The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.
Analytical Research & Development (AR&D) Department
Qualification : M.Pharm / M.Sc
AGM - OSD : M.Pharm with minimum 15-20 years of relevant experience. (1 Position)
• Responsible for all Analytical development activities. i.e. Method developments for Solid Orals like Tablets, Capsules etc.
• Responsible for procurement of new techniques and resources in time (i.e. Chemicals, Impurities, Columns, Instruments… Etc.).
• Responsible for review and approval of Standard Operating Procedures, Standard Test Procedures, Test Methods, Specifications and Guideline.
• To follow the applicable GXPs (GMP/GLP/GDP) compliance in laboratory.
• Responsible for Managing the maintenance & trouble shooting of various analytical instruments.
Manager - OSD : M.Pharm with minimum 10-12 years of relevant experience. (2 Positions)
• Expertise in Dissolution development should be in line with Canada, Europe Market.
• Expertise on the finalisation of Dissolution parameters like Selection of Media and Volume, Selection of Apparatus & RPM, Selection of surfactant concentrations for Poorly soluble drugs(BCS Class - ii & iv).
• Expertise in Stability indicating methods Assay, Related substances methods.
• Expertise on handling of HPLC,GC, Dissolution Apparatus, UV Visible spectrometer etc.
• Responsible for the Preparation and Review of SOP,STP, Technical Reports etc. Capable to lead about 10-15 scientists.
Manager - Semisolids : M.Pharm / Ph.D with minimum 10-12 years of relevant experience. (1 Position)
• New products method development for Semisolid dosage forms for regulated market.
• Expertise in Method development, Reverse engineering, and Characterisation of Semisolid products.
• Preparation, review and finalization of Specifications, STP’s, MDR’s and other technical reports required for CANADA and other regulated market.
• Expertise in Semisolid projects handling.
• Team handling experience is must, 5 - 7 Scientists.
Senior Executive - Method Validations (Reviewer) : M.Pharm / M.Sc with minimum 6-8 years of relevant experience.
(1 Position)
• Responsible for preparation and review of analytical method validation protocols and reports for various dosage forms.
• Responsible for preparation and review of analytical method transfer protocols and reports for various dosage forms.
• Planning analytical method validation activities and troubleshooting the problems during analytical method validation.
• Handling of Incidents, Change controls and Justification reports.
• GLP related activities in Laboratory.
Executive / Sr.Executive - OSD (Method Development) : M.Pharm / M.Sc with minimum 3-6 years of relevant experience. (6 Positions)
• Expertise in Dissolution development should be in line with Canada, Europe Market.
• Expertise on the finalisation of Dissolution parameters like Selection of Media and Volume, Selection of Apparatus & RPM, Selection of surfactant concentrations for Poorly soluble drugs (BCS Class - ii & iv).
• Good Knowledge on Stability indicating method development (like Assay, Related substances methods) & Regular analysis.
• Expertise on handling of HPLC,GC, Dissolution Apparatus, UV Visible spectrometer etc.
• Responsible for the Preparation and Review of SOP, STP, Technical Reports etc.
Executive - Semisolids : M.Pharm / M.Sc with minimum 3-5 years of relevant experience. (1 Position)
• New products method development of Assay, preservative contents and RS for Semisolid products.
• Routine and stability analysis for semisolid products.
• Expertise in IVRT/IVPT method development, method validation and comparative studies with reference product.
• Expertise in Reverse engineering by GC and HPLC technique.
• Should have knowledge of method development for Viscosity, Rheology, PSD/GSD by Microscopy etc.
Interested candidates can Walk-in for interview along-with their updated resume, passport size photograph
Walk in Interview
Date : Friday April, 12th 2024
Time : 10:00 AM to 03:30 PM
Venue : JAMP India Pharmaceuticals Pvt. Ltd. Plot No 40 & 41 (part), Phase 3, Biotech Park, Karkapatla (V), Hyderabad - 502281.
Candidates who are unable to attend the walk-in interview can send their profile to Mr. Satya Kiran (HR) at : skiran@jamppharma.com
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