18 Full-time mbbs dmo jobs in India.

This role is for one of Weekday’s clients Salary range: Rs 500000 - Rs 1800000 (ie INR 5 - 18 LPA) Min Experience: 5+ years Location: India, Bengaluru, Karnataka, NCR, Pune, Telangana, Hyderabad JobType: full-time We are looking for an experienced SAP DMS Consultant with strong hands-on experience in SAP Document

Salesforce Developer - DRO (Telco Order Management / orchestration) - 6 to 9 years Position Description Company Profile: Founded in 1976, CGI is among the largest independent IT and business consulting services firms in the world.

At Demo SA, one of EU’s largest pharmaceutical manufacturers for injectable products, we are looking for a talented Regulatory Affairs Senior Associate - Labeling to join our team.

Group Data Protection Officer (DPO) Location: Bengaluru (Hybrid) Role Type: Full-time Experience: 8 to 12 years The client is a UAE-headquartered fintech and digital asset infrastructure platform that enables traditional banks, fintechs, and enterprises to launch and embed regulated digital asset services through a

We're looking for an MBBS-qualified physician to deliver online consultations to patients through our platform. You'll manage a full consultation load independently — history taking, assessment, prescribing where appropriate, and knowing when a case needs in-person or specialist... Full time Shift work

Medical Officer - Mediclaim Process (MBBS/BAMS/BHMS ONLY) Start Date Starts  Immediately CTC (ANNUAL) Competitive salary Competitive salary ... Full time Immediate start

Full time Immediate start Remote job Working Monday to Friday

Full time Work at office Flexible hours

Position Overview Job Title: AI Full Stack Engineer Corporate Title: Associate Location: Bangalore, India Role Description Engineer is responsible for managing or performing work across multiple areas of the bank's overall IT Platform/Infrastructure including... SAS Full time Flexible hours

Role & responsibilities Team Leadership: Lead and train Lab Assistants and Analysts, ensuring everyone follows Standard Operating Procedures (SOPs) and maintains high discipline. Quality Standards: Strictly implement and maintain Good Laboratory Practices (GLP) to ensure... R&D Full time

Suggested Full time

Suggested Full time

The Regulatory Affairs Senior Associate will work at the interface of R&D and Regulatory, building a genuine technical understanding of the product's formulation and analytical profile to support sound regulatory strategy. This is not a document-processing role — it requires... Full time

Full time Immediate start

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented  Regulatory Affairs Associate to join our team. The job responsibilities for this position includes post-marketing regulatory submissions for Europe and... Full time

R&D Full time

R&D Full time

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team.