Skip to main content

Intas Pharma opens for Computerized System Validation

The Manager - IT CSV is responsible for end-to-end oversight of Computerized System Validation, equipmen/ utility qualifications, audit support, and quality systems compliance in a GxP-regulated pharmaceutical environment.
Dr. Reddy’s Laboratories invites applications for Program manager
Program Manager- R&D Transformation & Productivity, you will play a key role in supporting the execution of strategic transformation initiatives across the global R&D organization. Dr. Reddys Laboratories
BITS Pilani MPharm / M.S.Pharm / M.Tech Research Staff Openings
M.Pharm / M.S.Pharm / M.Tech with specialization in Pharmaceutics, Biotechnology, Medical Devices, Nanomedicine or equivalent. GPAT, GATE, NET will be preferred.
National AYUSH Mission Hiring Pharmacist
Diploma / Certificate in Ayurveda Pharmacist Course recognized by the Govt. of State.
Life Sciences, Biotechnology Fellowship at NIPER
First-class post-graduate degree (M.Sc./MS) in Life Sciences, (M. Tech.) in Biomedical Engineering / Bioengineering / Biotechnology / Medical Devices
Walk in drive for at Silver Oak University for Manufacturing Apprentice in Amneal Pharma
Looking for enthusiastic fresher candidates for production activities in the Manufacturing Department, who are eager to start and grow their career in the pharmaceutical industry.
Hetero looking for Medical & Scientific Support Executive
Support Medical Affairs objectives for assigned Cardio-Diabetes / Specialty therapies in emerging markets. Provide scientific and clinical inputs using current guidelines, clinical data, and real-world evidence.
PAREXEL Hiring Senior Regulatory Affairs Consultant
Contribute to preparation and delivery of regulatory submissions from a global and regional perspective. Preparation and review of Marketing Authorization Applications & Variations for filing in US, EU, Japan, Canada Switzerland, Australia.
Sun Pharma looking for Regulatory Affairs Executive
Adequate understanding on respective authority guidance and filing of new product and post approval changes. Review of documents related to product registration and dossier submission leading to faster approval
Work as MSAT Team member at Dr. Reddy’s Laboratories
Prepare, review, and approve technical protocols, reports, and product impact assessments related to product lifecycle management.