QC Analyst III (3rd Shift) - (30131)

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'RE LOOKING FOR

We’re looking for a skilled and motivated QC Analyst III to join our Quality Control team. In this role, you’ll perform a variety of analytical tests to evaluate the quality of materials and products in a regulated pharmaceutical environment. You’ll work closely with formulation, filling, and packaging teams to ensure product integrity and compliance with regulatory standards. This position is ideal for someone who thrives in a fast-paced lab setting, values precision, and enjoys contributing to continuous improvement and audit readiness.

This position is based in Raleigh, NC, with an on-site, 3rd shift schedule of 9pm-5am. Overtime and alternate hours may be required during peak production periods.

YOUR ROLE

• Perform wet chemistry tests and assays following SOPs and using laboratory instrumentation

• Review and revise testing procedures, instrument protocols, and lab documentation

• Support audit readiness and compliance with global regulatory standards

• Conduct experimental work on future products and testing procedures under supervision

• Record and report test results and significant observations accurately

• Assist with special testing and validation of instruments and processes

• Train new team members on lab procedures and compliance requirements

• Collaborate with internal teams to support production and quality goals

• Identify and report variations in test results, sample conditions, and equipment performance

• Maintain a safe and organized lab environment in accordance with safety and environmental regulations

YOUR BACKGROUND

Education

• Bachelor’s degree in Chemistry (preferred) or another science discipline with coursework in General, Organic, and Analytical Chemistry

Experience

• 2–3 years of analytical chemistry testing in an FDA-regulated environment (pharmaceutical manufacturing preferred)

Skills/Competencies

• Ability to manage multiple tasks with accuracy and precision

• Strong prioritization and leadership capabilities

• Self-motivated, energetic, and team-oriented

• Effective verbal and written communication skills

• Proficiency in data analysis and computer-based lab systems

• Knowledge of cGMPs, GLPs, FDA requirements, and laboratory safety standards