M.Pharm (Pharmaceutics) with about 2 - 5 yrs experience in R&D product development with injectable product development that includes liquid, lyophilized and complex injectables. …
POSITION SUMMARY Manage overall batch certification review of QC lab records, certificates of analysis/compliance and all related supporting documentation (i.e. documentation rev…
Literature search, product understanding, data interpretation for product to be undertaken for development. Design of primary product strategy, preparation of product strategy for…
POSITION SUMMARY Accountable for assuring the supply of high quality, GMP compliant drug products, define operational strategy for quality control system at site, facilitate in f…
Review of Raw Material/Packaging Material /Stability/ Microbiology/ Cleaning Method Validation/ Validation/ Finished Product Analytical data, Certificate of Analysis & related docu…
Review of Raw Material/Packaging Material /Stability/ Microbiology/ Cleaning Method Validation/ Validation/ Finished Product Analytical data, Certificate of Analysis & related docu…
Job Responsibilities: Responsible to take training before execution of allotted work Responsible to perform routine in-process sample analysis Responsible to perform Method De…
RESPONSIBILITY: * To manage activities of finished product & Stability section. Provide leadership and direction to ensure the achievement of all finish product & Stability sectio…
List of Responsibilities / Job function: To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to take training before execution of al…
DESIGNATION : Head - Microbiology DEPARTMENT & SUB AREA : Quality and Microbiology ACADEMIC QUALIFICATION : Minimum M.Sc. Microbiology TOTAL EXPERIENCE : Minimum 15 + Years …
GLP Bioanalytical To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw …
GLP Bioanalytical To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw …
To provide the value addition (technically) throughout the development process and to achieve successful on time filing. 2. To have strong execution skills and to interact cross fu…
GLP Bioanalytical To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw …
Job Description Experience in Formulation R&D product development with experience in Injectable product development in Novel drug delivery systems/ Lyophilized product/ Solution…
Role: To execute activities related to R&D Peptide Process Development & Scale-ups, along with a group comprising of Research Officers/ Research Assistants in co-ordination with …
Job Summary : Ensure adherence of overall GxP strategic direction for all IT Quality activities and ensure consistent compliance of GxP IT Systems with regulations and corporate qu…
Job description: Job Description Experience in Formulation R&D product development with experience in Injectable product development in Novel drug delivery systems/ Lyophilized pro…