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- ...development and approval of Quality Documents, the full-time Technical Procedure Writer will manage the controlled document approval process and... ...electronic document management systems; Veeva experience is a plus Basic knowledge of GMP, GCP, and GPvP processes is a plus...SuggestedFull timeLocal areaRemote work
- ...Onelims Em Project Technical Writer The OneLIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS... ...Prior work experience in a good manufacturing practices (GMP) environment Must possess sound interpersonal and information...SuggestedWork experience placement
- ...Technical Writer A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-... ...publishing tools. Create and maintain templates for both non-GMP and GMP documents. Draft documents from raw data. Verify...SuggestedWork at officeImmediate start
$40 - $44.97 per hour
...R&D Technical Writer Location: Salt Lake City, UT Type: Contract Compensation: $40 - $44.97/hr Work Model: Onsite Responsibilities... ...orders, and specifications, ensuring accuracy and compliance with GMP and QSR standards. Develop labeling designs using standard...SuggestedContract workWork at office- ...Technical Writer Location US-TN-Clinton ID 2026-2377 Category Manufacturing Position Type Full... ...Technical Services team, responsible for developing FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical...SuggestedFull timeWork at officeMonday to FridayDay shift
- ...Role : Technical Writer Location : Onsite in Lexington KY • A minimum of 2 years of life science experience • Prior experience working in a GMP manufacturing and lab setting • Prior experience reviewing existing SOPs and writing new SOPs for security,...Suggested
- ...Technical Writer Demonstrates knowledge of current Good Manufacturing Practice (FDA, EU and ICH) requirements and Quality Systems, with the... ...projects at the same time. Need to have an understanding of GMP Technical experience in MS Office and Adobe Acrobat is required...Suggested
- ...and QA management of designated clients. Working Conditions and Environment: Work is performed in an office, laboratory and/or GMP Depot environment. For laboratory positions, potential exposure to biological fluids with potential exposure to infectious organisms....SuggestedWork at office
- ...Excellent employment opportunity for a Analytical SME & CMC Technical Writer in the Ridgefield, CT area. (Remote) We are seeking an experienced... ...experience in regulatory submissions ~ Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)...SuggestedContract workWork experience placementRemote work
- ...Technical Writer Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional... ...the process. Complete all changes and related activities to GMP / ISO compliance. Identify and implement improvements in the...Suggested
- ...Technical Writer - Onsite in Clayton, NC This is a pharmaceutical technical writing position focused on developing, revising, and managing GMP documentation that supports manufacturing operations, process engineering, facilities, training, and quality systems. The role...Suggested
- ...MSAT Technical Writer, Cell Therapy Vector Support ,Support, Manufacturing Science and Technology (MSAT) The focus of the MSAT Technical... ...(s) to understand different failure modes - Works with GMP Quality Systems to deliver completed Root Cause Analysis investigation...Suggested
- ...Quality Technical Writer and Training Specialist Key Responsibilities: Documentation Development Create Highly detailed, clear step-by-step... ...manufacturing and quality-regulated operations, bio-pharmaceutical, GMP, and FDA environments. Experience with document control...Suggested
- ...expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled...SuggestedWork at office
- ...Laboratory Services. We are seeking a detail-oriented Validation Technical Writer to join our Validation team. In this role, you will play a... ...accuracy, clarity, and compliance of documentation related to GMP-regulated systems and facilities. Your expertise will support...Suggested
$40 per hour
...Job Description Job Description Job Title: Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.0... ...dispensing / manufacturing / packaging operations. Review GMP documents such as SOPs, Batch records, Logbooks to...Hourly payContract workLocal area$100k - $130k
...SUMMARY/OBJECTIVE: The Technical Writer, Analytical is responsible for supporting and coordinating Quality Management System (QMS) documentation... ...Assurance to draft, revise, route, and maintain compliant GMP laboratory documentation supporting analytical testing and development...Work at officeWork from home- ...Job Responsibilities: Author technical reports, policies, and Standard Operating Procedures. Author/review, format, and revise reports... ...with LIMS, SAP/SRM, Track Wise, and Veeva, Experience in GMP/GLP and/or a regulated industry. Education/Experience: At...
- ...Overview and Configuration, Validation and Security Plans required for GMP automation platforms. Middleware Application - 2 - Beginner... ...and easy-to-read approvable documents. Edit/write a variety of technical articles, reports, manuals, flow charts, and other documentation...Temporary workFor contractorsWork at office
$36 - $41 per hour
...Scientific community. We are currently looking for a Contract Technical Writer to work for a leading Greater Orange County area contract... ...On-site/Mon-Fri Responsibilities: Ensure compliance with GMP, ISO 90001, regulatory requirements, dept/bldg. Safety rules and...Contract workTemporary work$45 - $49.65 per hour
...tier global pharma leader in Branchburg, NJ, as a Supply Chain Technical Writer II. This 6-month extendable contract role offers an excellent... ...excellence, facilitate CAPA closures, and streamline critical GMP documentation within a dynamic supply chain environment. location...Hourly payContract workTemporary workWork experience placementWork at office- ...Job Description Job Description Maintenance Technical Writer | Employment Type | Contract-to-Hire | Location | Seabrook, NJ (on... ...food & beverage or food-grade manufacturing environments and GMP documentation requirements • Experience working alongside...Contract workWork at officeDay shift
- ...SUMMARY/OBJECTIVE: The Technical Writer is responsible for leading Quality Management System (QMS) documentation activities within Operations... ...and maintain controlled documentation in support of compliant GMP operations. This position serves as a key liaison between...Contract workWork at office
- ...This role will provide non-testing support to the QC Product Technical Support department. This scope includes coordination of generating... ...as the main job responsibility is data review and generation of GMP documentation A degree in science, preferably in microbiology or...
- Technical Writing Specialist Role Type: Contractor Location: Remote micro1 is seeking Technical Writing Specialists to support a customer project focused on developer and product documentation for AI training. No prior AI experience is required. Key Responsibilities Create...For contractorsRemote work
$65k - $85k
...Systems Planning and Analysis, Inc. (SPA) delivers high-impact, technical solutions to complex national security issues. With over 50... ...published product. SPA has an immediate need for a Technical Writer in San Diego, CA. #KS Responsibilities Responsibilities...Full timeWork at officeImmediate startFlexible hours- ...Job Title: Technical Writer/Editor Job Duration: 12 Months Contract on W2 Job Location: - Orlando, FL Note: US Citizen are required for this position. Job Description Write, rewrite and/or edit technical documents such as technical procedure manuals...Contract work
- ...with MANTECH! ***This is for a future opportunity*** MANTECH seeks a motivated, career and customer-oriented Technical Writer II to join our team in Crane, Indiana. This is an onsite position. As a core member, you will assist in the research &...Work at officeLocal area
- ...Technical Writer Summary of Position BQMI is adding to their growing team of professionals supporting government contracts across the United States. We are a well-established team who are known for being employee-focused while providing superior support to our...Contract workWork at officeRemote work
- ...national security and safeguard global assets. ESSENTIAL JOB FUNCTIONS: Job Summary: We are seeking a highly motivated technical writer to join our Kratos Defense & Rocket Support Services Division in Crane, Indiana. In this critical role, youill partner with...Work at office

