Author Jobs in Lexington (MA)
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Search Results - Author Jobs in Lexington (MA)
Katalyst Healthcares & Life Sciences-Lexington (MA)
spectroscopy, chromatography, protein analyzers, next gen sequencers, PCRs etc).
Consult clients on data integrity requirements in Analytical Instruments and perform verification of DI in the systems.
Author validation life cycle documents for client's review...
resume-library.com -
TalentCraft-Lexington (MA)
requirements.
• Investigate protocol nonconformances and site deviations.
• Initiate and manage validation-related change controls and corrective/preventive actions.
• Author SOPs related to validation practices.
• Conduct and document formal risk assessments...
mindmatch.ai -
Zifo-Lexington (MA)
of DI in the systems
Author validation life cycle documents for client’s review and approval
Perform Periodic review for the analytical instruments and conduct meetings with stakeholders to discuss on the remediations of observations from review
IT...
resume-library.com -
Lexington (MA)
efforts, author technical protocols, design and implement experimentation, generate technical reports, and author related CMC sections to support regulatory submissions. You will also need some background in Computer Science to be involved in the data...
pharmiweb.jobs -
Sunrise Systems Inc-Lexington (MA)
for descions, and clariffications as needed.
Must be able to juggle multiple projects and deliverables, and split billing time between projects where needed.
Experience with performing design testing of application to help author SDLC documents, including...
resume-library.com -
Zifo-Lexington (MA)
verification of DI in the systems
• Author validation life cycle documents for client’s review and approval
• Perform Periodic review for the analytical instruments and conduct meetings with stakeholders to discuss on the remediations of observations from...
workable.com -
Sunrise Systems Inc-Lexington (MA)
team members for descions, and clariffications as needed
Must be able to juggle multiple projects and deliverables, and split billing time between projects where needed.
Experience with performing design testing of application to help author SDLC...
resume-library.com -
Lexington (MA)
with others to develop key messages for complex clinical/regulatory documents
• Authors, reviews, and/or edits documents to support clinical trials and regulatory submissions, which may include:
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• Clinical summary and overview...
tiptopjob.com -
Randstad-Lexington (MA)
of application to help author SDLC documents, including SDCS, URS, FRA, Admin Sop, IQ, IOQ, ATR, Application Data Flow diagrams, etc.
• Must poses GXP experience with lab equipment.
Qualifications
Skills
• Quality
Experience
• Experienced
For certain...
randstadusa.com -
Lexington (MA)
cross:functional study teams, including personnel from Medical and Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Management, and Non:clinical Development.
Essential Functions
• Authors, edits...
tiptopjob.com -
LanceSoft Inc-Lexington (MA)
Experience with performing design testing of application to help author SDLC
documents, including SDCS, URS, FRA, Admin Sop, IQ, IOQ, ATR, Application
Data Flow diagrams, etc.
Must poses GXP experience with lab equipment.
Recommended Experience
Service...
resume-library.com -
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