Packaging Supervisor

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We are seeking a proactive and experienced Packaging Supervisor to lead operations in a pharmaceutical manufacturing environment. This role is essential in ensuring compliance with current Good Manufacturing Practices (cGMP), optimizing packaging processes, and mentoring a high-performing team. The ideal candidate will bring strong leadership, technical expertise, and a continuous improvement mindset to support production goals and regulatory standards.

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, and digital and AI solutions for diagnostic and interventional imaging. As a pioneer in contrast products for the last 95 years, we continuously innovate.

Customer centricity, Cooperation, Audacity, Focus, and Responsibility are the values we share and practice.

• Raleigh, NC

• First Shift, Monday–Thursday, 5:30 AM–3:30 PM (Overtime as needed, including weekends – flexibility required)

• Supervise daily packaging operations to meet or exceed production schedules and quality standards.
• Oversee filling, finishing, and formulation processes, with flexibility to support other production areas as needed.
• Ensure compliance with all regulatory requirements and cGMP standards.
• Train and mentor team members on equipment, processes, and safety protocols.
• Prepare and review process documentation, including deviations and change controls.
• Lead and participate in continuous improvement initiatives using Six Sigma and root cause analysis tools.
• Coordinate validation activities and support engineering studies.
• Identify and implement corrective and preventive actions (CAPA) to enhance efficiency and compliance.
• Collaborate cross‑functionally with Quality, Engineering, and Materials teams.
• Promote a culture of safety and actively participate in Environmental, Health & Safety (EHS) programs.

• Bachelor’s degree in Life Sciences or Engineering preferred

• 5 years of supervisory experience in a pharmaceutical manufacturing or FDA regulated environment.
• Experience with validation, CAPA, and regulatory compliance processes.

• Strong verbal and written communication skills, with the ability to present to large groups.
• Proficiency in desktop computer applications and documentation systems.
• Mechanical aptitude and familiarity with material handling equipment.
• Knowledge of Good Manufacturing Practices (GMP) and safety regulations.
• Six Sigma Green Belt or Lean Certification preferred.
• Ability to work cross‑functionally and lead teams effectively.
• Flexibility to work overtime and weekends as needed.

• Mid-Senior level

• Full‑time

• Management, Manufacturing, and Production

• Motor Vehicle Manufacturing