Date:  Jun 8, 2026
Location: 

Raleigh, US

Job Type:  Short-Term / Temporary

 Packaging & Labeling Systems Improvement Specialist

 

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.

 

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.

 

Achieve, Cooperate, Care and Innovate are the values ​​that we share and practice on a daily basis.

 

Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.

 

For more information on Guerbet, go to www.guerbet.com and follow Guerbet on Linkedin, Twitter, Instagram and Youtube

 

WHAT WE ARE LOOKING FOR

The Packaging & Labeling System Improvement Specialist will be operating in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.

This role focuses on improving packaging and labeling operations by translating regulatory requirements, system assessments, and operational insights into practical, sustainable enhancements. Working cross-functionally with Packaging, Production, Quality, and Supply Chain, the Specialist helps ensure labeling accuracy, error prevention, and compliance with GMP standards while improving efficiency. It is a hands-on position dedicated to implementing improvements and strengthening packaging and labeling systems. THIS IS A CONTRACT ROLE TO LAST 180124 MONTHS AND WILL BE ELIGIBLE FOR GUERBET BENEFITS.

YOUR ROLE

  • Lead and actively implement CAPAs and packaging/labeling improvements resulting from system assessments.
  • Translate regulatory and operational requirements into practical solutions embedded in daily packaging operations.
  • Monitor progress, support issue resolution, and verify effectiveness of implemented improvements.
  • Enhance packaging operations including line clearance, batch record compliance, reconciliation, and in-process inspection practices.
  • Improve label control systems, including label issuance, reconciliation, and verification processes.
  • Strengthen artwork management and change control processes to ensure accuracy and compliance.
  • Partner with Packaging, Production, and Quality teams to reduce human error and improve procedural compliance.
  • Performs other duties as assigned by management

Department Specific/Non-Essential Functions:

  • Support qualification activities for packaging lines and vision/inspection systems.
  • Provide training and coaching to operational teams on packaging and labeling processes and improvements.
  • Contribute to continuous improvement initiatives and packaging/labeling system optimization efforts.

YOUR BACKGROUND

Required Qualifications

  • Bachelor’s degree in Life Sciences, Engineering, or a related field (or equivalent combination of education and experience).
  • 10+ years of experience in packaging operations, labeling, or quality control within GMP-regulated environments.
  • Strong understanding of labeling controls, mix-up prevention, and packaging compliance requirements.
  • Experience implementing human error reduction strategies in operational environments.
  • Strong cross-functional collaboration, problem-solving, and hands-on operational implementation skills.

Preferred Qualifications

  • Experience in sterile packaging operations and associated regulatory expectations.
  • Familiarity with automation, serialization, barcoding, and vision/inspection technologies.
  • Knowledge of container closure integrity (CCI) and visual inspection standards for sterile products.
  • Experience supporting regulatory inspections, audit readiness, or packaging/labeling compliance programs.

 

Reason to join US

Much more than a Competitive salary,


We offer continued personal development. When you join Guerbet, you :

  • Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, 
  • Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient’s life all over the world,
  • Are joining a company where we value diversity of talents coming from various horizon.

 

We # Innovate # Cooperate # Care #Achieve at Guerbet. 

 

Guerbet is an Equal Opportunity Employer. As an organization, we believe that no individual should be discriminated against because of their differences, which includes the following: age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other basis as protected by federal, state, or local law. Guerbet is committed to diversity, equity, and inclusion.

 

Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to careers@guerbet.com or you can also call this number +19843443717