Regulatory Affairs Jobs in Pennsylvania
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Search Results - Regulatory Affairs Jobs in Pennsylvania
The Fountain Group LLC-Swiftwater (PA)
Currently I have an opening for a Regulatory Affairs Specialist located in Swiftwater, PA (Hybrid Schedule). Details for the position are as follows:
Job Description:
Will work closely with the Regulatory Site Office, Manufacturing and Supply...
resume-library.com -
IntePros-Exton
IntePros is currently looking for a Sr. Regulatory Affairs Project Management Specialist to join one of our growing medical device/manufacturing clients. The Sr. Regulatory Affairs Project Management Specialist is responsible for management...
mindmatch.ai -
HireTalent-Swiftwater (PA)
Job Title: Regulatory Affairs Specialist II (Clinical)
Job Location: Swiftwater, PA (Hybrid)
Job Duration: 6 Months
Overview of the Position
The Regulatory CMC Specialist will work closely with the Regulatory Site Office, Manufacturing...
resume-library.com -
Randstad-Swiftwater (PA)
documents/dossiers to be dispatched to regulatory affairs functions for submissions
• Coordinates CMC writing performed by another entity (internal or external)
• Optimizes the content of CMC dossiers to facilitate the management of future changes...
randstadusa.com -
Axelon Services Corporation-Pittsburgh
Job Title: Regulatory Affairs Assistant
1st Shift
Description:
Responsible for assisting with ensuring compliance with US OSHA and Canadian Workplace Hazardous Materials Information System (WHMIS). This includes gathering, maintaining...
resume-library.com -
Meet-Philadelphia
Collaborate closely with cross-functional teams, including Clinical Development, Regulatory Affairs, and Quality Assurance, to ensure alignment and adherence to project timelines.
• Oversee vendor selection and management, including CROs and other clinical...
mindmatch.ai -
V R Della Infotech Inc-Pittsburgh
for the preparation of Safety Data Sheets (SDSs), preparation of data for regulatory reports, and responding to customer requests for information regarding regulatory compliance and products.
This position is on-site.
Skills/Experience:
A minimum of a Bachelor's...
jobvertise.com -
Integrated Resources, Inc-Swiftwater (PA)
and approves CMC regulatory documents/dossiers to be dispatched to regulatory affairs functions for submissions
" Coordinates CMC writing performed by another entity (internal or external)
" Optimizes the content of CMC dossiers to facilitate the management...
resume-library.com -
Visron Technical LLC-Pittsburgh
Years of experience in a Product Safety and/or Regulatory Affairs role preferred....
smartsearchonline.com -
EPM Scientific-Philadelphia
Drive the preparation and submission of CMC sections for regulatory filings, including INDs, NDAs, BLAs, and MAAs, working closely with regulatory affairs teams.
• Collaborate with internal teams, including R&D, quality assurance, clinical...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-Swiftwater (PA)
documents/dossiers to be dispatched to regulatory affairs functions for submissions.
Coordinates CMC writing performed by another entity (internal or external).
Optimizes the content of CMC dossiers to facilitate the management of future changes.
Prepares...
resume-library.com -
EPM Scientific-Philadelphia
and ensuring compliance with regulatory standards.
Key Responsibilities:
• Lead the global medical affairs strategy for oncology, ensuring alignment with the companys overall business objectives and scientific goals.
• Oversee the development and execution...
mindmatch.ai -
Randstad-Souderton
be a plus.
• Knowledge and understanding of PPAP’s (i.e., production part approval process).
• Able to build process flow flowcharts in MS Visio or Excel.
• Some familiarity with OSHA safety and compliance requirements.
• Certifications in regulatory affairs...
randstadusa.com -
Michael Page-Philadelphia
Provide safety oversight and pharmacovigilance management to clinical development
3.
Regulatory Compliance:
• Work closely with regulatory affairs to ensure compliance with regulatory requirements throughout the development process.
• Provide medical...
michaelpage.com -
Collegeville (PA)
Ensure the development of appropriate global and/or regional regulatory strategy(s) and their execution for assigned asset(s) consistent with Medicines Development Strategy /Integrated Asset plan to ensure the development program meets the needs...
pharmadiversityjobboard.com -
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