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- ...Monday to Friday 8:30am to 5:00pm We are seeking a detail-oriented Technical Writer to support the development, revision, and management of manufacturing and engineering documentation within a GMP-regulated environment. This role will be responsible for converting...SuggestedHourly payContract workPart timeImmediate startRemote workMonday to Friday2 days per week1 day per week
- ...LanceSoft is seeking a Technical Writer II for an onsite role in Plainville, MA. You will collaborate with SMEs to build and revise manufacturing... ...from issuance to archival with QA. The role emphasizes GMP compliance, training junior associates on documentation standards...Suggested
- ...The Technical Writer is responsible for developing, editing, and maintaining Packaging Development documentation, including Package Development... ...and work instructions. • Ensure documentation complies with GMP, GDP, and quality standards. Qualifications Bachelor's...SuggestedFull time
- ...Job Title: Quality Control Investigation Writer Location: High Point, NC 27265 Duration... ...Quality Control department in support of GMP-regulated pharmaceutical manufacturing... ...investigation records for completeness, technical accuracy, regulatory compliance, and adherence...SuggestedContract work
- ...Title: QC Investigation Writer / Technical Writer – GMP | OOS/OOT Investigations Job Summary: Responsible for leading and authoring laboratory investigations in a GMP-regulated pharmaceutical environment. Investigate OOS/OOT results, environmental monitoring excursions...SuggestedFull time
- ...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...SuggestedFull timeWork at officeWork from home
- ...Position Overview The QC Senior Technical Writer authors, reviews, and manages Quality Control documents. This role collaborates with subject... ...at a global level Experience working in a regulated GMP environment Preferred Qualifications : ~10+ years of experience...SuggestedFull timeFlexible hoursShift 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
- ...Analytical Subject Matter Expert (SME) And CMC Technical Writer We are seeking an experienced Analytical Subject Matter Expert (SME) and... ...working experience in regulatory submissions • Familiarity with GMP and regulatory guidelines (e.g., ICH, FDA, EMA, USP, EP, etc.)...SuggestedContract workWork experience placement
- ...Technical Writer Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce... ...sectors and steadily grow. Job Description Looking for GMP experience in addition to tech writer experience. Also, this...Suggested
- ...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
$25 per hour
...organization in the food manufacturing industry, is seeking a Technical Writer to join their team. As a Technical Writer, you will be part of... ...safety, quality, sanitation, and regulatory standards such as GMP, HACCP, FSMA, and OSHA. Manage document workflows, revisions...SuggestedPermanent employmentPart timeWork at officeMonday to FridayFlexible hoursShift workWeekday work- ...to market. Position Summary We have an opportunity for a Technical Writer. This position is responsible for collecting, organizing,... ...administer quality system programs and resources Familiar with GMP documentation requirements Proficient with computer systems...SuggestedSeasonal workWork at officeLocal areaMonday to FridayShift work
$25 per hour
...organization in the food manufacturing industry, is seeking a Technical Writer to join their team. As a Technical Writer, you will be part of... ...safety, quality, sanitation, and regulatory standards such as GMP, HACCP, FSMA, and OSHA. Manage document workflows, revisions...SuggestedPermanent employmentPart timeWork at officeMonday to FridayFlexible hoursShift workWeekday work- ...Technical Writer Immediate need for a talented Technical Writer. This is a 06+ Months Contract opportunity with long-term potential and is... ...verify technical information. Ensure documentation aligns with GMP requirements, company standards, and document control...SuggestedContract workLocal areaImmediate start
$61.3k - $122.7k
...account or a CV. Get jobs like this by email Talentify emails you Technical Writer jobs in Madison. Job alerts Get jobs like this by email... ...equipment/hardware technical writing position. Experience in a GMP and/or ISO 13485 environment. Knowledge of ISO 17025:2005 and/...Work experience placementWork at officeShift workNight shift- ...Caguas, Puerto Rico | Posted on 10/07/2026 The Technical Writer will be responsible for authoring, reviewing, and updating high-quality technical... ...substances , ensuring all documents strictly adhere to GMP regulations and internal quality standards. The ideal candidate...
- Job Title: Technical Writer II Location: Plainville, MA 02762 (Onsite) Duration: 12month W2 contract with possible fulltime conversion... ...principles and processes and has a good understanding of current GMP and safety standards the RSO, Technical Writer II collaborates...Full timeContract workMonday to FridayShift workDay shift
- ...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...Full timeWork at officeMonday to FridayDay shift
$40 - $47 per hour
...Contract Technical Writer – CAPA/SOP Remediation Location: Raleigh, NC (On-site) Pay Rate: $40–$47/hour Engagement Type: Contract... ...backlog of CAPA-related documentation by updating and creating GMP-compliant technical documents. The team will work collaboratively...Contract workWork at officeImmediate startMonday to Friday$80k - $110k
...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...Full timeWork at office$83.3k - $125k
...Technical Writer III position at Thermo Fisher Scientific in Plainville, Massachusetts. Creates and maintains technical documentation including... ...s Degree with 4+ years, or Bachelor's Degree with 2+ years GMP/GLP regulations and quality system documentation expertise...Full timeWork at office- ...Technical Writer SetPoint Medical is seeking an experienced Technical Writer to support the Manufacturing Engineering and Operations organization... ...requirements. ~ Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). ~ Proficiency with...Hourly payContract work
$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$83.3k - $125k
...global health environmental protection and food safety. As a Technical Writer III youll create clear concise documentation that enables our... ...Degree with 2 years of experience. Demonstrated expertise in GMP/GLP regulations and quality system documentation Advanced proficiency...Full timeTemporary workWork at office- ...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...
- ...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...
- ...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...Full time
$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$90 - $140 per hour
...Job Description Journalist / Writer \n \n Position: Journalist / Writer \n \n Type: Contractor \n \n Compensation... ..., or published writing . \n Strong expertise in writing, technical writing, content evaluation, and critical analysis . \n...Remote jobFor contractors



