Customer Service Digitalization Specialist

at  Trasis

As an API Production Technician, you will produce pharmaceutical ingredients and/or reference standards in a GMP environment. You will be involved in analyzing the robustness of innovative processes on behalf of our internal and external customers.

Responsibilities

• You produce pharmaceutical ingredients and/or reference standards in accordance with the instructions on the Batch Record or other document, and in full compliance with applicable GMP procedures and rules.
• You carry out the synthesis experiments and quality controls required for your mission, in compliance with good practices and safety rules.
• You collect results and encode them in work files.
• You manage the laboratory log-books and take the necessary action in the event of any anomaly observed.
• You calibrate the equipment used and ensure its follow-up, maintenance and qualification.
• You ensure that equipment and utensils are maintained and available for analyses and experiments.
• You check items (starting materials, raw materials and production disposables) before production.
• You complete production-related documents.
• You are responsible for document management in relation to production activities (calculation sheets, QC forms).
• You carry out purification, quantification and isolation operations on the finished product.
• You check items and the Manufacturing Batch Record (MBR) at the end of production.

Profile

• You have a bachelor’s degree in chemistry, laboratory technologist or equivalent through experience.
• You have experience in chromatographic purification.
• You have a keen interest in organic synthesis.
• You have excellent organizational, analytical and critical skills.
• You are able to synthesize and analyze.
• You have a good command of English.
• You are familiar with the Office suite.

Do you want to become a major player in the global fight against cancer?
At Trasis, we give you the opportunity to work with cutting-edge technologies and to contribute to the improvement of cancer diagnosis and therapy techniques. Through your actions, you will have the opportunity to have a positive impact on the services provided to users and patients.
The opportunity to participate in building and improving processes in a growing company.
We offer a young and friendly work atmosphere, a flexible and dynamic environment.
An attractive and flexible salary according to your experience and performance, with extra-legal benefits

• You produce pharmaceutical ingredients and/or reference standards in accordance with the instructions on the Batch Record or other document, and in full compliance with applicable GMP procedures and rules.
• You carry out the synthesis experiments and quality controls required for your mission, in compliance with good practices and safety rules.
• You collect results and encode them in work files.
• You manage the laboratory log-books and take the necessary action in the event of any anomaly observed.
• You calibrate the equipment used and ensure its follow-up, maintenance and qualification.
• You ensure that equipment and utensils are maintained and available for analyses and experiments.
• You check items (starting materials, raw materials and production disposables) before production.
• You complete production-related documents.
• You are responsible for document management in relation to production activities (calculation sheets, QC forms).
• You carry out purification, quantification and isolation operations on the finished product.
• You check items and the Manufacturing Batch Record (MBR) at the end of production