Intern - CMC (Analytical) - Hyderabad

The Intern will assist in the development validation and optimization of analytical methods used for the analysis of pharmaceutical products raw materials and intermediates. · ...

+The Research Fellow will assist in the development, validation and optimization of analytical methods used for pharmaceutical products analysis.They will gain hands-on experience with modern analytical techniques and data interpretation contributing to drug development projects. ...

Job summary: The RA CMC Senior Manager is responsible for execution and/ or coordination of global regulatory CMC activities,... ...

Regulatory Affairs Manager facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. · ...

Responsible for CMC regulatory matters relating to registrations and/or life-cycle maintenance of business activities (including variations and renewals) for assigned product portfolio. · ...

We are looking for job Internal Medicine University :AIIMS,JIPMER ,PGIMER ,CMC Vellore MD OR DNB OR DRNB · ...

The Associate Director is a senior people leader responsible for the operational effectiveness, · staff engagement and strategic alignment of Amgen's CMC & Device Regulatory Team in Amgen India (AIN). · Key responsibilities include providing inclusive leadership for staff within ...

The Associate Director is a senior people leader responsible for the operational effectiveness staff engagement and strategic alignment of Amgens CMC Device Regulatory Team in Amgen India AIN. This role provides leadership across multiple functional interfaces and global sites en ...

Role & responsibilities · Achieve defined annual sales targets and drive revenue growth. · ...

About The JobOur Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. · Ready? As a Non-Clinical Senior Biostatistician within our Statistics Team in Hyderabad... ...

To manage and execute procurement activities related to biomedical equipment, consumables, spares and service contracts for the hospital ensuring cost efficiency quality compliance timely availability and adherence to statutory and hospital standards. · ...

The Associate Software Engineer is responsible for designing, developing, deploying, and maintaining software applications and solutions that meet business needs. · The role involves working closely with product managers, designers, and other engineers to create high-quality, · s ...

The Senior Manager Quality Compliance External Affairs will enhance quality, compliance and regulatory flexibility by providing leadership and support of external activities impacting Amgen's Operations function with link to Regulatory Affairs-CMC. · ...

We are seeking a talented · Insilico CMC Automation Jr. Product Owner · to drive digital transformation initiatives within our Research & Early Development laboratory environments. · This role serves as a critical bridge between laboratory scientists researchers and technology te ...

We are seeking a talented Insilico CMC Automation Jr. Product Owner to drive digital transformation initiatives within our Research & Early Development laboratory environments. · Analyze business needs and coordinate between stakeholder groups to address them and deliver prompt, ...

Radiopharmaceuticals company seeking General Manager for India platform at pivotal moment in radiopharmaceutical innovation. Key responsibilities include building and leading Actinium's India strategy, establishing manufacturing and clinical development capabilities, and partneri ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. ...

This is a hands-on non-supervisory non-laboratory role that serves as liaison between biopharmaceutical industry regulatory agencies USP departments Expert Committees. · Identifies opportunities for new standards solutions to address analytical challenges associated with next gen ...

As India's largest manufacturer of forklift trucks Godrej Material Handling offers an extensive range of forklifts warehouse trucks and specialised trucks for specific applications The business also designs and manufactures accessories to address a wide range of handling applicat ...

As a Senior Electronic Document Specialist within our Hyderabad Hub, you'll be responsible for managing documents for regulators. · ...