Author Jobs in Trenton
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Search Results - Author Jobs in Trenton
NavitsPartners-Trenton
regulatory submission strategies and timelines for pharmaceutical projects.
• Manage and author CMC dossiers, renewals, annual reports, variations, supplements, and responses to health authorities.
• Review technical reports and scientific data...
talentnest.com -
Katalyst Healthcares & Life Sciences-Trenton
Responsibilities and Requirements:
The position is at Roche Branchburg, NJ, Start date: Mid Jan / beginning of Feb.
They need to be good protocol authors, good communicators, and can draft, review and execute qualification protocols on process...
resume-library.com -
Tehk Recruitment Ltd-Trenton
author, and review any submissions to FDA to ensure company requirements and relevant FDA requirements are met.
• Liaise with Project Managers and participate on global client project teams to properly plan for and support client submissions...
jobvertise.com -
OPEN Health-Trenton
appropriate to the target audience, and that meet the authors’ communication objectives, client specifications, and industry guidelines
• Developing and maintaining in-depth knowledge in relevant therapy areas, including disease state, treatment guidelines...
workable.com -
Novo Nordisk A/S-Trenton
presenting external authors
• Develop local US publication plan (including encore abstracts, reviews, and supplements) in collaboration with Publications Manager
• Independent Medical Education (IME)
• Assist in developing medical education priorities...
appcast.io -
Pharma Universe-Trenton
and retest dates for all GMP raw materials through vendor COA and/or in-house COA.
• Review and release raw materials and critical materials for use in manufacturing.
• Author and review batch records, SOPs, and associated forms/formats required...
workable.com -
Integrated Resources, Inc-Princeton (NJ), 23 mi from Trenton
regulatory affairs,
global publication team, and commercial publications colleagues from market access and marketing.
The Manager - Publications is also expected to network effectively with external resources (e.g., authors) and work closely
with external...
resume-library.com -
Pharma Universe-Trenton
and retest dates for all GMP raw materials through vendor COA and/or in-house COA.
• Review and release raw materials and critical materials for use in manufacturing.
• Author and review batch records, SOPs, and associated forms/formats required...
workable.com -
LanceSoft Inc-West Point (PA), 40 mi from Trenton
Title: Design Verification Engineer II
Location: West Point, PA
Contract Duration: 12 Months
Pay Range: $35.00 - $44.00 USD hourly on W2
Job Description:
The basic function of this position is to author technical change assessment related...
resume-library.com -
eTeam Inc.-Rahway, 43 mi from Trenton
and effectively to manage and author regulatory CClient dossiers, renewals/annual reports, variations/supplements, and responses to authority questions as required in each country in order to gain new and maintain existing product registrations.
" Review...
resume-library.com -
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