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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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
Key Responsibilities: Having a Knowledge of Instrument operation like HPLC, GC, UV, IR, Karl Fischer, Auto Titrator Good knowledge of LIMS and Documentation having Experience of working with 21 CFR co
Description: This role ensures GMP and GxP compliance in dispensing, manufacturing, and packaging. Responsibilities include machine and area clearance, product sampling, in-process checks, batch recor
Key Responsibilities: Performing key activities of Supply Chain function To understand resource and capacity required to fulfill current and future demand Capacity Planning based on manufacturing capa
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
Key Responsibilities: Performing key activities of Supply Chain function Preparing Manufacturing Plan Coordinating for RM/PM delivery with SSSM (Purchase) team Coordinating for RM/PM release with QC t
Key Responsibilities: Experience of Analyst in physical activity like handling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and h
Key Responsibilities: Responsible for review of URS, DQ and vendor/ supplier's documents related to qualification. Responsible for preparation and review of Validation/ Qualification protocol and repo
Job Description (JD): Operate packing machines (blister/bottle/strip) as per SOPs Perform line clearance and batch changeover activities Ensure correct packing, labeling, and coding as per BMR/BPR Mai
Description: cGMP and compliance review in the GMP area as per cGMP guideline. 2 Machine and area clearance. 3 Sampling of blend, intermediate stages, AQL finished product, ANSI sample, reserve sample
To follow safety rules in the premises according to the company norms •Monitoring of DP, RH and temperature in aseptic processing area •To maintain the BMRs and other log books in the aseptic processi
Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment i
Essential Functions: To follow the safety rules in the premises according to the company norms. Monitoring of DP, RH and temperature area in their visual inspection Responsible for Operation and Clean
Description: This role is responsible for performing a diverse range of tasks related to the processing and assembly of pharmaceutical injectable products within a regulated sterile manufacturing envi
Prepare, Review and Finalize Regulatory strategies for Complex Products [like injectables that may include Peptides, Microspheres, Liposomes, Nano-suspensions etc./ Ophthalmic/ Otic/ Topical gel/ DDCP
Senior Officer – Manufacturing Process Operations is responsible for executing processes in the API manufacturing plant, ensuring product quality, regulatory compliance. This role includes operating k
1. Operation & Monitoring of Water system Ensure continuous and compliant operation of: Pretreatment, PW, WFI, pure steam, compressed air and gas distribution systems. Monitor critical parameters such
To perform sampling and analysis of water (Chemical and Microbiological testing) and record the relevant data To perform microbiological environmental monitoring of the clean area To perform Microbiol
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