About this opportunity
Guerbet lists this QC Sampling Specialist opportunity in raleigh, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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 100 years, we continuously innovate to improve the diagnosis, prognosis and quality of life of patients.
Customer Centricity, Cooperation, Audacity, Focus, and Responsibility are the values that we share and practice on a daily basis.
Working at Guerbet is not only being part of a multicultural team with nearly 3,000 people across more than 20 countries, but it is above all about playing a unique role in the future of medical imaging.
WHAT WE ARE LOOKING FOR
The QC Sampling Specialist will operate 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. The QC Sampling Specialist performs environmental, utilities, and product sampling in a GMP-regulated environment, ensuring compliance with approved procedures, aseptic techniques, and regulatory requirements. The role supports contamination control by conducting sampling in classified areas while adhering to strict gowning and aseptic practices. Working closely with QC Microbiology, Production, and QA, the specialist ensures reliable, compliant, and high-quality sampling activities.
YOUR ROLE
Perform routine environmental monitoring (EM) sampling in classified manufacturing areas according to approved plans
Conduct surface, air, and personnel monitoring using appropriate sampling techniques and equipment
Execute sampling activities using proper aseptic techniques while adhering to contamination control and cleanroom gowning requirements
Perform utilities sampling (e.g., purified water, WFI, gases) in accordance with approved procedures
Collect in-process and product samples while ensuring representativeness and minimizing contamination risk
Coordinate with manufacturing to perform sampling without disrupting operations
Ensure accurate sample identification, labeling, traceability, and timely transfer to the QC laboratory
Complete sampling documentation in compliance with GMP, GDP, and data integrity (ALCOA+) requirements
Follow all approved procedures related to sampling and contamination control
Report deviations, atypical observations, or potential contamination risks
Performs other duties as assigned by management
Department Specific/Non-Essential Functions:
Participate in investigations related to environmental monitoring or utilities results
Contribute to improvements in sampling procedures and contamination control practices
Support training activities related to sampling techniques and cleanroom behaviors
Assist with internal and external audits related to sampling activities
Performs other duties as assigned by management
YOUR BACKGROUND
Required Qualifications
Associate’s degree or technical training in microbiology, biology, biotechnology, or a related scientific discipline
Experience working in a GMP pharmaceutical, biotech, or sterile manufacturing environment
Experience with environmental monitoring or utilities sampling
Knowledge with cleanroom operations and aseptic techniques
Preferred Qualifications
Experience performing sampling in aseptic or Grade A/B cleanroom environments
Familiarity with Annex 1 expectations for environmental monitoring and contamination control strategies
Experience supporting regulatory inspections or audit readiness activities related to microbiology or sampling
Experience trending or reviewing environmental monitoring or utilities data
Familiarity with electronic systems such as LIMS or environmental monitoring data systems
Prior experience in sterile manufacturing or biologics environments
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Worksite address
raleigh, NC, 27601, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.