SENIOR SCIENTIST - PL&STABILITY

Senior Scientist - PL&Stability Evotec Verona, Italy We are currently looking for a highly motivated Scientist in the Analytical Development And Quality Control area, to join us for a position in our site in Verona.
He/She will work in a qualified team and will be responsible to.
Regulatory/Compliance Clear understanding of related SOPs, cGMPs and policies as necessary to accomplish daily tasks; Ensure full compliance with the quality system in place in CMC Aptuit Verona; Follow the safety guidelines; Support OOS and QI investigations if appropriate when involved in GMP activities.
Technical/Scientific Support the analysts with technical input during performance of analytical determinations on active drug substance, raw material, intermediates and final drug product in agreement with the client expectations; Support the development and validation of analytical methodology in accordance with ICH guidelines and client expectations; Support the technical side of new proposal when assigned as Technical Team Member; Accurately review analytical data, as required; Write and/or review scientific and technical documentation, with the full accountability for the data presented and the comments/conclusions driven, as well as for further discussion on reports content with the Customers; Give written/oral updates/presentations to the Customers as representatives of the technical area of expertise; Act as primary reference for all the analytical activities related to the assigned projects, with both internal and external clients.
Managerial Delegate to technical leader in scientific project leader absence; Manage in timely manner revenue closure and/or delays in revenues for the projects assigned for the analytical side; Understand the analytical activities to be performed and facilitate the scheduling of these activities to make sure they are completed within the due date; Be accountable and responsible for the analytical activities related to the assigned projects; Trainer for new associate (in those techniques for which has been received).
Administrative/General Open and clear communication; Keep supervisor informed of progress and activities; Communicates clearly with internal clients, both verbal and written; Listen carefully to others and responds appropriately; Cooperates with co-workers, team player; Willing to contribute to team activities; Demonstrates flexibility in organising work and priorities; Good problem solving skills and decision making skills to identify and solve work related issues.
Requirements.
Degree in Chemistry, Chemistry and Pharmaceutical Technology or similar.
MS and/or PhD will be considered a plus; Good written and spoken English; At least 5 years of work experience in the analytical sector of API/Drug Product development and/or manufacturing, in Pharmaceutical companies and GMP environment; Good analytical, interpersonal and teamwork skills, precision and flexibility; Consistent and reliable approach to work, diligent and precise management of activities.