Junior Officer, Autoclave
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. •Timely completion of SOPs train
Life Science Jobs in India
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Found 4490 jobs
Senior Manager, CSV IT
Key Responsibilities: 1. CSV Strategy & Governance - Develop and maintain the overall CSV strategy and validation master plans for global systems. - Ensure compliance with GAMP 5, USFDA, EU Annex 11,
General Manager, Plant Management
Description: Responsible to look after overall plant activities i.e. Regulatory Compliance and Quality Control, Strategic Planning and Management, Production Management, Financial Management, Human Re
Officer, EH&S
Description: Responsible for implementing and maintaining Process Safety Management (PSM) systems to ensure safe plant operations. Conducts hazard identification studies, risk assessments, HAZOP revie
Senior Executive, IPQA
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
Officer, IPQA
Description: This role supports the in-process quality assurance function within a pharmaceutical manufacturing environment, contributing to the definition and specification of activities, processes,
Senior Executive, IT User Support
Description: The role is responsible for ensuring effective day-to-day technical support to employees across a range of hardware and software systems. Handle QMS Activities. Support Laboratorty shop f
Assistant General Manager, Legal
Key Responsibilities: Secretarial Function: Manage the secretarial compliances. Board & Shareholder Meetings: Organize, conduct, and document meetings of the Board of Directors and shareholders. Compa
Executive, Procurement
Create and manage purchase orders of Excipients for all plants commercial requirements. Ensure timely follow-up and delivery coordination with SCE team to support uninterrupted production schedules. C
Senior Manager, QA Documentation
Responsible for overall QA function compliance with various regulatory guidelines and standard operating procedures in practice at the site. Review and monitor quality systems and provide guidance to
Senior Executive, Manufacturing Injectables
Responsible for document management like BMRs, BPRs, master SOPs etc.. Responsible for preparation & review of the master documents of production. Responsible to ensure UAF working in area. Responsibl
Executive, QC Environment Monitoring
Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validat
Executive, Quality Control
Description: To perform qualitative and quantitative analysis of raw materials and packaging materials In-process and Finished product as per applicable pharmacopeial standards, regulatory requirement
Associate, Manufacturing Injectables
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.
Executive, QC Instrumentation
Description: This role is responsible for managing, calibrating, and maintaining quality control instrumentation and equipment in compliance with established standards and regulatory requirements with
Senior Executive, Regulatory Affairs
Key Responsibilities Compile, prepare, review, and submit high-quality US ANDA and EU marketing authorization applications, including original submissions and amendments, for MDI/DPI inhalation produc
Senior Officer, Manufacturing Injectables
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
Associate, Packaging
Description: This role is responsible for supporting and monitoring pharmaceutical packaging operations while developing foundational competencies in packaging processes, equipment handling, and cGMP
Assistant Manager, Compliance
Assist Regional Compliance Lead in drafting / amending policies and procedures for the India Operations based on the changes in the regulatory environment Responsible for ensuring effective functionin
Assistant Manager, Regulatory Affairs
Description: Responsible for managing regulatory affairs activities and regulatory strategy execution to ensure compliance with global regulatory requirements, industry standards, and ethical practice
Looking for something specific?
Browse all job categories →