Gujarat

Execute manufacturing, processing, and packaging of commercial and stability batches as per BMR / BPR.

Analysis of Raw Material, In-process, Finish Products, Stability Tastings, Process Validation, Participate in Lab incident/OOS/OOT/Analytical Deviation.

Experience in HPLC, GC, Dissolution, UV, TOC, and Sterility Testing. Hands-on expertise in analytical method development and validation. Aculife Healthcare

RM Sampling and Analysis (Chemical & Instrumentation) HPLC, GC, IR, KF, UV, POLARIMETER, Dissolution Chemical Testing, FP/IP/Stability Analysis (Chemical & Instrumentation), Planning of AMT, AMV, API verification & Review

To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures.

M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma; Experience Into Analytical Validation. Finished Goods. Raw Material. Stability & CLP

M.Pharm. Exposure in EU/ US/ UK/ ROW market. Formulation patent exposure. Strong communication skills, Problem-Solving, & Adaptability.

Bachelors degree in Pharmacy or degree of Doctor of Pharmacy Pharm.D. obtained from any of the Universities established or incorporated by or under the Central or a State Act in India

MSc in Biotechnology / Life Science subjects, with 60% marks with at least one year of research experience.