5 - 7 years
5 - 7 Lacs
Posted:2 months ago|
Platform:
Work from Office
Full Time
Role & responsibilities 1. Candidate will be based at Pharma R&D Center at Thane and will Analytical Research and Development for US & Row Market with focus on OSD Dosage. 2. Candidate should have expertise in Analytical Method Validation and Method Development, Routine, Stability for Tablets and Capsules for US/ROW Market. 3. Experienced and responsible analytical development to develop and Validate new analytical methods for analysis of formulations (Solid, Semisolid and Liquid) dosage forms as per ICH guidelines. 4. Candidate have to support and troubleshooting in the development and validation of analytical methods working across the technical teams. (Routine, Stability, Method Development and Validation) 5. Candidate will be responsible for Routine and stability analysis as well as method development and method validation and method transfer for solid, semi solid and liquid dosage forms. 6. Shuld have skills in experimental designs, method validation, method development and documentation of Solid, Semisolid and liquid Formulations. 7. Candidate have to ensure documentation and reporting of experimental data in laboratory or electronic systems. Preferred candidate profile 1. Candidate should be MSc.Analytical Chemistry and with 6-8 Years of experience in Analytical and Development for ROW & US Markets and experience in OSD , InjectableDosage. 2. Candidate should have strong knowledge of GLP/ GMP ,ICH regulations. 3. Candidate should have experience of HANDLING Analytical Instuments like UV-Vis., FTIR, KF Titrator, GC, Dissolution Apparatus, HPLC & UPLC (Software: Empower-3, Lab Solution & Chromeleon). 4. Candidate should have good knowledge of Documentation. Perks and benefits
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