Responsibilities:
1. Assist the Global PQL in overseeing and executing the pharmaceutical quality improvement project
2. Provide project management support, including planning, scheduling, and coordinating project activities
3. Ensure compliance with regulatory requirements and quality standards
4. Facilitate communication and collaboration among project stakeholders
5. Monitor project progress and report on key performance indicators
6. Identify and mitigate project risks and issues
7. Support the development and implementation of quality improvement initiatives
Qualifications:
1. Completed University degree in a suitable subject (minimum 4 years full-time study), such as pharmacology, biochemistry, chemistry, chemical engineering or equivalent
2. Experience in Quality Assurance of commercial medicinal products under GMP
3. Proven experience in pharmaceutical project management and quality assurance, preferably working with complex supply chains and CMO/CLO management
4. Strong understanding of regulatory requirements and quality standards in the pharmaceutical industry
5. Excellent organizational, communication, and problem-solving skills
6. Ability to work collaboratively in a global team environment
7. Proficiency in project management tools and methodologies
8. Fluent in English, both written and spoken
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