Cipla

Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies

Graduate in Pharmacy or Life Sciences. 2 years in the field of Regulatory Affairs/ Quality Assurance/ Quality control/ Manufacturing/ Analytical Development/ R&D.

To drive end-to-end execution of new product launches for assigned geographies, ensuring timely delivery, commercial success, and alignment with revenue targets.

Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift.

M.Sc. / B. Pharma. Experience in QC department of a pharmaceutical organization with knowledge of latest regulatory standards and compliance norms.

Changes in the Regulatory guidelines: Keeping abreast with latest regulatory guidelines and interaction with RA department. Conflict regarding the priorities of samples: Interaction with cross-functional team along with the managers to prioritise the samples

Bachelor in Pharmacy. 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing

Perform chemical and physical analysis of raw materials, in-process samples, and finished products. Operate analytical instruments like HPLC, GC, UV Spectrophotometer, FTIR, Dissolution apparatus, etc.

Candidate having experience in Blister, Cartonator, Container, Topical, Labelling, Bottle, Filling & Counting machine operations + Sterile secondary packing.