Author Jobs in North Chicago
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Search Results - Author Jobs in North Chicago
AbbVie-North Chicago
Job Description
The Director II NBE Author leads the development and oversight of Chemistry, Manufacturing, and Controls (CMC) dossier strategy and authoring to support CMC regulatory deliverables such as INDs/IMPDs and Marketing Applications...
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Randstad-Lake Forest (IL), 5 mi from North Chicago
of Office 365 software such as PPT, Word, Excel, etc.
Preferred Qualifications:
• Experience with Adobe Illustrator
• Peer-Reviewed Publications as the first author
• Prior experience in AMCP Format and AMCP Dossiers
• Oncology Certification
#LI-AM1...
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AbbVie-North Chicago
by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question).
Author regulatory documents...
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Randstad-North Chicago
techniques, such as HPLC, GC, titration, and spectrometry. Author scientific protocols and reports.
• Use data interpretation ability and critical thinking skills to troubleshoot experiments and instrumentation, suggest, design, and conduct relevant...
randstadusa.com -
AbbVie-North Chicago
and/or isolations using expertise in reaction kinetics, transport phenomena, and mathematical modeling.
Author and/or review technical documents summarizing process development efforts and contribute to regulatory filings.
Exhibit a collaborative nature...
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Katalyst Healthcares & Life Sciences-North Chicago
Responsibilities:
Manage, compile, and author CMC sections of marketed product variations including CTD content, structural and formatting requirements are being met for assigned projects with minimal management oversight.
Manage assigned projects...
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AbbVie-North Chicago
key regulatory documents. Author technical memos and reports.
The position involves multi-disciplinary interactions with organic chemists, analytical chemists, engineers, drug product development, and program management.
The candidate will identify...
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AbbVie-North Chicago
and interpretation by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question).
Author regulatory...
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AbbVie-North Chicago
or development program.
A primary author of publications, presentations, regulatory documents and/or primary inventor of patents.
Demonstrates high proficiency across a wide range of relevant technologies.
Maintain a high level of productivity in the lab...
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AbbVie-North Chicago
meaningful, reliable, and can be incorporated directly into a research or development program.
A primary author of publications, presentations, regulatory documents and/or primary inventor of patents.
Demonstrates high proficiency across a wide range...
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AbbVie-North Chicago
Author of publications, presentations, technical reports, regulatory documents, and/or patents.
Demonstrate high proficiency across a wide range of relevant technologies.
Understand and adhere to corporate standards regarding code of conduct, safety...
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AbbVie-North Chicago
study findings to generate a pathology report as a component of the toxicology report.
Provides input to study protocols, supervise necropsies, perform histological examinations in rodent and non-rodent studies, author pathology reports, conduct peer...
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AbbVie-North Chicago
laboratories to ensure CMC timelines are met.
Interpret and identify data trends in key analytical release and stability assays.
Author and/or review key regulatory documents, laboratory data, technical memos and reports.
Proactively advise and share...
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AbbVie-North Chicago
sharing.
Leverage prior experience to author and review key regulatory documents, laboratory data, technical memos and reports.
The position involves multi-disciplinary collaborations across Discovery, Development, Manufacturing, and Regulatory...
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AbbVie-North Chicago
independently and providing technical support to a project team.
Provide individual technical support of all scale-up activities and maintain timelines for on-going projects.
Write/co-author process memos and scientific reports in support of Regulatory...
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