ROCHE: PTR International Operations Associate (contrato a término- aprox. 2 años-)

Para: At the Roche Group, about 80,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research focused healthcare groups.

Ref. R6375


Degree in relevant technical areas (Analytical, Biochemistry, Biology, Pharmacy, among others.).
At least 5 years of experience in the pharmaceutical industry.
Experience in Regulatory Affairs ideally.
Fluent in written and oral English (excluding).
Strong communication skills and excellent interpersonal skills.
Ability to influence and work both independently and collaboratively in a diverse team structure.
Critical thinking and problem solving skills a must, detail oriented.
Optimization and simplification mindset. Knowledge of Lean, Six Sigma, or Agile methodologies preferred.
Demonstrates effective problem solving ability, continuous improvement mindset, and has the ability to prioritize multiple tasks.
Knowledge of ICH and cGMPs, global regulations and health authority guidance.
Ability to work across various time zones.
Ability to travel according to the needs of the projects.

Objetivo de la posición

This position is responsible for the execution of Submission Enabling and Compliance Activities, for all Roche products in the countries covered by PTR International Operations.
Collaborates with the Centralized Activities department in the execution of all tasks (Renewals, CPP and samples management, translation of the Approval Letters, Information management activities, etc).
The role can take products and/ or countries under its responsibility, depending on the evolution of the previously mentioned activities.
Support departmental operational excellence and business process initiatives.
In collaboration with PDR ERAS, helps to develops and executes objectives and plans toward aligning one global regulatory voice/outlook to affiliates in the region.

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