ROCHE: PTR Associate- Global Position (3 years project)

"At Roche, 98,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we ´ve become one of the world´s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity".

Buscamos:

Advanced students or degree in a relevant technical area (Analytical, Biochemistry, Biology, Pharmacy, Computer science).
At least 2-3 years of experience in the industry or related job experiences.
Experience in LEAN and Agile Methodologies are an advantage.
Experience in Regulatory Affairs, development, manufacturing and/or quality assurance would be an asset.
Fluent written and oral English.
Ease of working with systems.
Proficient in Microsoft Office and Google Workspace.
Ability to work across various time zones.
Knowledge of ICH guidelines, GMP, global regulations and health authority guidance would be valuable.
Possibility to travel occasionally.
Strong communication skills.
Critical thinking and problem solving skills are a must.
Detail oriented.
Optimization and simplification mindset. Knowledge of Six Sigma, preferred.

Objetivos de la posición:

The heart of the role is the optimization, standardization and centralization of Pharma Technical Regulatory activities, ensuring increased efficiency while maintaining regulatory compliance.
In this position, you will be able to interact with different stakeholders from all over the world, working in close collaboration with cross-functional Global teams and Affiliates.
As soon as you start working, you will have the opportunity and responsibility to propose and execute specific process improvement projects, including standardization and automation of processes, in collaboration with other key functions, as applicable.
We are looking for a proactive, curious, eager to learn candidate, with a mindset focused on increasing productivity of work, ready to join a multicultural team. The candidate will interact with a diverse group of experts, in a competitive, motivating and dynamic work environment.
As primary duties of this position, we can highlight the centralization of cmc regulatory related activities for all our products worldwide, the responsibility to evaluate the processes with the explicit goal of making them lean and standardized leveraging automation and optimization opportunities, in collaboration with stakeholders and the identification of potential additional activities to be included in the scope of the team.