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New Jersey Staffing

Manager, Master Data Management / Serialization

New Jersey Staffing, Bound Brook, New Jersey, us, 08805

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Job Opportunity At Insmed

Insmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most valuable resource is our employees, and everything we do is motivated by a patients-first mentality. We are dedicated to growing our team with talented individuals from around the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values of collaboration, accountability, passion, respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up their sleeves. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career. Consistently Ranked Science's Top Employer Insmed is dedicated to creating a collaborative environment where our team can thrive. Every day, our employees turn their passion for science and research into innovative solutions for patients. That's why we've been named the No. 1 company to work for in the biopharma industry in Science's Top Employers survey for four years in a row. A Certified Great Place to Work We believe our company is truly special, and our employees agree. In July 2024, we became Great Place to Work-certified in the U.S. for the fourth year in a row. We are also honored to have been listed on the Best Workplaces in Biopharma, Best Workplaces in New York, PEOPLE Companies That Care, Best Workplaces for Women, Best Workplaces for Millennials, and Best Medium Workplaces lists. Master Data Manager

We are seeking a highly skilled and experienced Master Data Manager with an understanding of serialization and capacity planning in the pharmaceutical industry. The ideal candidate will be responsible for overseeing and managing critical data related to pharmaceutical product lifecycle, ensuring data integrity, accuracy, and regulatory compliance. This role requires a strong background in master data management (MDM), serialization processes, and capacity planning within the pharmaceutical supply chain. Key Responsibilities:

Master Data Management (MDM): Be responsible for and handle the creation, maintenance, and governance of all master data related to pharmaceutical products, including materials, products, packaging components, and suppliers. Ensure accuracy, consistency, and alignment of master data across multiple systems (ERP, Tracelink, etc.). Work closely with cross-functional teams (Quality, Regulatory, Manufacturing, and Supply Chain) to ensure proper data integration and standardization. Auditing capabilities / reporting post-changes Serialization Management: Handle the serialization process in compliance with global regulatory requirements (e.g., DSCSA and other relevant serialization laws). Ensure the timely implementation of serialization solutions and be responsible for serialization data flows from packaging through distribution and into the market. Collaborate with internal and external partners to ensure proper tracking, reporting, and data exchange for serialized products. Maintain and enhance the serialization system to ensure efficient and error-free operations. Capacity Planning: Lead and handle capacity planning efforts across manufacturing and packaging operations to ensure sufficient resources are available to meet production targets. Analyze historical data, current trends, and forecasted demand to drive strategic decisions on production capacity and resource allocation. Work closely with production, logistics, and supply chain teams to optimize plant capacity and minimize inefficiencies or bottlenecks. Data Governance & Compliance: Ensure data management processes are in full compliance with regulatory requirements and industry standard methodologies. Implement and carry out data governance standards, ensuring that all master data adheres to global regulatory standards. Perform regular audits and data reviews to ensure the highest level of data integrity and minimize risk. Continuous Improvement & Reporting: Lead continuous improvement efforts related to data management, serialization processes, and capacity planning to increase efficiency, reduce errors, and enhance overall productivity. Construct and deliver in-depth reports on important data points like data quality, serialization compliance, and capacity utilization for senior leadership. Collaborate with IT teams to implement and refine MDM and serialization systems, ensuring proper integrations and performance.