Guerbet
Join to apply for the
Filling Supervisor (2nd shift)
role at
Guerbet .
At Guerbet, we build lasting relationships so that we enable people to live better. We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, as well as digital and AI solutions for diagnostic and interventional imaging. As a pioneer in contrast products for the last 95 years, we continuously innovate.
What We’re Looking For We are seeking a dedicated and detail-oriented
Filling Supervisor
to lead operations in a pharmaceutical manufacturing environment. This role is critical in ensuring compliance with current Good Manufacturing Practices (cGMP), maintaining high-quality production standards, and fostering a culture of continuous improvement. The ideal candidate will bring strong leadership, technical expertise, and a proactive approach to problem‑solving, while also being comfortable working in a highly regulated, fast‑paced setting.
This position is located in Raleigh, NC and follows a 2nd shift schedule: Monday–Thursday, 3:30 PM–1:30 AM, with overtime as needed on weekends. Flexibility is essential.
Your Role
Supervise daily production operations, primarily in finishing, while supporting other areas as needed.
Ensure compliance with cGMP and all applicable regulatory requirements.
Prepare, review, and maintain accurate process documentation.
Train and mentor production personnel on equipment, procedures, and best practices.
Lead and support continuous improvement initiatives, including CAPAs.
Write and manage deviations (exceptions) and participate in change control processes.
Coordinate and oversee validation activities and engineering studies.
Collaborate with cross‑functional teams including Quality, Validation, Materials & Distribution, and Engineering.
Conduct manufacturing trend analysis and contribute to packaging capability improvements.
Promote and enforce safety standards, reporting any incidents or unsafe conditions promptly.
Your Background Education
Bachelor’s degree in Life Sciences preferred.
Experience
5 years of supervisory experience in a pharmaceutical manufacturing or FDA‑regulated environment.
Skills/Competencies
Strong verbal and written communication skills.
Effective interpersonal and leadership abilities.
Mechanical aptitude and comfort with hands‑on equipment use.
Proficiency in desktop computer applications.
Ability to read and follow SOPs, complete documentation accurately, and perform basic math.
Solid understanding of Good Manufacturing Practices (GMP).
Willingness and flexibility to work overtime as needed.
Referrals increase your chances of interviewing at Guerbet by 2x.
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Filling Supervisor (2nd shift)
role at
Guerbet .
At Guerbet, we build lasting relationships so that we enable people to live better. We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, as well as digital and AI solutions for diagnostic and interventional imaging. As a pioneer in contrast products for the last 95 years, we continuously innovate.
What We’re Looking For We are seeking a dedicated and detail-oriented
Filling Supervisor
to lead operations in a pharmaceutical manufacturing environment. This role is critical in ensuring compliance with current Good Manufacturing Practices (cGMP), maintaining high-quality production standards, and fostering a culture of continuous improvement. The ideal candidate will bring strong leadership, technical expertise, and a proactive approach to problem‑solving, while also being comfortable working in a highly regulated, fast‑paced setting.
This position is located in Raleigh, NC and follows a 2nd shift schedule: Monday–Thursday, 3:30 PM–1:30 AM, with overtime as needed on weekends. Flexibility is essential.
Your Role
Supervise daily production operations, primarily in finishing, while supporting other areas as needed.
Ensure compliance with cGMP and all applicable regulatory requirements.
Prepare, review, and maintain accurate process documentation.
Train and mentor production personnel on equipment, procedures, and best practices.
Lead and support continuous improvement initiatives, including CAPAs.
Write and manage deviations (exceptions) and participate in change control processes.
Coordinate and oversee validation activities and engineering studies.
Collaborate with cross‑functional teams including Quality, Validation, Materials & Distribution, and Engineering.
Conduct manufacturing trend analysis and contribute to packaging capability improvements.
Promote and enforce safety standards, reporting any incidents or unsafe conditions promptly.
Your Background Education
Bachelor’s degree in Life Sciences preferred.
Experience
5 years of supervisory experience in a pharmaceutical manufacturing or FDA‑regulated environment.
Skills/Competencies
Strong verbal and written communication skills.
Effective interpersonal and leadership abilities.
Mechanical aptitude and comfort with hands‑on equipment use.
Proficiency in desktop computer applications.
Ability to read and follow SOPs, complete documentation accurately, and perform basic math.
Solid understanding of Good Manufacturing Practices (GMP).
Willingness and flexibility to work overtime as needed.
Referrals increase your chances of interviewing at Guerbet by 2x.
#J-18808-Ljbffr