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inspire, and role model marketing excellence. You can thrive within a transformation culture. You are regarded as a marketing expert and gained your experience from Sanofi and/or other organizations. You have a strong understanding of Sanofi's Winning Ways of Marketing and the Marketing Excellence Tools (MEx).

You are highly customer centric, consultative, a strong collaborator, and passionate about professionalizing marketing and raising the marketing excellence capabilities across the US Vaccines Commercial Teams that ultimately delivers incremental growth. You have the ability to interact with all levels of leadership. You display a strong and genuine interest in helping US Vaccines

realize its Go-to-market transformation by inspiring and equipping marketers with leading edge capabilities to deliver impact and results. The Team: You will be joining the Marketing Excellence and Execution Team within US Sanofi Vaccines.

You will be an integral member of the team and will work closely with the US Marketing Franchises and the Global Marketing Excellence Team. Job Description Summary: The Director of Marketing Excellence is responsible for building marketing capabilities within the US Vaccines Commercial Team, assisting the Marketing Teams in leveraging the Sanofi MEx tools to make informed " where to play" and " how to win" choices based on strong

customer and market insights, and partnering with the Global Marketing Excellence Team to lead the US Vaccines annual brand planning process.

Essential Job Duties and Responsibilities: The successful candidate will be required to: Identify capability gaps within the US Vaccines Commercial Team and establish a roadmap for their resolution while simultaneously staying abreast of external best practices and raising internal standards accordingly Drive a marketing cultural change towards a truly customer-centric model that is insights driven and externally focused Lead the development and execution of foundational and advanced marketing capability building programs, training workshops, and " sprint solutions" like skill deep-dives Lead the development and implementation of a training curriculum for new and existing US Vaccines marketers that highlights the unique vaccine selling and B2B environment Continuously iterate and improve programs and curriculum to reflect feedback, evolving marketing excellence tools, and ever-changing US healthcare environment Facilitate MEx workshops with the US Vaccines Franchise Leads, constructively challenging and critiquing to deliver better quality thinking and results Champion and advocate the " Winning Choices Framework" (" where to play" and " how to win" ) and coordinate a consistent approach to annual brand planning Partner with the Global Marketing Excellence Team to magnify the impact of capability efforts within US Vaccines (e.

g. Marketing Skills Catalyst, Brand Planning, Circus Street, Positioning & Communication Excellence Deep Dives, Agency Transformation, Winning Way of Marketing, On-boarding, MEx Awards, MEx Hub etc. ) Collaborate with the US Vaccines Franchise Leads on strategic priorities, ensuring best practices are continuously shared within and outside of the US Vaccines Commercial Team Leverage the Vaccine MEx Champions network to embed change across the US Vaccines Commercial Team Provide marketing thought leadership with US Vaccines Franchise Leads Be a renowned and credible " go-to" expert for Marketers at all levels, coaching and sharing knowledge when and where required Champion a common, consistent Marketing language throughout the US Vaccines Commercial Team Manage and optimize assigned budget, if applicable This is not an exhaustive nor comprehensive list of key responsibilities as the candidate may perform other duties as assigned.

This role may also evolve over time. Key Relationships: Building collaborative partnerships and influencing key stakeholders is crucial in this role: US Vaccines Commercial Team Global Marketing Excellence Team Global Marketing Teams, as needed MEx Council Members and MEx Leads US Vaccines Annual Brand Planning Points Creative and Media Agencies, as needed Other external partners (e. g. capability partners), as needed Required Skills, Knowledge & Experience: Minimum of ten (10+) years of US medical or vaccine Marketing experience High aptitude to learn Sanofi's " Winning Choices" framework and MEx tools Strong strategic thinking, analytical, creative problem-solving and decision-making skills Proactive leadership and collaboration skills to establish strong networks Passion for transformation and coaching; a strong desire and curiosity to continuously learn and improve self and others Desire to help US marketers to do their " day jobs" better and committed to improving business performance and customer experience Strong organizational awareness; ability to navigate, leverage, collaborate and deliver results within the matrix and operating culture Excellent written and oral communication/presentation skills in English Preferred Skills, Knowledge & Experience: Minimum of five (5+) years US vaccine marketplace experience Expert working knowledge of Sanofi's " Winning Choices" framework, supporting tools, and systems Education: A minimum of a bachelor's degree is required MBA degree is preferred Critical Qualities: Ability to work in a fast-paced and ever-changing environment Strong sense of urgency, ability to effectively prioritize and operate calmly under pressure Positive " can-do" attitude, proactive, and a self-starter Ability to drive change with excellent communication and influencing skills A high degree of maturity and self-confidence Strong interpersonal and influencing skills Well organized, highly motivated, process-driven, results-oriented personality Ability to thrive and lead within a data-driven environment Creativity, curiosity, enthusiasm, analytical acumen, and exceptional overall business insights A desire to heighten enthusiasm by making work both fun and fulfilling Ability to work on-site in hybrid capacity Travel Expectations 10% Home Office Bridgewater, NJ #GD-SA #LI-SAAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.

We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.

We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. Director of Marketing Excellence To enable Sanofi's Play to Win ambition, and to compete and win in an ever-changing and increasingly competitive healthcare environment, we have created the Marketing Excellence and Execution Team, of which the Director of Marketing Excellence for US Vaccines plays a critical role.

Who you are: You want to coach, inspire, and role model marketing excellence. You can thrive within a transformation culture. You are regarded as a marketing expert and gained your experience from Sanofi and/or other organizations. You have a strong understanding of Sanofi's Winning Ways of Marketing and the Marketing Excellence Tools (MEx). You are highly customer centric, consultative, a strong collaborator, and passionate about professionalizing marketing and raising the marketing excellence capabilities across the US Vaccines Commercial Teams that ultimately delivers incremental growth.

You have the ability to interact with all levels of leadership. You display a strong and genuine interest in helping US Vaccines realize its Go-to-market transformation by inspiring and equipping marketers with leading edge capabilities to deliver impact and results. The Team: You will be joining the Marketing Excellence and Execution Team within US Sanofi Vaccines. You will be an integral member of the team and will work closely with the US Marketing Franchises and the Global Marketing Excellence Team. Job Description Summary: The Director of Marketing Excellence is responsible for building marketing capabilities within the US Vaccines Commercial Team, assisting the Marketing Teams in leveraging the Sanofi MEx tools to make informed " where to play" and " how to win" choices based on strong customer and market insights, and partnering with the Global Marketing Excellence Team to lead the US Vaccines annual brand planning process.

Essential Job Duties and Responsibilities: The successful candidate will be required to: Identify capability gaps within the US Vaccines Commercial Team and establish a roadmap for their resolution while simultaneously staying abreast of external best practices and raising internal standards accordingly Drive a marketing cultural change towards a truly customer-centric model that is insights driven and externally focused Lead the development and execution of foundational and advanced marketing capability building programs, training workshops, and " sprint solutions" like skill deep-dives Lead the development and implementation of a training curriculum for new and existing US Vaccines marketers that highlights the unique vaccine selling and B2B environment Continuously iterate and improve programs and curriculum to reflect feedback, evolving marketing excellence tools, and ever-changing US healthcare environment Facilitate MEx workshops with the US Vaccines Franchise Leads, constructively challenging and critiquing to deliver better quality thinking and results Champion and advocate the " Winning Choices Framework" (" where to play" and " how to win" ) and coordinate a consistent approach to annual brand planning Partner with the Global Marketing Excellence Team to magnify the impact of capability efforts within US Vaccines (e.

g. Marketing Skills Catalyst, Brand Planning, Circus Street, Positioning & Communication Excellence Deep Dives, Agency Transformation, Winning Way of Marketing, On-boarding, MEx Awards, MEx Hub etc.

) Collaborate with the US Vaccines Franchise Leads on strategic priorities, ensuring best practices are continuously shared within and outside of the US Vaccines Commercial Team Leverage the Vaccine MEx Champions network to embed change across the US Vaccines Commercial Team Provide marketing thought leadership with US Vaccines Franchise Leads Be a renowned and credible " go-to" expert for Marketers at all levels, coaching and sharing knowledge when and where required Champion a common, consistent Marketing language throughout the US Vaccines Commercial Team Manage and optimize assigned budget, if applicable This is not an exhaustive nor comprehensive list of key responsibilities as the candidate may perform other duties as assigned.

This role may also evolve over time. Key Relationships: Building collaborative partnerships and influencing key stakeholders is crucial in this role: US Vaccines Commercial Team Global Marketing Excellence Team Global Marketing Teams, as needed MEx Council Members and MEx Leads US Vaccines Annual Brand Planning Points Creative and Media Agencies, as needed Other external partners (e.

g. capability partners), as needed Required Skills, Knowledge & Experience: Minimum of ten (10+) years of US medical or vaccine Marketing experience High aptitude to learn Sanofi's " Winning Choices" framework and MEx tools Strong strategic thinking, analytical, creative problem-solving and decision-making skills Proactive leadership and collaboration skills to establish strong networks Passion for transformation and coaching; a strong desire and curiosity to continuously learn and improve self and others Desire to help US marketers to do their " day jobs" better and committed to improving business performance and customer experience Strong organizational awareness; ability to navigate, leverage, collaborate and deliver results within the matrix and operating culture Excellent written and oral communication/presentation skills in English Preferred Skills, Knowledge & Experience: Minimum of five (5+) years US vaccine marketplace experience Expert working knowledge of Sanofi's " Winning Choices" framework, supporting tools, and systems Education: A minimum of a bachelor's degree is required MBA degree is preferred Critical Qualities: Ability to work in a fast-paced and ever-changing environment Strong sense of urgency, ability to effectively prioritize and operate calmly under pressure Positive " can-do" attitude, proactive, and a self-starter Ability to drive change with excellent communication and influencing skills A high degree of maturity and self-confidence Strong interpersonal and influencing skills Well organized, highly motivated, process-driven, results-oriented personality Ability to thrive and lead within a data-driven environment Creativity, curiosity, enthusiasm, analytical acumen, and exceptional overall business insights A desire to heighten enthusiasm by making work both fun and fulfilling Ability to work on-site in hybrid capacity Travel Expectations 10% Home Office Bridgewater, NJ #GD-SA #LI-SAAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values.

We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.

We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. PDN-9addcbfa-aada-4a3c-b53b-dace190a92d1

systems and group purchasing organizations, leading health plans, shop benefit managers, and government health care institutions. The company also provides contract management, logistics and supply chain functions for the major Johnson & Johnson franchises.

ECM is a Center of Excellence delivering high quality, efficient and compliant Commercial and Government Contracting Services that enable Business Partners, leverages strengths, and harmonizes best practices to drive growth. ECM is divided into the following areas: Commercial Channel; Government Channel, Contracting Solutions and; and Risk Mitigation & Governance. The Senior Director, Contracting Solutions reports to the Vice President

of ECM and participates as a member of the Leadership Team, owning LT responsibilities across ECM. The Senior Director, ECM leads their team in creating the team's goals and objectives, while assisting all associates with their development plan.

The Senior Director is responsible for accurate operations and must certify every year from a SOX perspective that the people, process, and systems are compliant. The Senior Director is also responsible for reviewing the strategy, process, and data transacted by the team to identify opportunities and implement improvements in these spaces. In addition, the Senior Director will sponsor numerous projects associated with both the upstream and downstream

stakeholders who rely on ECM for contracting services. The Senior Director will also play an integral role in developing ECM's strategic plan.

Responsibilities: The Sr. Director will liaise with more senior counterparts within the Operating Companies (Op Co's), Internal Audit, the Global Legal Organization, J&J Technology, HCC, Customers, Distributors and Wholesalers on an ongoing basis. The Sr. Director will be partnering with all levels of the ECM organization to gain support and feedback on operating company strategies as required and will vary depending on business needs The Sr. Director will lead other People Managers in ECM and will be engaged in ECM projects as well as ECM engagements as needed.

The Sr. Director is also responsible for proactively identifying opportunities to drive and implement improvement processes or policies that will positively impact internal efficiencies, quality controls or the customer experience. Engage with cross-functional teams including Contracting, the Operating Companies and the Global Legal Organization. to ensure business objectives are met. Manage conflicting priorities and meet deadlines and deliverables sometimes with short turnaround times. Provide customer-focused, strategic, and analytical input to operating companies and internal management.

Demonstrate strong communication/presentation skills and conceptual abilities; capable of reviewing, understanding, and synthesizing large quantities of written contractual material or systems data. Maintain current knowledge and expertise on healthcare laws, regulations, and compliance. Manage relationships and provide direction to external vendors required to support the contracting and Records & Information Management systems. Education: A minimum of a bachelor's degree is required. An advanced degree is preferred. Experience and Skills: Required: A minimum of 10 years progressive business experience in sales, marketing, finance, government pricing, contracting, business development, Information Technology or other related areas in a healthcare industry or government agency is required.

People management experience is required, experience managing large teams is preferred. Demonstrated ability to align the goals of multiple stakeholders towards successful outcomes required. Strong skills with MS Office Suite required. Preferred: Experience in the US Healthcare marketplace including medicals and Medical Technology is preferred.

Experience with contracts (i. e. reading, interpreting, and negotiating) is preferred. Advanced competency in systems and demonstrated strong analytical skills preferred. ICS (Model N) and/or CORE (Model N) experience is preferred. Demonstrated leadership in project development and management, especially for large projects, including financials and capital request requirements is preferred. Working knowledge of Government and Commercial pricing, contracting and policy procedures is preferred. Vendor management and experience with procurement processes is preferred. Excellent knowledge of financial and audit controls is preferred.

Other: Position located in Raritan, NJ with up to 25% of domestic travel required. The anticipated base pay range for this position is $163,000 to $282,900. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.

careers.

on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research & Development, LLC. discovers and develops innovative medical solutions to address important unmet medical needs in the following therapeutic areas: immunology, oncology, neuroscience, infectious diseases & vaccines, cardiovascular & metabolism, and pulmonary hypertension.

Please visit http: // for more information. We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. We are guided by our Credo. Thriving on a diverse company culture,

celebrating the uniqueness of our employees and committed to inclusion. Proud to be an equal opportunity employer. Position Summary The Clinical Leader (CL) is responsible for leading the team for a number of Milvexian level activities across all LIBREXIA clinical trials (IDMC, CEC etc.

) and milvexian safety oversight across the program along with supporting other functional program needs. They will lead the Operational Alignment and Safety Integration Strategy Team (OASIS) for the LIBREXIA program within the CVMRPH Therapeutic Area. They will support the preparation of the compound and trial level documents, such as the Development Safety Update Report, Investigator Brochure, and Health

Authorities and Ethics Committees/Institutional Review Board responses.

In this role they may serve as Molecular Responsible Physician. The CL will lead their team to oversee and support the compound level safety and operational harmonization work across clinical trials, support the Independent Data Monitoring activities, the Joint Safety Monitoring Team and the emergency hotline service, Clinical Events Committee, development, and updates of the Clinical Development Plan within Compound Development Plan. They will contribute to protocol development, preparation of clinical study reports, and for the preparation and approval of essential documents for regulatory filings.

The CL may manage direct reports who are project physicians. They will operate in a matrix environment including external partners, and interact with different functions including project management, operations planning, project direction, regulatory affairs, data management, medical writing, biostatistics, benefit-risk management, pharmacogenomics, drug discovery, early clinical development, clinical pharmacology, clinical operations, health economics, epidemiology, worldwide medical affairs and other scientific and business-related disciplines. The CL is also expected to assist in the leadership of the evaluation of external scientific opportunities in the therapeutic area.

Major Duties & Responsibilities Responsible for medical monitoring/reporting and safety oversight; Evaluates adverse events (pre and post-marketing) for relationship to treatment and works closely with Global Medical Safety. Responsible for program medical monitoring/reporting and safety officer activities; Evaluates adverse events (pre and post-marketing) for relationship to treatment May support or assume responsibility for clinical development plans and participates in the design of clinical trials and development of the content of clinical study reports Interprets, reports and prepares results of product research in preparation for world-wide health authorities and submissions Assists Regulatory Affairs in determining requirement for any corrective actions or health authority reporting Acts as medical contact at company for worldwide health authorities concerning clinical/medical issues.

Assists Regulatory Affairs in the development of drug/device regulatory strategies May act as company spokesperson regarding publication of clinical research findings and presentations to relevant global health authorities and advisory committees Helps explore and evaluate new product ideas to assist in identifying new marketing opportunities Supports general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillance May support early clinical development and discovery activities involving product potential and development for registration Participates on evaluation of new product ideas, implement franchise business strategies, etc.

Responsible for backssment of medical publications emerging from the Team and its affiliates; Responsible, with appropriate colleagues, for review of Company advertising and promotion Recruitment, supervision, and development of junior medical staff, assuring diversity of candidates Maintain personal knowledge of assigned therapeutic indication(s) Recruit, supervise, and develop junior medical staff, assuring diversity of candidates Required Knowledge, Skills and Abilities: An MD (or international equivalent) is required.

Board Certification or Eligibility, experience in late development (ie, Phase II/III development experience including interactions with co-development partners) studies with cardiovascular outcomes preferred.

Additional education: Expertise in clinical drug development including demonstrated ability to develop clinical development plans meeting the highest standards is required. A minimum of 10 years Drug Development experience is required, safety review experience is preferred, as well as a minimum of 7 years medical industry experience. Highly successful managerial/supervisory experience is an asset. Also required is Phase II/III development experience including interactions with co-development partners. Worldwide registration experience strongly preferred as well as experience working or with the FDA is very strongly preferred.

Experience working in a Matrix environment and co-development partners is required. Up to 15-20% yearly travel is required (International as well as Domestic). • Fluent in written and spoken English • Working knowledge of the use of Microsoft software products including Excel, Powerpoint, and Word • Experience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings • Ability to work well in a dynamic environment and be able to prioritize and respond to changing needs of the business.

• Demonstrated ability to think strategically The anticipated base pay range for this position is $213,000 to $368,900. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, long term incentives, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans.

Additional information can be found through the link below. For additional general information on Company benefits, please go to: - www. careers. /employee-benefits At Johnson & Johnson, we're on a mission to change the trajectory of health for humanity. That starts by creating the world's healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love.

As such, depending on location and subject to local legislation, candidates offered employment may be required to show proof of COVID-19 vaccination or, in certain countries, secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. If you are invited to interview for the position, your recruiter will advise on the vaccine requirement status in your geographic location. Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.

every operating room around the world. We are redefining medical intervention by combining advancements in medical robotics, instrumentation, navigation and data science. Johnson & Johnson has made meaningful contributions to surgery for more than 100 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures.

Our continuing dedication to craft the future of surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. The Med Tech Quality & Compliance Quality Systems & Digital Services (QS & DS) organization is embarking on a digital innovation journey to transform the way quality

applications and transactions are completed. Project Qu In will be initiated in January 2024 with this role going through Phases 1 and 2 for a 2-year duration period.

The goal of this effort will be to transform our Med Tech Quality Management System (QMS) through the power of Artificial Intelligence (AI) and Machine Learning (ML), creating new value by eliminating transactional inefficiencies and complexity, empowering our teams to focus on our customers. As QS & DS Project Leader for Project Qu In you will make significant contributions towards the planning, development and deployment of Med Tech's solution to 100% Digital QMS. The role is responsible for maintaining a robust governance

and delivering key project objectives while supporting the project's adherence to scope, budget, communication plans, performance management and timeline.

Understanding the technical activities within the project, early identification of risks and their mitigations, and maintaining critical path are key criteria for the position. Key Responsibilities: Support the execution and overall management of the Project Qu In Phases 1 & 2. Support the process transformation for Complaints, Escalations and CAPA systems. Responsible for setting and maintaining the governance process for the management of AI & ML delivery activities that include discovery, analysis, design, build, test, deployment, and post launch automation support.

Ensures the speed and efficiency of the Agile/Scrum process in collaboration with the Product Owner, the Business Analyst and the Scrum Master. Support the delivery teams/squads, ensuring alignment to schedule, budget, and scope requirements. Owns quality by adhering to SDLC, Design & Code standards, security and compliance policies. Act as liaison between business process owners and the technology development team to ensure a healthy Product Backlog is built based on the business process owner's requirements. Lead resolution of customer issues to provide effective remediation in a timely manner, communicating out status and performance metrics to customers.

Partner with the Communications Leaders in the preparation and execution of the Change Strategies to ensure adequate communication is established at different levels of the organization, inclusive of analysis of feedback as an input to the project plan. Education: A minimum of a bachelor's degree in a technical field required (MS Preferred): Computer Science, Information Systems, Mathematics or STEM related fields. Experience and Skills: Required: A minimum of 4 years of experience in a Healthcare or related regulated industry is required.

A minimum of 2 years' experience in technology field and support models in a regulated environment. Solid understanding of Quality Processes and the interaction with Supply Chain processes is required. Successful track record in project execution against timelines and commitments required Experience and Expertise in Project Management with outstanding project coordination skills while being able to multi-task and meet multiple project timelines. Strong verbal and written communication, analytical/problem solving, interpersonal skills, capable of translating technical design ideas and proposals to both technical and non-technical group of customers.

Other: The salary for this position is anticipated to be between $75,000 and $115,000 This position may require up to 10% of domestic and international travel Training in " Intelligent Automation" technology (Certification Highly Desirable). Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers..

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This home is in preforeclosure, which means the homeowner is in default (missed payments).

Therefore, there could be an opportunity to strike a great deal with the owner and the bank.

This individual will partner with system functionality owners in collaboration with management in Operations to support personalized cell therapy production through safe and compliant operations according to c GMP requirements. The role will require technical experience, effective communication, leadership, coordination, and collaboration across relevant cross functional groups to enable robust systems training program for advancement of Raritan CAR-T Operators.

Key Responsibilities Leads, coaches and delivers a holistic, effective systems training program for Operations (Manufacturing) that support daily clinical and commercial production supply of a CAR-T product. Manages, plans, coordinates,

prepares and performs Instructor Led Training in areas of (but not limited to) to MES and S4. Manages the retention and archival of training related documents.

Collaborates and stays connected with System Subject Matter Experts on updates and changes to systems. Conducts knowledge and skill checks and independent performance qualifications for Operations. Works on training improvement projects that make a positive impact on the systems training program. Assists with writing or revising SOPs/Work Instructions, knowledge and skills backssments. Performs training backssments for new and updated procedures and implementations. Collaborates with Process Engineering and Technical Support on

implementation projects that may impact system functionalities.

Identifies technical training needs and expectations, monitors progress, addresses and resolves gaps in training requirements for Operations and other support areas. Optimizes the effectiveness and efficiency of systems training program in delivery of personnel who use systems day to day. Supports investigations and evaluates improvement opportunities for effective compliant training performance leading to sustained right first-time execution. Serve as back up to subject matter expert for Compliance & Training systems. Elevated access level in LMS to capture training compliance in real-time and assign training as needed.

Supports the maintenance and reporting of quality training metrics. Requirements A minimum of a Bachelor's Degree in Science, Information Science or equivalent technical discipline is required. A minimum of 5 years relevant work experience is required. Candidate must have experience working within an aseptic manufacturing facility, preferably in training/system applications, quality systems, or learning management systems. Knowledge of c GMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices.

Experience with training methodology, adult learning theory, instructional design and Train-the-Trainer programs. LMS experience Advanced computer skills and practical knowledge of MS Office Suite, Share Point, and other related systems. Good verbal and written communication skills Excellent organizational skills. Ability to effectively prioritize and execute tasks in a fast-paced environment. Works well in a team-oriented, collaborative environment. The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision.

Proactive and continuous improvement oriented. Ability to lead with influence. c GMP manufacturing. Able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members. Strong analytical, problem solving and critical thinking skills. Project management. Change management. Transparent, Passionate, Fearless and Accountable. #Li-Onsite#Li-JK2