Executive, IPQA
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitor
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Account Manager, Field Sales ( Ophthal )
Essential Functions: Promote and sell the ophthalmology segment portfolio to HCPs including institutions, hospitals, and private practitioners. Achieve monthly, quarterly, and annual sales targets wit
Assistant Manager, Quality Control
Responsible for Review of Quality Control documents and Electronic data. •Responsible for initiation, review and investigation related to Deviations, OOS, OOAL, CAPA & LIR. •Responsible for Review of
Senior Executive, IPQA EM
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitor
Executive Admin
Job Description for Admin Executive To develop and implement systems to control Man Movement, Material Movements, Visitors Movement and vehicle Movements. To Prepare, Implement, followed and maintaine
Executive/ Senior Executive - Water System & HVAC
Key Responsibilities: Equipment Operation & Maintenance: Overseeing the operation, maintenance, and repair of Water systems, Which shall include Pretreatment, PW generation, storage and distribution,
Executive_ IP-FP-ST_ HPLC Analyst_ shift duty
Experience: Analyst in physical activity like Handling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and having knowledge of LIMS.
Senior Executive- Filling Inj Manufacturing
Key Responsibilities: Responsible for document management like BMR's, BPR's, master SOP's etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF wor
Executive, IPQA EM
Key Responsibilities: Environment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualificat
Assistant / Associate - Filling & Sealing
Key Responsibilities: Responsible to attend the training as per schedule and to ensure the training and work as per TNI. Responsible to perform and monitoring all the activities related to Aseptic are
Sr. Executive in QC.Microbiology_Injectable , SEZ_Matoda
Key Responsibilities: Water sampling and analysis Microbial Limit Test Sterility test Bioburden test Preservative efficacy test Bacterial endotoxin test. Qualification: M.Sc. (Microbiology) Experience
Senior Executive- Filling Inj Manufacturing
Responsible for document management like BMR's, BPR's, master SOP's etc. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsi
Executive Manufacturing QMS and compliance Injectable
Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements
Senior Assistant, Granulation
Operate and monitor granulation machines to ensure the production of high-quality granules. Perform routine equipment maintenance and troubleshooting during production. Follow Good Manufacturing Pract
Deputy Manager - Manufacturing QMS
Key Responsibilities: Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturin
Deputy Manager, QA Validation
Responsible for review of URS, DQ and vendor/ supplier's documents related to qualification. Responsible for preparation and review of Validation/ Qualification protocol and report. Responsible for ex
Associate - Packing & Visual Inspection
Key Responsibilities : Responsible to operate the machines Responsible for cleaning and sanitization of visual inspection and Packing area. Responsible to all packing related activities. Responsible t
Senior Executive - Packing
Key Responsibilities: Responsible for preparation, review, revision, control, and implementation of standard operating procedures of packing department. Responsible for preparation & review of the mas
Executive-QCC-INJ-IP-FP-STABILITY
Person having minimum experience of analysis and processing of In process and Finished product and handling of HPLC,UV,FTIR,K/F,AAS,IC,Dissolution (Sotax) and other instruments Qualification: Master's
Associate - Manufacturing
Replacement is required to perform Aseptic area activities i.e., Aseptic batch mfg., Filtration, filling activities, Operation of manufacturing /Filtration vessels CIP and area cleaning activity in as
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