Genom Biotech Pvt. Ltd is a leading pharmaceutical and biotech company operating in 17countries spread across CIS, Middle East, Africa and Latin America and has over 118 Brandscatering to all the therapeutic segments. Genom manufactures a wide range of products like Injectable, Tablets, Capsules, Liquids and Ointments, catering to various illnesses such as Cardiovascular, Neurological, Gastrointestinal and covering all the major therapeutic segments.
Post : Quality Assurance/STP/Change Control/Deviation/Sr. Executive
Job Description
To prepare and checking of BMR & BPR, To prepare Protocols & reports of process validation, To review BMR & BPR cum batch release, To prepare Annual Product Quality Review Reports, To handle deviations, To handle change control, non conformance, out of specification, internal audit report and QMS system,To maintain overall cGMP in the plant, To perform overall documentation regarding PIC/S, WHO, cGMP, cGLP, ISO 9001:2008, To set analytical method validation protocol, report type setting, stability protocol type setting, BMR/ BPR type setting.
Candidate Profile
To prepare and checking of BMR & BPR, To prepare Protocols & reports of process validation, To review BMR & BPR cum batch release, To prepare Annual Product Quality Review Reports, To handle deviations, To handle change control, non conformance, out of specification, internal audit report and QMS system,To maintain overall cGMP in the plant, To perform overall documentation regarding PIC/S, WHO, cGMP, cGLP, ISO 9001:2008, To set analytical method validation protocol, report type setting, stability protocol type setting, BMR/ BPR type setting
Additional Information:
Experience: 3-7 Years.
Qualification: B.Pharm / M.Pharm
Location: Nashik
Industry Type: Pharma
Functional Area: Quality Assurance
End Date: 18th July, 2017
Send your CV to hr@genompharmacopoeia.com
Posted By,
Praveen Patnaik,
Genom Biotech
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