Architect and engineer állások, munkák egészségügy, gyógyszeripar területen

For each assigned therapeutic project (synthetic or biologic molecule) and once agreed with the CMC Project Team actors, the CMC OPCM is the single accountable person for the accuracy of the entered plan and regularly updated in the planning tool (Planisware solution). The CMC OPCM ensures that the...

Subject-Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer....

Do you want to join Philip Morris? We're looking for a  Senior Laboratory Technician - Exploratory Analytical Chemistry Laboratory YOUR DAILY TASKS 1. Perform autonomously laboratory tests to generate accurate, high-quality data supporting exploratory analyses, special projects, and/or proficiency...

Conduct Interoperability Testing: Perform comprehensive testing of medical imaging devices and software to ensure compatibility and compliance with DICOM standards....

• Contribute to all phases of medical device development, from architecture concepts to design verification and design transfer
• Design and develop low-power medical embedded systems, with a strong focus on safety, reliability and regulatory compliance (IEC13485, IEC60601, ISOetc.)

• Lead contamination control program, risk assessments and strategies in line with cGMP, Johnson & Johnson, and regulatory standards.
• Drive initiatives to reduce contamination risks and enhance microbiological hygiene practices.

• Technical responsibility in development projects in the field of Intraocular Lenses (IOL)
• Responsibility for the technical support of existing products throughout their entire lifecycle and assistance with approval in international markets

• Manage and validate embedded computerized systems integrated into industrial equipment.
• Execute validation activities specifically related to embedded systems, in compliance with applicable regulations and internal procedures.

• Contributing to the research, development, verification, validation, and industrialization of our devices.
• Supporting the creation and implementation of design control, risk management, quality and regulatory documentation related to the devices and manufacturing processes.