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Clinical Packaging Technician - 2nd Shift

ICON Clinical Research

West Point, PAJobSeen 2w agoSeen in employer's feed 1w ago

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At a glance

Compensation
No compensation found
Location
West Point, PA
Work Authorization
Not specified

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Job overview

ICON plc seeks a detail-oriented Packaging Label Print Technician for its Clinical Supplies team on the 2nd shift, working in a cross‑functional, GMP‑regulated environment to handle clinical label production, packaging, equipment setup, documentation, inventory management, and quality compliance.

Skills & qualifications

RequiredNice to have

Skills

Attention to DetailOrganizational SkillsMechanical AptitudeEquipment OperationBasic TroubleshootingFollow Detailed ProceduresDocumentationVerbal CommunicationWritten CommunicationMulti‑TaskingGMP KnowledgeGDP KnowledgeLabel Printing SystemsPackaging EquipmentQuality Documentation PracticesProblem SolvingContinuous ImprovementTeamworkCollaborationCustomer Service

Qualifications

High School DiplomaBachelor’s Degree0-3 Years Relevant Experience With Degree or 3+ Years Without Degree

Benefits

Medical Insurance
401(k) Match
Paid Time Off

Full job description

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

Your Profile:

You will bring relevant executive support and administration experience, along with the following qualifications and skills.

Required qualifications and experience:

  • 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.

Preferred

  • 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.

What You'll Bring

  • 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.

What ICON can offer you:

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 work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply

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