QA

Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQL inspections and periodic inspections of control samples

Responsible for implementation of quality systems within the site. Review of Change controls, Deviations, Investigations, CAPA, OOS and OOT reports. Responsible for review of validation protocols and reports.

Review of environment monitoring records. Sterility testing of the finished products and sterile API. Should have good knowledge in QMS activities.

Bliss GVS is a fast-growing Pharmaceutical Company with a proven track record of developing, manufacturing and marketing high quality pharmaceutical formulations at affordable prices for the global market.

Candidate should have experience in Oral formulations Solid and liquid for Handling of APQR, IPQA activity and Process Validation. Candidate should have experience in regulatory plant with hand on experience in Raw Material and Packing Material in formulation unit.

Analyst Finished, Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromele on Software. Require good exposure in Lab QA related work. D.Pharma / B.Pharma / M.Pharma 

Experience in Pharmaceutical Company in Parental, responsible for line clearance activity, responsible for in process checks, responsible for sampling. Finished product checking before release, management and execution of process validation & media fill simulation.

Candidate acquainted of Quality Management System Document like Change control, Deviation and their Investigations, CAPA and Audit Management. This role will focus on ensuring the highest standards of quality throughout the manufacturing process, specifically for active pharmaceutical ingredients

You will be responsible for executing or assigning in-process activities during shifts, conducting line clearances, material verification, overseeing start-up of machines, and coordinating sampling activities to ensure product quality and compliance.