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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

 

QC Micro Supervisor

Guerbet is a leader in the medical imaging field offering health professionals innovative and effective contrast agents, medical devices and innovative solutions indispensable to diagnostic and interventional imaging to improve patients' prognosis for all major diseases and quality of life. 

Working at Guerbet means joining a human-scale company that aims to become a new global leader in Medical Imaging. 

 

Achieve, Cooperate, Care and Innovate are the values that we share and practice every day.

 

A vacancy now exists for the role of QC Microbiology Supervisor reporting to the QC Lead.  

This role is a Full Time- Permanent position and the primary responsibilities will be to manage the analytical testing in the QC Lab.  This will involve overseeing the timely completion of all raw materials, in process, finished product, microbiology and stability testing.

 

Principle Accountabilities include but are not limited to:                                                                             

  • Day to day management of the QC group including:
  • Planning and coordination of all analytical testing - QC and Microbiology
  • Perform testing as assigned
  • Ensuring that analytical testing is carried out in compliance with all site SOPs and GXP standards
  • Ensuring that all QC Chemists are trained in appropriate test methods and procedures
  • Liaising with Production to ensure an efficient and effective testing service 
  • COA generation for product release and shipment
  • Other project work as determined by QC Lead
  • Technical Support/coaching for QC Chemist group
  • Support the Supervisory and Management teams as a member of the extended Leadership Team.
  • Ensure that EHS roles and responsibilities are complied with as per the requirements of the site Safety Statement & EHS Management System
  • Delegation of QC Lead’s duties in their absence or as assigned

 

Continuous Improvement

 

Lead the QC team in continuously improving the efficiency and performance of the QC laboratory through:

  • Facilitating and driving the implementation of modifications, improvements and work simplifications as appropriate
  • Ensuring that investigations and root cause analysis are completed to drive improvements and determine root causes where required

 

Compliance

 

  • Promote the site safety programme within the QC group
  • Actively participate in QC cost improvement programmes

 

People Management

 

  • To foster a positive team environment through regular coaching and feedback to help team members improve performance and conduct tasks effectively
  • To manage employee relations issues at a local level communicating with the QC Lead to achieve best solutions at all times

 

Applicants must have the following:

  • Bachelors Degree in Analytical Science / Chemistry.  
  • Minimum 4 years relevant laboratory experience, using hands-on analytical techniques
  • Aptitude for computer operations essential including LIMS / Empower experience 
  • Previous Supervisory experience is an advantage
  • Strong technical Microbiology/Chemistry and instrumentation background is essential
  • Demonstrated ability to manage and deliver projects on target.
  • Demonstrated ability to implement improvements, complete thorough root cause analysis and work through management systems.
  • Willingness to learn,  with a Can Do-Will Do Approach
  • Positive approach to safety
  • Continuous Improvement Mindset

 

Training

 

Full training on all the responsibilities of this role will be provided. Successful applicants can expect to join an enthusiastic, energetic and hard working team.

 

 

Guerbet is an equal opportunities employer and welcomes applications from all sections of the community.