Technical Writer Salary at Upswot Inc BETA

Pay Rate : $ 37.00 to $ 42.00 Per Hour Technical Writer, Analytical Outsourcing, Biopharmaceutical Development Candidates must be local and able to work onsite ~2-3 days per week. May be more, as needed. M-F 8-5 regular schedule. Scientific background, ideally pharma experience Job Qualifications •BS in Chemistry, Biology or a related scientific discipline. •At least 2-3 years scientific/analytical lab experience, preferably in the field of protein therapeutics or monoclonal antibody therapies. •Proficient in scientific/technical writing. ***Experience in Empower chromatographic data system •Experience with LIMS, SAP/SRM, TrackWise, and Veeva. •Excellent oral communication, interpersonal and technical writing skills. •Excellent organizational skills, demonstrate attention to detail. •Experience in GMP/GLP and/or a regulated industry. •Strong background in Microsoft applications such as Word, Excel, SharePoint a must. •Advanced Excel knowledge is a plus. Job Description •Author technica

The Technical Writer will support the Naval Surface Warfare Center in Philadelphia, PA, by creating and maintaining technical documentation, including policies, procedures, strategic plans, and cybersecurity documentation. The ideal candidate will be responsible for writing clear, concise, and accurate technical content, ensuring that documentation meets high standards and aligns with the needs of the organization and its stakeholders. Additionally, the Technical Writer will present technical documents and strategic plans to executives, facilitating effective communication across teams. **This position is contingent upon award of contract** Key Responsibilities: Write and update policies, technical documents, strategic plans, designs, cybersecurity operations, and procedures. Collaborate with subject matter experts (SMEs) to gather information and ensure technical accuracy in documentation. Review and revise existing documents to ensure they remain up to date and compliant with organiz

Job: Technical Writer,-Analytical Outsourcing, Biopharmaceutical Development Location: Exton, PA/Hybrid- 2-3 Days Duration: 12 Months+ Candidates must be local and able to work onsite ~2-3 days per week. May be more, as needed. M-F 8-5 regular schedule. Scientific background, ideally pharma experience. Must HAVE: • BS in Chemistry, Biology or a related scientific discipline. • At least 2-3 years scientific/analytical lab experience, preferably in the field of protein therapeutics or monoclonal antibody therapies. • Proficient in scientific/technical writing. ***Experience in Empower chromatographic data system Job Qualifications: • Experience with LIMS, SAP/SRM, TrackWise, and Veeva. • Excellent oral communication, interpersonal and technical writing skills. • Excellent organizational skills, demonstrate attention to detail. • Experience in GMP/GLP and/or a regulated industry. • Strong background in Microsoft applications such as Word, Excel, SharePoint a must. • Advanced Excel knowled

TECHNICAL WRITER Exton PA 1-3 year contract $40-$50 an hour Scientific background, ideally pharma experience Job Qualifications • BS in Chemistry, Biology or a related scientific discipline. • At least 2-3 years scientific/analytical lab experience, preferably in the field of protein therapeutics or monoclonal antibody therapies. • Proficient in scientific/technical writing. ***Experience in Empower chromatographic data system • Experience with LIMS, SAP/SRM, TrackWise, and Veeva. • Excellent oral communication, interpersonal and technical writing skills. Job Description • Author technical reports, policies, and Standard Operating Procedures. • Author/review, format, and revise reports, protocols, analytical method validations, and CMC sections for regulatory submissions. • Author investigations, deviations, change controls, and other non-conformance records. • Work with vendors to coordinate testing and arrange shipments as needed. • Compile and review scientific data for completeness

The Technical Writer is responsible for developing instructional and informational materials that ensure the safe, appropriate, and effective use of scientific and technological products and services. This role involves creating and managing technical documentation, manuals, and work instructions while ensuring compliance with company documentation and quality assurance standards. Key Responsibilities: Develops and manages user documentation projects, including work instructions, style guides, and process documentation. Collaborates with technical teams to gain in-depth product knowledge. Reviews, revises, and approves existing documentation for consistency and quality improvement. Investigates issues (INVs/CAPAs) and recommends documentation changes to address root causes. Supports project teams by coordinating documentation timelines and deliverables. Manages translation projects and vendor communications as needed. Oversees documentation workflows through regulatory submission and p

Job Description Job Description Position Type: Contract Hybrid - Local and able to work onsite 2-3 days per week. May be more, as needed. Required: BS in Chemistry, Biology or a related scientific discipline. Scientific background, ideally pharma experience. At least 2-3 years scientific/analytical lab experience, preferably in the field of protein therapeutics or monoclonal antibody therapies. Proficient in scientific/technical writing. Experience in Empower chromatographic data system. Experience with LIMS, SAP/SRM, TrackWise, and Veeva. Excellent oral communication, interpersonal and technical writing skills. Excellent organizational skills, demonstrate attention to detail. Experience in GMP/GLP and/or a regulated industry. Strong background in Microsoft applications such as Word, Excel, and SharePoint a must. Advanced Excel knowledge is a plus. Responsibilities: Author technical reports, policies, and Standard Operating Procedures. Author/review, format, and revise reports, protoco

Technical Writer Job Category: Engineering and Technical Support Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 25% Type of Travel: Continental US * * * CACI is seeking a cleared Technical Support Analyst who will be providing writing and editing services across Intel Enablers/Mounted Systems. This position is based at Aberdeen Proving Ground, MD and is **Hybrid!** What Youll Get to Do: + Producing/Rewriting tech manual content or performing editing and formatting to ensure it passes quality checks before review and signature + Create line art (2D, isometric) from CAD renders, exploded views, to support detailed parts information and maintenance procedures + Compose and edit computer-generated flat line, isometric drawings. + Serves as command expert on technical data media innovation + Develops requirements and provides technical guidance and direction for preparation of technical publications + Assisting le

Position Summary: We are seeking an experienced Technical Writer with a strong background in defense contracting, aerospace, or other related technical fields. The ideal candidate will be responsible for creating, editing, and maintaining technical documentation that meets industry standards and supports the needs of both internal and external stakeholders. This role requires exceptional attention to detail, technical acumen, and the ability to translate complex information into clear, concise documentation. Key Responsibilities Develop, write, and edit technical documents, including user manuals, standard operating procedures, installation guides, and training materials, with a primary focus on technical reports and proposals. Collaborate with subject matter experts (SMEs), engineers, and project teams to gather and verify technical information. Create and maintain document templates and style guides to ensure consistency and compliance with industry standards and customer requirement