Gujarat

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. 

To support for commercial troubleshooting/remediation/Market complaints for Non-Oral manufacturing sites. To support for timely investigation/execution and to resume commercial manufacturing and to meet market/ sales requirement.

Dissolution apparatus, GC, IR and AAS and Documentation related to QMS. To review respective GMP Documents of QC department such as analytical / worksheet of In Process and Finished Product.

M.Pharm/B.Pharm/M.Sc/B.Sc Review of BMR/BPR and process validation reports, in process testing, sampling and line clearance, Media Fill. Emcure