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Guerbet is a leader in medical imaging worldwide, offering a wide range of pharmaceutical products, medical devices, digital and AI solutions for diagnostic and interventional imaging, to improve the diagnosis and treatment of patients.

A pioneer since more than 90 years in the field of contrast media, Guerbet is continuously innovating with 9% of revenue dedicated to Research & Development and four centers in France, Israel and the United States.

Guerbet (GBT) is listed on Euronext Paris (segment B – mid caps) and generated €817 million in revenue in 2019 with a global workforce of over 2,800 employees.

Achieve, Cooperate, Care and Innovate are the values that Guerbet's employees share and practice every day. Working at Guerbet means playing a unique part in the future of medical imaging. Passionate about its business, the company strive day in, day out to combine performance, quality and sustainable development.

For more information about Guerbet, please go to www.guerbet.com  and follow Guerbet on Twitter @GuerbetGroup

 

Production Supervisor - 2nd Shift

The Production Supervisor is responsible for all aspects of maintaining current Good Manufacturing Practices into the pharmaceutical production environment. This includes monitoring current processes, adapting new processes, training personnel, and ensuring regulatory compliance.

Position Responsibilities

  • Supervise production operations in a pharmaceutical manufacturing environment to meet or exceed production schedules/goals.
  • Primarily oversee filling, finishing, and or formulation operations but support other production operations during absences.
  • Prepare/review process documentation
  • Train and manage training of personnel on new/existing processes and equipment
  • Develop and mentor operations personnel in their career.
  • Apply six sigma tools and root cause analysis to improve processes and resolve problems.
  • Identify and implement improvements for existing processes (Corrective and Preventative Actions-CAPA)
  • Ensure compliance with all regulatory agencies
  • Write Exceptions (Deviations)
  • Participate and own actions to support change control initiatives.
  • Oversee engineering studies
  • Coordinate validation activities
  • Propose, Evaluate and Implement improvements to current operations to reduce cost and improve compliance.

Position Requirements


Education required/ preferred:

BS Degree in Life Sciences or Engineering preferred. 

Experience:

Minimum of 3 years of supervisory experience in a pharmaceutical environment.

Preferred Skills/Qualifications:

  • Six-Sigma Greenbelt or Lean Certified preferred
  • Must have excellent verbal and written communication skills
  • Must have ability to present information to large groups
  • Must have good interpersonal skills
  • Mechanical aptitude requiredWillingness to work overtime / off-shift

Skills/Competencies:

  • Ability to interact with all Quality, Materials and Distribution, and Engineering.
  • Advance desktop computer skills