About the Department
At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world.
As a part of Novo Nordisk, Catalent, Indiana LLC. in Bloomington, Indiana, is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product fill / finish and packaging. The Bloomington campus is a recognized facility where talented teams work with innovators to help develop, manufacture and supply products to patients around the world.
What we offer you :
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.
Our state-of-the-art facility in Bloomington, Indiana provides a fully integrated model from process and formulation development to clinical and commercial biomanufacturing and drug product fill / finish and packaging. Bloomington’s main campus has been recognized as Facility of the Year in both 2007 and 2017 by the International Society of Pharmaceutical Engineers (ISPE), INTERPHEX, and Pharmaceutical Processing magazine.
The Senior Manager – Supply Chain Planning will be responsible for leading the planning and coordination of all supply chain activities to ensure the timely and efficient production of pharmaceutical products, ensuring schedule adherence, and optimizing resource utilization. This role requires strategic thinking, cross-functional collaboration, and a deep understanding of the unique challenges within the pharmaceutical manufacturing environment.
The Position
The Senior Manager of Supply Chain is responsible for the execution that must comply with GMPs, EHS, and the company's internal policies and procedures.
Relationships
Reports to : Director or above
Direct Reports : 5 – 12
Total Site Staff (includes directs) : 5 – 25
Essential Functions
Lead the development of demand forecasts and production plans in collaboration with Commercial, Manufacturing, and Supply Chain teams to meet customer requirementsOversee the creation and management of master production schedules to optimize resource utilization and ensure alignment with customer delivery timelinesCoordinate with production teams to translate forecasts into detailed schedules, setting clear production goals while considering equipment availability, staffing, and regulatory constraintsMonitor production schedules, ensuring adherence to established timelines, and proactively addressing any deviationsCollaborate with Manufacturing, Quality, and Engineering teams to identify root causes of schedule deviations and implement corrective actions to minimize disruptionsImplement strategies to maintain optimal inventory levels of raw materials, intermediates, and finished goods while minimizing excess stock and reducing inventory risksMonitor and present monthly supply chain performance reports, including metrics such as on-time delivery, schedule adherence and forecast accuracyWork closely with Manufacturing, Quality, Procurement, and Regulatory teams to resolve supply chain issues and ensure material availability for productionIdentify and implement continuous improvement initiatives to optimize planning processes, enhance supply chain efficiency, and reduce costsDevelop strategies to mitigate supply chain risks, including disruptions, delays, and regulatory changesMonitor the external environment for potential impacts on the supply chain and adjust plans accordinglyLead, mentor, and develop the Supply Chain Planning team, providing guidance on best practices, process improvements, and career developmentFoster a culture of collaboration, accountability, and continuous learning within the teamStrong understanding of ERP / MRP systems and supply chain planning toolsDevelop and measure supply chain metrics that drive continuous improvementProve timely, accurate data to support scenario planning, root cause analysis, and decision makingEstablish a process and rhythm to review forecast and actual, develop required digital toolsIdentify capacity / capability gaps in Supply Chain, establish metrics that support monitoring of the planSupport Supply Chain Directors in SQDC and other global forumsFollow company policies, guidelines, and work instructionsOther duties as assignedMaterials)(Batch Release)
Lead the development of demand forecasts and production plans in collaboration with Commercial, Manufacturing, and Supply Chain teams to meet customer requirementsOversee the creation and management of master production schedules to optimize resource utilization and ensure alignment with customer delivery timelinesCoordinate with production teams to translate forecasts into detailed schedules, setting clear production goals while considering equipment availability, staffing, and regulatory constraintsMonitor production schedules, ensuring adherence to established timelines, and proactively addressing any deviationsCollaborate with Manufacturing, Quality, and Engineering teams to identify root causes of schedule deviations and implement corrective actions to minimize disruptionsImplement strategies to maintain optimal inventory levels of raw materials, intermediates, and finished goods while minimizing excess stock and reducing inventory risksMonitor and present monthly supply chain performance reports, including metrics such as on-time delivery, schedule adherence and forecast accuracyWork closely with Manufacturing, Quality, Procurement, and Regulatory teams to resolve supply chain issues and ensure material availability for productionIdentify and implement continuous improvement initiatives to optimize planning processes, enhance supply chain efficiency, and reduce costsDevelop strategies to mitigate supply chain risks, including disruptions, delays, and regulatory changesMonitor the external environment for potential impacts on the supply chain and adjust plans accordinglyLead, mentor, and develop the Supply Chain Planning team, providing guidance on best practices, process improvements, and career developmentFoster a culture of collaboration, accountability, and continuous learning within the teamStrong understanding of ERP / MRP systems and supply chain planning toolsDevelop and measure supply chain metrics that drive continuous improvementProve timely, accurate data to support scenario planning, root cause analysis, and decision makingEstablish a process and rhythm to review forecast and actual, develop required digital toolsIdentify capacity / capability gaps in Supply Chain, establish metrics that support monitoring of the planSupport Supply Chain Directors in SQDC and other global forumsFollow company policies, guidelines, and work instructionsOther duties assignedAll other Supply Chain Functions)
Direct responsibility over the Warehouse, Materials Control, Logistics, and InventoryCross-functional collaboration with Procurement, Ops Planning, Project Management, Manufacturing, Engineering, Validation, Technical Services, Finance, Security, Legal, Quality Control, and Quality AssuranceCoaches, mentors, and teaches employees, colleagues, and / or customersOther duties as assignedQualifications
Education / Experience :Bachelor’s degree required
Master’s Degree preferredMinimum of 5 years progressive leadership experienceRelated experience in a regulated industryStrong understanding of pharmaceutical industry, and GMPs, preferredTechnical Requirements :Ability to use Excel, Word, and other Office systems
Ability to attend training and apply learning on routine operation, maintenance, SOPs, and regulatory guidelinesAbility to peer review data to ensure data is well organized with complete documentationAbility to provide ideas, introduce new technology, and drive process improvementsBehavioural Requirements :Ability to see and hear, read, and write clear English
Requires adaptability, analyzing, assessing, calculating, decision making, dependability, good judgment, reading, memorizing, social skills, speaking, and stress controlAbility to communicate effectively in English and follow / retain detailed written and verbal instruction in an accurate, timely, safe, and professional mannerAbility to manage time effectively to complete assignments in expected time frameDetail oriented with ability to work effectively under high pressure with multiple deadlinesStrong ability to multi-task in a fast-paced environmentLeadership Requirements :Monitors quality of others’ work within group and mentors others regarding project or task requirements
Establishes an effective, professional, and positive relationship with employeesClarifies responsibilities and expectations and holds employees accountableWe commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
