At Zentiva, we are a team of 5.400 unique talents bonded together by our common mission. We believe our diversity is a source of great energy and strength, and we create a work culture and ethics where everyone feels appreciated, can be their true selves, and contribute to the best of their ability. Seeking for a balanced team across the company we welcome applications from all qualified candidates with various educational and industry experiences, cultural or ethical backgrounds, and different life experiences or abilities, regardless of their religious or philosophical beliefs or whomever they choose to love.
Our team serves as a strategic link between the Research & Development division and Manufacturing, with a focus on solid dosage forms. We ensure a smooth transition of products from late-stage development into full-scale commercial production. Our responsibilities include process scale-up, troubleshooting of manufacturing challenges, assessment and optimization of technologies and procedures, as well as coordination of product transfers between production sites. We collaborate closely with cross-functional partners such as Controlling, Quality Assurance, Regulatory Affairs and others to secure seamless delivery and compliance.
We are currently seeking a highly capable professional to manage the technology transfer activities within solid dosage forms. In this role, you will be responsible for resolving unexpected technical issues in production, aligning manufacturing and regulatory documentation, implementing process and formulation changes, qualifying new suppliers of active substances and primary packaging materials, and ensuring contract manufacturing and product validation in accordance with GMP standards.
University degree in chemistry or pharmaceutical technology/manufacturing.
Fluency in Czech/Slovak as well as good knowledge of English.
Organization and prioritization skills with strong sense of reliability.
Passion to learn new things.
An advantage might be the knowledge of given professional area - Pharmaceutical Technology, API Technology and Production or knowledge of GMP rules and authorities requirements.
An opportunity to work for a successful international pharmaceutical company.
An opportunity to learn newest approaches in managing creative and highly adaptive business organizations.
Pleasant and dynamic working environment.
Continuous personal development.
An attractive compensation & benefits package.
Above standard social and benefit program.