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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
- Indotronix is seeking a Technical Writer to develop and revise procedures used in manufacturing processes. You will collaborate with area SMEs... ...from issuance to archival with Quality Assurance, maintaining GMP SOPs, and training staff on writing standards. Fully onsite in...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
- ...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
$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,...SuggestedPart timeWork at officeMonday to FridayShift workWeekday work$40 per hour
...Immediate need for a talented Technical Writer . This is a 06+ Months Contract opportunity with long-term potential and is located in Fort... ...technical information. Ensure documentation aligns with GMP requirements, company standards, and document control procedures...SuggestedContract workLocal areaImmediate start- ...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
$38 - $41.96 per hour
...We are seeking a contract Technical Writer / Deviation Specialist to support the Manufacturing Science and Technology (MSAT) team within our... ...ideal candidate is detail-oriented, comfortable working in a GMP manufacturing environment, and able to translate complex manufacturing...SuggestedHourly payContract workTemporary workLocal areaRemote work- ...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
- ...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...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...Work at office
$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- ...for an average of 10+ years. Job Description Job Title: Technical Writer Location: Plainville, MA 02762 Duration: 12 Months Responsibilities... ...Assurance Responsibilities may include maintaining the GMP manual of Standard Operating Procedures and management of...Monday to FridayShift workDay shift
- ...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...Seasonal 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...Permanent employmentPart timeWork at officeMonday to FridayFlexible hoursShift workWeekday work- ...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- ...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...
$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$33 per hour
Technical Writer I - Manufacturing Sciences About the Role We are seeking a detail-oriented Technical Writer I to join our Manufacturing Sciences... ...a Science or Engineering degree and experience working with GMP documentation, manufacturing records, quality systems, and...Contract workTemporary workWork at office$36 - $43 per hour
Technical Writer Location: Torrance, CA | Employment Type: Full-Time Turn Complex Manufacturing Processes Into Clear, Reliable GMP Documentation At PolyPeptide, we partner with pharmaceutical and biotech companies to support the development and manufacturing of peptide...Full timeWork 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...
$83.3k - $125k
...global health, environmental protection, and food safety. As a Technical Writer III, you'll create clear, concise documentation that enables... ...Degree with 2 + years of experience. • Demonstrated expertise in GMP/GLP regulations and quality system documentation • Advanced...Full timeTemporary workWork at office$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


