Supply Chain Consultant jobs at Eikon Therapeutics - 223 jobs

The Head of Supply Chain Solutions and Fulfillment is responsible for driving operational excellence across ResMed's global logistics, distribution, and trade networks. This role ensures that customer orders are executed flawlessly, cost-effectively, and in alignment with strategic business objectives. The Head of Supply Chain Solutions and Fulfillment will work across regions (Americas, EMEA, and APAC) to deliver consistent performance, improve customer experience, and create value through optimized fulfilment practices. Reporting directly to the Global Vice President of Distribution Operations, this role provides governance, oversight, and leadership for critical fulfilment initiatives, while partnering with commercial, operations, and corporate stakeholders to achieve measurable business outcomes. **Key Responsibilities** Support short- and long-term operational strategies including customer experience, operational excellence, cost savings, and talent development. **Skills & Competencies** **Communication:** Strong written, verbal, and presentation skills with the ability to influence at all levels. **Problem Solving:** Analytical and detail-oriented with the ability to manage ambiguity and find solutions. **Innovation:** Promotes process improvements and adapts quickly to changing requirements. Strong understanding of supply chain, logistics, and trade, with the ability to connect operations to P&L impact.**Qualifications & Experience** Bachelor's degree in Business, Supply Chain, or related field, or 10+ years' relevant management experience.6-10 years' experience in supply chain, logistics, distribution, or order fulfilment, preferably within the medical device or healthcare sector.Minimum of 5 years of direct leadership experience in a global or matrixed organization. Demonstrated experience in building governance, process discipline, and fulfilment performance metrics. Strong financial acumen with proven ability to connect operational outcomes to business results. Experience managing global order fulfilment operations, including trade compliance and customer delivery. Ability to travel globally up to 30%. Experience with large-scale process design and transformation programs. We are shaping the future at ResMed, and we recognize the need to build on and broaden our existing skills and continue to attract and retain the world's best talent. We work hard to offer holistic benefits packages, provide flexible work arrangements, cultivate a workforce culture that allows employees to grow personally and professionally, and deliver competitive salaries to our team members. Employees scheduled to work 30 or more hours per week are eligible for benefits. This position qualifies for the following benefits package: comprehensive medical, vision, dental, and life, AD&D, short-term and long-term disability insurance, sleep care management, Health Savings Account (HSA), Flexible Spending Account (FSA), commuter benefits, 401(k), Employee Stock Purchase Plan (ESPP), Employee Assistance Program (EAP), and tuition assistance. Employees accrue fifteen days Paid Time Off (PTO) in their first year of employment, receive 11 paid holidays plus 3 floating days and are eligible for 14 weeks of primary caregiver or two weeks of secondary caregiver leave when welcoming new family members.Individual pay decisions are based on a variety of factors, such as the candidate's geographic work location, relevant qualifications, work experience, and skills.At ResMed, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range for this position is: $167,000 - $251,000Client-facing or commercial partnership experience. #J-18808-Ljbffr

Top Requirements (Must haves) 10+ years of experience in Project Management, with experience managing large, highly visible software and application development projects Retail experience is required - these are application development projects within supply chain domain, related to merchandising systems, order management, and retail concepts like pricing, promotions, purchase orders, etc. Full-funnel/cross domain experience is expected (understanding how the backend influences the front end/ecommerce experience) Ability to be hands on - partnering with stakeholders to create a detailed project plan, break program into multiple tracks, manage different work streams, and manage those tracks of work as needed, as well as manage risk/budget/resources and partner with other leaders on prioritization. Strategically partner with delivery leaders on prioritization and program delivery Highly hands-on. Confident and mature attitude. Additional Qualifications A strong Project Manager that is involved in all PM responsibilities and PM fundamentals from detailed project plans, budget, scope, resource and timeline management, status reports, risk and issue logs and management, deployment planning Strong Project management experience with a proven track record of working cross functionally Clear, precise communication is a must for this role as she would be speaking to VPs and above in steering committee meetings and other settings. Demonstrated SDLC project experience with experience working in an Agile environment is required Should be able to excel in a fast paced environment, deal with and be able to steer team in ambiguous situations. Need a strong, edge of your seat, engaging personality type person Bachelor's Degree, preferably with a technical focus

Top Requirements (Must haves) 10+ years of experience in Project Management, with experience managing large, highly visible software and application development projects Retail experience is required - these are application development projects within supply chain domain, related to merchandising systems, order management, and retail concepts like pricing, promotions, purchase orders, etc. Full-funnel/cross domain experience is expected (understanding how the backend influences the front end/ecommerce experience) Ability to be hands on - partnering with stakeholders to create a detailed project plan, break program into multiple tracks, manage different work streams, and manage those tracks of work as needed, as well as manage risk/budget/resources and partner with other leaders on prioritization. Strategically partner with delivery leaders on prioritization and program delivery Highly hands-on. Confident and mature attitude. Additional Qualifications A strong Project Manager that is involved in all PM responsibilities and PM fundamentals from detailed project plans, budget, scope, resource and timeline management, status reports, risk and issue logs and management, deployment planning Strong Project management experience with a proven track record of working cross functionally Clear, precise communication is a must for this role as she would be speaking to VPs and above in steering committee meetings and other settings. Demonstrated SDLC project experience with experience working in an Agile environment is required Should be able to excel in a fast paced environment, deal with and be able to steer team in ambiguous situations. Need a strong, edge of your seat, engaging personality type person Bachelor's Degree, preferably with a technical focus

Synthekine is a Menlo Park, CA based biotechnology company focused on discovering and developing best in class cytokine therapeutics to treat cancer and autoimmunity. We use our unique insights on how cytokines bind to their receptors and tune these systems through protein engineering to generate therapeutics that have transformative potential. Synthekine was formed in 2019 and has raised $313M from leading biotech investors. We are advancing a deep pipeline of therapeutics against some of the most important cytokine targets. Come join us and help us give patients and physicians better options to treat disease and advance cytokine science along the way. Position Summary We are seeking an Associate Director/ Director of Supply Chain to provide support for the PH2/3 product development of cytokine therapeutics to treat cancer and autoimmune diseases. This individual will work closely with the technical operations leadership team and functional heads by providing supply chain and logistics expertise for the Synthekine Phase 2 and 3 clinical product development programs. This is a highly visible role that will interact with the full range of functions within the company. This position will report to the Chief Technical Officer and will be based in Menlo Park. Job Responsibilities Establish the procedures and manage the drug substance, drug product, and labeled/packaged product chain of custody and logistics Manage various products and sample shipping and receiving from and between CMOs Work with Clinical operations to provide appropriate management of study supplies and product distribution Manage the GMP production inventory control, material management, and shipping/receiving operations Maintain the US/EU sourcing, material supply, production capacity, logistics, and availability to meet forecast. Collaborate with our external partners to integrate timelines and deliverables with the overall Synthekine project plans Provides oversight for the development and implementation of the operations systems into the technical operations functions. Manages Supply chain budgets for logistics and distribution Ensures that all records for state, federal, and insurance inspections are accurate and up to date. Operates within compliance with FDA and ISO requirements and guidelines. Partner with other departments Position may require some travel Qualifications BS degree with 8+ years (Associate Director); 10+ years (Director) in Operations, supply chain management, and/or business systems experience Strong leadership, communication (both verbal and written) skills Excellent business, financial and negotiating skills are required along with knowledge of quality systems, lean manufacturing processes and project management knowledge Strong working knowledge of automated supply chain systems Knowledge of current requirements for GLP, cGMP, and GCP is also required Experience with regulatory submissions Forward-thinking and creative with high ethical standards Team player with leadership skills with ability to influence others Well organized and self-directed Strong interpersonal skills with an ability to communicate with people at all levels of an organization Preferred Qualifications Experience with handling GMP DS, DP, and labeled/packaged product logistics to support clinical studies Strong Supply chain background and prior experience working with CMO/CRO is a plus Expertise in using and/or developing clinical supply and inventory systems Prior experience setting up and/or supporting clinical study distribution systems and procedures The anticipated salary range for the position of Associate Director based in our Menlo Park, CA office is $180,000-200,000; The anticipated salary range for the position of Director is $220,000-240,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, education, etc. Synthekine is a multi-state employer, and this salary range may not reflect positions that work in other states. We comply with all state, federal and local laws regarding pay practices. Synthekine is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Synthekine requires all new hires to be fully vaccinated prior to the first date of employment (subject to any legally required exemptions). #J-18808-Ljbffr

Top Requirements (Must haves) 10+ years of experience in Project Management, with experience managing large, highly visible software and application development projects Retail experience is required - these are application development projects within supply chain domain, related to merchandising systems, order management, and retail concepts like pricing, promotions, purchase orders, etc. Full-funnel/cross domain experience is expected (understanding how the backend influences the front end/ecommerce experience) Ability to be hands on - partnering with stakeholders to create a detailed project plan, break program into multiple tracks, manage different work streams, and manage those tracks of work as needed, as well as manage risk/budget/resources and partner with other leaders on prioritization. Strategically partner with delivery leaders on prioritization and program delivery Highly hands-on. Confident and mature attitude. Additional Qualifications A strong Project Manager that is involved in all PM responsibilities and PM fundamentals from detailed project plans, budget, scope, resource and timeline management, status reports, risk and issue logs and management, deployment planning Strong Project management experience with a proven track record of working cross functionally Clear, precise communication is a must for this role as she would be speaking to VPs and above in steering committee meetings and other settings. Demonstrated SDLC project experience with experience working in an Agile environment is required Should be able to excel in a fast paced environment, deal with and be able to steer team in ambiguous situations. Need a strong, edge of your seat, engaging personality type person Bachelor's Degree, preferably with a technical focus

A leading supply chain consulting firm based in San Jose, California, is seeking an Associate Manager - Consulting to oversee the transformation of sourcing and procurement processes. The ideal candidate will have at least 5 years' experience in supply chain management with a strong focus on sourcing and vendor management, proficiency in SAP S/4, and excellent analytical and communication skills. You will collaborate with cross-functional teams to implement innovative practices, ensuring alignment with global standards. The role offers numerous opportunities for professional growth and impact. #J-18808-Ljbffr

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer-working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Director, Global Clinical Supply Chain is an end-to-end clinical supply planning leader that provides relevant expertise in a fast-paced biopharmaceutical environment. The Director works with Global Supply Chain (GSC) and other Gilead functions (Clinical Development, Clinical Operations, Product Development & Manufacturing, Quality Assurance, Regulatory, and PMO) to develop and formulate supply chain strategies, meet project deliverables, solve business problems and create competitive advantage. This role covers all elements of clinical supply planning from protocol design through manufacturing to distribution and inventory management of clinical supplies at clinical sites worldwide. The individual has expert knowledge of clinical supply chain best practices in a GxP environment and strong cross-functional, multi-cultural communication skills to lead in a fast-paced, global company. Essential Job Functions & Focus Area Serves as the clinical supply lead on PDM sub-teams for complex development programs (late phase, acquisition, partnership/alliance, new modality, etc.). Leads development and execution of overall clinical supply strategy and management for clinical development programs, including management of investigational medicinal product (IMP) for assigned global trials. Oversees and supports clinical study planners in a matrix environment; facilitates issue and risk identification, mitigation, resolution and communication. Drives decision-making at cross-functional teams (ClinOps, PDM sub-teams) to support the long-term vision. Identifies, manages and mitigates supply risks at the program level; leads process improvements and organizational imperatives. Authors, revises and reviews SOPs, work instructions and business policies. Accountable for the clinical supply budget of assigned development programs. Reviews and approves statements of work, purchase orders and invoices. Influences program allocations at partners and CMOs as needed. Leads or contributes to strategic initiatives including due diligence resource pool, global drug delivery community, clinical supply integration due to M&A, and support for the External Advocacy Steering Team (EAST). Education & Experience Requirements 12+ years of relevant experience in related field with a BS/BA; or 10+ years of relevant experience with an MA/MBA. Key Knowledge and Skills Ability to develop complex concepts, techniques, and standards. Ability to develop solutions to complex problems requiring ingenuity, creativity and innovativeness. Solutions may set precedents affecting the entire organization; typically unique challenges. Recommends organizational objectives and interprets company policies. Establishes organizational policies in a major segment of the company. Interprets, executes, and recommends modifications to department policies. Demonstrates a comprehensive understanding of the financial aspects of supply chain operations. Specific Job Responsibilities Manage planning, development, implementation, administration and budgeting of production planning, purchasing, material control, inventory control and shipping/receiving functions. Coordinate activities and resolve issues related to production planning, procurement, and material management; make decisions aligned with strategic direction. Implement and maintain material control systems, policies, processes and procedures to ensure timely material flow to meet production requirements. Ensure adequate personnel, equipment, material and services to maintain inventory levels. Coordinate interdepartmental activity with Quality Assurance, Manufacturing, Engineering and Contract Administration. Provide guidance in establishment and maintenance of the production control system. May liaison with governmental/regulatory agencies as required. Review, approve and implement changes to controlled documents as needed. Develop new applications for the department and monitor cost, schedules and performance of major contracts as applicable. The salary range for this position is: $210,375.00 - $272,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility varies by role), paid time off, and a benefits package, including medical, dental, vision and life insurance plans. Eligible employees may participate in benefit plans subject to plan terms. For additional benefits information, visit: ****************************************************************** EEO Notice (US) Gilead Sciences is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national origin, sex, age, sexual orientation, disability, genetic information, gender identity or other non-job related characteristics or prohibited grounds by applicable law. Our environment respects individual differences and recognizes each employee as an integral member of our company. We promote a work environment free of harassment and discrimination and celebrate diversity of thought and opinion. For current employees and contractors: please apply via the Internal Career Opportunities portal in Workday. #J-18808-Ljbffr

A leading biopharmaceutical company is seeking a Vice President of Global Supply Chain to manage end-to-end supply chain activities for clinical and commercial products. This role requires extensive experience in supply chain management, particularly within the pharmaceutical industry. The successful candidate will lead a global team and ensure the timely supply of products across various clinical studies. This position offers a competitive salary and a hybrid working model in San Francisco. #J-18808-Ljbffr

United States - California - Foster City Manufacturing Operations & Supply Chain Regular Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. As part of our rapidly growing science-driven organization, colleagues at Gilead are revolutionizing healthcare by bringing urgently needed medicines to patients in the areas of HIV/AIDS, liver diseases, hematology and oncology, inflammation and respiratory diseases and cardiovascular conditions. We are proud to have some of the most talented colleagues from across the research, healthcare, pharmaceutical, biotechnology & business sectors, working together and supporting each other to help make a real difference to the lives of patients. Exec Director, Global Supply Chain Strategic Sourcing and Supplier Management FOSTER CITY, CA Key Responsibilities: Reporting to the SVP of Global Supply Chain, and part of the larger Pharmaceutical Development and Manufacturing organization (PDM), the ED Strategic Sourcing and Supplier management will lead a team of Supply chain professionals sourcing and leading our outsourced CMO network. This role is accountable for the strategic business relationships with external suppliers of both Development and Commercial services and/or materials. This includes ownership of the strategy, selection, and performance management of all suppliers providing API, SDD, OSD, BDS, sterile DP, and secondary packaging services as well as all suppliers of direct materials including medical devices, primary packaging, excipients, and manufacturing consumables. This role collaborates closely with all PDM functional groups including RA, Tech Dev, Mfg. Ops, QA, Product & Portfolio Strategy, and Global Supply Chain and is accountable for continuous improvement and ongoing collaboration with our suppliers through product lifecycle. Responsibilities: Development and Commercial Programs: Own the strategic business relationship with suppliers of manufacturing services and direct materials including but not exhaustive: Accountable for sourcing of strategic partners, contract negotiation and ongoing business relationship with the suppliers. (MSAs, SOWs, Supply Agreements, Pricing, etc.) Lead strategic business discussions, long range supply and/capacity planning, and business development, through the product lifecycle and ensure financial discipline, win win and savings opportunities. Participate and contribute into CD & OP and S & OP. Management of supplier performance (monthly/annually) Key KPI: i.e., OTD, Batch Release First Time %). Deviation on time Closure (%), Batch Rejection Rate (%), Deviations per batch The escalation points for Mfg. Ops team members for recurrent or chronic performance issues from suppliers Lead quarterly / annual business review meetings (BRMs) with strategic/high suppliers Lead the assessment and mitigation of supplier risks through regular supplier risk management processes BCP plans with suppliers articulated and desk top exercises completed to ensure robustness Responsible for preparation and tracking of RFPs/RFQs for new business with external suppliers and in consultation with functional stakeholders (Mfg. Ops, Tech. Dev. QA, etc.) In collaboration with Product and Portfolio Strategy team members, identify and manage strategic suppliers of manufacturing services in alignment with network supply chain strategies Own the development and execution of supplier strategies for direct material suppliers Identify and manage strategic suppliers of direct materials in alignment with approved CMT strategies Establish quality and technical execution expectations with vendors Segment our supplier and have a strategy for strategic and tiered suppliers. Articulate digital roadmap and integration with key suppliers, plan and execute against it Sustainability and resilience strategy articulated with key suppliers Development/Clinical Programs: Providing intel, options, and solutions; staying informed and knowledgeable of relevant Development CDMO and material supplier capabilities, offerings, capacities, etc. as they relate to potential or known Gilead pipeline needs Leading site assessment teams (SATs) and/or category management teams (CMTs) for the assessment and selection of new service or material suppliers to meet Development program needs Ensuring the full scope of supplier selections made during Development align with Commercial manufacturing and/or network strategies, as necessary. Establish quality and technical execution expectations with vendors Prepare and/or review agreements covering confidentiality, supply terms & conditions, and quality Commercial Programs: Providing intel, options, or solutions; staying informed and knowledgeable of relevant Commercial CMO and material supplier capabilities, offerings, capacities, etc. as they relate to Gilead Commercial supply needs Leading site assessment teams (SATs) and/or category management teams (CMTs) for the assessment and selection of service or material suppliers to meet commercial Program needs Qualifications: Primary degree in Business, Science or Engineering discipline. Master's degree and/or professional qualifications in supply chain management desired. 15+ years of biopharmaceutical industry experience with at least 5 years of experience focused on management and leadership roles with contract manufacturers in a supply chain capacity. Experience developing, implementing, and executing strategic plans and objectives for organizations and departments. Solid understanding of current industry trends. Leadership qualities of the successful candidate include the following: collaboration, building and developing high performing teams, accountability, cross functional engagement and influence, program management, strategic vision, executive presence, coaching, goal setting and performance management. Strong business acumen. Capability to navigate and lead in a highly matrixed environment. Demonstrated ability to understand complex and complicated situations and to strip out complications. Effective communication skills, both written and verbal. Can make convincing arguments, inspire action, and bridge diverse cultures. Capable to communicate the world of PDM to people outside of PDM, and to communicate about the world outside of PDM to those inside. Negotiation and conflict resolution skills. A proven capability to contribute to your team's success through servant leadership. A proven capability to contribute to the success of PDM and Gilead as a senior leader. Gilead Core Values Integrity (Doing What's Right) Inclusion (Encouraging Diversity) Teamwork (Working Together) Excellence (Being Your Best) Accountability (Taking Personal Responsibility) #J-18808-Ljbffr

A leading biopharmaceutical company is seeking a Director, Global Clinical Supply Chain in Foster City, CA. This role is responsible for managing the supply chain for clinical development programs and requires 12+ years of experience in a related field. The ideal candidate will have strategic leadership capabilities and a proven track record in supply chain management. The position offers a comprehensive salary package and benefits, alongside the opportunity to impact health innovations. #J-18808-Ljbffr

United States - California - Foster City Manufacturing Operations & Supply Chain Regular Gilead's Director, Global Clinical Supply Chain is an end-to-end clinical supply planning leader that provides relevant expertise in a fast-paced biopharmaceutical environment. The Director works internally with other members of Global Supply Chain (GSC) and other Gilead functions - e.g., Clinical Development, Clinical Operations, Product Development & Manufacturing (PDM), Quality Assurance, Regulatory, and Project Management Office - to develop and formulate supply chain strategies, meet project deliverables, solve business problems and create competitive advantage. This position includes all elements of the clinical supply planning from the protocol design through manufacturing to the ultimate distribution and inventory management of clinical supplies at clinical sites worldwide. The individual has an expert working knowledge of clinical supply chain best practices and experience working with a GxP environment. Has strong cross‑functional, multi‑cultural awareness and communication skills to lead in a fast‑paced, global company. ESSENTIAL JOB FUNCTIONS & FOCUS AREA Serves as the clinical supply lead on PDM sub‑teams especially for complex development programs - e.g., late phase, acquisition, partnership/alliance, new modality, etc. Leads the development and execution of overall clinical supply strategy and management for clinical development program(s), including management of investigational medicinal product (IMP) for assigned global trials. Often in a matrix environment, oversees and supports clinical study planners. Facilitates issue and risk identification, mitigation, resolution and communication. Drives decision‑making at cross‑functional teams (ClinOps, PDM sub‑teams) supporting the long‑term vision. Identifies, manages and mitigates supply risks at clinical development program level. Leads and drives visible, impactful process improvements, change business and organizational imperatives. Authors, revises and reviews standard operating procedures (SOPs), work instructions and business policies. Accountable for clinical supply budget of assigned clinical development program(s). Reviews and approves statement of work, purchase orders and invoices. Influences, at times drives, program allocations at partners, contract manufacturing organizations (CMOs). Lead or a contributing member to GCSC, GSC or PDM strategic initiatives including and not limited to due diligence resource pool, global drug delivery community, clinical supply integration due to M&A and policy topic member supporting the External Advocacy Steering Team (EAST). Key Knowledge and Skills Able to develop complex concepts, techniques, and standards. Able to develop solutions to complex problems which require an in depth degree of ingenuity, creativity and innovativeness. Challenges are frequently unique and solutions may serve as precedent for future decisions, which affect the entire organization. Recommends organizational objectives and interprets company policies. Establishes organizational policies in a major segment of the company. Able to interpret, execute, and recommend modifications to department policies. Demonstrates a comprehensive understanding of the financial aspects of Supply Chain operations. Specific Job Responsibilities Manages the planning, development, implementation, administration and budgeting of the production planning, purchasing, material control, inventory control and shipping/receiving functions. Provides department management with the coordination of activities and resolution of issues and potential problems related to production planning, procurement, and material management, making or recommending appropriate decisions consistent with strategic direction. Implements and maintains material control systems, policies, processes and procedures ensuring that a controlled flow of approved materials timed to meet production requirements. Ensures that personnel, equipment, material and services are provided as needed to maintain acceptable inventory levels. Coordinates interdepartmental activity with Quality Assurance, Manufacturing, Engineering and Contract Administration. Provides expertise and guidance in establishment and maintenance of the production control system. May serve as liaison between the company and the various governmental agencies. Directly interfaces with regulatory agencies as required. Reviews, approves and/or implements changes to controlled documents as needed. Develops new applications for the department, based on professional principles and theories. May negotiate major contracts involving large financial amounts. Monitors cost, schedules and performance aspects of major contracts. Education & Experience Requirements 12+ years of relevant experience in related field and a BS or BA; OR 10+ years of relevant experience and a MA/MBA OR 8+ years of relevant experience and a PhD Job Level: Director Job Type: Full Time Location: United States - California - Foster City Legal note: Equal Employment Opportunity (EEO) applies. #J-18808-Ljbffr

Associate Director, End-to-End Commercial Supply Planner plays a critical role developing and executing supply plans for commercial small molecule and biologics products. This role partners closely with regional commercial supply chain leads to deeply understand demand planning trends, market dynamics, and promotional activities, ensuring these inputs are fully incorporated into global supply plans. Reporting to the End-to-End Commercial Supply Chain Product Lead, the role leverages tools such as SAP ERP and Kinaxis Rapid Response to enable accurate, responsive supply planning and ensure product availability across diverse markets. Key Responsibilities Collaborative Demand-Supply Alignment Act as a primary partner to regional commercial supply chain leads to understand regional demand planning trends, market access changes, promotional campaigns, and product lifecycle events. Ensure demand signals from regional planning teams are accurately reflected and integrated into the end-to-end supply plans. Facilitate regular communication and alignment sessions with regional leads to validate assumptions, reconcile forecast discrepancies, and adjust supply plans accordingly. Supply Planning & Execution Develop, maintain, and execute detailed commercial supply plans that reflect the latest demand insights and manufacturing capacities. Utilize SAP ERP and Kinaxis RapidResponse to build and monitor supply plans, adapting quickly to changes in demand or supply constraints. Work closely with internal and external manufacturing sites to confirm production schedules support demand trends and commercial priorities. Inventory & Allocation Management Collaborate with regional supply leads to optimize inventory positions, balancing customer service levels with cost efficiency. Support supply allocation decisions during constrained supply scenarios by leveraging insights from demand trends. Cross-Functional Engagement Partner with Commercial Operations, Quality, Manufacturing, and Finance teams to ensure supply plans support overall business objectives. Participate in regional and global S&OP processes, providing supply planning expertise and demand-supply reconciliation. Support change management initiatives impacting supply plans resulting from commercial or regulatory changes Performance Monitoring & Reporting Track and report key supply planning metrics including supply plan adherence, inventory levels, and service performance. Provide timely updates and escalations to leadership and stakeholders based on supply-demand alignment. Basic Qualifications Doctorate and 5+ years of relevant experience OR Master's and 8+ years of relevant experience OR Bachelor's and 10+ years of relevant experience OR Preferred Qualifications Experience in supply planning or related roles within pharmaceutical or biopharmaceutical commercial supply chains. Proven experience partnering with regional commercial supply chain leads to incorporate demand planning insights into supply plans. Strong experience with SAP ERP and Kinaxis RapidResponse or equivalent supply planning tools. Knowledge of commercial supply chain dynamics in small molecule and/or biologics product sectors. Excellent interpersonal and communication skills to foster collaboration with regional teams. Strong analytical skills with the ability to interpret demand data and translate into executable supply plans. Ability to manage competing priorities and work effectively in a global, matrixed environment. Proactive problem-solving mindset and customer-focused approach. #J-18808-Ljbffr

United States - California - Foster City Manufacturing Operations & Supply Chain Regular Director E2E Product Supply Chain-Foster City, CA Reports To: VP, Global Commercial Supply Chain & Strategy Gilead Sciences is seeking a highly experienced and strategic E2E Product Supply Chain Director to lead and optimize our end-to-end supply chain operations. This role is critical in ensuring the seamless delivery of products from manufacturing to the end customer, while maintaining high standards of quality, efficiency, and compliance. Strategic Leadership Develop and implement supply chain strategies that align with Gilead's business objectives and growth plans. Collaborate with commercial teams to understand product strategy, launch plans, and promotional activities. Translate brand needs into supply chain requirements, identifying potential challenges and solutions. Provide supply chain insights and expertise during brand strategy development. Demand and Supply Planning Oversee demand and supply planning for commercial products, ensuring the availability of necessary materials and resources. Align long‑range planning (LRP) with financial planning, capacity assessments, and market forecasts to ensure readiness for future demands. Collaborate with cross‑functional teams to integrate LRP into overall business strategy. Monitor global supply chain trends and potential disruptions, proactively adjusting plans to mitigate risks. Develop and manage demand forecasts for assigned brands, considering market dynamics and promotional plans. Ensure forecast accuracy and alignment with inventory targets. Coordinate with the planning team to ensure optimal supply availability. Monitor product availability and proactively manage potential supply disruptions. Coordinate with production, quality, and logistics teams to ensure seamless supply chain operations. Drive end‑to‑end supply chain efficiency and effectiveness for the assigned brand. Operational Excellence Oversee the entire supply chain process, including manufacturing, logistics, and distribution, ensuring efficiency and cost‑effectiveness. Monitor and analyze supply chain performance for the assigned brands. Identify areas for improvement and propose corrective actions. Develop and present reports and metrics to track performance. Establish and monitor key performance indicators (KPIs) to track and improve supply chain performance. Drive continuous improvement initiatives and adopt new technologies to enhance supply chain capabilities. Monitor inventory levels for assigned brands. Identify slow‑moving or excess inventory and propose mitigation strategies. Implement optimized inventory strategies to maximize product availability. Quality Assurance Ensure all supply chain activities comply with regulatory requirements and quality standards. Identify and mitigate risks within the supply chain to ensure continuity and reliability. Develop and implement long‑term supply chain strategies that support the company's growth and product pipeline. Develop and recommend strategies to enhance supply chain resilience, including risk assessment, contingency planning, and diversification of supply sources. Work closely with cross‑functional teams, including R&D, manufacturing, and commercial, to ensure alignment and support for product launches and ongoing operations. Establish and maintain relationships with the Gilead Sites and Global External Manufacturing. Work closely with CMC to understand batch sizes and manufacturing complexities for each product and oversee comprehensive plans for API and DP production, ensuring alignment with commercial timelines. Collaborate with the NPI Team on supply chain activities for new product launches, ensuring a smooth transition and consistent supply. Serve as the primary supply chain point of contact for brand and commercial teams. Maintain regular communication with stakeholders, sharing updates and proactively addressing issues. Qualifications Education: Bachelor's degree in Supply Chain Management, Business Administration, or a related field; MBA or advanced degree preferred. Experience: Minimum of 10 years of progressive experience in Supply Chain, Planning, Manufacturing, or other Supply Chain discipline, preferably in the Biotechnology / Pharmaceutical industry, with at least 5 years in a leadership role. Skills: Strong analytical, problem‑solving, and decision‑making skills; excellent communication and interpersonal skills; proficiency in supply chain software and technologies. Leadership: Proven ability to lead and inspire teams, drive change, and achieve results in a fast‑paced environment. Knowledge: Deep understanding of global supply chain dynamics, regulatory requirements, and industry best practices. Certifications: Supply chain certification is a plus (e.g., APICS, CPIM, CSCP). Additional Skills: Ability to manage complex projects and drive cross‑functional initiatives; experience with regulatory requirements related to pharmaceutical supply chains; ability to manage multiple projects in a fast‑paced environment; strong interpersonal communication skills; proven ability to build and maintain collaborative, effective internal and external relationships; excellent written, oral communication, and presentation skills; ability to collaborate effectively in a dynamic, cross‑functional matrix environment. Job Requisition ID R0045258 Full Time/Part Time Full-Time Job Level Director #J-18808-Ljbffr

A leading biopharmaceutical company in California is seeking an experienced Supply Chain Leader to oversee clinical and commercial supply planning. The role requires extensive experience in cGMP operations and the ability to drive operational improvements. Candidates must have a strong background in strategic planning, leadership, and exceptional communication skills. If you are passionate about making a meaningful impact in patient lives and have a proven track record, we encourage you to apply. #J-18808-Ljbffr

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.The Associate Director of Operational Excellence (OpEx) is a key leadership role responsible for driving end-to-end process improvement, operational efficiency, and organizational capability building across Supply Chain, External Manufacturing, and Technical Operations within the pharmaceutical manufacturing network. This role will partner with internal and external stakeholders to deliver transformational initiatives, ensure robust supply performance, and enhance the company's ability to deliver high-quality medicines to patients reliably and cost-effectively.The ideal candidate brings expertise in Lean Six Sigma, pharmaceutical manufacturing processes (including cGMP), and the unique challenges of managing a global external manufacturing and supply network.**Responsibilities****Lead Operational Excellence Strategy & Execution*** Develop and execute the Operational Excellence roadmap for Supply Chain, External Manufacturing, and Technical Operations, aligned with business goals and priorities.* Drive transformational initiatives that enhance reliability, agility, and cost-effectiveness of the end-to-end supply network.* Embed a culture of continuous improvement across internal teams and external partners.* Monitor industry trends and benchmark performance to sustain competitive advantage in operational practices.**Process Improvement & Performance Optimization*** Identify, prioritize, and implement process improvement opportunities to enhance service, reduce costs, and ensure compliance across planning, sourcing, manufacturing, and distribution.* Facilitate cross-functional projects using Lean, Six Sigma, Value Stream Mapping, and other proven methodologies.* Support Technical Operations in problem-solving initiatives by coaching team leads to effectively utilize fit-for-purpose frameworks for identifying root cause(s).* Standardize and digitize key supply chain and manufacturing processes to improve visibility, control, and decision-making.**External Manufacturing & Supplier Excellence*** Collaborate with CMOs/CDMOs and internal stakeholders to assess and improve external manufacturing performance through systematic KPI reviews and improvement plans.* Lead joint improvement initiatives with external partners while ensuring cGMP and regulatory compliance.* Build strong relationships and foster a culture of collaboration and continuous improvement with suppliers and contract manufacturers.**Tier Management & Visual Performance Management*** Design, implement, and sustain a Tiered Management System (Tier 1-3) across Supply Chain, External Manufacturing, and Technical Operations to enable effective daily, weekly, and monthly performance management.* Deploy visual management tools and performance dashboards at each tier level to drive accountability, transparency, and fast problem resolution.* Train and coach teams and partners in daily management practices, visual controls, and structured problem-solving.* Ensure escalation processes and feedback loops are effective and standardized across the network.**Capability Building & Change Leadership*** Build organizational capabilities by developing and delivering training on Operational Excellence tools and methodologies to internal teams and external partners.* Coach functional and site leaders in OpEx mindset and practices to enable self-sufficiency and sustained improvements.* Lead change management efforts to overcome resistance and embed new ways of working.* Act as a role model for continuous improvement, demonstrating a data-driven, collaborative, and solution-oriented approach.**Qualifications & Experience*** Bachelor's degree in Engineering, Supply Chain Management, Life Sciences, or related field required; Master's degree or MBA preferred.* Minimum 8-10 years of experience in a regulated healthcare industry segment (e.g., pharmaceutical development, supply chain, manufacturing, medical device, or technical operations, with at least 3-5 years in operational excellence, continuous improvement, or similar leadership roles.* Strong understanding of manufacturing and supply chain processes, cGMP, regulatory requirements, and the complexities of external manufacturing.* Certified Lean Six Sigma Black Belt (or equivalent) strongly preferred.* Proven track record of delivering measurable improvements in operational performance, cost reduction, and process efficiency.* Experience managing and improving external manufacturing or supplier relationships in a regulated industry.* Exceptional project management, change management, and facilitation skills.* Excellent communication, influencing, and stakeholder management abilities across all organizational levels and with external partners.* Ability to thrive in a fast-paced, matrixed, and global environment.**Competencies*** Strategic thinking with a hands-on approach.* Results-oriented and data-driven decision-making.* Strong analytical and problem-solving skills.* Ability to lead without authority and drive collaboration.* Passion for excellence and continuous improvement.**Pay Range:**In the U.S., the hiring pay range for fully qualified candidates is $189,900-$221,550 per year. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors.*Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.***Please review our PRIOR to applying.**Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do - all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.Here are some ways to check for authenticity:* We do not conduct job interviews through non-standard text messaging applications* We will never request personal information such as banking details until after an official offer has been accepted and verified* We will never request that you purchase equipment or other items when interviewing or hiring* If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at ************************************Please visit our website at:****Cytokinetics is an Equal Opportunity Employer** #J-18808-Ljbffr

The Head of Global Supply Chain Solutions and Fulfillment is responsible for driving operational excellence across ResMed's global logistics, distribution, and trade networks. This role ensures that customer orders are executed flawlessly, cost-effectively, and in alignment with strategic business objectives. The Head of Global Supply Chain Solutions and Fulfillment will work across regions (Americas, EMEA, and APAC) to deliver consistent performance, improve customer experience, and create value through optimized fulfilment practices. Reporting directly to the Global Vice President of Distribution Operations, this role provides governance, oversight, and leadership for critical fulfilment initiatives, while partnering with commercial, operations, and corporate stakeholders to achieve measurable business outcomes. Key Responsibilities Strategic Leadership & Alignment Negotiate with key business partners globally to gain alignment on fulfilment vision, priorities, and project selection. Lead cross-functional collaboration across logistics, distribution, and trade to ensure delivery of strategic initiatives. Align fulfilment strategies with overall business objectives, building strong partnerships with commercial, corporate, and operations teams. Balance global strategy with regional execution to ensure consistent and scalable fulfilment outcomes. Order Fulfilment Excellence Oversee the global order fulfilment process to ensure accuracy, timeliness, and efficiency. Drive initiatives that improve service levels and customer satisfaction across all channels and regions. Solve complex fulfilment issues by identifying and addressing root causes to improve accuracy, productivity, and quality. Champion process standardization, compliance, and scalability across the global fulfilment network. Business Performance & Governance Develop, track, and report performance metrics (OKRs, KPIs) that drive fulfilment excellence and business value. Support short- and long-term operational strategies including customer experience, operational excellence, cost savings, and talent development. Collaborate with Finance and Operations to ensure fulfilment performance is tied to measurable ROI and P&L impact. Lead executive-level reporting, translating data and insights into clear business narratives. People Leadership & Development Provide vision and direction for fulfilment teams globally while fostering bottom-up input and continuous improvement. Build and lead a diverse and inclusive team, with an emphasis on developing future leaders and exporting talent across the organization. Inspire teams to stay focused and motivated during periods of organizational complexity and change. Position Challenges Navigating a complex and evolving fulfilment landscape across culturally diverse global teams. Delivering measurable improvements in customer value while balancing cost, quality, and speed. Managing the trade-offs between short-term operational needs and long-term sustainable growth. Leading through ambiguity while providing clarity and discipline to global fulfilment processes. Skills & Competencies Leadership: Inspires teams to achieve excellence, empowers others, and builds trust through performance. Communication: Strong written, verbal, and presentation skills with the ability to influence at all levels. Results Orientation: Highly motivated to deliver on commitments with accountability for outcomes. Problem Solving: Analytical and detail-oriented with the ability to manage ambiguity and find solutions. Collaboration: Effective at working across boundaries and building partnerships globally. Innovation: Promotes process improvements and adapts quickly to changing requirements. Business Acumen: Strong understanding of supply chain, logistics, and trade, with the ability to connect operations to P&L impact. Qualifications & Experience Required: Bachelor's degree in Business, Supply Chain, or related field, or 10+ years' relevant management experience. 6-10 years' experience in supply chain, logistics, distribution, or order fulfilment, preferably within the medical device or healthcare sector. Minimum of 5 years of direct leadership experience in a global or matrixed organization. Demonstrated experience in building governance, process discipline, and fulfilment performance metrics. Strong financial acumen with proven ability to connect operational outcomes to business results. Experience managing global order fulfilment operations, including trade compliance and customer delivery. Ability to travel globally up to 30%. Preferred: MBA or advanced degree in Business, Supply Chain, or related field. Experience with large-scale process design and transformation programs. Client-facing or commercial partnership experience. We are shaping the future at ResMed, and we recognize the need to build on and broaden our existing skills and continue to attract and retain the world's best talent. We work hard to offer holistic benefits packages, provide flexible work arrangements, cultivate a workforce culture that allows employees to grow personally and professionally, and deliver competitive salaries to our team members. Employees scheduled to work 30 or more hours per week are eligible for benefits. This position qualifies for the following benefits package: comprehensive medical, vision, dental, and life, AD&D, short-term and long-term disability insurance, sleep care management, Health Savings Account (HSA), Flexible Spending Account (FSA), commuter benefits, 401(k), Employee Stock Purchase Plan (ESPP), Employee Assistance Program (EAP), and tuition assistance. Employees accrue fifteen days Paid Time Off (PTO) in their first year of employment, receive 11 paid holidays plus 3 floating days and are eligible for 14 weeks of primary caregiver or two weeks of secondary caregiver leave when welcoming new family members. Individual pay decisions are based on a variety of factors, such as the candidate's geographic work location, relevant qualifications, work experience, and skills. At ResMed, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range for this position is: $167,000 - $251,000 Joining us is more than saying “yes” to making the world a healthier place. It's discovering a career that's challenging, supportive and inspiring. Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates. If this sounds like the workplace for you, apply now! We commit to respond to every applicant.

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. Affiliate Overview Eidos Therapeutics, an affiliate within BridgeBio Pharma, is a commercial-stage biopharmaceutical company focused on Transthyretin Amyloid Cardiomyopathy (ATTR-CM). What You'll Do The Vice President of Global Supply Chain will be responsible for global end-to-end clinical supply chain activities related to managing supply of Investigational Product (IP) including packaging, labeling, distribution and demand forecasting for multiple clinical studies through all stages of clinical development. The role will also have responsibility for global end-to-end commercial supply chain activities, including the management of S&OP, Supply planning, Supplier (CMO, CPO, 3PL) management, inventory management, and partnership with Global Trade for Finished Good distribution. The role will partner closely with CMC/Manufacturing, Commercial, Clinical, and Quality Assurance teams and partner stakeholders to ensure timely and uninterrupted supply of clinical and commercial product. The individual must have the ability to manage global teams, experience in GxP industry, be an effective leader, and work efficiently in a fast-paced environment. Responsibilities Manage a global team of supply chain professionals, responsible for both clinical and commercial end-to-end supply chain Manage all aspects of commercial supply chain, including Drug Substance and Drug Product Contract Manufacturing Organizations (CMOs), Packaging and Labeling activities with Contract Packaging organizations (CPOs), Finished Good receiving, put away, storage and distribution activities at Third Part Logistics Providers (3PLs) Coordinate logistics of material transfer for clinical and commercial drug substance, drug product and components to/from international CMOs/CPOs, managing exportation, applicable USDA/FDA licenses and permits, VAT recovery and customs brokers Own the global Sales & Operations Planning (S&OP) process for all commercial products, coordinating with global market access team for demand planning, finance team for financial planning and driving ownership of final supply plan to be communicated to global partners Own and actively manage the commercial supply plan, all commercial inventory, both in process and finished goods; manage shelf life and expiration Own and manage all serialization activities for commercial products globally Manage clinical packaging and labeling activities including label design, translation, production, distribution and inventory management Provide clinical demand signals, translate the total demand into a demand forecast over time based on a clinical protocol or study overview Prepare a clinical supply plan to support the demand, including determination of supply overage amounts, monitor inventory and provide regular inventory update to project teams Monitor clinical drug expiry/retest dating; initiate inventory release and re-supply, serving as the unblinded inventory manager Manage domestic and international distribution and logistics for clinical programs, including importing and exporting clinical supplies and developing distribution instructions with clinical supply vendors Support budget activities, including managing supplier contracts, PO generation and invoicing approvals for clinical and commercial purchases Work collaboratively with QA to manage supply chain activities such as batch release, final release, temperature excursions and to support the investigation of any deviations in a timely manner Work with CMC as a liaison to clinical operations and also on the evaluation of new CMOs or CPOs for commercial supply chain Work with Global Trade & Distribution and global Finance teams to manage global 3PLs, ensuring quality Finished Good inventory management, distribution and logistics, sales and revenue reporting Generate and maintain global SOPs in Veeva QMS and ensure updates and compliance with industry standards Develop and maintain strong internal cross-functional collaboration with stakeholders, such as CMC, Clinical Operations, Market Access, Finance, Quality, and Regulatory Affairs Where You'll Work This is a hybrid role and requires in-office collaboration 2-3x per week in our San Francisco Office. Who You Are At least fifteen (15) years of experience in Supply Chain Management and/or Manufacturing functions in the pharmaceutical and/or biotechnology industries. Title based on experience Bachelor's or Master's Degree in a scientific discipline Detailed understanding of the pharmaceutical business, including both clinical development and manufacturing and commercial manufacturing and supply chain Proven experience with forecasting, demand/supply planning, inventory management, packaging, labeling and distribution including cold chain, import/export and reverse logistics Proven experience managing and developing a team of professionals Experience with SAP or similar ERP platform Experience with product serialization, TraceLink or other similar platform and DSCSA standards Experience with Veeva, or other similar QMS platform Experience with clinical blinding practices Experience in assisting set-up of IRT Systems for global clinical studies Demonstrated skills in project management and vendor management Working knowledge of drug development process (Phase I-IV) Working knowledge of current GMP/GCP/GDP guidance and regulations Familiar with US and EU import/export regulations Excellent attention to detail, strong data analysis, problems solving and decision-making ability all while working in a fast-paced and dynamic environment Proven ability to effectively develop, communicate, and gain support for execution plans with a wide range of stakeholders Ability to handle multiple projects simultaneously APICS certification or supply chain education preferred Other Information: Position may require occasional evening and/or weekend commitment Position may require occasional travel (up to 20%), domestic and international Salary is competitive and commensurate with experience and qualifications Rewarding Those Who Make the Mission Possible We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return. Financial Benefits: Market leading compensation 401K with 100% employer match on first 3% & 50% on the next 2% Employee stock purchase program Pre-tax commuter benefits Referral program with $2,500 award for hired referrals Health & Wellbeing: Comprehensive health care with 100% premiums covered - no cost to you and dependents Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions) Hybrid work model - employees have the autonomy in where and how they do their work Unlimited flexible paid time off - take the time that you need Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents Flex spending accounts & company-provided group term life & disability Subsidized lunch via Forkable on days worked from our office Skill Development & Career Paths: People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities #LI-NT1 At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states. Salary $335,000 - $392,500 USD

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a "moneyball for biotech" approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. Affiliate Overview Eidos Therapeutics, an affiliate within BridgeBio Pharma, is a commercial-stage biopharmaceutical company focused on Transthyretin Amyloid Cardiomyopathy (ATTR-CM). What You'll Do The Vice President of Global Supply Chain will be responsible for global end-to-end clinical supply chain activities related to managing supply of Investigational Product (IP) including packaging, labeling, distribution and demand forecasting for multiple clinical studies through all stages of clinical development. The role will also have responsibility for global end-to-end commercial supply chain activities, including the management of S&OP, Supply planning, Supplier (CMO, CPO, 3PL) management, inventory management, and partnership with Global Trade for Finished Good distribution. The role will partner closely with CMC/Manufacturing, Commercial, Clinical, and Quality Assurance teams and partner stakeholders to ensure timely and uninterrupted supply of clinical and commercial product. The individual must have the ability to manage global teams, experience in GxP industry, be an effective leader, and work efficiently in a fast-paced environment. Responsibilities * Manage a global team of supply chain professionals, responsible for both clinical and commercial end-to-end supply chain * Manage all aspects of commercial supply chain, including Drug Substance and Drug Product Contract Manufacturing Organizations (CMOs), Packaging and Labeling activities with Contract Packaging organizations (CPOs), Finished Good receiving, put away, storage and distribution activities at Third Part Logistics Providers (3PLs) * Coordinate logistics of material transfer for clinical and commercial drug substance, drug product and components to/from international CMOs/CPOs, managing exportation, applicable USDA/FDA licenses and permits, VAT recovery and customs brokers * Own the global Sales & Operations Planning (S&OP) process for all commercial products, coordinating with global market access team for demand planning, finance team for financial planning and driving ownership of final supply plan to be communicated to global partners * Own and actively manage the commercial supply plan, all commercial inventory, both in process and finished goods; manage shelf life and expiration * Own and manage all serialization activities for commercial products globally * Manage clinical packaging and labeling activities including label design, translation, production, distribution and inventory management * Provide clinical demand signals, translate the total demand into a demand forecast over time based on a clinical protocol or study overview * Prepare a clinical supply plan to support the demand, including determination of supply overage amounts, monitor inventory and provide regular inventory update to project teams * Monitor clinical drug expiry/retest dating; initiate inventory release and re-supply, serving as the unblinded inventory manager * Manage domestic and international distribution and logistics for clinical programs, including importing and exporting clinical supplies and developing distribution instructions with clinical supply vendors * Support budget activities, including managing supplier contracts, PO generation and invoicing approvals for clinical and commercial purchases * Work collaboratively with QA to manage supply chain activities such as batch release, final release, temperature excursions and to support the investigation of any deviations in a timely manner * Work with CMC as a liaison to clinical operations and also on the evaluation of new CMOs or CPOs for commercial supply chain * Work with Global Trade & Distribution and global Finance teams to manage global 3PLs, ensuring quality Finished Good inventory management, distribution and logistics, sales and revenue reporting * Generate and maintain global SOPs in Veeva QMS and ensure updates and compliance with industry standards * Develop and maintain strong internal cross-functional collaboration with stakeholders, such as CMC, Clinical Operations, Market Access, Finance, Quality, and Regulatory Affairs Where You'll Work This is a hybrid role and requires in-office collaboration 2-3x per week in our San Francisco Office. Who You Are * At least fifteen (15) years of experience in Supply Chain Management and/or Manufacturing functions in the pharmaceutical and/or biotechnology industries. Title based on experience * Bachelor's or Master's Degree in a scientific discipline * Detailed understanding of the pharmaceutical business, including both clinical development and manufacturing and commercial manufacturing and supply chain * Proven experience with forecasting, demand/supply planning, inventory management, packaging, labeling and distribution including cold chain, import/export and reverse logistics * Proven experience managing and developing a team of professionals * Experience with SAP or similar ERP platform * Experience with product serialization, TraceLink or other similar platform and DSCSA standards * Experience with Veeva, or other similar QMS platform * Experience with clinical blinding practices * Experience in assisting set-up of IRT Systems for global clinical studies * Demonstrated skills in project management and vendor management * Working knowledge of drug development process (Phase I-IV) * Working knowledge of current GMP/GCP/GDP guidance and regulations * Familiar with US and EU import/export regulations * Excellent attention to detail, strong data analysis, problems solving and decision-making ability all while working in a fast-paced and dynamic environment * Proven ability to effectively develop, communicate, and gain support for execution plans with a wide range of stakeholders * Ability to handle multiple projects simultaneously * APICS certification or supply chain education preferred * Other Information: * Position may require occasional evening and/or weekend commitment * Position may require occasional travel (up to 20%), domestic and international * Salary is competitive and commensurate with experience and qualifications Rewarding Those Who Make the Mission Possible We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return. Financial Benefits: * Market leading compensation * 401K with 100% employer match on first 3% & 50% on the next 2% * Employee stock purchase program * Pre-tax commuter benefits * Referral program with $2,500 award for hired referrals Health & Wellbeing: * Comprehensive health care with 100% premiums covered - no cost to you and dependents * Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions) * Hybrid work model - employees have the autonomy in where and how they do their work * Unlimited flexible paid time off - take the time that you need * Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents * Flex spending accounts & company-provided group term life & disability * Subsidized lunch via Forkable on days worked from our office Skill Development & Career Paths: * People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility * We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching * We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities #LI-NT1

We are seeking an experienced and visionary Vice President of Supply Chain to join our leadership team. This role offers a unique opportunity to build and shape a world-class supply chain function that supports both commercial and clinical production objectives. The ideal candidate will be a strategic architect and operational leader, responsible for designing scalable systems, establishing integrated business planning processes, and driving alignment across the organization to ensure supply chain excellence. **Key Responsibilities:** As the Vice President of Supply Chain, you will: + **Build and establish a robust supply chain function** that delivers operational scalability and efficiency to meet evolving business needs. + Lead the development and implementation of **integrated business planning processes** to align supply chain operations with corporate objectives, production schedules, and market demand. + Establish and refine **strategic raw material planning models** to ensure alignment with clinical and commercial production forecasts. + Design and implement systems, tools, and procedures that optimize material planning, procurement, outsourcing, and risk management. + Develop and execute strategies to **optimize vendor capacity, quality, schedule, and cost** while mitigating supply chain risks. + Collaborate cross-functionally to establish proactive risk management frameworks and ensure raw materials availability to meet production goals. + Drive operational excellence by identifying and executing continuous improvement initiatives for scalability and performance. + Represent the supply chain function in high-level discussions with external stakeholders, including customers, vendors, and regulatory agencies. + Prepare and contribute to regulatory submissions, including BLA documentation, ensuring compliance and readiness. + Partner with other departmental leaders to align supply chain strategies with broader organizational goals and initiatives. + Recruit, mentor, and develop a high-performing supply chain team, fostering leadership and growth within the department. + Develop and manage operational schedules, budgets, and long-term strategic plans for the supply chain function. **To be considered for this role, you must have:** + A Bachelor's degree in Management or a related field, with 20+ years of supply chain experience and 5+ years in the biopharmaceutical industry (or an equivalent combination of education and experience). + Advanced degrees, such as an MBA, are a plus. **What you'll bring:** + A proven track record of **building and scaling supply chain functions** in dynamic, fast-paced environments. + Expertise in designing and implementing **integrated business planning processes** to align operations and strategy. + Innovative problem-solving and creative thinking to address complex supply chain challenges. + High level of integrity, transparency, and effective communication skills. + Strong knowledge of business continuity, risk management, and long-term planning. + Ability to lead and influence cross-functional teams and drive organizational alignment. + Familiarity with global supply chain trends and industry best practices. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit ********************************************************************* For other countries' specific benefits, please speak to your recruiter. Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron's roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and expectations for your role and your location. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc. **Salary Range (annually)** $300,000.00 - $500,000.00