2-3

Person should have the worked on Peptide Manufacturing & Peptide Synthesis and Exposure to Peptide Synthesis, purification, filtration and drying processes and Peptides synthesis, Peptide purification, Lyophilization.

RPG LIFE SCIENCES LIMITED, ARE INVITING CANDIDATURE FROM PROFESSIONALS FOR BELOW MENTIONED POSITIONS

Responsible for development, optimization, and scale-up of tablet formulations, ensuring product quality, stability, and regulatory compliance.

Should have hands on experience in Water samples analysis, In-process Bioburden and BET analysis, MLT analysis of Raw material and Packing material, Antibiotic assay by Microbial method and Sterility testing.

B.Pharm / M.Pharm; Experience in Market Complaint / Investigation / Audit Compliance / Cleaning Validation / Process Validation. Micro Labs Limited

Preparation and control of SOPs, STPs, specifications, formats, and master documents. Review of BMR, BPR, deviations, change controls, and CAPA records. CLAPS Industries require QA Documentation professional

Preparing & Reviewing Manuscript, research papers, review articles, abstracts, posters, slide sets/ oral presentations. Managing Activities like Writing, review, literature search.

Akums Plant 1 specializes in the production of Oral Solid Dosage Forms, including tablets and capsules.

Oversee IPQA activities during injectable manufacturing & packaging Review and approve BMR/BPR ensuring cGMP compliance Handle deviations, CAPA, and audit readiness (QMS) Lead QA team activities and drive continuous improvement initiatives