Clinical Packaging Technician - 2nd Shift
Listed on 2026-09-12
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Manufacturing / Production
Production QC/QA, Packaging Engineer
Clinical Packaging Technician - 2nd Shift
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are seeking a detail-oriented and motivated Packaging Label Print Technician to join our Clinical Supplies team on the 2nd shift. In this role, you will work as part of a cross-functional team supporting clinical packaging, labeling, and printing operations in a regulated GMP environment. The successful candidate will be responsible for clinical label production, packaging activities, equipment setup and operation, documentation, inventory management, and adherence to quality and safety standards.
This is an excellent opportunity for individuals looking to build a career in pharmaceutical, biotechnology, or clinical supply operations while contributing to the successful delivery of clinical trial materials.
Key responsibilities include:- Execute clinical packaging and labeling operations in accordance with GMP requirements.
- Stage materials, equipment, and rooms for production activities, including handling materials with restricted environmental exposure requirements.
- Set up, operate, disassemble, and clean production equipment.
- Perform and document packaging, labeling, sampling, and de‑packaging activities.
- Print, inspect, proofread, reconcile, and maintain accountability of clinical product labels.
- Maintain label inventory and ensure appropriate material control throughout the production process.
- Process packaging and labeling documentation in compliance with GMP and GDP requirements.
- Conduct in‑process quality inspections to ensure label accuracy and product integrity.
- Verify equipment calibration status before use.
- Perform facility and equipment cleaning activities and complete verification procedures.
- Identify, document, and report quality events, deviations, or non‑compliance observations.
- Maintain compliance with all site safety, quality, and training requirements
You will bring relevant executive support and administration experience, along with the following qualifications and skills.
- High school diploma or equivalent required. Bachelor’s degree preferred.
- 0 to 3 years of relevant experience with a degree, or 3+ years of relevant experience without a degree.
- Strong attention to detail and organizational skills.
- Mechanical aptitude with equipment operation and basic troubleshooting skills.
- Ability to follow detailed procedures and accurately complete documentation.
- Strong verbal and written communication skills
- Ability to manage multiple priorities in a fast‑paced environment.
- Experience working in GMP‑regulated pharmaceutical, biotechnology, clinical supply, manufacturing, or packaging environments.
- Experience with label printing systems, packaging equipment, and quality documentation practices.
- Familiarity with GMP, GDP, and quality compliance requirements.
- A strong commitment to quality, safety, and compliance.
- A proactive approach to problem solving and continuous improvement.
- The ability to work effectively as part of a team while maintaining accountability for individual responsibilities.
- A focus on accuracy, operational excellence, and customer service
- Demonstrated teamwork and collaboration skills.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and…
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