0.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Site Name: Bengaluru Luxor North Tower Posted Date: Oct 21 2025 Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. We're uniting science, technology, and talent to get...

Posted 3 days ago

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Dam Safety Specialist (International Expert) SMEC

15.0 - 17.0 years

0 Lacs

delhi, india

On-site

Position Title: Dam Safety Specialist (International Expert) Key Qualifications/ Requirements: He/ She should have a degree in civil engineering and have at least experience of 15 years experience in dealing with construction supervision and quality assurance, safety evaluation, preparation of guidelines/manuals, design experience, past member of any safety inspections and remedial measures etc. He/ She should have worked in at least 5 large dam projects. Job Descriptions Serve as the Nodal Expert for reviewing all dam safety aspects across project activities. Conduct CS&QA visits and prepare official transmittals for onward submission. Perform dam safety inspections and provide expert opini...

Posted 4 weeks ago

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G.M. - CLINICAL RESEARCH Panacea Biotec

15.0 - 20.0 years

0 Lacs

delhi

On-site

As a General Manager reporting to the Sr. VP of Clinical Research, you will be responsible for overseeing various aspects of clinical trials and BA-BE studies. With an educational background of MBBS and MD, you are expected to bring 15-20 years of experience to the role. Your primary duties will include preparing, reviewing, and approving clinical trial documents, providing medical support to the study team, and assisting in regulatory approvals in NDAC Meetings. Your role will also involve CRO evaluation and selection for outsourcing clinical research projects, as well as preparing and implementing CAPA. Real-time management of SAEs and monitoring responsibilities will be crucial aspects of...

Posted 1 month ago

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