QA

Experience in analysis of Solid Oral - FP, Instrumentation, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC & Dissolution. 

Shodhana Laboratories is a pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) and Intermediates. Established in 2000, they cater to both generic and custom requirements for well-known pharmaceutical brands

MSc / MPharm. in Pharmaceutical Chemistry, Analytical Chemistry,Chemistry, Pharmaceutical Analysis, Quality Assurance, or allied areas from a recognized University or equivalent.

B.Pharm / M.Pharm / M.Sc . Expertise in analysis on HPLC, GC, Assay, Dissolution. Method Validation Protocol creation and execution, Expertise in handling HPLC, ICPMS, GC etc. USV Private Limited

The ideal candidate must have hands-on exposure to ophthalmic formulations, along with practical experience in autoclave operations and batch manufacturing processes. A strong understanding of GMP and quality compliance is essential.

Responsible for execution and review support of Quality Assurance activities including document review, shop-floor QA support, deviation handling, and quality systems support to ensure compliance with cGMP and regulatory requirements.

M.Pharm with 8-12 Yrs experience Ph.D in Pharmaceutics with 5-10 Yrs Experience

Strong knowledge of Quality Agreement / Technical Agreement drafting and review. Practical experience in vendor risk assessment, approved vendor list management and periodic vendor requalification.