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Pharmaceutical Serialization Jobs (NOW HIRING)

Trioptus

Packaging Technician

Wilson, NC · On-site

$14.75 - $18.25/hr

Experience in OSD pharmaceutical packaging . * Experience with serialization equipment and processes. * Previous manufacturing or packaging experience in a regulated industry. Physical ...

Artius Solutions

Packaging Supervisor

Fall River, MA · On-site

$72K - $93K/hr

Strong knowledge of pharmaceutical packaging machinery and cGMP protocols. * Familiarity with serialization tools like Systech and ERP systems like SAP. * Proficient in Microsoft Office tools (Excel ...

TriOptus LLC

Packaging Technician

Wilson, NC · On-site

$14.75 - $18.25/hr

Experience in OSD pharmaceutical packaging . * Experience with serialization equipment and processes. * Previous manufacturing or packaging experience in a regulated industry. Physical ...

TriOptus LLC

Packaging Technician

Wilson, NC · On-site

$14.75 - $18.25/hr

Experience in OSD pharmaceutical packaging . * Experience with serialization equipment and processes. * Previous manufacturing or packaging experience in a regulated industry. Physical ...

Purple Drive Technologies

SAP S4 HANA

Indianapolis, IN · On-site

Knowledge of serialization, track trace, and cold chain compliance in pharmaceutical distribution is a plus. Excellent communication and interpersonal skills, with the ability to translate technical ...

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Pharmaceutical Serialization information

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How much do pharmaceutical serialization jobs pay per hour?

As of Jun 9, 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 a Pharmaceutical Serialization role?

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 the Pharmaceutical Serialization position, and why are they important?

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 a Pharmaceutical Serialization job?

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
Process Engineer III - Packaging

Process Engineer III - Packaging

RESILIENCE

West Chester, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

A career at Resilience is more than just a job - it's an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
For more information, please visit www.resilience.com
Position Summary
The Process Engineer III - Packaging is a technical leader responsible for validated packaging processes supporting combination products and pharmaceutical-device systems within a GMP-regulated manufacturing environment.
This role leads the long-term strategic packaging initiatives and provides advanced technical support to Packaging Engineers and Operations. The position serves as the primary technical contact for packaging-related issues and partners cross-functionally with Manufacturing, Quality, Validation, Regulatory, Technical Operations, Supply Chain, and Facilities to ensure compliant, efficient, and inspection-ready packaging processes.
Key Responsibilities
Process Ownership & Technical Leadership
  • Own validated primary and secondary packaging processes, including serialization and aggregation systems where applicable.
  • Ensure control of critical process parameters (CPPs), critical quality attributes (CQAs), and established operating ranges.
  • Maintain packaging processes in a state of control through continued process verification and performance monitoring.
  • Serve as the technical subject matter expert (SME) for automated and semi-automated packaging lines (cartoning, labeling, blistering, pouching, case packing, serialization systems, etc.).
  • Lead complex troubleshooting and root cause investigations for packaging deviations and line performance issues.
  • Provide mentorship and technical guidance to Packaging Engineers and Operations teams.
  • Provide on-call support as required.

Validation & Compliance
  • Author and/or approve URS, FAT/SAT documentation, commissioning plans, and IQ/OQ/PQ protocols and reports for packaging equipment.
  • Lead packaging process validation and revalidation activities.
  • Initiate and lead investigations related to deviations, non-conformances, serialization discrepancies, and packaging complaints.
  • Support and manage change control activities, ensuring appropriate risk assessments and validation strategies.
  • Serve as technical SME during regulatory inspections and audits.

Continuous Improvement & Strategic Projects
  • Lead long-term capital and packaging line improvement initiatives focused on:
    • OEE optimization
    • Yield improvement
    • Scrap and material waste reduction
    • Changeover time reduction
    • Serialization and aggregation efficiency
    • Line reliability and uptime improvement
  • Support new product introductions (NPI), artwork updates, and packaging component changes.
  • Manage lifecycle planning and obsolescence strategies for packaging equipment and serialization systems.
  • Support technology transfers and line expansions.

Cross-Functional Collaboration
  • Partner with Quality, Regulatory Affairs, Serialization/IT teams, Supply Chain, Manufacturing, and Facilities.
  • Collaborate with packaging material suppliers and equipment vendors to resolve technical issues and enhance material compatibility and machine performance.
  • Provide technical input for packaging component specifications and supplier qualifications.
  • Support capital procurement and supplier FAT activities.

Minimum Qualifications
  • Significant experience in pharmaceutical or combination product packaging within a GMP-regulated environment.
  • Experience with automated packaging equipment and line integration.
  • Experience with process validation (IQ/OQ/PQ) and lifecycle validation principles.
  • Demonstrated experience leading investigations, root cause analysis, and change control processes.

Preferred Qualifications
  • Bachelor's degree in engineering (Mechanical, Chemical, Industrial, Biomedical, or related discipline).
  • Experience with serialization and aggregation systems.
  • Experience supporting regulatory inspections.
  • Project management experience in capital equipment or long-term improvement initiatives.
  • Lean manufacturing or Six Sigma certification.

Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $80,000.00 - $121,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.

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