Expected M.Pharm by education with 3+ years experience for Document requisition and review, Dossier Preparation, CTD, ACTD, Country specific for ROW Market

Knowledge & hands-on experience of equipment qualification & validation of sterile manufacturing of USFDA approved sterile facility only.

Knowledge of injectable plant aseptic practices, BMR, PFS Filling, Cartridge Filling, Lyophilization, SVP/LVP Line etc.

Granulation / Compression / Packaging / Coating/ Capsule Filling

Hands-on experience with analytical instruments such as Particle Size Distribution (PSD) analyzer (Malvern), Zeta Sizer, and Dissolution Apparatus I, II, and IV will be considered an added advantage.

D.Pharma / B.Pharm from a recognized institution. The age of the applicants should not exceed 35 years as of 01.01.2020.

B.Pharm / Bachelors degree in Engineering or Technology or Medicine, from a recognized University or equivalent.

M.Pharm, M.Tech with minimum 2 years experience in procurement / logistics / supply chain management in reputed institute / organisation.

Master of Social Work/BSW/M.Sc. in Allied Health Sciences (M.Sc. Clinical Embryology/Echo-Cardiography/Forensic Odontology/Medical Genetics & Counselling/Respiratory Therapy/Medical Anatomy/Clinical Research

1st class Post Graduate Degree, Including the integrated PG Degree in Life Sciences with 3 years’ Experience or PhD

Scheduled Castes candidates who have already secured admission and qualify NET examination will be given preference. Such candidates will be required to join the fellowship within 3 months of the issue of the JRF award letter. 

Post Graduate Degree, including the integrated PG degrees in any of Life Sciences.

Coordinate method development and validation for trace-level nitrosamine detection using LC-MS/MS.

Packing Material | Raw Material | Receipts | Dispensing | Storage | Finishing Goods

Senior, Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.

Change Control Management, Deviation Management, Quality Risk Assessment. EU, MHRA, USFDA & ANVISA audits / regulatory exposure is MUST required

Sterile dosage form product development, execution and CMC submission experience for regulated markets is basic requirement.

Analytical Method Validation, HPLC - Dissolution, GC. and Analytical data review, QMS. RM & PM testing.