Walk-In Interview - 12th April, 2024 (Friday)
Inviting proficient Analytical Research & Development (AR&D) experts! Seize the opportunity as we are expanding our Analytical Research & Development team in Hyderabad.
Company : JAMP India Pharmaceuticals Pvt. Ltd.
Venue : JAMP India Pharmaceuticals Pvt. Ltd., Plot No 40 & 41 (part), Phase 3, Biotech Park, Karkapatla (V), Hyderabad - 502281.
Time: 10:00 AM to 03:30 PM
Location : Hyderabad
Contact Person: Mr. Satya Kiran(HR) 8978944466
Vacany Details:
1. Designation & Qualification:AGM- OSD (M.Pharm)
Experience:15-20 yrs
Position:01
Responsibilities:
Responsible for all Analytical development activities. Le. 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
2. Designation & Qualification: Manager - OSD (Dissolution Development) (M.Pharm)
Experience:10-12 yrs
Position:02
Responsibilities:
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.
3. Designation & Qualification: Manager - Semisolids (M.Pharm / Ph.D)
Experience:10-12 yrs
Position:01
Responsibilities:
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.
Experience-12+ Years of which minimum 50% exp, in Semisolid projects handling.
Team handling experience is must, 5-7 Scientists.
New products method development for Semisolid dosage forms for regulated market.
4. Designation & Qualification: Senior Executive - Method Validations (Reviewer) (M.Pharm / M.Sc)
Experience:6-8 yrs
Position:01
Responsibilities:
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.
5. Designation & Qualification: Executive / Sr.Executive - OSD (Method Development)
Experience:3-6 yrs
Position:06
Responsibilities:
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.
Expertise in Dissolution development should be in line with Canada, Europe Market.
6. Designation & Qualification: Executive - Semisolids (M.Pharm / M.Sc)
Experience:3-5 yrs
Position:01
Responsibilities:
Routine and stability analysis for semisolid products.
Expertise in Reverse engineering by GC and HPLC technique.
Expertise in IVRT/IVPT method development, method validation and comparative studies with reference product.
Should have knowledge of method development for Viscosity, Rheology, PSD/GSD by Microscopy etc.
New products method development of Assay, preservative contents and RS for Semisolid products.
JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma generic products, our Orimed Pharma branded products, our Wampole and Laboratoire Suisse natural health products, and our Cosmetic Import beauty and personal care products.
JAMP Pharma Group has also made a recent major investment in biosimilars , one of the fastest growing markets in the industrywith the launch of its BIOJAMP division. For nearly 35 years, we have been committed to supporting healthcare professionals so that they may focus on what matters most: the well-being of Canadians. We have made healthcare solutions more accessible and affordable for both patients and consumers.
