SAVA Medica Limited is a leading pharmaceutical company based in India.
Human life is precious to us. That is why we, at SAVA Medica, are committed to provide such products which can improve human health & life at affordable cost.
To accomplish our aim we, at SAVA Medica, are engaged in manufacturing & marketing of the branded generic medicines at affordable prices.
Post: Executive Regulatory Affairs
Job Description:
CO-ORDINATION WITH QUALITY ASSURANCE, QUALITY CONTROL, R&D, PACKING, PRODUCTION FOR TECHNICAL DATA ENSURING PREPARATION OF DOCUMENTATION ACCORDING TO THE REQUIREMENTS OF MOH OF THE CONCERNED COUNTRY
ENSURING EFFECTIVE AND PROMPT ATTENTION AND HANDLING OF QUERIES FROM MOH OF VARIOUS COUNTRIES.
CO-ORDINATING VARIOUS MANUFACTURING LOCATIONS AND LEGAL DEPARTMENT.
MAINTAIN THE RECORDS OF REGISTERED PRODUCTS FOR RENEWAL OF REGISTRATION
RESPONSIBLE FOR SUBMISSION OF TECHNICAL TENDER DOCUMENTS FOR INTERNATIONAL AND DOMESTIC TENDERS
DMF DOSSIER ACTIVITY
Candidate Profile:
MONITORING AND CHECKING OF REGISTRATION AND RE-REGISTRATION DOSSIERS OF FORMULATIONS INCLUDING PRESCRIPTION PRODUCTS, OTS PRODUCTS, SEMI - REGULATED COUNTRIES AND NON-REGULATED COUNTRIES
SORTING OUT TECHNICAL QUERIES RECEIVED FROM AGENTS AND HEALTH AUTHORITIES OF RESPECTIVE COUNTRIES FOR REGISTRATION OF PRODUCTS
Additional Information:
Experience: 1-4 Years
Location: Pune
Education: B.Pharm, M.Pharm
Indusrty Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
End Date: 21st Oct., 2011
Forward Your Resume Here, jobs@savaglobal.com
See All SAVA Global B.Sc Alerts B.Pharm Alerts M.Pharm Alerts Pune Alerts
See All Other Jobs in our Database