Responsibilities:
Assist the Global PQL in overseeing and executing the pharmaceutical quality improvement project
Provide project management support, including planning, scheduling, and coordinating project activities
Ensure compliance with regulatory requirements and quality standards
Facilitate communication and collaboration among project stakeholders
Monitor project progress and report on key performance indicators
Identify and mitigate project risks and issues
Support the development and implementation of quality improvement initiatives
Qualifications:
Completed University degree in a suitable subject (full-time study), such as pharmacology, biochemistry, chemistry, chemical engineering or equivalent
Experience in Quality Assurance of commercial medicinal products under GMP
Proven experience in pharmaceutical project management and quality assurance, preferably working with complex supply chains and CMO/CLO management
Strong understanding of regulatory requirements and quality standards in the pharmaceutical industry
Excellent organizational, communication, and problem-solving skills
Ability to work collaboratively in a global team environment
Proficiency in project management tools and methodologies
Fluent in English, both written and spoken.
Company Benefits:
A very renowned company
Good infrastructure
Possibilities to work in a home office
Continuous support during the assignment
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