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 Brands catering 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.
Genom Pharmaceutical is committed to deliver healthy life to all the strata of the society and this endeavor of the company is adequately supported by strong F&D, Operations and Marketing teams.
Post: AMD Sr Officer/Executive
Job Description
Method development through trials & errors for different dosage forms & preparation of complete Method of Analysis & send to RA Department, To suggest necessary changes in the Methods of Analysis received from registration department for new registration & re-registration,To solve the analytical queries by practical experiments this helps in registration of products, Successfully Transfer of analytical method from transferring laboratory to receiving laboratory providing with all documents, Analytical Method validation for Assay/ Dissolution/ Content uniformity/Degradation product/Dissolution profiling/cleaning validation as per regulatory requirement,To prepare Raw Material Specification & Finish product specifications for new products developments,To prepare the protocol and report of validation (including Assay/Preservative/Related substance/ Dissolution with profiling/ content uniformity/ Force degradation study/ cleaning validation etc.) as per ICH or Pharmacopeia.
Candidate Profile
Method development through trials & errors for different dosage forms & preparation of complete Method of Analysis & send to RA Department, To suggest necessary changes in the Methods of Analysis received from registration department for new registration & re-registration,To solve the analytical queries by practical experiments this helps in registration of products, Successfully Transfer of analytical method from transferring laboratory to receiving laboratory providing with all documents, Analytical Method validation for Assay/ Dissolution/ Content uniformity/Degradation product/Dissolution profiling/cleaning validation as per regulatory requirement,To prepare Raw Material Specification & Finish product specifications for new products developments,To prepare the protocol and report of validation (including Assay/Preservative/Related substance/ Dissolution with profiling/ content uniformity/ Force degradation study/ cleaning validation etc.) as per ICH or Pharmacopeia..
Additional Information:
Experience: 3 - 6 Years
Qualification: B.SC / M.SC., M.Pharm
Location: Nashik
Industry Type: Pharma
Functional Area: AMD
Salary: 2.5 to 3.5 L
End Date: 18th April, 2017
Send your CV to recruitment@genompharmacopoeia.com
Posted By,
Vishwajeet Kumar,
Genom Biotech
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