Soft Skills:

1. Attention to Detail: Precision and thoroughness in executing tasks (actively used when dealing with quality assurance processes and regulatory documentation).

2. Communication Skills: Effectively conveying complex information to various audiences, including government Health Authorities and colleagues from different departments).

3. Problem-Solving: Flexible and sometimes creative attitude to occuring tasks.

4. Time Management: Juggling multiple tasks and priorities to meet deadlines and maintain the efficiency of quality assurance processes.

5. Teamwork: Collaborating with cross-functional teams to ensure a seamless flow of information and processes between different departments.

6. Adaptability: Being flexible and adaptable to changes in regulations, industry standards, and company procedures.

7. Ethical Judgment: Demonstrating a strong sense of ethical responsibility when dealing with issues related to drug quality and safety.

8. Continuous Learning: Willingness to learn and grow on both personal and professional levels, to enhance the already existing skills and get new knowledge and experiences.

Hard Skills:

1. Regulatory Compliance: Developing a keen understanding of pharmaceutical regulations and ensuring adherence to standards set by regulatory authorities.

2. Document Management: Proficiently managing and organizing documentation, including batch records and quality records.

3. Analytical Techniques: Using theoretical knowledge in various analytical techniques, such as chromatography, spectroscopy, and microbiological assays, for thorough revision and preparation of Quality Documentation for pharmaceutical products.

4. Product Release: Active and keen participation in the preparations of imported medicinal products (vaccines, immunology, rare diseases) to be released in Ukraine.