Regulatory Affairs Jobs in Arizona
1 - 15 of 71
Search Results - Regulatory Affairs Jobs in Arizona
Tucson Medical Center-Tucson
Overview
In this role, you lead the health system’s clinical risk management and regulatory affairs to reduce liability and ensure readiness. You will advise executives and clinical leaders, coordinate regulatory responses, and drive a proactive...
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YO AI Labs-Phoenix
Job Description
Job Description
Job Title: Regulatory Affairs Specialist
Location: Remote
Job Type: Contract Job Description
We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing...
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Insmed-Chandler
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
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Innovative Health LLC-Scottsdale
Job Description
Job Description
The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.
• Responsible...
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Insmed-Phoenix
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
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System One-Tucson
Job Description
Job Description
Job Title: Regulatory Affairs Manager - PHCS Location: Tucson, AZ Type: Contract Compensation: $45-55.00/hr Work Model: Onsite – onsite Hours: 40.0
Overview As a key member of the Regulatory Affairs team, you...
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Quest Global-Chandler
and approval
What You Will Bring:
• Bachelor’s degree or equivalent experience
• 3+ years in technical writing, proposal development, quality documentation, regulatory affairs, contracts administration, or paralegal work
• Demonstrated ability to produce...
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Insmed-Tucson
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
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Quest Global-Gilbert
and approval
What You Will Bring:
• Bachelor’s degree or equivalent experience
• 3+ years in technical writing, proposal development, quality documentation, regulatory affairs, contracts administration, or paralegal work
• Demonstrated ability to produce...
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Insmed-Tucson
correspondence and submissions accurately; ensure lifecycle management activities
Key requirements
• Bachelor’s degree in a scientific discipline
• 10+ years in Global CMC Regulatory Affairs or relevant pharma/biotech development experience
• 5+ years of gene...
Read more
Quest Global-Tempe
and approval
What You Will Bring:
• Bachelor’s degree or equivalent experience
• 3+ years in technical writing, proposal development, quality documentation, regulatory affairs, contracts administration, or paralegal work
• Demonstrated ability to produce...
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Rock Pros USA-Mesa
Compliance & Regulatory Affairs
• Ensure compliance with applicable federal, state, and industry regulations
• Maintain required records, reports, and documentation
• Coordinate and support regulatory inspections and audits
• Monitor regulatory changes...
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Quest Global-Surprise
and approval
What You Will Bring:
• Bachelor’s degree or equivalent experience
• 3+ years in technical writing, proposal development, quality documentation, regulatory affairs, contracts administration, or paralegal work
• Demonstrated ability to produce...
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Arizona Liver Health-Tucson
Bachelor's Degree in healthcare, regulatory affairs, biosciences, or other related field required.
• Master's Degree in healthcare, biosciences, or other related field preferred.
• Good Clinical Practice (GCP) certification required.
Benefits & Perks...
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Quest Global-Mesa
and approval
What You Will Bring:
• Bachelor’s degree or equivalent experience
• 3+ years in technical writing, proposal development, quality documentation, regulatory affairs, contracts administration, or paralegal work
• Demonstrated ability to produce...
Read more
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