MedinCell® is a pharmaceutical company at commercial stage that develops innovative long-acting injectable medicines in many therapeutic areas based on our BEPO® technology.
We are looking for a Senior Analytical Scientist to join our Analytical Development & Testing team, based in Montpellier!
As Senior Analytical Scientist, you will be responsible for the development (design of experiments, data generation and interpretation), pre-validation, and implementation of analytical methods using UPLC/HPLC systems to support our development projects.
Design and perform quality scientific experiments to develop robust analytical chromatographic methods. Implement risk assessment and Quality-by-Design (QbD) concepts during analytical method development whenever possible. Make sound scientific conclusions and decisions.
Coordinate and ensure successful timely completion of experiments alone or with the support of team members
Perform & document chromatographic method development, method check / pre-validation and transfer within the appropriate quality framework in adherence with company quality management system and ICH guidelines.
Compile, analyze and interpret data to achieve a robust and fit-for-purpose chromatographic methods. Present to the team during technical meetings.
Write/update or review SOPs related to equipment use and analytical methods.
If required or necessary, interact with other departments for supporting activities such as project managers, R&D team, regulatory affairs, process development, transfer team and CDMOs.
Participate in client meetings and / or teleconferences when required, communicating in English.
Support the subsequent transfer of chromatographic test methods to both internal and external (CDMO) end users.
Support continuous improvement efforts in lab procedures, develop best practices and ensure compliance with the Quality Management System.
Identify and evaluate new analytical technologies. Expand existing analytical capabilities.
Design and perform quality scientific experiments to develop robust analytical chromatographic methods. Implement risk assessment and Quality-by-Design (QbD) concepts during analytical method development whenever possible. Make sound scientific conclusions and decisions.
Coordinate and ensure successful timely completion of experiments alone or with the support of team members.
Perform & document chromatographic method development, method check / pre-validation and transfer within the appropriate quality framework in adherence with company quality management system and ICH guidelines.
Compile, analyze and interpret data to achieve a robust and fit-for-purpose chromatographic methods. Present to the team during technical meetings.
Write/update or review SOPs related to equipment use and analytical methods.
If required or necessary, interact with other departments for supporting activities such as project managers, R&D team, regulatory affairs, process development, transfer team and CDMOs.
Participate in client meetings and / or teleconferences when required, communicating in English.
Support the subsequent transfer of chromatographic test methods to both internal and external (CDMO) end users.
Support continuous improvement efforts in lab procedures, develop best practices and ensure compliance with the Quality Management System.
Identify and evaluate new analytical technologies. Expand existing analytical capabilities.
Strong work ethic.
Autonomous, analytically minded, rigorous, methodical, perseverant.
Effective functioning in a rapidly changing environment and adherence to the values, principles and mission of the company.
Excellent interpersonal skills and an ability to work with others in a highly collaborative environment.
Openness and ability to adapt to changing situations.
Desire to continuously improve and progress.
If this mission sounds appealing to you, we’d love to hear from you!
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