Manager, Quality Control Scheduling

The RoleIn this role, you will be responsible for performing multiple activities in support of Moderna’s cGMP Quality Control (QC) Laboratories; maintaining the QC site execution schedule, at a daily and shift level, for all resources to ensure on-time, in-full delivery of results to support lots release and the Stability Program at Moderna’s Norwood site. The scheduler is also expected to maintain and communicate testing metrics from the QC group and highlight constraints to functional management. The incumbent of this role will work in close cooperation with multiple stakeholders to ensure that the testing and reporting schedule is set against company priorities.Here’s What You’ll DoWork directly with the project management, supply chain, QA and manufacturing teams to capture all required commercial and clinical lot testing needs for the site.Develop the laboratory testing schedule to meet demand and communicate capacity constraints.Responsible for the maintenance and continuous improvement of Scheduling software systems.Create and maintain detailed plan to support the testing needs of the stability and technical development groups.Lead meetings with QC laboratory sub-teams to align and facilitate discussions on priorities, quality events and overall deliverables.Communicate KPI’s and metrics that track the effectiveness of planning and testing execution.Serve as a point of contact for information requests on status into the QC team and respond, or route accordingly.Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.Additional duties as may be assigned from time to time.Here’s What You’ll Need (Basic Qualifications)Education: BA/BS DegreeExperience: 2 to 3 years of experience of planning in QC Laboratories planning inside a Supply Chain or QA organizations.Here’s What You’ll Bring to the Table (Preferred Qualifications)Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards).A desire to make an impact as part of a high-growth, transformational company that is

Bold, Relentless, Curious, and Collaborative.About ModernaSince our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit

modernatx.com/careers

to learn more about our current opportunities.Moderna is a smoke-free, alcohol-free and drug-free work environment.

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