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 -
Symbotic-Lexington (MA)
technicians and contractors conducting hands-on mobile robot testing.
• Validate the test fixtures, stimulus, and automated software to meet test requirements across multiple manufacturing locations.
• Author comprehensive repair test specifications...
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)
perspective, including but not limiting to: study design and sample size determination; author/review statistics section in the protocol, SAP and DMC charter; create/review study randomization files; develop TFL shell and specification; review CRFs and other...
tiptopjob.com -
Katalyst Healthcares & Life Sciences-Lexington (MA)
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.
Service now, Veeva, Trackwise, Active Directory, firewall rules, My Access, NTFS permissions...
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 -
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 -
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...
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Eurofins USA PSS Insourcing Solutions-Cambridge, 7 mi from Lexington (MA)
resource for potency assays.
Execution of complex GMP release and stability assays such as cell based functional assays, flow cytometry methods, ddPCR, ELISA, and NGS assays.
Author and review SOPs and technical reports.
Work with cross-functional groups...
resume-library.com -
Lexington (MA)
documents
• Authors, reviews, and/or edits documents to support clinical trials and regulatory submissions, which may include:
stylelist:style:type:circle:
• Clinical summary and overview documents in eCTD format for global regulatory submissions, including...
tiptopjob.com -
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