At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.
We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 100 years, we continuously innovate to improve the diagnosis, prognosis and quality of life of patients.
Customer Centricity, Cooperation, Audacity, Focus, and Responsibility are the values that we share and practice on a daily basis.
Working at Guerbet is not only being part of a multicultural team with nearly 3,000 people across more than 20 countries, but it is above all about playing a unique role in the future of medical imaging.
WHAT WE'RE LOOKING FORThe Packaging Supervisor is responsible for overseeing the packaging operations within a pharmaceutical production environment. This includes ensuring compliance with current Good Manufacturing Practices (cGMP), managing packaging processes, training personnel, and maintaining regulatory compliance.
YOUR ROLE
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Supervise packaging operations to meet or exceed production schedules/goals.
Oversee the packaging of pharmaceutical products, ensuring adherence to quality standards and regulatory requirements.
Prepare/review packaging process documentation.
Train and manage training of personnel on new/existing packaging processes and equipment.
Develop and mentor packaging personnel in their career.
Apply root cause analysis to improve packaging processes and resolve problems.
Identify and implement improvements for existing packaging processes (Corrective and Preventative Actions-CAPA).
Ensure compliance with all regulatory agencies.
Write Exceptions (Deviations) related to packaging operations.
Participate and own actions to support change control initiatives.
Oversee engineering studies related to packaging.
Coordinate validation activities for packaging processes.
Propose, evaluate, and implement improvements to current packaging operations to reduce cost and improve compliance.
Performs other duties as assigned by management.
YOUR BACKGROUND
Education
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Bachelor’s degree in Life Sciences or Engineering preferred
Experience
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5 years of supervisory experience in a pharmaceutical manufacturing or FDA regulated environment
Experience with validation, CAPA, and regulatory compliance processes
Skills/Competencies
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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
