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.
Our Bloomington, Indiana site 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.
The Position
The Planner is a key individual contributor to the success of the Company. The Planner supports the execution of the Master Production Plan for the entire site to achieve 100% on-time delivery of scheduled batches. The Planner leads all tasks associated with the planning and purchasing of raw materials, scheduling of customer orders, including projects, equipment availability, promise dates and working with procurement and materials management when the need for expediting of any material necessary to start the order.
Relationships
Reports to Manager, Supply Chain
Essential Functions
Performs analysis to determine optimal production schedule of customer orders and combination of key inputs, including Customer requirements from the Project Management personnel, production sequencing raw material and equipment availability based on their own assessmentInterprets and communicates special requirements to appropriate personnelUpdates new plans and changes in the inventory management systemSupports new product introduction, BOM's and item master as neededVerifies availability of material and capacity before reschedulingEnsures schedule stability by minimizing short term changes to the schedule where possibleCreates, monitors and updates manufacturing work orders and parts lists in the systemMaintains effectiveness of the Quality System components relevant to this positionResponsible for updating existing reports and developing new onesResponsible for tracking departmental performance metrics, as requiredWork closely with all internal and external suppliers and vendorsMaintain work area to 5S standards as posted in work areaMaintain SOPs (Standard Operating Procedure) for all duties and tasksFollow all safety and environmental requirements in the performance of dutiesOther duties as assignedPhysical Requirements
Frequent sitting, standing, walking, reading of written documents and use of computer monitor screen, reaching with hands and arms, talking, writing, listening. Occasional stooping, kneeling, crouching, bending, carrying, grasping. Frequent lifting and/or moving up to 10 pounds and occasional lifting and/or moving up to 50 pounds. Comply with EHS responsibilities of the position. Working in a lab environment will require working with skin irritants, lung irritants, electrical equipment, sharp instruments, toxic materials, and hazardous waste. Safety procedures will be followed to minimize exposure, including clean room gowning. Working conditions will be Heating Ventilation and Air Conditioned controlled.
Qualifications
- High School/GED required
- Bachelor's degree preferred
- ASCM or ISM certification preferred
- 2 or more years of experience required
- Must be able to read and understand English-written job instructions and safety requirements
- Successful experience interacting and liaising with internal and external clients, customers, and/or suppliers required
- Experience using electronic ERP and Material Management systems required
- Prior experience in a cGMP environment preferred
- Technical Requirements:
- Ability to use Excel, Word, and other office systems
- Demonstrates theoretical understanding of the work tasks assigned
- Maintains high quality documentation in accordance with applicable regulatory guidance and Site SOPs
- Computer literate with experience creating and developing complex spreadsheets
- Prior work experience with ERP software (e.g. JD Edwards )
- Ability to learn, retain, and apply technical information on multiple topics
- Develop and execute complex procedures with high quality
- Basic understanding of the supply chain in a pharmaceutical laboratory and / or production operation
- Capable of rapid learning of unfamiliar principles or techniques with minimum training
- Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
- Ability to problem solve to initiate and execute/monitor corrective action
- Ability to independently interpret data, analyze trends and provide insight into potential issues and subsequent solutions
- Mathematical reasoning ability
Behavioral Requirements:Ability to see and hear, read and write clear EnglishRequires adaptability, analyzing, assessing, calculating, decision making, dependability, good judgment, reading, memorizing, social skills, speaking, stress control, writingAbility to communicate effectively and follow/retain detailed written and verbal instruction in an accurate, timely, safe, and professional manner with supervisor, group members, and other departments as necessary, in a professional and accurate mannerAbility to manage time effectively to complete assignments in expected time frame and independently seek out additional work when tasks are completed ahead of timeAbility to cooperate with coworkers within an organized team environment or work aloneDetail oriented and well organized with ability to work effectively under high pressure with multiple deadlinesAbility to put aside personal opinions and focus on business needs, department needs or group needsPositive attitude and ability to work with othersAbility to process a large volume of workAbility to effectively carry out and implement changeAbility to transfer knowledge to others via training or mentoring of staff; demonstrated ability to guide others through communication and learningAbility to make decisions which have moderate impact on immediate work unitAbility to understand opposing points of view on highly complex issues and to negotiate and integrate different viewpointsAbility to make decisions which have significant impact on the department's credibility, operations, and servicesWe 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-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.