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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

MSc / MPharm in Chemistry, Analytical Chemistry. Pharmaceutical Analysis or related field. 1 - 4 years of relevant experience in Analytical Development

D.Pharm / B.Pharm Freshers can apply, with minimum 2-8 years post qualification experience in retail pharmacy

B.Pharma/Msc Executive/Sr.Executive 06 to 08 Yrs of Experience in manufacturing/Packing External preparation

Drug product packaging, Viol labeling machine, PFS lobeling. Carton coding, and Visual Inspection, Batch Execution.

Exposure to Manufacturing operations like Granulation, Compression, Coating, Capsule filling eBMR/ eBPR/ eLog/ Sap/QMS/trims and handling of SCADA