Main responsibilities
- Development of internal documents in the field of quality management (SOP, STP, production protocols, instructions, etc.)
- Reviews of quality of manufactured products
- Records of defects and inconsistencies, analysis of their causes
- Management of the enterprise documentation system
Our expectations
- Completed higher specialized education (pharmaceutical, chemical and technological)
- Work experience in pharmaceutical production for at least 1 year or at enterprises with a functioning quality system
- Knowledge of the process of developing documents in the field of quality
- Knowledge of the basic provisions of GMP and the ability to implement them in practice
We offer
- Official competitive salary
- The prospect of career growth due to the personnel reserve program
- The VMI program
- Personal Birthday Award
- Cozy dining room
- Soft adaptation under the guidance of an experienced mentor
- Active corporate life
- Service delivery from the Rybatskoe metro station, travel time from the metro to the place of work – up to 15 minutes
Working hours
- 5/2 from 09.00 to 18.00
- 5/2 from 08.00 to 17.00
Place of work
- St. Petersburg, Metallostroy settlement, road to Metallostroy, 5A
Service shuttle from metro station "Rybatskoye"
