Writer Salary at Swedenborg Foundation BETA

Immediate need for a talented Technical Writer. This is a 12+months contract opportunity with long-term potential and is located in Philadelphia, PA (Hybrid). Please review the job description below and contact me ASAP if you are interested. Job ID:25-63787 Pay Range: $50 - $55/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Writes and maintains robust documentation that focuses on the OTT app onboarding, development, and deployment experience (e.g., feature explanations, developer guides, API references, business requirements). Partners with Product to define documentation strategy, establish writing guidelines, and formalize operational processes. Acts as a content subject matter expert that proactively gathers information from adjacent teams about upcoming platform features and improvements. Incorporates feedback from external partners and interna

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 Title: Technical Writer Location: Exton, PA Hours/Schedule: M-F 8-5 Type: Contract, Potential for extension or conversion to permanent Responsibilities 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 as needed. Perform trending and evaluation for continuous monitoring of stability data and shelf-life extension. Use of LIMS database including protocol setup, data entry/approval, and data trending. Process invoices, purchase orders, and other agreements. Interact with finance and vendors to confirm work and adjust budget forecasts. Coordinate document review, approval, and archiving. Participate in analytical testing lab acti

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

About Us: At SHELLBACK, we believe there is a better way to provide semiconductor capital equipment. A more valuable way where customers are earned. We work for our customers and we're obsessively passionate about it, and our mission is to help achieve their goals through collaboration, trust, and transparency. Serving both traditional semiconductor fabs, as well as emerging technologies, SHELLBACK is a cost-effective single source for fully integrated equipment solutions. We are seeking a Technical Writer to document the intricate details of our product manuals, manufacturing processes and equipment operation. This role is key in ensuring that complex procedures are communicated clearly through well-crafted process documentation and user guides. This is a fully on-site position, and applicants must be located in the Coopersburg, PA area. Your Impact: The Technical Writer will work closely with engineers, manufacturing teams, and product managers to capture detailed information about n