3-4

Sterile, parenteral operations including aseptic processing, filling, sealing, filtration, production, QMS, batch manufacturing, autoclave, terminal sterilization, and packing. Production lines : Ophthalmic, Vial, PFS, LYO, Cartridges, and Bag. Machine exposure: Groninger, Optima, Dyno Truking, Bosch filling machines, Fedegari sterilizer, Steriline, Plumat, Pharmalab, and packing and labelling machines.

Expertise in compounding, aseptic operations, and troubleshooting the equipment, with a focus on solution-oriented approaches.

Candidate having experience of Bio-similar product manufacturing. Large scale bioreactor, Continuous centrifuge Trouble shooting, risk assessment, root cause analysis.

Should have knowledge of country specific dossier preparation. Should have knowledge of country specific dossier preparation

UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines

As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.

Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software. Strong analytical and problem- solving skills.