program activities to make recommendations for changes in policy and procedures.</li><li>Conducts technical engineering research and provides technical assistance to consulting engineers, contractors and construction managers.</li></ul>Qualifications &amp; Experience <ul><li>Education and Experience requirements at this level consist of pursuing a bachelor’s degree in engineering from a college or university which is recognized by the New Jersey State Board of Registration for Professional Engineers and Land Surveyors, in accordance with the standards of the Accreditation Board of Engineering Technology or a bachelor’s degree in construction management.</li><li>Skills and Abilities required to perform duties at this level include knowledge; of basic engineering principles and techniques; of engineering planning; of equipment and materials used in engineering operations; of specialized subjects used in the fields of engineering, such as mathematics, statistics, mechanics, power, physics and chemistry; and of strength of materials.</li><li>Ability is required to apply engineering principles to practical engineering problems; to use engineering equipment and tools, including computer applications; to make, read and interpret engineering drawings and specifications; to express ideas clearly and concisely, both orally and in writing; to relate abstract ideas to actual needs and adopt an effective course of action; and to establish and maintain effective working relationships with others.</li><li>All candidates must be authorized to work in the US at the time of hire.&nbsp; Please note that immigration or visa sponsorship is not available for this position.</li></ul>If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Global Capital Project Engineering Internship

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 rich in diversity. 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.RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.The Sr. Quality Engineer will work cross-functionally to develop and implement engineering solutions that enhance compliance and reliability. &nbsp;This position will be responsible for providing quality oversight on the execution and update of the Validation Master Plan and site metrics.&nbsp; This position provides guidance on CAPA plans and use statistical tools to identify trends and promote continuous improvement.&nbsp; The Sr. Quality Engineer will be responsible for leading root cause analysis efforts using risk management principles. Supporting a Multi-phase to commercial facility. This position reports directly to the Associate Director, of Quality, Indianapolis.*This is an onsite position located at Rayzebio's Indianapolis, IN site*Job Responsibilities:<ul><li>Provide quality support and oversight of equipment validation, computer systems validation, and change management.</li><li>Provide quality review and support for the calibration and preventive maintenance programs.</li><li>Lead continuous improvement initiatives through cross-functional support and project management techniques.</li><li>Participate with the Facilities, Engineering and MS&amp;T teams on new installations/systems and innovation.</li><li>Leads cross-functional efforts for process improvement projects through use of statistical tools and various risk analysis tools.</li><li>Apply current industry standards and regulations to ensure procedures and policies are compliant with FDA, EU and ISPE GAMP-5 guidelines.</li><li>Support the enrollment and approval of assets in the asset management system.</li></ul>Education and Experience:<ul><li>BS/MS in Science related discipline preferred with 5-6+ years of quality assurance or quality engineering experience</li><li>Experience working in a GMP aseptic manufacturing environment preferred</li><li>Experience working with FDA and EU regulations.</li><li>ASQ or ISO certification and previous auditing experience a plus</li></ul>Skills and Qualifications:<ul><li>Highly motivated and organized professional with the ability to work independently</li><li>Working knowledge of 21 CFR Parts 11, 210, 211 and EU annex</li><li>Very personable with strong communication skills &nbsp;</li><li>Ability to read and interpret technical documents</li><li>Excellent professional ethics, integrity, and ability to maintain confidential information</li></ul>Physical Demands:While performing the duties of this&nbsp;job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this&nbsp;job&nbsp;include&nbsp;close vision and distance vision.&nbsp;This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Senior Engineer, Quality

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 rich in diversity. 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.Job Description: Software Engineer, Finite SchedulingWorking With UsChallenging. 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 rich in diversity. 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-usAt Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.Position Summary At BMS, digital innovation and Information Technology are central to our vision of transforming patients’ lives through science. To accelerate our ability to serve patients around the world, we must unleash the power of technology.  We are committed to being at the forefront of transforming the way medicine is made and delivered by harnessing the power of computer and data science, artificial intelligence, and other technologies to promote scientific discovery, faster decision making, and enhanced patient care.    Bristol Myers Squibb is advancing new and next-generation therapies while exploring and investing in technologies&nbsp;to optimize the planning processes&nbsp;to meet future needs. This role will serve as the delivery lead for Supply Planning and help in driving optimized solutions in the planning space while ensuring SLA compliant system support. If you want an exciting and rewarding career that is meaningful, consider joining our diverse team!Key ResponsibilitiesServe as the Finite Scheduling systems analyst of Emerson RTMS system in supporting and delivering digital capabilities. Collaborate with IT and business stakeholders in reviewing business requirements for new capabilities, enhancements, system upgrades or new deployments. Deliver the IT solutions following best practices and aligning People, Process, Technology &amp; Data. Engage with IT and Mfg. Ops. colleagues in exploring cost-effective and sustainable solutions. Actively participate in various meetings with internal and external stakeholders in driving timely closure of support activities. Ensure timely resolution of outstanding tickets (bug-fixes, enhancements) as per the SLA guidelines. Monitor and provide system support ensuring system operates under the service level agreement around availability, performance, accuracy &amp; reliability. Perform unit and integration tests and assist with user acceptance testing. Provide system training on new capabilities to the business stakeholders.Qualifications and Experience1-3 years of experience working as a system analyst or developer. Bachelor’s Degree in technical engineering, science field or related discipline is required. Basic understanding of scheduling and planning algorithms in addition to ERP and manufacturing systems (e.g., MES, DCS, Process Historian) is a plus. Agile and critical thinker with a passion for innovation and learning new skills. Excellent verbal, written and interpersonal communication skills; ability to strategically collaborate and influence in the defined area of scope. Ability to easily navigate through multiple tasks and initiatives. Ability to balance strategic awareness &amp; direction setting with consistent tactical results. Good planning, problem solving, analytical, time management and organizational skills.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Software Engineer Finite Scheduling

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 rich in diversity. 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.Summary:The Automation Systems Engineer will support the successful implementation and operation of Process Automation / OT Systems through interaction with internal team members, peer, and higher-level customers as well as external service providers. The individual is responsible for development of and adherence to system governance procedures.&nbsp;Reporting into the B&amp;IT organization this candidate will be primarily responsible to own activities and deliverables for the Operational Technology and Automation systems across the site and working with a team of cross functional engineers that support on-going improvement and maintenance of these systems.The candidate should have at least 2+ years of experience in pharma/biotech with exposure or expertise in Automation, Hardware, System infrastructure, exposure to Supply Chain, Manufacturing and Quality System disciplines. The candidate needs to understand Good Manufacturing Practices (GMPs).Required Competencies:&nbsp; Knowledge, Skills, and Abilities:<ul><li>Exposure computerized system projects.</li><li>Excellent communication skills including oral, written, and formal presentations.</li><li>Exposure to Process Automation Systems like PLC, DCS, equipment and data collection (i.e. OSI PI).&nbsp;</li><li>Understanding of engineering documentation such as P&amp;IDs, process flow diagrams and standard operating procedures.&nbsp;</li><li>Ability to troubleshoot control systems from the field element up through operator interfaces and databases.&nbsp;</li><li>Strong interpersonal skills and the ability to work in a team environment.&nbsp;</li><li>Ability to work effectively in a fast-paced multi-tasking environment.&nbsp;</li><li>Ability to work in a diverse work environment, manage multiple priorities, and be self-directed.</li></ul>Education and Experience:<ul><li>Bachelor’s degree in engineering, IT, Science field or equivalent experience.</li><li>Experience with PLC, SCADA systems, Automation hardware, DeltaV and Site Historian highly valued but not required</li><li>Minimum 2+ year’s relevant industry experience.</li><li>Prior Biologics/Cell Therapy experience is highly valued but not required.</li><li>Understanding of supply chain, manufacturing domains and supporting technology including manufacturing and supply chain MES and ERP systems (e.g. Oracle, SAP) is highly valued but not required.</li><li>Working knowledge of regulatory requirements and how they relate to existing and new business systems and practices, primarily GxP.</li></ul>Duties and Responsibilities:<ul><li>Will work on and contribute to the Libertyville, IL Facility Process Automation Systems, the data collection (OSI PI) and analytics deliverables.</li><li>Will work with a team of automation and cross functional engineers.</li><li>Partner with Mfg. Operations colleagues (Manufacturing, MS&amp;T, Quality, Site Engineering), Enterprise teams (Global MS&amp;T, Enterprise MES), Enterprise Business teams and local system Digital Capability Managers to deliver the requirements for the Libertyville therapy facility for the following:</li><li>Delivering the requirements for the Process Automation Systems (Infrastructure as well as the Unit operations within the Process automation system).</li><li>Integration needs with the Manufacturing Execution System (Syncade) &amp; Data Historian (OSI PI)</li><li>Help execute the PAS priorities for the Libertyville CTF and work on the delivery of these priorities.</li><li>Develop presentations for the endorsement of OT / Automation projects.</li><li>Work with the technical teams to develop the requirements, code and test the deliverables and drive execution of system testing at the site level.</li><li>Network and work with other cell therapy members to proactively identify issues with cell therapy-based requirements and drive the resolutions.</li><li>Will support the troubleshooting, maintenance, validation, and administration of the following systems: SCADA systems, OSI PI, and DeltaV, Building Automation System. Systems may be added to scope as new installs are completed on-site.</li><li>Support other CTF sites in the BMS network as needed.</li></ul>Working Conditions:This is an office-based role and will spend most of the time seating at desk in an office environment. Individual may be required to gown and enter clean rooms to assist with project work. This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to <a href="mailto:adastaffingsupport@bms.com" target="_blank">adastaffingsupport@bms.com</a>. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:&nbsp;<a href="https://careers.bms.com/california-residents/" target="_blank">https://careers.bms.com/california-residents/</a>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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