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Faberco Life Sciences Incorporated-Parañaque
that all pharmaceutical products comply with applicable regulations in the Philippines. This role involves overseeing regulatory submissions, managing relationships with regulatory agencies such as the Food and Drug Administration (FDA) Philippines...
Unlimited Network of Opportunities International Corporation-Quezon City
for food supplements and other food products , as well as other licenses such as License to Operate (LTO), free sale certificates, promo permits from the Food and Drug Administration (FDA) and trademark certificates from Intellectual Property Office (IPO)....
jobstreet.com -
WSAudiology-Carmen
Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
• Creation and maintenance of Engineering/Product work instruction to ensure Operative compliance.
• Lead projects and product transfer, test deployment...
Luxasia Group-Taguig
in the Philippines. This includes handling FDA product notification and compliance and adherence to the Extended Producer Responsibility (EPR) Act. This position will play a key role in ensuring both product and environmental regulatory obligations are fulfilled...
appcast.io -
WSAudiology-Silang
planned output. Working with IMI to support assets/equipment inventory.
Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
Creation and maintenance of Engineering/Product work instruction to ensure...
Dexcom Inc.-Manila
on a global scale stands before us.
Position Summary:
This position will support quality activities and projects to successfully meet department and corporate goals. This position will require a mastery of understanding, interpreting, and implementing FDA...
appcast.io -
WSAudiology-Calamba
Working with IMI to support assets/equipment inventory.
Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
Creation and maintenance of Engineering/Product work instruction to ensure Operative compliance...
PSC Biotech-Philippines
and a deep understanding of calibration processes and preventative maintenance protocols.
Key Responsibilities:
• Lead and support validation activities, ensuring compliance with all applicable regulatory requirements (cGMP, FDA, EMA, etc.) and industry...
appcast.io -
WSAudiology-Carmen
and meet daily planned output. Working with IMI to support assets/equipment inventory.
• Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
• Creation and maintenance of Engineering/Product work...
The Medical City-Pasig
Maintenance of Equipment
• Skills in calibrating and maintaining radiation detection instruments and linear accelerators.
Knowledge of Regulatory Standards
• Understanding of local (e.g., DOH, FDA) and international (e.g., IAEA, AAPM) regulations...
YSU Marketing Corporation-Opol
Protection (BFP)
• Department of Environmental & Natural Resources (DENR)
• Food and Drug Administration (FDA)
• Other Barangay / Municipal Entities
• Relays result of inspection, findings and citations (if any) to ManCom and/or concerned department...
mynimo.com -
WSAudiology-Biñan
and meet daily planned output. Working with IMI to support assets/equipment inventory.
• Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
• Creation and maintenance of Engineering/Product work...
appcast.io -
ICON-Manila
9. Provide innovative solutions to generate metrics reports meeting business requirements
10. Create compliance reports to confirm standards compliance
2. End-to-end knowledge of the drug development process
3. Understanding of FDA/ICH guidelines...
Syneos Health, Inc.-Mandaluyong
the clinical trial industry is required.
• Pharma/CRO experience is required, to include client relationship management.
• Thorough knowledge of FDA regulations, drug development, and clinical monitoring procedures is necessary.
• Must have demonstrated...
appcast.io -
WSAudiology-Philippines
planned output. Working with IMI to support assets/equipment inventory.
• Ensure all technical documentation and procedures are in compliance with ISO 13485 and FDA CFR 21 820.
• Creation and maintenance of Engineering/Product work instruction to ensure...
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