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Pharmaceutical Serialization Jobs (NOW HIRING)

Robert Half

Systems Engineer

Bridgewater, NJ · On-site

$38 - $44/hr

Help manage serialization and track-and-trace solutions by supporting compliance with global standards such as GS1 and applicable pharmaceutical supply chain regulations. * Assist with the ...

Infosys Limited

SAP ATTP Consultant

Raleigh, NC · On-site

$106 - $167/hr

Strong understanding of pharmaceutical supply chain and logistics processes. * Working knowledge of global serialization regulations such as DSCSA, EU FMD, India DAVA, Russia Chestny ZNAK, and other ...

FurstStaffing

Serialization Manager

South Beloit, IL

$105K/yr

This role is critical to ensuring the integrity, safety, and transparency of the pharmaceutical supply chain. The ideal candidate will have deep expertise in serialization systems, regulatory ...

Infosys

SAP ATTP Consultant

Raleigh, NC · On-site

$61.25 - $83.50/hr

... pharmaceutical supply chain and logistics processes. • Working knowledge of global serialization regulations such as DSCSA, EU FMD, India DAVA, Russia Chestny ZNAK, and other country-specific ...

Infosys Limited

SAP EWM Consultant

Foster City, CA · On-site

$114 - $167/hr

SAP EWM and ATTP integration experience, Pharmaceutical Serialization regulatory knowledge is a plus. * Proven track record of leading large‑scale SAP implementations, upgrades, and enhancements.

Infosys

SAP EWM Consultant

Foster City, CA · On-site

$73.50 - $100.25/hr

Preferred Skill and Experience • Experience working in highly regulated industries, especially pharmaceuticals. • Deep knowledge of serialization, compliance frameworks, and data integrity ...

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Pharmaceutical Serialization information

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How much do pharmaceutical serialization jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for pharmaceutical serialization in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What are the main responsibilities and challenges faced in pharmaceutical serialization?

In a Pharmaceutical Serialization role, your primary responsibility is to implement and manage systems that uniquely identify and track pharmaceuticals across the supply chain, ensuring data integrity and regulatory compliance. Common challenges include keeping up with evolving global serialization requirements, integrating diverse technologies across manufacturing sites, and troubleshooting data mismatches or system errors. You’ll often collaborate with IT, quality assurance, packaging, and regulatory teams to ensure smooth operations. Success in this role relies on attention to detail, proactive problem-solving, and effective teamwork.

What are the key skills and qualifications needed to thrive in pharmaceutical serialization?

Excelling in Pharmaceutical Serialization requires knowledge of regulatory compliance, supply chain logistics, and pharmaceutical manufacturing processes, often supported by a degree in life sciences or engineering. Familiarity with serialization software platforms (such as SAP ATTP or TraceLink), barcode/RFID technologies, and regulatory standards (like DSCSA or EU FMD) is crucial. Strong attention to detail, analytical thinking, and effective cross-functional communication are valuable soft skills in this field. These competencies ensure that pharmaceutical products are accurately tracked through the supply chain, maintaining product integrity and regulatory adherence.

What is pharmaceutical serialization?

A Pharmaceutical Serialization job involves managing and implementing track-and-trace systems to ensure compliance with regulations like the Drug Supply Chain Security Act (DSCSA) or EU Falsified Medicines Directive (FMD). Professionals in this role oversee serialization processes, ensuring that each drug package is assigned a unique identifier to prevent counterfeit medications from entering the supply chain. They work with regulatory bodies, IT systems, and production teams to maintain data accuracy and integrity. This role is critical for enhancing patient safety and improving supply chain transparency.

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Pharmaceutical Serialization jobs near you
Infographic showing various Pharmaceutical Serialization job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Senior Pharmaceutical Automation Engineer

Visium Resources, Inc.

Clayton, NC • On-site

$88K - $116K/yr

Contractor

Posted 26 days ago

Job description

Introduction
Visium Resources has been asked to identify qualified candidates for this Senior Pharmaceutical Automation Engineer position. This position is a 12 month contract with anticipated renewals at a large Pharmaceutical company in Clayton, NC. This position is 5 days per week onsite.


Summary

We are seeking an experienced Senior Pharmaceutical Automation Engineer to support the implementation, commissioning, qualification, startup, and operational readiness of automated manufacturing systems for a major Fill Finish Expansion (FFEx) project within a state-of-the-art pharmaceutical manufacturing facility.

This role will provide technical automation support across multiple production and packaging systems, ensuring automation platforms are installed, tested, validated, and transitioned into reliable manufacturing operations while meeting FDA, cGMP, GAMP 5, and corporate quality standards. The ideal candidate possesses strong PLC, SCADA, MES, and pharmaceutical manufacturing automation experience with demonstrated success supporting highly automated production environments.


Primary Responsibilities
  • Provide automation engineering support for pharmaceutical manufacturing and packaging equipment throughout installation, commissioning, qualification, startup, and production support.
  • Troubleshoot and resolve automation-related issues impacting manufacturing operations.
  • Support Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.
  • Review, troubleshoot, and modify PLC, HMI, SCADA, MES, and industrial network configurations as required.
  • Coordinate automation activities with engineering, validation, manufacturing, quality assurance, vendors, and system integrators.
  • Support change controls, deviations, CAPAs, and root cause investigations related to automation systems.
  • Participate in startup planning and execution while minimizing production downtime.
  • Develop and maintain automation documentation including:
    • Functional Specifications
    • Design Specifications
    • Software Change Documentation
    • Test Protocols
    • SOPs
    • System Configuration Documentation
  • Assist in cybersecurity, backup, disaster recovery, and system lifecycle management.
  • Ensure automation systems comply with FDA 21 CFR Part 11, cGMP, GAMP 5, and data integrity requirements.
  • Support long-term reliability improvements and continuous process optimization.
Manufacturing Equipment Supported
The Automation Engineer will support automation systems associated with highly automated pharmaceutical manufacturing and packaging equipment including:
Assembly OperationsFlexTouch (FxT) Assembly Lines
  • Mikron Assembly FlexCells
  • Mikron Handling Units
    • HUGP - Good Pen
    • HUMM - Motor Module
    • HUSA - Sub Assembly
  • Automated Palletizer
SDD Assembly Line
  • Cell 10 & 20 - Load SU/FA & Laser Mark
  • Cell 30 & 35 - Load Syringe
  • Cell 38 & 40 - Device Assembly
  • Cell 50 - Load RA
Packaging Operations
Support multi-vendor automated packaging equipment including:
  • Pester Depalletizer
  • Bausch + Stroebel Labeler
  • Fargo (Koerber) Transfer Unit
  • Dividella Cartoner
  • Robomat NeedlePak
  • Uhlmann Unit Serialization Platform (USP)
  • Uhlmann Track & Trace
  • Pester End-of-Line Palletizer
Automation Systems
Candidates should have experience with several of the following technologies:
PLC Platforms
  • Schneider Electric
  • B&R Automation
  • Allen-Bradley ControlLogix
  • Siemens PLCs
SCADA & HMI
  • FactoryTalk View
  • FactoryTalk Services
  • SCADA troubleshooting
  • Industrial HMI development
Manufacturing Systems
  • PAS-X Manufacturing Execution System (MES)
  • Historian systems
  • SQL Server
  • AVEVA PI System
Vision Systems
  • Cognex
  • Keyence
  • Vision Automation
Serialization
  • Uhlmann Track & Trace
  • Pharmaceutical serialization systems
Infrastructure
  • ThinManager
  • Octoplant
  • Industrial Ethernet networks
  • Virtualized automation environments
  • Windows Server administration (automation-related)

Required Qualifications
  • Bachelor's degree in Engineering, Automation Engineering, Electrical Engineering, Computer Engineering, or related technical discipline.
  • 5+ years of pharmaceutical or biotechnology automation engineering experience.
  • Experience supporting FDA-regulated manufacturing facilities.
  • Strong PLC troubleshooting experience with one or more major PLC platforms.
  • Experience supporting SCADA systems in pharmaceutical manufacturing.
  • Working knowledge of MES integration.
  • Experience supporting commissioning and qualification activities.
  • Understanding of ISA-88 and ISA-95 principles.
  • Familiarity with 21 CFR Part 11 and electronic records compliance.
  • Excellent troubleshooting and root cause analysis skills.
  • Strong communication and cross-functional collaboration abilities.
Preferred Qualifications
  • 8+ years of pharmaceutical automation engineering experience.
  • Experience supporting Fill Finish manufacturing facilities.
  • Experience with device assembly or high-speed packaging equipment.
  • Previous Novo Nordisk project experience.
  • Experience with PAS-X MES.
  • Experience with FactoryTalk SCADA architecture.
  • Knowledge of serialization systems.
  • Experience with AVEVA PI Historian.
  • Familiarity with ThinManager and Octoplant.
  • Experience supporting validated manufacturing environments.
Knowledge & Skills
  • PLC programming and troubleshooting
  • Industrial automation architecture
  • SCADA systems
  • MES integration
  • Industrial networking
  • Validation support
  • Commissioning and startup
  • Equipment integration
  • Root cause analysis
  • Change management
  • Vendor coordination
  • Continuous improvement
  • Pharmaceutical manufacturing operations
  • Data integrity and compliance
  • Technical documentation
Work Environment
  • On-site support within an active pharmaceutical manufacturing facility.
  • Frequent interaction with manufacturing, engineering, validation, quality, and equipment vendors.
  • Ability to support commissioning, startup, off-shift troubleshooting, and occasional weekend activities during project milestones.
  • May require gowning and work within classified manufacturing areas.

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Visium Resources is an award-winning employment firm with a mission to match talented individuals with highly successful organizations. At Visium, our company"s success is based on your success. When you work with us, you are never 'just a number'. You are our most important asset. Here, you will know us by name through our regular visits to client sites and even occasional luncheons. We will always be there when you need assistance and will always go the extra mile to ensure that you are as successful as possible. Whether you're looking for contract, contract-to-hire or permanent opportunities, we firmly believe there is no employment agency that will work harder for you than Visium.
Visium Resources is an equal opportunity employer and values diversity. All employment is decided based on qualifications, merit and business need.

Education:BS/BA DegreeEmployment Type: CONTRACTOR

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