The Position
The Project Clinical Data Programmer Specialist is overall accountable and responsible for implementation and adherence to project standards template in EDC and DMW. Demonstrates subject matter expertise and equips in-depth knowledge and...
...We are seeking a talented UI/UXDesigner to join our team and play a crucial role in... ...for our digital applications
As a UI/UX Designer , youwill collaborate clo...
...analysis, and tools to support drug development.
Role Description
This is a full-time remote role for an Entry-Level Software Engineer at SecureGen. The Software Engineer will be responsible for developing s...
....
Role Description
This is a full-time remote role for a Generative AI Engineer. The Generative AI Engineer will be responsible for developing the generative models used to generate chemical
Company Description
Jaidev Pharma Placement is a pharmaceutical sales and human resources agency with over two decades of expertise. We focus on offering exceptional human resources services across India at highly competitive rates.
Role Des...
JOB DESCRIPTION
Position Title: Research Student in next-generation technology R&D
Training Duration: 1 month
Training Location: Remote
Stipend: Yes (after promotion)
We are seeking talented and motivated trainees to join our laboratories. The t...
As a Design Engineer specializing in fabrication and mechanical systems, you will be responsible for conceptualizing, designing, and developing mechanical components and systems for fabrication processes. You will work closely with cross-functional t...
Dispensing Medications: Review prescriptions from healthcare providers to verify their accuracy and appropriateness. Dispense medications to patients, ensuring the correct dosage and instructions are provided.
Patient Counseling: Offer counseling ...
...Relocation Authorized: None
Grade: 23
Position to be Panel Interviewed No
Telework Type:Part-Time Telework
Employee Referral Amount:
Bechtel India is a global operation that supports execution of pro...
Perform testing on Raw materials, in-process material, finished drug product, and stabilities in support of production and regulatory filings.
Experience
2 - 7 years experience in a cGMP laboratory
Familiar with cGMP and FDA requirements
...
