Objective of the role: Because this company has EUGMP consult-er & start to by production equipment from European country to archive EUGMP certificate, therefor we need technical person that know production machines & equipment, respect & implement EUGMP & Iran MOH rules. .
List of responsibilities:
1- Control the line of production.
2- Implement & do cGMP in the production line.
3- Handel workers at the policy of cGMP.
4- Respect & do the order of top manager & responsible pharmacist
Reporting to: Senior Operation Manager, responsible pharmacist.
Subordinates: 25-30 workers & their supervisions.
Length of Probation Period: 1 month.
Working hours: Saturday to wens day 7:00AM to 16:00 PM .maybe we need over time.
Travel requirements: may be for FAT of machines need to go to for foreign country...
Commission / Bonus / Benefits: will have EUGMP training .participate in FAT & SAT...
University Qualifications: MA of chemistry.
Other certifications obtained: cGMP training.
Nature and length of previous experience: at least 5 years in the field of pharmaceutical company.
Specialist knowledge: GMP, know raw & finish products & packaging materials. ICDL.
Soft Skills and Personality traits: good in English language, team work skills, willing to learn, respect to hierarchy, communicate with workers.
what is your experience in pharmaceutical productions?
How necessary is it for you to be creative on your job?
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Ofogh Tolid Darou Pars (Ofogh Pharma)
Ofogh Pharma is a private pharmaceutical manufacturing company .Its partners are several international pharmaceutical companies.
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