Preparation of the Standard Operating Procedures and batch manufacturing record as per current good manufacturing practices.
Execution of the approved standard operating Procedure and batch manufacturing record.
Day to Day Planning of the batches as per production schedule given by the Production head.
Manufacturing of the biotech formulation as per instruction given into the batch manufacturing record.
Strictly follow up the Aseptic Operation and Practices with Procedures in critical Area.
Overall Supervision in Production area activities like washing/sterilization, Disinfection , Manufacturing of the biotech formulation, aseptic Filling Operation, Collection and leak testing and visual inspection of the small volume parental Preparation.
On line completion of the production documents like batch manufacturing record and log books etc.
Keeping ready and supporting for facility qualification and validation.
Ensuring of the preventative maintenance is followed by engg. as per given schedule.
Timely completion of cGMP and On job training schedule.
Effective utilization of the production consumables like disinfectant, filters and hand gloves etc.
Person should be able to speak, write and understand English.
Candidate should have Pharmacist degree.
He should have at least three to five years’ experience in formulation /sterile area.
Trustworthy and Accurate
Able to work under pressure
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VitanePharmed pharmaceutical company, working under license of VitanePharmaGmbH, has been established in 2009 to supply high quality medicines in various therapeutic lines including internal medicine, Endocrinology, Gynecology and Oncology.
VitanePharmed manufacturing facility is being constructed near Tehran to meet cGMP guidelines according to US-FDA & EMA standards, to do produce Biologic, Hormonal & Oncologic finished products to be exported to regulated markets.
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