Dmitrijs Ruskovs Email & Phone Number

C#, Java

Riga, Latvia

C++, Git, C#, .NET, Relational Databses & SQL, HTTP & Web API Basics, Unit Testing, Test Driven Development, Clean Code, SOLID, Design Patterns, HTML & CSS, VueJS, TypeScript & NodeJS basics

Riga, Latvia

20 subordinates. Quality assurance. GMP, ISO standardization. Coordination of quality assurance, process validation, equipment qualification specialists, auditors. Handling of company lead and accepted Inspections, audits, training for company employees; complaint, manufacturing change and deviationmanaging. Elaboration of Technical agreements, quality agreements, distribution agreements (quality part).

13 subordinates. Development and supervision of analytical documentation and documentation for registration for development of new Final dosage forms. Communication with clients, registration specialists and authorities. Development of technical agreements, evaluation of Licensed product quality,partner product, API and excipient quality, analytical, development, elucidation and productiondocumentation. Evaluation and elaboration of Drug Master files and Module 3 documentation.

10 subordinates. Development and supervision of analytical documentation and documentation for registration for development of new Active Pharmaceutical Ingredients (API), intermediates and raw materials. Communication with clients, registration specialists and authorities. Development of technicalagreements, evaluation of API and raw material quality, analytical, development, elucidation and production documentation. Evaluation and elaboration of Drug Master files and API parts for Module 3 documentation.

GLP, ISO standardization. European co-project managing and supervising, Quality system assurance supervising and improvement.

Project managing and supervision for new Active Pharmaceutical Ingredients (API). Performance of analysis, development of analytical methods for API, validation of Analytical procedures. Elaboration of analytical and registration documentation for Drug Master Files and Module 3 documentation.

Performance of HPLC, spectral and other analysis, development of analytical methods for API, validation of analytical methods. (specialization HPLC)

Organic synthesis, project managing, preparation and presentation of development reports to the customer

Riga, Latvia

Organic synthesis: synthesis of new potential Active Pharmaceutical Products for Novel drugs (mostlyanticancer drugs for brand European pharmaceutical companies and research Institutes), projectmanaging, preparation and presentation of development reports to the customer

Master Of Science - Ms, Organic Chemistry

Bachelor Of Technology - Btech, Food Science And Technology, Additional Education

Bachelor Of Science - Bs