Formulation Technician - 3rd Shift

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 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.

Achieve
, Cooperate
, Care and Innovate are the values that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.

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The Formulation Technician operates in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.

The Formulation Technician is responsible for the processing and preparation of pharmaceutical formulations within a cGMP regulated production environment. The role also provides operational support to filling team members, ensuring a smooth transition of materials and consistent execution of upstream and filling processes. The Formulation Technician will alsobe responsible for completing allnecessarydocumentationrelatedto the manufacturing processwhileadheringto cGMP andGDPguidelines.

• Demonstrate understanding of Current Good Manufacturing Practices (cGMP) and applicable regulatory guidelines (FDA, EMA, etc.) in a clean room environment requiring aseptic behavior.
• Prepare media according to approved batch records, SOPs, and cGMP requirements. Verify material identity, lot numbers, expiration dates, and required quantities through inventory systems, such as SAP
• Perform controlled transfers of API into designated formulation vessels or staging containers while adhering to segregation, containment, and safety procedures.
• Prepare and review process documentation to ensure accuracy, completeness, and compliance with cGMP and GDP requirements.
• Ensure compliance with all applicable regulatory agencies and cGMP requirements. Sanitize hold tanks, formulation tanks, process equipment, utensils, and conduct general cleaning of formulation processing areas according to cGMP and sanitation procedures.
• Maintain strict adherence to aseptic techniques during all operations within a controlled environment.
• Ensurea highlevel of safety, quality, and productivity tomaintaina reliable supply of products to patients.
• Promptly report andassistin investigation of any contamination events or deviations.
• Performs other duties as assigned by management

• Collaborate with Engineering, Validation, and otherdepartmentsininitiating and implementingprograms such as Continuous
  
  Improvement (Leanand 5S) and Total Productive Maintenance.
• Prevent excess wasteofproduct and/or components by operating the equipment in an efficient manner.
• Report all safety and/or environmental incidents to management immediately.
• Cross-training to perform tasks and roles outside of the primary responsibilities
• Performs other duties as assigned by management

Required Qualifications

• High School diploma, GED or equivalent.
• 1-3 experience in pharmaceutical manufacturing (preferred).
• Compounding or formulation experience (preferred)
• Strong knowledge of aseptic processing, cleanroom standards, and sterile techniques.
• Knowledg…