Medical Writer Jobs in Zug
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Suchergebnisse - Medical Writer Jobs in Zug
GlaxoSmithKline-Zug
to achieve our goals:
• MD/MBBS/PharmD or PhD in clinical / scientific discipline related to hematology.
• 5 + years of experience in Medical Affairs including roles in LOCs and in global teams supporting pre/peri launch phases of assets.
• Writing, speaking...
Coopers Group AG-Zug
Develop and execute comprehensive tests to verify code functionality.
• Regulatory Compliance Documentation: Provide detailed and precise documentation in alignment
with the medical device software development process standards (such as IEC 62304, ISO...
Hays-Zug
Software Development Engineer C++ RT (m/f/d)
We are looking for a Software Development Engineer C++ RT for one of our clients in the medical device industry. The perfect candidate has a Master or bachelor degree in software engineering and 5+ years...
Coopers Group AG-Zug
and execute comprehensive tests to verify code functionality.
Regulatory Compliance Documentation: Provide detailed and precise documentation in alignment
with the medical device software development process standards (such as IEC 62304, ISO 13485...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets.
Responsibilities
• Leads the pharmacovigilance agreement negotiation...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets
Responsibilities
Leads the pharmacovigilance agreement negotiation...
Tbwa Chiat/Day Inc-Zug
medical monitors, clinical operations, biostats, regulatory, medical writing, medical liaisons, call center, and QA.
• Experience in investigating and managing potential product quality defects.
• Management of compliance deviations and formulations...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets.
Responsibilities
Leads the pharmacovigilance agreement negotiation...
BridgeBio Pharma-Zug
will be responsible for collaborating with Clinical Operations, QA, Clinical Research, Regulatory Affairs, and Medical Writing to determine safety strategy for all international expansion markets .
Responsibilities
• Leads the pharmacovigilance agreement negotiation...
RMIT Professional Resources AG-Zug
in defining work packages, estimation, planning, and execution within an agile development team to meet feature objectives and deadlines.
4. Writing high-quality, maintainable C++ code and performing comprehensive testing to verify functionality, ensuring...
Flexsis-Zug
with the medical device software development process standards (such as IEC 62304, ISO 13485).
• Quality Assurance: Conduct thorough reviews of application design, functionality, usability, and performance, and propose enhancements for continuous improvement...
Blueprint Medicines-Zug
and coordinate the preparation, including writing as necessary, assembly, review, and timely submission of regulatory dossiers as required for registration of products in the UK, supporting for Europe, and International markets, as needed.
• Work to prepare...
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