Packaging Specialist -Weekends Night Shift
Novartis Pharmaceuticals Corp.
Posted Wednesday, April 15, 2026
Posting ID: REQ-10069973_crt:1774954959693
Indianapolis, IN
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Summary
Primary responsibility is finish secondary packaging of manufactured product, literature and labeling appropriately in accordance with GxP procedures for shipment to customer. Packaging inventory management (receipt, stocking, replenishment etc.), support shipping/receiving areas, and final product packaging.
SHIFT: 12:00pm-12:00am. Thursday-Sunday one week, Friday-Sunday the next week and alternating.
About the Role
Major accountabilities:
• Executes all activities related to the packaging of RLT products. Responsibilities include prep and fulfillment of customer orders focusing on KPI goals as well as ensuring all state, federal and Novartis radiation safety guidelines are adhered to.
• Responsible for successful on-time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role.
• Supports all technical aspects related to packaging readiness including prep of chill packs, printing/organizing of all shipping documents, GPS programming, prep of all shipping materials.
• Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
• Ensures all cGMP compliance activities are followed.
• Participation in assigned qualification/validation activities, and assist on deviation investigations and inspections, as necessary.
• Prepares applicable documents and records such as batch records, shipping documents, and training materials.
Minimum Requirements:
Benefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & Reasonable Accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Primary responsibility is finish secondary packaging of manufactured product, literature and labeling appropriately in accordance with GxP procedures for shipment to customer. Packaging inventory management (receipt, stocking, replenishment etc.), support shipping/receiving areas, and final product packaging.
SHIFT: 12:00pm-12:00am. Thursday-Sunday one week, Friday-Sunday the next week and alternating.
About the Role
Major accountabilities:
• Executes all activities related to the packaging of RLT products. Responsibilities include prep and fulfillment of customer orders focusing on KPI goals as well as ensuring all state, federal and Novartis radiation safety guidelines are adhered to.
• Responsible for successful on-time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including HSE for the specific role.
• Supports all technical aspects related to packaging readiness including prep of chill packs, printing/organizing of all shipping documents, GPS programming, prep of all shipping materials.
• Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure.
• Ensures all cGMP compliance activities are followed.
• Participation in assigned qualification/validation activities, and assist on deviation investigations and inspections, as necessary.
• Prepares applicable documents and records such as batch records, shipping documents, and training materials.
Minimum Requirements:
- High school diploma or equivalent
- 1+ yr in distribution, warehousing, manufacturing experience in a regulated industry
- Hazardous shipping training is a plus
- Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted.
- Ability to lift or carry up to 35 pounds
- Radio Pharma experience preferred.
- General HSE Knowledge
Benefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accessibility & Reasonable Accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
On-SiteInventory ManagementPharmaceuticalsPackaging And LabelingKey Performance Indicators (KPIs)Standard Operating ProcedureInnovationEnvironment Health And SafetyGood Manufacturing PracticesVisual AcuityAsepsisShipping And ReceivingRadiation ProtectionDeviation InvestigationsProduct LiteratureShipping Documents
