of trust between our internal and external stakeholders. Position Description The Quality-Medical Affairs Professional (Q...-MAP (Quality Medical Affairs Professional)) is a therapeutically aligned clinical scientist focusing on the quality...
engineering or (medical) informatics You can offer extensive professional experience in regulatory affairs for Software...Job Title: Regulatory Affairs Professional Job Location: Bengaluru, Karnataka, India Job Location Type: On-site...
while maintaining quality. Lead capacity planning for the Medical Affairs Quality LCCI Team through data-driven decisions by collecting...Job Title: Manager - Medical Affairs (Medical Writing / Medical Editing) Job Location: Bengaluru, Karnataka, India...
efficiency and quality for maximum productivity while maintaining quality. Lead capacity planning for the Medical Affairs... and stressed health system, Lilly Medical Affairs (MA) can provide clear, credible answers that will set Lilly apart...
creation, identification, collection and entry of regulatory affairs information of medical devices. Support related regulatory... years Regulatory Affairs experience in medical device companies including international product registrations, new product...
in Regulatory Affairs for medical devices > You have > 3 years of relevant professional experience in the field... of Siemens Healthineers > You support in the creation of quality requirements and guidance documents for Regulatory Affairs...
creation, identification, collection, and entry of regulatory affairs information of medical devices. Support related... years Regulatory Affairs experience in medical device companies including international product registrations, new product...
. Professional Experience 2-4 years Regulatory Affairs experience in medical device companies including international product... creation, identification, collection, and entry of regulatory affairs information of medical devices. Support related...
in Regulatory Affairs for medical devices > You have > 3 years of relevant professional experience in the field... of Siemens Healthineers > You support in the creation of quality requirements and guidance documents for Regulatory Affairs...
You support in the creation of quality requirements and guidance documents for Regulatory Affairs topics You support the...: You have a degree in natural sciences or engineering; alternatively, you have a master's degree in Regulatory Affairs for medical...
of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution..., engineering, bioengineering, biology, or chemistry. Professional Experience: 2-4 years Regulatory Affairs experience...
of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution..., engineering, bioengineering, biology, or chemistry. Professional Experience: 2-4 years Regulatory Affairs experience...
of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution..., engineering, bioengineering, biology, or chemistry. Professional Experience: 2-4 years Regulatory Affairs experience...
of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution..., engineering, bioengineering, biology, or chemistry. Professional Experience: 2-4 years Regulatory Affairs experience...
of regulatory affairs information of medical devices. Support related regulatory affairs activities, such as assessment, execution..., engineering, bioengineering, biology, or chemistry. Professional Experience: 2-4 years Regulatory Affairs experience...
We are currently looking to strengthen our business quality and regulatory affairs team in Bangalore. The role requires... of experience in Quality Assurance/Production Quality in Medical Devices/ Equipment Industry is preferred. Strong communication...
We are currently looking to strengthen our business quality and regulatory affairs team in Bangalore. The role requires... of experience in Quality Assurance/Production Quality in Medical Devices/ Equipment Industry is preferred. Strong communication...
Clinical Development and Regulatory Affairs, to ensure high-quality scientific writing and timely reporting of safety data...Job Title: Senior safety medical writer Job Location: Bengaluru, Karnataka, India Job Location Type: On-site...
requirement: 3-8 years of experience in medical device & drug regulatory Affairs Specific experience in Indian Medical Device...Job Purpose Ensure pharmaceutical and medical device product application submissions and approvals from Central Drugs...
Evidence Operations team in the Regions & Operations Department of Global Medical Affairs, Global Business Services (GBS.... Stakeholder Management: Build strong relationships with key stakeholders, including clinical operations, medical affairs...