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January 2026

Apply Online for Senior Clinical Research Associate at Takeda

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Work as Trials and Publication Project Manager at AstraZeneca
Works in close collaboration with the external service provider and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner.
Regulatory Professional Wanted at Novo Nordisk - BPharm, MPharm Apply
Managing initial clinical trial application submissions in the EU according to the Clinical Trial Regulation and all changes during the life cycle of clinical trials.
TCS Hiring Clinical Data Reviewer
Preparing eCRF specifications, Edit check specification and other study specific set up documents.
Openings in Quality Control and Manufacturing (Nasal) at Dr. Reddy’s
Should be well-versed with techniques such as Spraytech, and Sprayview8t Pattern, Pump delivery test also good working knowledge of HPLC. 
Teva looking for Regulatory Coordinator
Regulatory Coordinator will support the Director, Regulatory Affairs and other Senior Directors in International Markets to organize and perform required tasks for regulatory affairs in order to maintain compliance with current regulations and in-house standards.
Bristol Myers Squibb Require Safety Data Sheet Specialist Writer
Bachelors degree in chemistry, toxicology, product stewardship, industrial hygiene or related discipline required
Career opportunities with V-Ensure Pharma Technologies for Pharmacy candidates
Handling of production machines such as BQS, Coating, Granulation. Bottle line packing machine primary and secondary.
CuraTeQ Biologics gets Health Canada NOC for Pegylated Filgrastim Biosimilar Dyrupeg

CuraTeQ Biologics Private Limited, a wholly owned subsidiary of Aurobindo Pharma Ltd, has received a Notice of Compliance (NOC) from Health Canada’s Biologics and Radiopharmaceutical Drugs Directorate (BRDD) for Dyrupeg™, its pegylated filgrastim biosimilar.

Biocon Pharma Secures USFDA Approval for Everolimus Tablets for Oral Suspension

Biocon Pharma Limited, a wholly owned subsidiary of Biocon Limited, has received approval from the U.S. Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Everolimus Tablets for Oral Suspension. The approval covers 2 mg, 3 mg and 5 mg strengths.