Good understanding on formulation & Development for regulated market/Should have experience on product technology transfer at plant side/ Knowledge on QBD,Good documentation practice/literature survey/ICH guidelines/ Solid Oral/Injectables/ OSD Required Candidate profile Execution of process evaluation, optimization, scale-up and exhibit batches. Meeting product development timelines/ Solid Oral/ Injectable Candidate can share their CV on stuti.naik@enaltec.com
Knowledge of Process development for APIs and intermediates/Trouble shooting of products at plant level/Planning and executing the experiments/Technology transfer to plant level/Handling reactions from mg to gram scale/ API R&D Required Candidate profile Cost reduction and plant troubleshooting/OD at plant site for technology transfer as & when required/ Chemistry/Regulatory Guidelines/GMP/GLP/ Timely delivery/ Compound interpretation NMR/LCMS/HPLC
Follow- GLP/ GDP/Preparation-Perform AMV & AMD/ Verification protocol & Report/ Calibration of Instrument & Equipments/Support Process Development team/Development of using Analytical instrumentation technique/ Develop method of impurity isolation Required Candidate profile Review & execute-Specification/STP/SOP/calibration documents/Routine samples( Sample for process development, IPQC, complete analysis/stability samples/outside samples/Supporting for TTD/ GC/ HPLC
Assist in formulation development of solid, liquid, semi-solid & parenteral/ Injectable dosage forms. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Injectable/Solid Oral Share CV- stuti.naik@enaltec.com
Assist in formulation development of parenteral/ Injectable dosage forms. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Injectables- Share CV- stuti.naik@enaltec.com
Method Development & Method Validation on HPLC. Stability Studies. Method transfer. Core API Experience. API R&D Preferred Immediate Joiner. Experience- 3-5 Yrs Required Candidate profile Good Experienced with Analytical Method Development & Validation on HPLC. Stability Studies Samples. Calibration.Good Knowledge of Analytical Technics. API R&D.
Candidates should have good hands on Experience on HPLC, GC, Stability, Wet Lab, RM Sampling & Analysis, Documentation, Standardization of Karl fisher Titrator. Responsible for Calibration of Instruments. Can handle QMS & AMV activities Required Candidate profile Preferred immediate Joiners. USFDA preferable. Interested candidate can share CV on sachin.kapte@enaltec.com Mob.8976826875
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