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Clinical Packaging Technician - 2nd Shift

ICON plc
Posted 5 days ago, valid for a month
Location

Blue Bell, SD, US

Salary

$42,600 - $53,250 per year

Contract type

Full Time

Retirement Plan
Life Insurance
Employee Assistance

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Sonic Summary

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  • ICON is seeking a Clinical Packaging Technician for the 2nd shift, focused on supporting clinical operations and project management.
  • The role involves organizing meetings, managing study information, overseeing project reporting, and assisting with financial tasks.
  • Candidates should have a Bachelor's degree in a relevant field and experience in a CRO, pharmaceutical company, or clinical research is preferred.
  • Proficiency in MS Office applications, especially Excel and PowerPoint, is required, along with skills in taking meeting minutes and scheduling meetings.
  • The position offers a competitive salary range of $42,600.00 to $53,250.00 and emphasizes the importance of inclusion and accessibility in the workplace.
Clinical Packaging Technician - 2nd Shift

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


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.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Salary Range

$42,600.00-$53,250.00

Are you a current ICON Employee? Please click here to apply




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