iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.
We are looking for: Project Manager in the Pharmaceutical Industry - VIE Contract (W/M)
Target start date: 01/06/2023
Responsibilities:
Ensure the management and monitoring of pharmaceutical industrial projects in compliance with good manufacturing practice (GMP) and Health, safety, and environment (HSE) standards
Product transfer projects
Quality Projects (Product Quality review (PQR), Quality Compliance, Audit Preparation)
Supply Chain projects
HSE projects (Audit preparation, implementation of HSE system)
Perform industrial feasibility studies for projects
Collect and provide other services with the elements necessary for the realization of new projects
Monitor, consolidate and document all the information needed to launch new projects
Define the needs necessary for the realization of the projects
Participate in project planning while respecting deadlines
Monitor projects, report anomalies, and participate in their treatment with the managers concerned.
Check protocols and reports
Ensure compliance with the HSE policy
Ensure compliance with GMP and quality guidelines
Requirements:
Master’s Degree ideally in science, engineering, or health field (e.g., Chemistry, Pharmacy, Biology, Chemical Engineering)
Experience in Pharmaceutical industrial experience (chemical, analytical, pharmaceutical, manufacturing) desirable
Fluency in English
At ease with Ms-Office skills (Word, Excel, PowerPoint etc.,)
Knowledge / understanding of current Good manufacturing practice (cGMP) regulations, requirements, and expectation
Able to comprehend pharmaceutical Quality operations / pharmaceutical manufacturing and supply tools
Ability to work and cooperate seamlessly with people at different levels of an organization
Ability to manage multiple projects
Excellent interpersonal skills: a strong collaborator and problem-solver
Solid understanding of pharmaceutical industry is beneficial
Good listening and organizational skills
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
DATE POSTED
12/14/2022
CONTRACT TYPE
Full time
JOB ID
R2667943
LOCATION
Casablanca, Morocco