Cerus
Remote Jobs
2 Jobs
About Cerus: Cerus aims to be the global leader and trusted partner of blood centers and hospitals whose technology, services, and commitment are the lifeblood of safe and accessible blood for patients around the world. This is a US based remote opportunity. Candidates who currently reside in the US will be considered. Summary: Manage an assigned set of suppliers globally, with activities including planning, purchasing, supplier governance, inventory management and related system transactions. Responsibilities: - Primary contact for a specific number of suppliers. - Ensure the achievement of targets assigned to supplier management. - Organize, set-up, and prepare meetings, based on specific needs such as (but not limited to) monthly business reviews, quarterly business reviews, issues management, etc. - Execute supplier performance evaluations and initiate required improvement plans. - Manage supplier-related operational processes as required. - Identify and drive implementation of cost improvement initiatives. - Ensure Cerus’ internal alignment with suppliers, supporting new product development, and other changes required to support the organization. - Manage forecasting, planning, purchasing and inventory requirements. - Manage activities related to risk mitigation and business continuity plans, including formulating solutions and gaining internal support to implement such activities. - Collaborate with manufacturing development and quality teams on global forecasting and capacity plans with suppliers. - Create purchase orders to replenish inventory based on business rules. - Manage Request for Proposal (RFP) activities in support of new products and alternative vendor selection processes. - Partner with Customer Care and support customer requirements. - Chair cross functional project meetings with Clinical Ops, Finance, CMC, Customer Care, Manufacturing development and Quality on routine matters involving new product introductions and general supply chain projects. - Suppliers and internal stakeholders are in different time zones and requires a high level of flexibility in attending meetings and supporting the organization before or after regular business hours. - As a Supply Chain Manager supporting critical medical production and its manufacturing operations, this position requires a high level of sense of urgency. - Comply with QMS and SOX requirements. - Roughly 10-20% domestic and international travel. Qualifications: - Bachelor’s degree with a minimum of 5 years experience of supplier management, supply chain, planning, and inventory management - Understanding of Finance, Operations, Inventory Management, Supply Chain, Quality and Administration processes - Strong problem solving, communication, and interpersonal skills to collaborate with stakeholders on all levels of the business - Experience conducting project presentations to executive level management - Must be able to work in a fast-paced environment with demonstrated ability to effectively manage multiple competing tasks and demands - Good organizational skills, self-directed, and attentive to detail - Strong user of Microsoft Office Suite, with emphasis on Excel, PowerPoint and Visio - ERP system experience (preferably Oracle) We understand that our people are essential to our success. This philosophy is revealed in our competitive benefits package, designed to improve employees’ lives both on and off the job. Benefits plans: medical, dental, vision, domestic partner benefits, paid maternity and paternity leaves, healthcare and dependent care flexible spending, life and accidental death insurance, long-term and short-term disability insurance, matching 401(k), RSUs Work and family: EAP, legal and financial services, health club membership discounts, tuition reimbursement Compensation: The base salary range for this position in the selected city is $124,000-$156,000 annually. Base pay is one part of the total package to compensate and recognize employees for their work. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.
About Cerus: Cerus aims to be the global leader and trusted partner of blood centers and hospitals whose technology, services, and commitment are the lifeblood of safe and accessible blood for patients around the world. Summary & Scope of Position: Coordinate and prepare documents for submissions to regulatory agencies worldwide, as appropriate by project. Primary Responsibilities: - Coordinate and prepare regulatory submissions for EMEA, LATAM, and APAC regions, including planning, authoring, and reviewing submission documents. Interface cross-functionally to obtain required components and ensure submissions meet applicable regulatory requirements and timelines. - Review submission-related documentation from clinical, pre-clinical, research, development, and manufacturing functions to ensure consistency with regulatory filings and compliance with applicable regulations. - Maintain current knowledge of EU and international regulatory requirements, guidelines, and trends. Assess the impact of regulatory changes on assigned projects and provide recommendations to regulatory and cross-functional teams. - Support and contribute to the development and execution of regulatory strategies in collaboration with senior Regulatory Affairs personnel. - Participate in and/or represent Regulatory Affairs on cross-functional project teams, ensuring regulatory considerations are appropriately integrated into project plans. - Maintain accurate and up-to-date regulatory records and documentation, including submission archives and agency correspondence. - Work independently on routine assignments, with general guidance provided for new or complex tasks. - Perform other related duties as assigned. Qualifications/Requirements/Skills: - Bachelor’s degree in a related scientific discipline with a minimum of 5 years regulatory experience in a biotechnology, pharmaceutical, or medical device company. - Proven ability to work effectively in a fast-paced environment, managing multiple competing priorities and deadlines. - Demonstrated ability to work independently, take initiative, and drive tasks to completion within established timelines. - Strong communication skills, including interpersonal, written, verbal, and active listening abilities. - Effective time management skills, with the ability to plan, prioritize, and manage multiple tasks and schedules. - Highly detail-oriented with a strong focus on accuracy and quality. We understand that our people are essential to our success. This philosophy is revealed in our competitive benefits package, designed to improve employees’ lives both on and off the job. Benefits plans: medical, dental, vision, domestic partner benefits, paid maternity and paternity leaves, healthcare and dependent care flexible spending, life and accidental death insurance, long-term and short-term disability insurance, matching 401(k), RSUs Work and family: EAP, legal and financial services, health club membership discounts, tuition reimbursement Compensation: The base salary range for this position in the selected city is $150,000-165,000 annually. Base pay is one part of the total package to compensate and recognize employees for their work. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.