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
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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
Description: This role supports the in-process quality assurance function within a pharmaceutical manufacturing environment, contributing to the definition and specification of activities, processes,
Description: This role is responsible for performing a diverse range of manufacturing operations related to the processing and assembly of injectable pharmaceutical products within a regulated manufac
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated sterile manufacturing envir
Description: This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products
Description: This role is responsible for conducting environmental monitoring activities and quality analyses in compliance with established standards and regulatory requirements within a global pharm
Responsible as Department training coordinator (DTC). •Responsible for training management activities. •Responsible to upload training copy of SOP in training software •Responsible to provide training
Description: Responsible for Preparation and Implementation of SOP's. Viable monitoring in clean area of manufacturing and warehouse as per the defined schedule. Responsible for personnel monitoring.
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of pharmaceutical ingredients and finished products while contributing to operational exc
To analyse In-Process, Finished Product, Stability, Process validation samples as per current STP/SOPs/ Specifications & Pharmacopoeias. To operate analytical instruments like Rheometer, Viscometer, U
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment.
Description: This role is responsible for conducting in-process and final product quality analyses and inspections within a quality control laboratory in strict compliance with established standards a
To follow the safety rules in the premises according to the company norms. •To handle Quality Management Documents like Change Control, Deviation etc •To prepare Failure Investigation Reports against
Description: •To follow the safety rules in the premises according to the company norms. •To maintain online the BMRs and other log books in the respective area as per cGMP and SOP. •Responsible for m
Description: The role is responsible for leading, governing, and optimizing pharmaceutical manufacturing processes across production operations. The role ensures process design integrity, validation c
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a glob
Description: This role is responsible for conducting in-process and final product quality testing and analyses in strict compliance with established standards and regulatory requirements within a glob
Description: The role is responsible for delivering responsive, day-to-day IT technical support to employees across the organization, ensuring stable and secure operation of hardware and software syst
Description: Sampling and analysis of water (Chemical and Microbiological testing) and record relevant data. Microbiological environmental monitoring/compressed air monitoring of the clean area. Micro
To prepare validation documents such as Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and other Qualification documents for equipment /utilities/fac
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