Skip to main content

RCB invites applications from Doctoral degree in Science candidates

A Doctoral degree in Science or a Master’s degree in Engineering/ Technology from a recognized university or equivalent. Regional Centre for Biotechnology
Life Sciences, Biochemistry, Biotechnology Fellowship at Institute of Science, BHU
Life Sciences, Biochemistry, Biotechnology Fellowship at Institute of Science, BHU
The candidate should have a first-class post-graduate degree in Biochemistry/ Biotechnology/ Molecular & Human Genetics/Zoology / Animal Science / Life Sciences with qualified NET/GATE or equivalent examination. Department of Molecular and Human Genetics, Institute of Science, BHU
Applications are invited for Scientist at Department of Microbiology, SGPGIMS
Applications are invited for Scientist at Department of Microbiology, SGPGIMS
Setting up of Nation-wide Network of Laboratories for Managing Epidemics and National Calamities — Virus Research & Diagnostic Laboratory (VRDL) funded by the Department of Health Research (DHR), Government of India
Walk In Drive at Baddi for Pharma and Science candidates at Intas Pharma
Walk In Drive at Baddi for Pharma and Science candidates at Intas Pharma
Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.
Openings for Pharma and Science candidates in Purchase, Quality Control, Formulation R&D at Aneta Pharma
Openings for Pharma and Science candidates in Purchase, Quality Control, Formulation R&D at Aneta Pharma
End-to-end product & process development, pilot-scale manufacturing, technical documentation, regulatory compliance.
Multiple Positions for Pharma and Science candidates at Intas Pharma
Multiple Positions for Pharma and Science candidates at Intas Pharma
Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.
Job for Pharmacy graduates in Production and Quality Assurance at Rusan
Job for Pharmacy graduates in Production and Quality Assurance at Rusan
Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates.
Analytical Research and Development Jobs at Anthea Pharma
Analytical Research and Development Jobs at Anthea Pharma
Hands-on experience in Analytical Method Development, Method Validation, and Routine Analysis. 
APDM Pharma Hiring Formulation Development Sr. Officer / Executive
APDM Pharma Hiring Formulation Development Sr. Officer / Executive
Development and optimization of parenteral and ophthalmic formulations. Planning and execution of formulation development trials.  Scale-up and technology transfer activities. APDM Pharmaceuticals
Sun Pharma Require Regulatory Operations & Publishing Manager
Sun Pharma Require Regulatory Operations & Publishing Manager
To collaborate with internal and external stakeholders like CMC team, supply, commercial, IPR, legal, CROs, Consultants etc to ensure smooth regulatory submissions process
Novo Nordisk looking for Clinical Trials Senior Manager
Novo Nordisk looking for Clinical Trials Senior Manager
Senior Manager CETA, you will drive Therapeutic Area performance for CDC India by providing strategic trial insights, leading portfolio planning and execution, and ensuring operational excellence across clinical trial activities.
Hiring Senior Regulatory Affairs Specialist at Medtronic
Hiring Senior Regulatory Affairs Specialist at Medtronic
Bachelors degree in medical, Mechanical, Electric Life Science or other healthcare related majors. Set up new process for entering new data - Regulatory Information Management System.
Work as Senior GRA Labeling Specialist at Sanofi
Work as Senior GRA Labeling Specialist at Sanofi
Coordination of labeling review and approval throughout the E2E labeling process, which includes preparation of labeling components for submission to regulatory agencies, participation in labeling negotiations with agencies resulting in product approvals or labeling updates, and release of labeling for use throughout the company for marketed and LCM products
USFDA Inspection at Aurobindo Pharma’s Lannett Facility Concludes With Four Observations
USFDA Inspection at Aurobindo Pharma’s Lannett Facility Concludes With Four Observations

A routine inspection by the United States Food and Drug Administration (US FDA) at Lannett Company LLC, a wholly owned step-down subsidiary of Aurobindo Pharma USA, Inc., has concluded with four observations.

The inspection was conducted at Lannett Company’s manufacturing facility in Seymour, Indiana, USA, from August 17 to August 21, 2026. According to the company’s regulatory filing, the inspection was carried out as part of the US FDA’s routine inspection process.

Robot-assisted surgery shows clinical advantages over laparoscopic surgery for gastric cancer
Robot-assisted surgery shows clinical advantages over laparoscopic surgery for gastric cancer
Surgery remains the primary curative treatment for gastric cancer, with laparoscopic gastrectomy (LG) established as a standard minimally invasive approach. While LG offers faster recovery than open surgery, it remains technically demanding because surgeons must operate within a confined space using rigid instruments that can amplify hand tremors.
ICON plc Hiring Senior CDC
ICON plc Hiring Senior CDC
Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. Manage clinical and third-party data reconciliation based on edit specifications and data review plans. ICON plc
Orion Pharma looking for Product information Specialist
Orion Pharma looking for Product information Specialist
Bachelors / Master s degree in life sciences, B.Pharm/M.Pharm or health-related field from a reputed college. Orion Pharma
Site Start Up EUCTR II Specialist Post at PAREXEL
Site Start Up EUCTR II Specialist Post at PAREXEL
Triage and manage Requests for Information (RFI) from regulatory authorities, coordinating responses with relevant stakeholders. Collect required documents for IVDR (In Vitro Diagnostic Regulation) ethics submissions and ensure compliance with country requirements
Work as Pharmacovigilance Operations Senior Associate at Amgen
Work as Pharmacovigilance Operations Senior Associate at Amgen
Support ICSR processing to ensure high-quality cases in a timely manner to meet all worldwide regulatory authority requirements
CDSCO Flags 239 Drug Samples as Not of Standard Quality in July 2026 Alert
CDSCO Flags 239 Drug Samples as Not of Standard Quality in July 2026 Alert

The Central Drugs Standard Control Organization (CDSCO) has released its July 2026 Not of Standard Quality (NSQ) drug alert, listing a large number of medicine samples that failed to meet specified quality standards during testing by state and CDSCO laboratories.

Subscribe to