Packaging Supervisor - (30084)

 

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.   

  

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

  

For more information on Guerbet, go to www.guerbet.com and follow Guerbet on LinkedIn, X, Instagram, and YouTube. 

 

WHAT WE'RE LOOKING FOR

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.

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

 

YOUR ROLE

• 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.

 

YOUR BACKGROUND

Education

• Bachelor’s degree in Life Sciences or Engineering preferred

Experience

• 5 years of supervisory experience in a pharmaceutical manufacturing or FDA regulated environment

• Experience with validation, CAPA, and regulatory compliance processes

Skills/Competencies

• 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 a