QA

Dissolution apparatus, GC, IR and AAS and Documentation related to QMS. To review respective GMP Documents of QC department such as analytical / worksheet of In Process and Finished Product.

M.Pharm/B.Pharm/M.Sc/B.Sc Review of BMR/BPR and process validation reports, in process testing, sampling and line clearance, Media Fill. Emcure

EXPERIENCE INTO RECEIPT & DISPENSING ACTIVITY, INWARD & OUTWARD ACTIVITY

Exposure to OSD Manufacturing operations like Granulation, Pellet coating, Compression, Coating, Capsules, Primary Packing (Blister Packing, Sachet Filling, Secondary Packing (Cartonator & Labelling)

Audit exposure in USFDA/ EUGMP approved company. Exposure of Material Handling / Electronic Batch Record filling and review / Good Knowledge of SAP System & Their T Codes for PPPI / Machine Alarms handling / QMS / Deviation / Change Control / SOP / Daily Reports Preparation/ Manpower Handling.

Handling and Reviewing of the documents related to instrument i.e HPLC- Dissolution, Candidate having experience in AQA (Lab QA) and IPQA

Conduct thorough visual inspections of products to identify defects, damages, or inconsistencies, ensuring they meet company quality standards before packaging as per SOP.

Hetero is one of worlds leading producers of key Active Pharmaceutical Ingredients (APIs) and generic formulations with presence in 140 countries and backed by 30 years of experience in the pharma sector.

B. Pharmacy/M. Pharmacy; Self Inspection Audit, Audit trail, Electronic data management, Qualification (Shift Working). Finished Products & Analytical Method Validation