BRIC-inStem invites applications (online) from eligible candidates for contractual position of following Scientific position in the laboratory of Dr Reena Singh. We are looking for dedicated professionals who are result-oriented, can assimilate, analyze and communicate data effectively and are excellent team players capable of working in a fast-paced, multi-disciplinary environment.

Finished Products, Stability Studies, Instrumental Analysis (GC, HPLC, KF), Raw Material. Alkem Laboratories Limited is organizing a walk-in interview drive to source candidates for its Baddi manufacturing facility.

Experience in a formulation plant and knowledge of tablet packing, including primary & secondary packing areas. Hands-on experience in Propix Track & Trace system

USV Private Limited is a prominent Indian multinational pharmaceutical and biotechnology company founded in 1961, specializing in diabetes and cardiovascular therapeutics.

Established in 2016, ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.

Responsible for monitoring of cGMP activities at site and to have the oversight, monitoring and compliance with quality system.

Monitor and route incoming safety information to the appropriate project teams. Record all ICSR documentation and track cases in accordance with sponsor/customer specifications; distribute incoming mail and faxes.

The ideal candidate will have expertise in Pharma Research & Development and proficiency in MS Excel. Experience in PV Case Processing and Pharmacovigilance & Safety Ops is a plus. The role involves a hybrid work model with rotational shifts.

Formulation Analytical Method development using HPLC/GC/IC/Potentiometry, Brazil-Regulatory analytical experience is mandatory

The Clinical Data Manager is responsible for working with the Clinical Data Management team and other internal project team members to provide data management services for our customers to ensure on time and accurate deliverables.

The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.The role is critical to meet planned Site Ready dates

Xogene combines regulatory expertise with advanced technology to automate complex processes in clinical trial disclosure. As trusted experts with comprehensive knowledge of global regulatory frameworks, we deliver efficient data transformation and regulatory compliance for our clients, streamlining workflows through our AI and agentic networking capabilities. We're committed to leveraging technological solutions to advance clinical trial transparency.

Responsible for ensuring operating state of cGMP compliance in Solution/Emulsion preparation, vial/ampoule washing, Depyrogenation, Filling, Capping and Collection operations.

Adverse Event Reporting Officers must have strong organizational, communication and problem-solving skills. In addition, they are responsible for daily source document quality reviews. Adverse Event Reporting Officer report directly to Team Lead, AERO.

Master / Integrated Masters in Organic / Pharmaceutical / General Chemistry with experience in organic synthesis. CSIR-National Chemical Laboratory, Pune

Institute of Bioresources and Sustainable Development Fellowships | 41 fellowships in different research

M.Sc./ B.E./ B.Tech. or equivalent degree with at least 55% marks and one publication in Science Citation Indexed Journal and should have completed at least two years of post-M.Sc./ B.E./ B.Tech. Human Resource Development (HRD) Group of COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (CSIR), New Delhi

Smart Diagnostics of Rotating Machinery: A Digital Twin Approach for Industries using Physics-Based Simulation and AI/ML. IIT Bombay

Diploma in Ayurvedic Pharmacy from any recognized University/ institution or Board or faculty of Indian System of Medicine established by law in India or recognized by the Govt. Shri Krishna AYUSH University, Kurukshetra