Hyderabad

Responsible for Formulation Development of Oral Liquid and Nasal Formulations. Responsible for conducting Formulation Development Trials and documenting the details in LNB.

M.Pharm, B.Pharm, M.Sc ; Stability, HPLC, GC, Wet Analysis, Dissolution, IP/FP, RM, LIMS, Microbiology.

Having Injectable Experience of Shop floor and supervising activities like filtration, filling and Stoppering, Sealing, Lyophilizer Operations and Training and QMS

Maintain smooth collaboration and works closely with key stakeholders across the globe to develop reference standards for biotechnology pharmaceutical products including proteins, peptides, heparins, antibiotics, and advanced therapies.

Quality Assurance - in process - Drug Substance Manufacturing, Upstream, Downstream

Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information

B.Pharmacy, M.Sc Analytical, M.Pharmacy Analytical ; Selected candidates must commit to a three-year service agreement.

Support a discipline and or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility

post graduate degree, preference given for Ph.D. in Organic Chemistry or Medicinal, Pharmaceutical Chemistry area. National Institute of Pharmaceutical Education and Research