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- ...Job Title - OneLIMS EM project technical writer Location: Swiftwater, PA 18370 Duration: Contractual till Mar 2027 with the possibility of... ...LIMS) pharmaceutical, or biotech environments (e.g., Veeva, GMP) Description The OneLIMS EM project technical writer is responsible...SuggestedWork experience placement
Aequor
Swiftwater, PA9 hours ago - A pharmaceutical company in New Jersey is seeking a detail-oriented GMP Pharmaceutical Technical Writer. This role involves creating and maintaining controlled documentation to meet GMP regulations. The ideal candidate will collaborate with internal teams to ensure the...Suggested
- An established industry player is seeking a Technical Writer with extensive experience in GMP laboratory environments. The role involves writing and revising standard operating procedures (SOPs) and collaborating with cross-functional teams to translate complex technical...Suggested
- Overview Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled...SuggestedWork at office
- Indivior PLC in Raleigh, NC is seeking a Production Investigator/Technical Writer to investigate manufacturing deviations and report on customer complaints. You will create and update SOPs, work instructions, and participate in audits. The ideal candidate has at least...Suggested
- ...Position: Technical Writer- GMP Manufacturing Documentation Location: Houston, TX (100% On-Site) Length: 6 Month Contract Please no agencies. Direct employees currently authorized to work in the United States – no sponsorship available Job Description:...SuggestedContract workTemporary work
Digital Prospectors
Houston, TX3 days ago - ...Gmp Pharmaceutical Technical Writer Reporting to the appropriate department based on area of 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...SuggestedWork at office
Cedent Life Talent
Springfield, NJ4 days ago $30 - $40 per hour
...VA Order: 2160737 Order Type : Temp Technical Writer-SOP Specialist Our client, a local company, is seeking a... ...Ensure all documentation adheres to regulatory requirements (e.g., GMP,ISO), safety standards, and company policies. Documentation...SuggestedTemporary workPart timeLocal areaRemote workRobbins Staffing Solutions Inc
Charlottesville, VA3 days ago- ...an experienced Analytical Subject Matter Expert (SME) and CMC Technical Writer to support external drug substance (DS) and drug product (DP)... ...working experience in regulatory submissions • Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)...SuggestedContract workWork experience placement
Patel Consultants Corporation
Danbury, CT1 day ago $35 - $40 per hour
...Technical Writer Kenosha County, WI $35-40 AN HOUR On site The ideal candidate will be responsible for creating and writing various... ...Technical writing experience in pharma manufacturing (GMP environment) Background in Quality and/or Operations Experience...SuggestedMedasource
Pleasant Prairie, WI4 days ago- ...Job Title: SOP Technical Writer Contract Length: 3-months Location: Remote Hours: 40 hours per week Start Date: 7/6/26 Client... ...in farm animals and pets. Operating in a highly regulated, GMP-driven environment, our client emphasizes quality, compliance,...SuggestedContract workRemote workWorldwide
Medasource
Iowa2 days ago - ...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...SuggestedWork at officeWork from home
Experic
Cranbury, NJ9 hours ago - ...fields. This has helped us expand into new sectors and steadily grow. Job Description Job Description: Looking for GMP experience in addition to technical writing experience. The candidate will also be summarizing metrics for the site, involving data extraction and spreadsheet...Suggested
- Responsibilities Develop, edit, and maintain technical documentation including SOPs, work instructions, validation protocols, and reports... ...Manufacturing, and Engineering teams to ensure documentation aligns with GMP standards and operational processes Support documentation...SuggestedWork at office
- ...Duties Write and revise standard operating procedures (SOPs) for GMP Analytical and Microbiology laboratory operation and instruments... ...manage competing deadlines and balance priorities. Excellent technical writing skills, close attention to detail and excellent follow up...Suggested
- ...and dependent care), and disability coverage. Position Technical Writer Location Vandalia, Ohio Summary The Technical... ...guidelines. Follow and observe all regulatory requirements (GMP's, ISO, FDA, internal policies) applicable to area of...Contract workWork at officeFlexible hours
Adare Pharma
Vandalia, OH1 day ago - ...Job Description Job Description TECHNICAL REPORT WRITER JOB SUMMARY Responsible for reporting scientific and technical information in a manner that can be understood by an average reader. Responsible for research and preparing technical reports to support due...Work at officeLocal area
August Mack Environmental, Inc.
Independence, OH6 days ago $40 - $48 per hour
...Immediate need for a talented USA-Technical Writer II (IT) . This is a 12 Months Contract opportunity with long-term potential and is located... ...Prior work experience in a good manufacturing practices (GMP) environment Must possess sound interpersonal and information...Contract workWork experience placementLocal areaImmediate startMonday to FridayWeekend workAfternoon shiftPyramid Consulting, Inc
Swiftwater, PA9 hours ago$28 - $36 per hour
QMS Technical Writer - Temporary QMS Technical Writer - Temporary is responsible for directly participating in a Quality Systems Integration... ...related experience. 3-5 years of technical writing experience in a GMP, Biotechnology, Pharmaceuticals or another regulated industry....Temporary workFlexible hoursShift work- Overview TITLE: Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients... ...deadlines and company and departmental metrics. Conduct GMP, GDP, SOP, and awareness training as needed for deviation resolution...Worldwide
- ...Technical Writer/ Editor Job ID#: 26-2280 Clearance: Ability to successfully complete applicable background investigations and comply with organizational security requirements. Location: Remote Who We Are: Since our inception back in 2006, Navitas has grown...Local areaRemote work
Navitas Business Consulting
United States4 days ago $40 - $45 per hour
...We are seeking a mid-level Technical Writer that will be responsible for planning, writing, editing, and verifying high-quality technical documents! The ideal candidate will be: Responsible for researching, writing, editing, and verifying high-quality technical...Hourly payRemote workAdaptation
United States1 day ago- ...MSAT - Process Lead Technical Writer Location: On-site, Portsmouth, NH. The MSAT Process Lead Technical Writer is responsible for the... ...0 years in a production environment. ~ Working knowledge of GMP / Biotechnology manufacturing background referred, some...Work experience placement
Lonza
Portsmouth, NH4 days ago - ...Compliance Technical Writer Sr: The Compliance Technical Writer Sr is responsible for producing, editing, and maintaining high quality, audit ready NERC compliance documentation for the Enterprise NERC Reliability Assurance (ENRA) organization. This role operates in...
Insight Global
Columbus, OH4 days ago $90k - $110k
...cross-functional environment, takes pride in delivering high-quality, user-focused documentation, and enjoys translating complex technical information into clear, approachable content. To be successful, the candidate must utilize our products in a laboratory environment...Work at officeAdaptiva
Washington DC2 days ago- ...document control, versioning, and consistency standards Assist in transitioning QMS documents into ETQ What We’re Looking For Technical writing or process documentation experience Background in Supply Chain, Warehouse, Quality, or Manufacturing environments...Work at office
Mastech Digital
Tolleson, AZ2 days ago - ..., MOPs, runbooks, and knowledge base articles. Lead SME working sessions to capture requirements, clarify intent, and validate technical accuracy for publish-ready documentation. Standardize content using approved templates and consistent structure to improve readability...Work at office
CyrusOne
Carrollton, TX9 hours ago $50 per hour
...Now Hiring: Technical Editor & Writer (Contract) – Elkridge, MD Area I’m working with a leading company to identify a Technical Editor & Writer with a strong engineering or military systems background. This is a great opportunity for someone who can turn complex technical...Contract workImmediate startTAD PGS, Inc.
Elkridge, MD9 hours ago- ...received by our participants and is a viable tool for our instructors. AVO Training is currently looking for an experienced Technical Writer to create high-quality content for our publications and instructional programs, which contribute to the success of our...Work at office
AVO Training Institute | Electrical Safety
Dallas, TX3 days ago $30 - $35 per hour
...Kelly Engineering is seeking a Technical Writer to join one of our leading clients in the Chemical/Composite/Materials manufacturing industry at their Anaheim, CA location. Please apply to learn more! Ideal candidate: Manufacturing or Production industry experience...Kelly Science, Engineering, Technology & Telecom
Anaheim, CA2 days ago
