Technical Writer Salary at Centerline BETA

Job Description Job Description OVERVIEW The Technical Writer is responsible for creating, managing, and maintaining clear, concise, and user-focused documentation for Passport Technology's software, hardware, and systems. This role ensures customers, employees, and stakeholders have access to accurate and helpful resources, such as user manuals, API guides, troubleshooting instructions, and training materials. Working closely with cross-functional teams, the Technical Writer bridges the gap between technical complexity and user understanding, contributing to the overall success of Passport Technology's innovative products. DUTIES AND RESPONSIBILITIES Key Responsibilities: • Develop and maintain high-quality documentation, including user manuals, API references, installation guides, and internal knowledge bases for Passport Technology's products. • Collaborate with engineering, product development, and quality assurance teams to gather and verify technical information. • Research and t

BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Contract Technical Writer to work for a leading Greater Orange County area contract development and manufacturing organization. Salary: $75k-85K/yr. Contract: 3+ months Summary: Responsible for writing a variety of technical documents.Deviations, SOP’s, Protocols, Batch Record creations, Process observations and documentation, reports, procedures, forms, work instructions, drawings, specifications that are used in a cGMP production environment. Responsibilities Ensure compliance with GMP, ISO 90001, regulatory requirements, dept/bldg. Safety rules and applicable company policies and procedures Support cross functional teams by providing technical writing of required documents in a timely and accurate manner. Support departments cross functionally for their departmental technical writing needs. Manufacturing, QA, QC, Engineering, Project

Company Description Jobs for Humanity is collaborating with Upwardly Global and with Unclassified to build an inclusive and just employment ecosystem. We support individuals coming from all walks of life. Company Name: Unclassified Job Description Job Description: Alignerr.com is a community of subject matter experts from several disciplines who align AI models by creating high-quality data in their field of expertise to build the future of Generative AI. Alignerr is operated by Labelbox. Labelbox is the leading data-centric AI platform for building intelligent applications. Teams looking to capitalize on the latest advances in generative AI and LLMs use the Labelbox platform to inject these systems with the right degree of human supervision and automation. Whether they are building AI products by using LLMs that require human fine-tuning, or applying AI to reduce the time associated with manually-intensive tasks like data labeling or finding business insights, Labelbox enables teams t

Seeking a highly motivated individual with late-phase CMC technical experience, including technical and regulatory submission experience. This position is part of the Process Development organization and in this role, this individual will be supporting the internal Process Development teams. In the near-term, this role will support time critical CMC Regulatory submissions. Longer-term, this individual will be embedded in technical teams within the Process Development department supporting CMC aspects of our growing pipeline projects. Responsibilities (include but are not limited to): Author and Finalize appropriate Module 3 documents and Response to Agency Questions in collaboration with Regulatory CMC and Technical Subject Matter Experts Experience in analytical method development of vector and T cell, extended characterization of vector and T cell products, awareness of ICHs and global compendial requirements governing analytical development and characterization/comparability of Adva

Source One is a consulting services company and we’re currently looking for the following individual to work as a consultant with our direct client, a global medical device manufacturer, in Lake Forrest, CA. Candidates must be available to support west coast hours with the ability to work onsite occasionally. No sponsorship or C2C Title: Technical Illustrator Location: Lake Forrest, CA Remote must be available to support west coast hours with the ability to work onsite occasionally. Contract Length: 12 months – likely to be extended w2 Rate: $42-$50 per hour Our client is looking for a technical illustrator with experience in technical illustration, image editing, CAD model illustration, and video creation to support printed and digital manuals or other guides with visual aids. An ideal candidate works with minimal supervision to create a library of reusable vector-based drawings of electromechanical hardware products as well as enhance user and service personnel comprehension of both

Company Description For more than 25 years, MSX International has been a dedicated partner to leading automotive brands around the world. We support them in transforming their businesses and in managing their operations across the areas of Customer Experience, Repair Optimization, Learning and Insights. We focus on helping our clients generate more value for their customers. With over 5,000 employees based in more than 80 countries worldwide, our teams provide industry-leading expertise. We have combined our deep industry expertise with cutting-edge technology solutions to help our automotive clients increase revenue and reduce costs, while enhancing operational efficiency and improving customer satisfaction. Our goal is to help our customers reach their full potential and to excel as their global partner of choice. Job Description Currently seeking a professional Technical Writer to join the expanding Engineering team. The successful applicant will be responsible for creating, confirm

Job ID: 25-08218 Title: CMC Technical Writer Location: Santa Monica, CA , Onsite Duration: 7 Months Assignment Responsibilities (include but are not limited to): •Author and Finalize appropriate Module 3 documents and Response to Agency Questions in collaboration with Regulatory CMC and Technical Subject Matter Experts •Experience in analytical method development of vector and T cell, extended characterization of vector and T cell products, awareness of ICHs and global compendial requirements governing analytical development and characterization/comparability of Advanced Therapy Medicinal Products and vector intermediates. Requirements: •Bachelor's, Master's Degree, or PhD in Biochemical Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, Biology, Biochemistry or equivalent with 7+ years (Bachelors), 5+ years (Masters), 3+ years (PhD) of relevant experience •Experience CMC/Module 3 regulatory submissions •Experience in technical writing and proficient in high qual

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A