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
Conduct literature survey, analyze samples (innovator, developmental, stability), Method Development & Validation, Product analysis, documentation, reports, instrument handling & troubleshooting. Required Candidate profile . M.Pharm/ M.Sc./ Skilled in LNB/logbook documentation, test methods, validation/verification, instrument calibration, troubleshooting & data review.
Assist in formulation development of Solid Oral Dosage form. 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/Solid Oral- Share CV- stuti.naik@enaltec.com
Manage & guide team, coordinate with all concerned department, supervise method development/validation, review data/docs, oversee calibration, method transfers, customer calls & team training. Required Candidate profile M.Pharm/ M.Sc with team management skills in AR&D. Strong in method development/validation, data review, calibration, training juniors, client coordination.
Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com
Job Description: Assist in literature and patent searches, pre-formulation studies, and characterization of drug substances and innovator products. Support formulation development for solid oral dosage form for global markets products. Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines. Ensure compliance with SOPs and laboratory guidelines. Compile and document data as per guidance and support all formulation development activities as needed. Preferred Immediate Joiner.
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