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54 Technical Writer Jobs in Cranbury, NJ + Post a Job

Technical Writer-CMC Lead

Confidential Princeton Meadows, NJ

Working in collaboration with global regulatory and safety (GRS) CMC teams and bioprocess manufacturing/process development technical experts… Monster

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Medical Information Developer/Technical Writer

Systems Documentation Inc 4 Reviews Princeton Meadows, NJ

technical writer • Experience as a technical… We are currently looking for a medical information developer/technicalJobsite.com

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PHARMA Technical writer – new

Auritas 2 Reviews Edison, NJ

validation reports and SOPs. Maintains standardized and consistent documentation practices. Writes and revises cGMP documents including batch records… Dice

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Pharma Technical Writer – new

Super Technology Solutions, Inc. Middlesex, NJ

validation reports and SOPs. Maintains standardized and consistent documentation practices. • Writes and revises cGMP documents including batch… Dice

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Supply Chain Process Facilitator and Technical Writer Intern

Hamilton Sundstrand 100+ Reviews Princeton, NJ

Sensors Unlimited, a UTC Aerospace Systems company is the leading developer and manufacturer of shortwave infrared (SWIR) one and two dimension focal… Beyond.com

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Supply Chain Process Facilitator and Technical Writer Intern - ReqCode 112462-01

UTC Aerospace Systems 16 Reviews Princeton, NJ

Sensors Unlimited, a UTC Aerospace Systems company is the leading developer and manufacturer of shortwave infrared (SWIR) one and two dimension focal… America's Job Exchange

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Technical Writer (5m) – easy apply

inVentiv Health 82 Reviews Bridgewater, NJ

Contribute to R&D, LCM and Industrial Development and Innovation projects (in-licensing, partnership projects) by planning, writing and delivering… CareerBuilder

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LEAD TECHNICAL WRITER CMC

Bristol-Myers Squibb 100+ Reviews Hopewell, NJ

Working in collaboration with GRS CMC teams and BMPD technical experts. Creates final drafts of Regulatory documents for submission to GRS and… Bristol-Myers Squibb

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Technical Writer/ Senior Technical Writer

Roche 90 Reviews Branchburg, NJ

Responsible for ensuring that labeling produced is within global regulatory, FDA, ISO, IVDD, CE and legal guidelines. * Responsible for obtaining… Beyond.com

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Technical Writer

Rose International 28 Reviews Raritan, NJ

• Create and Update existing Quality System Documentation like ( SOPs, WIs, Policies and others). • Experience in working with Electronic Document… CareerBuilder

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Technical Writer Pharma

Confidential Company Middlesex, NJ

validation reports and SOPs Maintains standardized and consistent documentation practices Writes and revises cGMP documents including batch records… Dice

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Updated May 18, 2013