Guerbet
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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.
Location Raleigh, NC
Schedule First Shift, Monday–Thursday, 5:30 AM–3:30 PM (Overtime as needed, including weekends – flexibility required)
Responsibilities
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.
Qualifications 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.
Seniority Level Mid-Senior level
Employment Type Full‑time
Job Function Management, Manufacturing, and Production
Industries Motor Vehicle Manufacturing
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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.
Location Raleigh, NC
Schedule First Shift, Monday–Thursday, 5:30 AM–3:30 PM (Overtime as needed, including weekends – flexibility required)
Responsibilities
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.
Qualifications 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.
Seniority Level Mid-Senior level
Employment Type Full‑time
Job Function Management, Manufacturing, and Production
Industries Motor Vehicle Manufacturing
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