Author Jobs in New Brunswick
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Search Results - Author Jobs in New Brunswick
ECLARO-New Brunswick
comments to the matrix teams.
Facilitate data verification to ensure accuracy of submission data following the internal standard operating procedure.
Author CMC elements of regulatory filings with supervision.
Participate on various cross-functional...
resume-library.com -
BCforward-New Brunswick
comments to the matrix teams.
• Facilitate data verification to ensure accuracy of submission data following the internal standard operating procedure.
• Author CMC elements of regulatory filings with supervision.
• Participate on various cross-functional...
BCforward-New Brunswick
comments to the matrix teams.
• Facilitate data verification to ensure accuracy of submission data following the internal standard operating procedure.
• Author CMC elements of regulatory filings with supervision.
• Participate on various cross-functional...
BCforward-New Brunswick
comments to the matrix teams.
• Facilitate data verification to ensure accuracy of submission data following the internal standard operating procedure.
• Author CMC elements of regulatory filings with supervision.
• Participate on various cross-functional...
mindmatch.ai -
Stage Solutions Inc-New Brunswick
/facilitating consensus meetings, distributing review comments to the matrix teams.
• Facilitate data verification to ensure the accuracy of submission data following the internal standard operating procedure. Author CMC elements of regulatory filings...
jobvertise.com -
Stack Builders-New York, 28 mi from New Brunswick
We're currently seeking an experienced AEM Lead Author to join us!
In this remote contract position, you'll collaborate with a client project team to boost brand visibility, optimize their website, engage visitors, and lead a team of AEM authors. You...
workable.com -
Katalyst Healthcares & Life Sciences-South Plainfield, 7 mi from New Brunswick
Consultants on execution responsibilities & be direct interface to customer FT team.
Support Engagement Lead with resource interviews, allocation, utilization, schedule forecasting & adjustments as required.
Author the following CSV Deliverables: Initial...
resume-library.com -
GForce Life Sciences-Princeton (NJ), 14 mi from New Brunswick
document development and management.
Description
• U.S. policy and SOP lifecycle document development and management.
• Includes tracking documents during the review/approval process, direct engagement with authors and teams, and following up with authors...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-Rahway, 12 mi from New Brunswick
Principal Scientist is also responsible for the preparation and review of information required for development of regulatory CMC dossiers for new and existing commercial products.
Work independently and effectively to manage and author regulatory CMC...
resume-library.com -
Clinical Resource Network (CRN)-Princeton (NJ), 14 mi from New Brunswick
product as assigned).
• Author and review all related documentation for the Quality group including Protocols, Reports, SOPs, Risk Management, Quality Agreements, Instruction Manuals, CAPAs, Deviations, Specifications and Change Controls.
• Collaborate...
mindmatch.ai -
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