Ekspert upravljanja kakovosti za proces proizvodnje bioloških učinkovin (m/ž/d) / QA expert for the production process of biological agents (m/f/d)
Novartis
Quality Assurance
Slovenia
Posted on May 23, 2024
Summary
Prinašamo življenjsko pomembna zdravila milijonom ljudi. Smo na stičišču najnovejših dosežkov medicinske znanosti in inovativne digitalne tehnologije. Vse kar počnemo je usklajeno z našo zavezo h kakovosti in zagotavljanju varnih učinkovin za bolnike. Naša zaveza kakovosti temelji na znanosti, prinašamo inovativnost in naše delo je usmerjeno k bolnikom. Ne glede na to, ali sodelujete v razvoju, proizvodnji, vzdrževanju, skladnosti ali analizi, bo vaš prispevek neposredno vplival na bolnike." Brez preverjanja in zagotavljanja kakovosti v vseh točkah procesa ne moremo zanesljivo graditi zaupanja bolnikov. Vam to poslanstvo predstavlja vrednoto?
Kot Ekspert upravljanja kakovosti za proces proizvodnje bioloških učinkovin skupaj z sodelavci zagotavljate, da se uresničujejo zahteve po skladnosti dobre proizvodne prakse. Vaša vloga vključuje pobudo, usklajevanje in izvajanje vseh potrebnih aktivnosti za doseganje skladnosti. V tej vlogi imate kot strokovnjak tudi svetovalno vlogo v zadevah GMP za vse zaposlene v vrednostnem toku.
We bring life-saving medicines to millions of people. We are at the crossroads of the latest advances in medical science and innovative digital technology. Everything we do is in line with our commitment to quality and to providing safe active substances for patients. Our commitment to quality is based on science, we innovate and our work is patient-centred. Whether you are involved in development, production, maintenance, compliance or analysis, your contribution will have a direct impact on patients. ” Without quality checks and quality assurance at all points in the process, we cannot reliably build patient trust. Do you value this mission?
As the QA expert for the production process of biological agents, you and your colleagues ensure that GMP compliance requirements are met. Your role includes initiating, coordinating and carrying out all necessary activities to achieve compliance. As an expert, you also have an advisory role on GMP matters for all employees in the value chain.
Kot Ekspert upravljanja kakovosti za proces proizvodnje bioloških učinkovin skupaj z sodelavci zagotavljate, da se uresničujejo zahteve po skladnosti dobre proizvodne prakse. Vaša vloga vključuje pobudo, usklajevanje in izvajanje vseh potrebnih aktivnosti za doseganje skladnosti. V tej vlogi imate kot strokovnjak tudi svetovalno vlogo v zadevah GMP za vse zaposlene v vrednostnem toku.
We bring life-saving medicines to millions of people. We are at the crossroads of the latest advances in medical science and innovative digital technology. Everything we do is in line with our commitment to quality and to providing safe active substances for patients. Our commitment to quality is based on science, we innovate and our work is patient-centred. Whether you are involved in development, production, maintenance, compliance or analysis, your contribution will have a direct impact on patients. ” Without quality checks and quality assurance at all points in the process, we cannot reliably build patient trust. Do you value this mission?
As the QA expert for the production process of biological agents, you and your colleagues ensure that GMP compliance requirements are met. Your role includes initiating, coordinating and carrying out all necessary activities to achieve compliance. As an expert, you also have an advisory role on GMP matters for all employees in the value chain.
