Main responsibilities
- Development of internal documents for the quality control department of a pharmaceutical enterprise (SOP, STP, protocols, specifications, etc.)
Our expectations
- Higher specialized education (pharmaceutical, chemical technology, quality management)
- Experience in pharmaceutical production for at least 3 years or in enterprises with a functioning quality system GMP, ISO, CDP, etc.
- Experience in an analytical laboratory is desirable
- Experience in developing documents in the field of quality is required
- Knowledge of the basics of GMP provisions
- Ability to navigate legislation, regulatory documentation and standards related to the production of medicines
We offer
- Work in an actively developing company, interesting professional tasks, modern equipment
- Registration in accordance with the Labor legislation of the Russian Federation
- Stable salary payments (2 times a month)
- VHI policy after the probationary period
- Birthday bonuses for employees
- Nutrition compensation
- Corporate sports activities
Working hours
- 5/2 from 09.00 to 18.00
Place of work
- St. Petersburg, Metallostroy settlement, road to Metallostroy, 5A
Service shuttle from metro station "Rybatskoye"
