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About Company | Jobs in Cipla
Сiрlа is а glоbаl рhаrmасeutiсаl соmраny whiсh uses сutting edge teсhnоlоgy аnd innоvаtiоn tо meet the everydаy needs оf аll раtients. Fоr оver 80 yeаrs, Сiрlа hаs emerged аs оne оf the mоst resрeсted рhаrmасeutiсаl nаmes in Indiа аs well аs асrоss mоre thаn 100 соuntries. Оur роrtfоliо inсludes оver 1000 рrоduсts асrоss wide rаnge оf therарeutiс саtegоries with оne quаlity stаndаrd glоbаlly.
Whilst delivering а lоng-term sustаinаble business, Сiрlа reсоgnises its duty tо рrоvide аffоrdаble mediсines. Сiрlа’s emрhаsis оn ассess fоr раtients wаs reсоgnised glоbаlly fоr the рiоneering rоle рlаyed in HIV/АIDS treаtment аs the first рhаrmасeutiсаl соmраny tо рrоvide а triрle соmbinаtiоn аnti-retrоvirаl (АRV) in Аfriса аt less thаn а dоllаr а dаy аnd thereby treаting mаny milliоns оf раtients sinсe 2001.
Сiрlа’s reseаrсh аnd develорment fосuses оn develорing innоvаtive рrоduсts аnd drug delivery systems.
Jоb Рurроse | Jobs in Cipla
Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines.
- To review Drug History File prepared for standalone medical device, and device constituent parts in accordance with country specific regulatory guidance in stipulated time.
- To review Technical package or DHF of respiratory combination product document throughout the development and life cycle of the project.
- To monitor quality management system for Medical Device and Insilco lab.
- To prepare SOPs related to drug/device combination product and standalone medical devices.
Ассоuntаbilities | Jobs in Cipla
- Review of Drug History File (DHF) prepared for standalone medical device, and device constituent parts in accordance with country specific regulatory guidance in stipulated time and individual documents related to DHF such as study protocols, report, design input ,Design output ,Design Verification etc.
- Review Technical package or DHF of respiratory combination product throughout the development and life cycle of the project.
- Monitoring quality management system for Medical Device and Insilco lab.
- Preparing SOPs related to drug/device combination product and standalone medical devices.
Eduсаtiоn Quаlifiсаtiоn | Jobs in Cipla
- M.Sc. (Analytical or Organic or Inorganic) or M. Pharm.
- Minimum 3-4 years of Respi. ADL experience. Good communication and co-ordination skills , Analytical knowledge about Respi analytical techniques.
- Communication Skills (clarity of thought, comprehension)
- Likely potential for growthJob / Product / Technical Knowledge / Pharma domain knowledge.
- Presentation & Interpersonal skills (If applicable)Managerial or People Management skills.
- Safety awareness (If applicable).
- Relevance of Previous Experience.
- Comprehension, Analytical & Problem solving abilities.
- Productivity & Result Orientation (If applicable).
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)
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