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Serialization Manager Jobs in Indiana (NOW HIRING)

aan

Warehouse Associate

Plainfield, IN · On-site

$20/hr

May or may not operate equipment, determined by management and operates equipment only with Aarons provided PIT training completion and certification * Labeling and serialization of product * Picking ...

aan

Warehouse Associate

Plainfield, IN · On-site

$20/hr

May or may not operate equipment, determined by management and operates equipment only with Aarons provided PIT training completion and certification * Labeling and serialization of product * Picking ...

Aaron's

Warehouse Associate

Plainfield, IN · On-site

$20/hr

May or may not operate equipment, determined by management and operates equipment only with Aarons provided PIT training completion and certification * Labeling and serialization of product * Picking ...

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Serialization Manager information

What does a serialization manager do?

A Serialization Manager oversees the process of assigning unique serial numbers to products, typically in the pharmaceutical or manufacturing industries, to ensure traceability and compliance with regulatory requirements. They manage serialization systems, coordinate with IT and production teams, and ensure all products are properly serialized and tracked throughout the supply chain. Their role is crucial for preventing counterfeiting, supporting product recalls, and meeting government regulations.

What are the key skills and qualifications needed to thrive as a serialization manager?

To thrive as a Serialization Manager, you need in-depth knowledge of pharmaceutical supply chain regulations, serialization processes, and compliance standards, typically supported by a degree in a scientific, engineering, or related field. Familiarity with serialization software (such as SAP ATTP, TraceLink), data management systems, and regulatory compliance tools is crucial. Strong project management, problem-solving skills, and effective communication enable successful cross-functional collaboration and issue resolution. These skills and qualifications are vital to ensure products meet regulatory requirements, prevent counterfeiting, and maintain supply chain integrity.

How does a serialization manager typically interact with cross-functional teams to ensure compliance with global pharmaceutical regulations?

A Serialization Manager regularly collaborates with quality assurance, IT, supply chain, and regulatory affairs teams to ensure all serialized products meet global regulatory requirements. This includes coordinating system integrations, aligning on data standards, and troubleshooting issues that could impact product traceability. Effective communication and project management skills are essential, as the role often requires leading cross-functional meetings, providing training, and ensuring any changes in regulations are quickly implemented across all departments involved in the serialization process.

What are popular job titles related to Serialization Manager jobs in Indiana?

For Serialization Manager jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Serialization Manager jobs in Indiana look for?

The top searched job categories for Serialization Manager jobs in Indiana are:

Serialization Manager jobs near you
Infographic showing various Serialization Manager job openings in Indiana as of September 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution.

Drug Product Manufacturing Scientist - Advanced Therapies Manufacturing

Lebanon, IN • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$66K - $171K/yr

Other

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Position DescriptionDrug Product Bioprocess Scientist – Technical Services/Manufacturing Scientist (TS/MS)

Responsible for providing technical support for the development, implementation, and execution of compliant manufacturing of gene therapy drug product (initial focus: formulation, media & buffer preparation, drug product filling & packaging, and visual inspection operations; from facility startup through validation and commercial manufacturing).

Key Objectives/Deliverables
  • Provide technical support for TS/MS activities (tech transfer, process validation, investigation, media & buffer recipe, formulation, filling & packaging, visual inspection)
  • Apply scientific principles for gene therapy drug product manufacturing (chemistry, equipment, aseptic processes, container closure systems)
  • Address and resolve formulation issues
  • Own/steer media and buffer preparation formulations
  • Prepare/review/approve technical documents (change controls, regulatory submissions, deviation investigations, validation protocols & summary reports, processing records, process descriptions, annual reports)
  • Support/lead TS/MS technical projects to improve startup, process control, yield, product quality and/or productivity; implement technical process changes
  • Develop/monitor statistically based real-time process variability/capability metrics
  • Support daily manufacturing operations via process knowledge and data analysis
  • Serve as technical interface external to the Lebanon site; provide audit support as needed
  • Work/lead cross-functional teams; ensure safe working environment
Basic Requirements
  • BS in Chemical Engineering, Biochemical Engineering, Chemistry, Biochemistry, or related quantitative field
  • 3+ years cGMP manufacturing experience (Operations, Validation, TS/MS, Engineering, or Quality Assurance)
  • 3+ years parenteral drug product manufacturing (formulation, tech transfer, visual inspection, statistical trending/analysis, process risk assessment e.g., FMEA)
  • Authorized to work in the U.S. full-time; Lilly does not sponsor work authorization/visas
Additional Preferences
  • In-depth gene therapy manufacturing knowledge; AAV formulation/media/buffer experience
  • Solution filling and/or isolator technology; serialization/packaging experience
  • Interpersonal/teamwork, self-management/organization, strong oral/written communication
  • Data trending/analysis; complex data problem-solving; cross-functional leadership
Compensation/Benefits (if applicable)
  • Anticipated wage: $66,000 - $171,600; company bonus eligibility and comprehensive benefits (401(k), medical/dental/vision, flexible benefits, life insurance, time off/leave, well-being benefits).
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