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Grifols · 8 hours ago

Sr. Manager Supply Chain Projects

NC-Clayton

Full-time

Onsite

Senior Level, Lead/Staff

10+ years exp

Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. The Sr. Manager Supply Chain Projects is responsible for managing a wide range of projects related to product supply, requiring independent decision making and effective communication at all levels. This role involves coordinating new product launches, managing implementation schedules, and ensuring compliance with regulatory requirements.

BiotechnologyHealth CareManufacturing

Responsibilities

Coordinate and manage implementation of new projects impacting supply planning activities

Participate or lead teams to coordinate new product launches, new component implementation and new regulatory requirements

Represent Supply Chain in procedures or system changes

Coordinate and manage implementation of new and/or modified packaging materials and BOMs related to Regulatory Notifications of Changes

Develop implementation schedule with Sr. Supply Planner, Label Development and Procurement

Issue Change Controls

Issue Master Data Requests

Issue Quality Master Data Requests

Issue requests to inactivate materials and BOMs no longer required as a result of changes

Coordinate and manage Purchasing Specifications for new and/or modified packaging materials for Grifols and various Grifols products packaged at locations like GWWO

Initiate Commodity Evaluation Request process for new components, if applicable

Initiate new and/or modified purchase specifications using Document Change Request in DCM

Qualified Author for Planning, Label Development and Procurement owned controlled documents

Initiate and manage revisions to current documents

Monitor document status to ensure required review timelines are met

Create new documents following approved DCM procedures as required

Coordinate and manage implementation of new and/or modified BOMs related to major site validation projects

Develop implementation scope and schedule with Project Lead, Project Owner, and/or Supply Chain representative(s)

Issue Master Data Requests

Issue Quality Master Data Requests

Issue requests to inactivate materials and BOMs no longer required as a result of changes

May represent Supply Chain on projects, committees, and/or teams

May also lead complex projects independently

May lead participate on cross-functional teams

Qualification

CGMP knowledgeSAP ERPProject managementChange control systemsRegulatory experienceCommunicationNegotiation skillsOrganizational skillsDecision making

Required

Bachelor's degree in Business, Science or related field required

At least ten (10) years applicable work experience in a cGMP role with NLT two (2) years direct experience with cGMP documentation

Strong knowledge of cGMP documentation and change control systems including experience with DCM

Proficient in SAP ERP system and Microsoft Office

Excellent oral and written communication skills, adaptable to different audiences

Agile and able to manage complex and dynamic variables

Excellent organizational skills, the ability to manage multiple concurrent projects and deadlines, and the ability to develop alternate strategies and influence others

Ability to develop customer relationships through collaboration, respect, professionalism, trust, and integrity

Strong decision making skills. Makes key decisions impacting overall business objectives