B.Sc

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

Preparing eCRF specifications, Edit check specification and other study specific set up documents.

Should be well-versed with techniques such as Spraytech, and Sprayview8t Pattern, Pump delivery test also good working knowledge of HPLC. 

Bachelors degree in chemistry, toxicology, product stewardship, industrial hygiene or related discipline required

You will be responsible for preparation, review, and approval of Cleaning Master Validation Plan, Cleaning Validation and Verification Protocols and Reports, Acceptance Criteria documents, Cleaning Validation matrix, and Periodic Monitoring Schedule

Degree in Pharmacy from an Institute / University recognized by All India Council of Technical Education. Public Service Commission

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

clinical data cleaning and reconciliation activities performed with high accuracy and in accordance with GCP, SOPs/WPDs, and study protocols. experience in RAVE / Veeva EDC