Packaging Supervisor

Packaging Supervisor Guerbet - 3.6 Raleigh, NC Job Details Full-time 3 days ago Qualifications Quality control corrective actions Manufacturing management Document review (document control) EHS Six Sigma Green Belt 5 years Pharmaceutical regulatory compliance Engineering Six Sigma methodology implementation Corrective and preventive actions (CAPA) GMP Improving operational efficiency Supervising experience Bachelor's degree in engineering Bachelor's degree Continuous improvement Production planning Packaging Mentoring Pharmaceutical plant experience Quality standards in production Technical skills instruction Materials handling Manufacturing Root cause analysis Senior level Cross-functional collaboration Leadership Communication skills Technical Proficiency Full Job Description 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 as needed