Gehaltsübersicht für Development in Boudry

Technical Sales Support Engineer (m/f)Apply DivisionAutomationFunctionSales/MarketingRelated locationSwitzerland, Boudry Your main tasks Review the customer specifications and products in order to develop an assembly concept based on our standard assembly platforms Provide our customers with product design support to improve the assembly process Organize feasibility studies in collaboration with our internal engineering services so as to address specific design concerns or issues Obtain quotes and manage subsystem deliveries through direct contact with suppliers Establish a detailed project estimate as the basis for the sales price Write quotations and present your solution to our customers as part of the sales team Your profile Mechanical engineer (HND, university degree or equivalent) with relevant experience High degree of analytical skills while maintaining a creative approach to your work Ability to meet objectives without getting lost in the details Open-minded personality with communication, negotiation, and persuasion skills Ability and willingness to travel Fluent language skills in German / Swiss-German is a must, any other language is a plus What we offer A career opportunity providing interesting and varied work in the French-speaking region of Switzerland The opportunity to work in a multinational company that offers a wide range of development and training A position in a passionate company with a competitive salary Apply

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. We are seeking a highly motivated Digital & IT Omnichannel Capability Intern to join our international team. The Digital & IT Omnichannel Capability Intern will work closely with Global and in-Market functions to support the development and implementation of our OMNI channel strategy. The role supports as well the continues harmonization of digital design standards to foster an aligned corporate branding and digital best practices across all supported channels, to gain efficiencies across the supported market and beyond. The successful candidate will have a strong interest in technology, data analytics, and customer experience. Key Responsibilities: Assist in the development and implementation of our OMNI channel strategy for International Markets Collaborate with delivery teams to create and localize digital assets, content, and campaigns that resonate with the target audience and adhere to cultural sensitivities and leverage enterprise platforms Conduct research and analysis on customer behavior and preferences across different channels and Markets Monitor and analyze the performance of our digital channels and provide recommendations for improvement Collaborate with cross-functional teams to ensure alignment and consistency across all channels and markets Stay up to date with the latest trends and best practices in digital marketing and customer experience Qualifications / Experience: Currently pursuing a bachelor's or master's degree in a related field Strong interest in technology, data analytics, and customer experience Analytical and problem-solving skills Excellent written and verbal communication skills Proficient in Microsoft Office, particularly Excel and PowerPoint Plus: Experience with digital marketing tools, tactics and platforms This is a great opportunity for someone who is passionate about digital marketing technology and customer experience to gain hands-on experience in a fast-paced and dynamic environment. If you are a self-starter who is eager to learn and grow, we encourage you to apply for this exciting internship opportunity. 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

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. Widespread IT technical knowledge such as Operating System, Infrastructure and Networking. Programming is excluded and development of script is very limited. Proficiency into Computer System Validation in the pharmaceutical environment is required. The accountability of the worker is the improvement or full implementation of off-the-shelf and configurable (Gamp3 and 4) standalone and interconnected standalones, regulated by the GmPs. To a lesser extent, he will collaborate on (Gamp5) worldwide/interconnected systems. Skills/Knowledge Required Pharmaceutical, Biotechnology, Life Science industry experience is a must. 3-5 years’ experience as an IT Engineer running project from requirements to delivery of final product and documentation included. Familiar with Change Management tools and regulated document authoring. COTS and Web-based requirements, architecture, Agile/SCRUM methodology. Real Time Data Management and Interfaces (e.g.: Kepware, OSI PI) a strong plus Serialization technologies (Laetus) a strong plus Six Sigma, Lean or Business Process Change Techniques a plus Technical diploma in Information Systems or equivalent experience Experience in Computer System Validation Awareness of 21-CFR Part 11, Eudralex, MHRA Awareness of business and enterprise architecture Fully operational in French and English Business acumen Autonomous in analysis, problem solving and achieving deliverables Oral and Written communication Constructive influencing of colleagues to positive outcome Duties and Responsibilities Information Technology Requirements, GmP Regulation, must be explained and obtained from the vendor of system. When necessary, the Engineer, may have to customize the system, or adapt the process, to comply the GmPs. Guarantee Data Integrity of the system into its environment and process. Design through elicits, analyzes, documents, and validates detailed user / functional / non-functional requirements; identify gaps between system capabilities and requirements to ensure that business needs are met. Adjust the number of deliverables, their quality and complexity to guarantee the respect of timelines and fit to validation approach. Facilitate meetings with business colleagues on IT topics Assist the translation of compliance requirements into test conditions and expected results for application functionality, and acceptance testing (IQ, OQ, PQ, FAT, SAT) Understand business objectives, processes, and strategies. Drive development and execution of change management and training throughout the organization during the implementation and ongoing use of system applications Ability to work strategically and independently with internal and external groups on multiple simultaneous projects Understand and ensure the use of existing standards for design and governance. Architect system specific topology and adapt/integrate it into existing infrastructure. Collaborate with IT groups to ensure standards are applied for technological tools. Use existing standard to capitalize on lessons learned. Define new versatile solutions covering abstract User Requirements to fulfill unmet needs. Implement specific standalone and interconnected computerized system supporting activities like Production (e.g.: Laetus Track & Trace, Blending, Encapsulation, Tablet Press, Blistering, Bottling, Cartoning, Room Monitoring System and other various equipment used for the manufacturing, packaging and Quality Control of drug products. Usage of a wide variety of Information Technology skills to configure systems, implement backup mechanism for flat files, databases, etc. Deploy proper privileges on Operating System (Windows) and File Systems. Develop governance and “how to” Work Practices, including their Configuration Specifications to allow the operational team to support and administer the newly integrated system. Transmit information and follow up with specialists to obtain required configuration of the global network, backup tool and infrastructure. Configure and setup local network, infrastructure, computers and applications. Preparation and configuration of interfaces between multiple system may be required. Usage of Kepware technology and OPC protocol will be required. 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

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 Summary The Senior Scientific Advisor (sSA) is responsible to actively engage with Thought Leaders (TL), Health Care Professionals (HCPs) to serve as the Therapeutic Area (TA) reference point within their geographic scope. The sSA is responsible to design and deliver a medical plan, consistent with global medial strategic imperatives and in collaboration with local Representatives (Partners). sSA provides medical support to internal matrix Local Representatives (Partners) as well as fosters effective and open relationships with them. sSA supports Brand Strategies development in collaboration with BMS Marketing by communicating medical insights and drug or disease area knowledge with reference to patients’ needs and treatment trends. Key Responsibilities External Environment and Customer Focus Profile the medical landscape in the focused countries within the Disease Area and continuously update this knowledge, including knowledge and expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities, Role model in developing and maintaining peer-to-peer relationships and close contacts with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer unsolicited product and HEOR related questions, Master proficiency in available scientific resources and presentations and effectively present information to HCPs, as appropriate, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives, Actively profile the medical and competitive landscape to effectively evolve planning at the market level within the medical team and matrix leadership teams, as appropriate. Collect, analyze and present meaningful medical insights back to the medical and commercial organizations at brand team meetings to be actioned in support of the strategy development, Identify the need for and execute local Advisory Boards, Propose scientifically meaningful medical programs such as Continuous Medical Educational (CME) programs and Symposia and ensure flawless execution of such activities, Provide scientific information to and collaborate with Local Representatives-Partners (LR-P) relevant functions. Support Clinical Trial Activities Contribute to the “early prioritization” of development programs of Local Representatives countries by collating and integrating data on disease incidence/prevalence, treatment patterns, unmet medical needs and interest from the scientific community, as appropriate. Serve as point of reference for compounds in early development Actively track study performance and contribute with insights and solutions Ensure that BMS Pharmacovigilance procedural documents are understood and applied by Investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events. Medical Planning/Execution Deliver scientifically meaningful medical programs and ensure flawless execution of medical activities to support overarching medical plan execution (e.g. Advisory Boards, Expert Exchange Meeting, Satellite Symposia, etc.), Contribute to the development of Brand Plans and Brand Strategies by communicating medical insight and product or disease area knowledge with reference to patients needs and treatment trends, Participates in the development of the Local Medical Plan, work with local representatives (partners) to deliver Local Medical Plan, contribute to the overall Marketing Plan by leveraging medical insight and product or disease area knowledge of recent scientific publications, Discuss and deliver Health Economics and Outcomes Research (HEOR) evidence-based information reactively (ie, to government agencies, healthcare organizations, and payers), as appropriate, Work with the PV responsible to help ensure that all the information regarding AEs in the field is collected, to facilitate the correct and transparent communication of AEs internally and to the competent Health Authorities externally. Medical support for internal stakeholders Contribute to the initial and ongoing medical/scientific disease area and product-specific training of internal BMS stakeholders (specifically to Commercial, Regulatory, Pharmacovigilance, Legal Counsel and Market Access), Investigational Site staff, Site Managers and Monitors in BMS products, Contribute to, supervise and coordinate the development of the medical / scientific sections of pricing and reimbursement files, Contribute to the development and review of non- promotional material (consistent with the Non-Promotional Review SOP) and participates in the review process of Risk Minimization Materials/ARMA materials. Compliance Endorse and implement a culture of compliance, Adhere to all internal and external rules and regulations, Alert management or the Compliance Department to any possible compliance issues, Act as a role model who demonstrates consistent ethical and professional behavior. Qualifications & Experience Advanced scientific or medical degree (PharmD, PhD, MD), Experience Requirements Relevant industry experience in Medical Affairs/Clinical Development. Experience in a customer-facing role with thought leaders and key customers preferred, Ability to work effectively with cross functional teams including clinical, commercial, regulatory, pharmacovigilance and health outcomes as well as and market-based medical colleagues, Ability to communicate scientific or clinical data in an understandable and valuable manner to help HCPs best serve their patients, Broad experience in Immune/Inflammatory disease area with specific expertise in clinical development is preferred, Experience with investigator sponsored research, non-registrational studies, and early patient access programs preferred, Highly organized and motivated individual possessing excellent communication, presentation and interpersonal skills. Key Competency Requirements Expert knowledge in Immunology & Inflammatory disease area, ideally Psoriasis, scientific or clinical area, Experience in the EMEA (LR-EU) region health care environment & knowledge of local regulations, Developing field medical plans aligned with medical and overall disease & product objectives, Strong communication and presentation skills, Fluent in English, Compliance & Integrity. Travel Requirement Extensive travel (30% time). 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:0126 Bristol-Myers Squibb Kft

Fullstack Software Developer (m/f)Apply DivisionAutomationFunctionInformation Technology/ITRelated locationSwitzerland, Boudry Making complexity accessible Mikron Automation is your worldwide partner for advanced automation solutions. At Mikron we are committed to delivering the best assembly systems and all needed services throughout your product’s entire life cycle. With our extensive engineering know-how, complex process expertise, scalable platforms, and lifelong support we are driving lasting success for your business. Your main task Understand internal users’ and customers’ requirements and provide solutions to answers their needs. Design, develop and maintain new features on the existing platform. Help improve the development team best practices and processes. Work with the agile iterative/incremental mindset and participate actively in the different ceremonials. Your profile Proven experience in software environment development. Good knowledge of web application concept. Good Knowledge of C# Good Knowledge of databases concept: an asset Expertise in network’s architecture, security and cloud concepts: an asset Strong motivation for complex challenges and learning new technologies Mindset for continuous improvement, lean thinking, and high-quality work Excellent communication and teamwork skills. Native speaker of English or French, with excellent knowledge of the other language What we offer A motivating, challenging position with progression opportunities inside a company which pays attention to the continuous training needs of its staff, quality and customer satisfaction A multicultural, collegial, dynamic, teamwork-focused and continuous improvement oriented environment The opportunity to tackle a large number of challenges in a technical and software environment An open-minded and human company culture If you are interested what you have read and want to join our team, we would be keen to hear from you! Apply

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 Summary The Principal Process Engineer/Scientist acts as a technology transfer lead in the parenteral manufacturing MS&T group. This position is accountable for the technical interface between the sending and receiving sites to ensure design and transfer of robust manufacturing processes for new products and key lifecycle parenteral products. Ensures processes are designed and validated per applicable cGMPs, BMS procedures, and that processes are defined consistent with regulatory filings. This position must comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices. The role will also be responsible for review and authoring of key CMC submissions, along with setting relevant standards and creating /maintaining associated tech transfer business processes. Key Responsibilities Leads parenteral technology transfer projects for key lifecycle biologic parenteral products, including the establishment of the process/parameters for each unit operation of the process, and up until the completion of process performance qualification and subsequent CMC filing activities. Development, characterization, optimization and troubleshooting product and manufacturing processes of parenteral dosage forms. Performs Design of Experiments and Process Risk Assessment (FMEA) activities to establish appropriate process control strategies. Designs, prepares, and reviews technology transfer protocols, methods/processes, experimental and/or authoring plans and/or templates as appropriate. Responsible to create, maintain and harmonize key tech transfer business processes. Partners with the management team in the identification of best practices in industry related to technology transfers, pharmaceutical technology to create a competitive advantage. Partners with site operations to provide a parenteral manufacturing process that is sustainable for future product supply. Partners with existing sites in the network to incorporate lessons learned from ‘sending’ sites for an optimized manufacturing process. Representative on global supply strategy groups/site forums and to relevant stakeholders across the company. Leads, motivates, mentors, and develops team members to meet and exceed plant and company goals and objectives. Develops and maintains effective working relationships with other division groups in support of technology transfer, validation, and process support activities. Responsible to review and co-author key CMC sections. Requires approximately ~20% travel. Requirements Bachelor’s degree in Pharmacy, Biochemistry, Chemical Engineering or related Pharmaceutical sciences. Seven years of directly related experience in Technical Services work within the pharmaceutical industry. Three years experience in parenteral manufacturing of protein therapeutics (biologics) strongly preferred, along with demonstrated knowledge of how these products behave in parenteral processes. Subject matter expert in parenteral operations: aseptic processing, sterilization, sterile filtration, isolator technology, lyophilization, pre-filled syringe operations. Strong knowledge of global regulatory requirements related to the design and control of these processes. Knowledge of SOPs, cGMPs and GLPs and the ability to work and manage within a regulatory environment. Demonstrated experience with the execution of technology transfer and scale up programs for commercial drug product manufacturing processes. Strong oral and written communication skills. Ability to work within and lead cross-functional technical teams. Familiarity with Design of Experiments, Quality by Design, and Quality Risk Management concepts commonly employed in pharmaceutical manufacturing. Strong understanding of project management systems and tools is preferred. Excellent organizational skills and the ability to successfully manage a multitude of technical projects. Ability to work in a fast paced, complex and changing environment. Excellent analytical, technical and strategic thinking skills and experiences. Demonstrated management, interpersonal and teamwork skills. Strong mentor, with excellent people development skills and track record. 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:0422 Swords Laboratories Unlimited Company, Dublin, Boudry Branch

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 Summary The Clinical Development Lead sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. CDLs are matrix leaders and managers who lead, develop, motivate and achieve results through teams; demonstrate a commitment to the development of a resilient attitude, embrace change and have an unwavering commitment to our People Strategy Serves as the clinical point of accountability for the Development Team and is responsible for the overall clinical development plan for asset(s) in one or more indication(s)/tumor type(s) Ensures studies are aligned with target label indications and are designed to meet regulatory, quality, medical, and access goals Serves as a matrix leader to lead, develop, motivate and achieve results through teams, and is the direct manager to Clinical Trial Physicians (CTPs) Key Responsibilities Accountable for the clinical contribution to the development of each indication strategy, including registrational and non-registrational studies, with the support of the CTPs and Clinical Scientists (CS) within the asset and/or indication Responsible for managing clinical trial physician(s); attracting, developing and retaining top talent; ensuring appropriate training and mentoring of clinical trial physicians May serve as CTP as necessary Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by the CTPs and CSs. Should work to proactively partner with these roles Accountable for clinical content for CSRs, regulatory reports, briefing books and submission documents Champions a quality-focused mindset and ensures adherence to GCP and compliance obligations for clinical conduct Represents Clinical Development in both internal and external forums as the consulted authority for the disease area, including within Business Development function Partners with Worldwide Patient Safety physicians in the ongoing review of safety data Serves as the (co-)leader of the cross-functional Clinical Development Team Provides clinical leadership and disease area expertise into integrated disease area strategies Partners closely with KOLs in specific indications Serves as Primary Clinical Representative in Regulatory interactions Evaluates strategic options against a given Target Product Profile (TPP) Collaborates with Global Development Operations/Global Compliance Group to develop asset level risk management plan, resolves issues with Quality/CS, and raises to DT as needed Sets executional priorities and partners with CTP and CS to support executional delivery of studies Accountable for top line data with support of CTP, CS, and Statisticians Qualifications & Experience MD required with a deep understanding of the clinical principles of the area of interest or equivalent therapy area knowledge At least 10 years of relevant experience Experience Requirements: CDL has demonstrated leadership in the design and execution of multiple clinical trials (e.g. significant experience as a senior clinical leader), and exhibits all of the following attributes: Able to synthesize internal and external data to produce a clinical strategy Able to ensure that the clinical program will result in a viable registrational strategy Able to assess personnel needs, translate into a hiring strategy, and lead the hiring efforts Able to work with other stakeholders to ensure a robust enterprise level strategy for asset(s) and indication(s) including early, late and post-marketing development, as well as awareness of the enterprise disease area portfolio CDL has demonstrated, sustained excellent performance as Clinical Trial Physician, Clinical Scientist, or equivalent Verifiable track record of successful people management and development, or leadership in a matrix team (e.g. mentoring junior colleagues) Key Competency Requirements: CDL has demonstrated excellent skills in clinical development strategy including the clinical components of regulatory submission(s) External focus to understand the trends in the disease area treatment paradigms and ability to build relationships with external partners, thought leaders and collaborators outside of BMS Partner and interact with colleagues from Early Development who design and implement first in human through proof of concept trials and will to assure a seamless transition into late stage development (Phase II-III trials) Ability to lead and develop a group of CTPs to ensure scientific and technical excellence of clinical development programs and deliverables Travel Required Domestic and International travel may be required. The starting compensation for this job is a range from $308,000-354,000 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 the where the job is performed. Final individual compensation will be decided based on demonstrated experience. For more on benefits, please visit our https://careers.bms.com/working-with-us. Eligibility for specific benefits listed on our BMS Careers site may vary based on the job and location. 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1525 JuN - Seattle Dexter

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. The Senior Director, Vendor & Digital Health Quality is a critical management position in the Clinical Development and Operations Quality Operations (CDOQ) team within the R&D Quality organization that is responsible for the development and implementation of Quality Strategy and strategic oversight for all clinical vendors and digital health activities in the context of clinical trials. The position provides leadership for the identification and resolution of critical quality risks and issues that may affect BMS. The Senior Director, Vendor and Digital Health Quality is also responsible for effectively engaging with various stakeholders in R&D, Digital Health and Strategic Sourcing & Procurement. The Senior Director Data & Vendor Quality will act as Quality Culture ambassador within R&D R, with responsibility for influencing senior leadership across BMS with respect to the importance of building continuous quality enhancements into the organization. Key Responsibilities and Major Duties Oversees/provides GCP consultation to stakeholders on quality issues and risksand process enhancement/compliance - ensuring consistent quality standards and fostering strong working relationships. Promotes high standards of quality, compliance, and process excellence through oversight of procedure development/enhancement as well as by leading or contributing to strategic initiatives to ensure delivery of business goals. Develop and implement quality strategy to oversee clinical vendor and digital health activities in the context of clinical trials Oversee vendor quality oversight activities and manage external quality (e.g., quality agreements with vendors) Oversee the incorporation of new technology and innovation (e.g., digital health technology tools, CDx etc.)) in clinical trials ensuringreliability of trial results. Oversees the development and implementation of the digitalization strategy for CDOQ including automation, virtual reality, and chat bots. Incorporate global regulatory trends and changes into the organization as applicable. Engage with executive management and cross functional business partners to identify areas of greatest compliance risk and obtain information and feedback relevant to process improvement; drive issue resolution Continually evaluate the strategic approach, drive changes in RDQ processes, and modify the RDQ program to meet the changing needs of the organization, regulatory environment and industry best practice Ensure rapid communication of quality issues, including potential misconduct or issues of significant deviations with project/products, to business partners and senior management Talent Development/Management Build and maintain a Vendor and Digital Health Quality organization by creating an environment that attracts, develops and retain high-quality employees Develop hiring plans to staff critical areas in R&D Quality and establish the necessary infrastructure to ensure alignment with corporate objectives Provide leadership, coaching, professional development, mentoring, and support for direct and indirect reports, including talent planning and performance management Develop, motivate, and empower direct reports to have a high degree of accountability for performance and the oversight of key deliverables Engage and energize employees through communication of goals, priorities, and other business critical information as well as recognizing and celebrating success and achievements Attract high-caliber talent and facilitate functional talent development through coaching and provision of challenging assignments to promote individual and team development Lead performance management processes to ensure that individuals are held to appropriate, consistent standards and that key leadership development and succession plans are established Promote a high-performance, externally-focused operating culture throughout organization which emphasizes customer, teamwork, personal accountability, and commitment to quality Model desired behaviors personally and reinforce desired behaviors at all levels in organization. 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 Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. 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 [email protected]. 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. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1057 Celgene R&D Sarl

Working 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-us .The Senior Clinical Scientist reports through the Clinical Science function which provides scientific expertise necessary to design and deliver clinical studies and programs.Position Responsibilities:+ Maintain a thorough understanding of assigned protocols and protocol requirements; educate supporting team members+ Plan and lead the implementation all study startup/conduct/close-out activities as applicable+ Evaluate innovative trial designs (collaboration with Medical Monitor/Clinical Development Lead)+ Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing)+ Site-facing activities such as training and serving as primary contact for clinical questions+ Activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by supporting CS team+ Clinical data trend identification; provide trends and escalate questions to Medical Monitor+ Develop clinical narrative plan; review clinical narratives+ Provision of information required by Protocol Manager for development of trial budget, CRO scope of work, etc.+ Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities+ Drafting/review and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)Collaborate and serve as primary liaison between external partners for scientific adviceDegree Requirements:+ Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred)Experience Requirements:+ Strong experience in clinical science, clinical research, or equivalent+ Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations+ Proficient knowledge and skills to support program specific data review, trend identification, data interpretation+ Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committeesKey Competency Requirements:+ Excellent verbal, written, communication and interpersonal skills+ Must be able to effectively communicate and collaborate across functions and job levels+ Ability to assimilate technical information quickly+ Routinely takes initiative+ Detail-oriented+ Strong sense of teamwork; ability to lead team activities+ Proficient in Medical Terminology and medical writing skills+ Proficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile)+ Proficient critical thinking, problem solving, decision making skills+ Understanding of functional and cross-functional relationships+ Commitment to Quality+ Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism+ Proficient planning/project management skills (ability to develop short to mid-range plans that are realistic and effective in meeting goals)Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools_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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.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 [email protected] . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.Company: Bristol-Myers SquibbReq Number: R1577835Updated: 2024-02-01 04:56:57.010 UTCLocation: Boudry,SwitzerlandBristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.Über das Unternehmen:Bristol Myers Squibb

Bristol Myers Squibb weiß um die Bedeutung von Balance und Flexibilität im Arbeitsumfeld. Wir bieten daher eine Vielzahl von attraktiven Benefits, Dienstleistungen und Programmen an, die unseren Mitarbeitern die Ressourcen bieten, ihre Ziele sowohl bei der Arbeit als auch in ihrem Privatleben zu verfolgen.Bristol-Myers Squibb SAVeröffentlicht:26 Januar 2024Pensum:100%Vertrag:FestanstellungArbeitsort:BoudryDirector Global Digital Transportation SolutionsBei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu Innovationen bei, die bedeutende Veränderungen vorantreiben. Wir verleihen jeder Therapie, für die wir Pionierarbeit leisten, eine menschliche Note. Kommen Sie zu Bristol Myers Squibb und machen Sie einen Unterschied.The Global Director Digital Transportation Solutions is responsible for advancing and managing process and system solutions to support the seamless delivery of products on a global scale. One of the immediate focus areas will be the leadership of the Logistics Control Tower Program which aims at developing a single Transportation system solution that holistically manages the Transportation Operations processes from booking, execution, monitoring and analysis of freight for all 3 business areas of BMS.You will be accountable for developing global cross-functional Transportation strategies, programs, and policies to ensure a successful and compliant Logistics operation providing leadership and direction to Global teams based in the US, Europe, Asia-Pac and Latin America. Working as a key member of the Delivery Excellence Team, you will proactively recognize and address any technical, compliance, and regulatory issues associated with systems, processes, and product quality.Key Responsibilities Lead the Global Logistics Control Tower Program through all stages of the initiative cycle from business case development, vendor selection to global implementation and operations support. Global Process Owner for supporting the advancement of digital and process solutions across all aspects of Transportation. Prepare and Execute Strategic Roadmap for Digital Transportation systems following Gartner maturity model and other industry maturity thought leaders. Work in close partnership with Global Distribution Services (GDS) Team and other stakeholders to develop and deliver on the overall process and digital strategic priorities for the Global Delivery Excellence organization, including strategies for Transportation, Logistics, Distribution, and all other aspects of global drug delivery. Collaborate closely with other functions in developing and executing major strategic initiatives. Lead the application portfolio of data and technologies including but not limited to SAP, cloud computing, cogitative computing, advanced analytics, machine learning to enhance supply chain business processes for Global Distribution Services (GDS). Define process effectiveness monitoring methods, including establishment of metrics and associated targets, data collection and analysis, measurement and reporting mechanisms. Provide appropriate process guidance and instruction. Seeks to automate and simplify repetitive tasks, promoting operational excellence, process standardization and harmonization where appropriate. Qualifications & Experience B.S. or BA in supply chain, management and/or engineering Advanced certification in Supply Chain Management strongly preferred (e.g. APICS CSCP/ CPIM). Operational excellence experience (Green/Black belt or equivalent) preferred. 10+ years of experience in Supply Chain or Logistics Management in the biotech/pharma industry, or comparable. Deep Knowledge or industry expert in Logistics Control Tower Implementation and / or operations. Excellent knowledge of Logistics and IT processes ideally with experience in the design, development, testing, deployment of SAP ERP system. Self-starter who takes initiative and creates novel solutions to problems. Additional professional and personal requirements include: Business Acumen: Has a strong understanding of the key business drivers of the industry/organization. Persuades others with fact-based judgments of the business situation. Executing for Results : Maintains high standards of performance for himself/herself and others and follows through on commitments. Leading Cross Functional Project Teams: Holds people accountable for agreed-to results. Identifies and keeps others focused on the most important metrics to drive the business. Building Relationships & Influencing: Establishes credibility and earns respect with a diverse set of internal and external cross functional stakeholders. Enterprise Mindset: Understands the big picture, beyond their own functional area. Leads within the broader internal and external network and seeks to have impact on organization-wide performance. Change Agility: Creates a vision for the future by spotting strategic opportunities for breakthrough performance. Translates the case for change into actionable plans for the organization. Digital Dexterity : Possesses strong desire to exploit existing and emerging technologies for better business outcomes, is a digital adopter and a flexible learner. Wir setzen uns auf der ganzen Welt leidenschaftlich dafür ein, das Leben von Patienten mit schweren Krankheiten zu beeinflussen. Unsere gemeinsamen Werte Leidenschaft, Innovation, Dringlichkeit, Verantwortlichkeit, Inklusion und Integrität befähigen uns, unsere individuellen Talente und unterschiedlichen Perspektiven in einer integrativen Kultur einzusetzen und bringen das höchste Potenzial jedes unserer Kollegen hervor.