FAVEA projects
A A A
Vacancies

Position: Head of Design Department


Place of business: Zlнn, the Czech Republic

Roles and responsibilities:
  • Organization of activities pursued by departments in preparing projects of reconstructions of pharmaceutical and biotechnological productions,
  • Distribution of responsibilities between employees within the department,  Development of design solutions;
  • Distribution of responsibilities between subcontractors;
  • Supervision of the progress of works;
  • Expertise, expert’s opinion on designs;
  • Defence of own design solutions with the client;
  • Attendance at foreign business trip.

Required education:
graduate from college of technology.

Knowledge of foreign languages:
English or Russian.

Preferred are candidates skilled in designing pharmaceutical or biotechnological productions.

Contact:
This e-mail address is being protected from spam bots, you need JavaScript enabled to view it
tel. +420 577 211 049

Position: Designer-Production Engineer (pharmacy, microbiology, biotechnology, chemist-production engineer)


Place of business: Zlнn, the Czech Republic

Roles and responsibilities:
  • Full development and implementation of the technological section of reconstruction projects for various pharmaceutical productions.
  • Development and expertise of technological section of the project: technical report, technical diagrams and designs, assembly plan, equipment specifications, etc.
  • Preparation of technical roles for designing, selection of equipment, installation of equipment;
  • Development of technological diagram, calculation of technological process for selection of equipment, equipment specifications;
  • Room designing and composition of equipment;
  • Co-ordination of design construction, air conditioning and electro-technical works;
  • Co-ordination of design documentation with senior professionals of the company;
  • Participation in preparation of ordered specifications for technical equipment;
  • Consultations for clients regarding usage and deployment of equipment;
  • Review of equipment validation documentation,
  • Placing orders for equipment;
  • Extension of a new facility to the existing manufacturing plant (designing, technological approach);
  • Maintenance of Rule of Procedure;
  • Supervision during assembly and test operation;
  • Selection of equipment and necessary options (pumps, valves, flaps, etc.);
  • Connection of media to tanks and barrels;
  • Assigning tasks to subcontractors;
  • Attendance at foreign business trips.

Contact:
This e-mail address is being protected from spam bots, you need JavaScript enabled to view it
tel. +420 577 211 049
 



This year “Platinum Ounce” award in the special category of the organizing committee for the “Successful implementation of projects on modernization of pharmaceutical production in Russian Federation in accordance with the standards GMP” received company FAVEA

Video

Opening of a new pharmaceutical production in Kazan

Opening of a new pharmaceutical production in Kazan

The new production of growth hormone RASTAN in Ufa

The new production of growth hormone RASTAN in Ufa

GMP Standard

The worldwide most important document in determining the requirements for production and quality control of medicines for humans and animals is "Good Manufacturing Practice for Medicinal Products (GMP)".

 

Validation

In the methodological guidance we take into account the most recent issues of the national normative documents, the recommendations of the World Health Organization (WHO) and the Convention on mutual recognition of inspections in ...

GMP Training

The purpose of this training is to deepen the fundamental knowledge and expertise on the development of modern pharmaceuticals, manufacturing and quality control. Important objective is to train the personnel, ...

Rambler's Top100