Senior Officer, Quality Control
Description: This role involves performing complex routine and non-routine analytical testing on various pharmaceutical materials and products using a wide range of analytical techniques (Simple: HPLC
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Description: This role involves performing complex routine and non-routine analytical testing on various pharmaceutical materials and products using a wide range of analytical techniques (Simple: HPLC
Description: The position is responsible for in-process and final product quality analyses and inspection in compliance with established specifications, standards, and regulatory requirements. The rol
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
Job Responsibility: Technical Writing & Documentation: Development Key Responsibilities Lead the preparation of comprehensive documentation for complex R&D projects , including new formulations, emerg
Description: Responsible to perform sterility testing, bacterial endotoxins testing, LBPC and bioburden testing of raw material, in-process, packing material, finished products, Stability samples and
Review analytical data for Raw Materials (RM), Packaging Materials (PM), in-process samples, Finished Products (FP), stability samples, working standards, reference standards, and other test samples.
Description: The position provides enterprise leadership for Quality Assurance (QA) governance, regulatory compliance, and Quality Management Systems (QMS) across pharmaceutical manufacturing operatio
Key Responsibilities To prepare and review of URS, DQ, QRM, FAT, SAT, and vendor/ supplier's documents related to qualification. To execute Qualification / Re-Qualification and Validation activities o
Description: Responsible for managing advanced regulatory affairs, regulatory operations support, eCTD publishing / submission for US market and compliance activities to ensure adherence to global reg
Job description: Operate and monitor granulation equipment and related manufacturing apparatus in accordance with validated procedures and GMP standards. Supervision of Mfg activities (Equipment like
Description: This role is responsible for performing a variety of tasks related to the compression and coating of pharmaceutical tablets within a regulated manufacturing environment. The incumbent ope
Description: This role supports manufacturing operations for oral solid dosage (OSD) products by executing routine production activities in a regulated pharmaceutical environment. The role involves op
Description: This role is responsible for conducting in-process and final product quality analyses and inspections in strict compliance with established standards and regulatory requirements within a
Description: This role is responsible for executing manufacturing and packaging operations within a regulated pharmaceutical environment, ensuring products are packed accurately, efficiently, and in c
Key Responsibilities 1. Dossier Preparation & Submissions Prepare, review, and submit CTD / ACTD / country‑specific dossiers for: New product registrations Line extensions (strength, pack size, shelf
Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality a
Description: This role is responsible for managing and overseeing pharmaceutical manufacturing operations at a deputy manager level within a regulated manufacturing environment, ensuring that all prod
Plan, coordinate and execute mechanical engineering activities for projects (greenfield/brownfield) Review BOQs, layouts, specifications and ensure installation of HVAC, utilities and cleanroom system
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
Description: The position is responsible for in-process and final product quality investigations in compliance with internal standards and global regulatory requirements. The role focuses on interpret
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