Job Description

Come join us in reshaping the future with Atkins Ralis.

Atkins Ralis is dedicated to engineering a better future for our planet and its people.

Role Overview

Your role within the team: Provides technical and project leadership with a comprehensive understanding of the pharmaceutical industry design/build/validation processes and how they relate to Canadian, EU, and US FDA cGMP regulation requirements.

Responsibilities

• Develops/reviews technical documentation for clients in regulated industries including qualification and validation protocols and reports, criticality assessments, risk assessments, validation master plans, user requirements specifications, standard operating procedures, and quality plans and policies.
• Coordinate and execute testing of systems and processes from test protocols to assess compliance against requirements.
• Analysis of test data, including that derived from complex pro...