Technical Manager

Syria

Pharmacy

Finished or Exempted (For male)

1-Direct supervision in collaboration with the QC, R&D and Production directors
To develop the necessary specifications for the APIs, recipients and Finished
Products, within the constitutional specifications as mentioned in the Master
Drug file.
2. Supervise directly and in collaboration with the production director, in all the
Manufacturing operations of the products and make sure that it matches
Licensed specifications in the master drug file.
3. Develop and adopt the necessary formulations and study new formulations
For the manufacturing department in cooperation with R&D and production
Directors and study its stability and to provide protocols to the Ministry of
Health and cooperate in the field of documentation and quality assurance of
Products

4. Supervise directly along with the Quality assurance director, as he is
Responsible for the quality in all preparations and procedures along with the
Quality assurance team .
5. Follow-up technical manners with the Ministry of Health and the union to
Obtain the necessary permits for the plant varieties in all its forms and other
Licenses required for manufacturing.
6. Supervise directly on manufacturing department, warehouses, maintenance
And Quality control sections in compliance with the GMP and ISO quality
Requirements
7. Work directly on the issuing of some of the work instructions and standard
Methods of work (SOP) relating to production, hygiene, warehouses and
Control of the various versions issued by the managers and representatives
Of the ISO system
8. Cooperation with the directors and heads of departments to train technicians
And workers and supervise the rehabilitation work.
9. Follow-up hygiene, environmental and all health regulatory and enforcement
Of safety and lab systems
10. Follow-up to the new Master Drug Files, books of the Ministry of Health and
The terms of ISO and documentation

Competitive Package
Medical Insurance

1

Jun 10, 2017