B.Pharm / M. SC in Chemistry / Biotechnology; Experience into Media Fill Activities Exposure into EM Monitoring as QA Knowledge about Sterility, MLT, BET, Water Analysis, Media Preparation; Analysis of Raw Material / Finished product / Intermediates / Stability / Instrumentation / Sampling
M.Pharm or Ph.D. in Pharmacy with industrial experience in pharmaceutical development and scale-up of products. Preferred area of expertise is Oral Dosage forms and Injectable formulations. Perform formulation development activities on differentiated formulations and innovative technologies to achieve Product development.
Ensuring all equipment and materials used in the filling process are properly sterilized and sanitized to maintain aseptic conditions and prevent contamination. Quality Assurance, Conducting in-process checks and inspections to verify product integrity, including visual inspections, measurement checks, and sampling for microbiological testing.
B. Pharm with 2 to 7 years of experience supervising and controlling Packing areas. Should have exposure of handling packing machine PFS, Vial, Cartridge automatic packing line.
Evaluate the change control requests and the impact on the stability of the products. Review the stability data of the products and issue recommendations for the shelf life Prepare the stability protocols and annual stability summary review for finished products
To prepare documents like BMRs. BPRs. protocols and reports for trial batches, scale-up batches, exhibit batches, process validation batches. To-coordinate and execute scale up, exhibit, process validation batches. To prepare and review the departmental standard operating procedures.
Hiring Candidates for Apitoria Pharma Private Limited & Auroactive Pharma Private Limited 100% subsidary of Aurobindo Pharma Limited to fill the following Positions in API Division for Srikakulam & Visakhapatnam, Andhra Pradesh, India.