Technical Writer Salary at Adelfi Llc BETA

Role: Technical Writer Location: onsite in Burbank, CA Duration: Contract can last up to 1 year Job Description: Focus> technical writer for policy procedures Tech writing, word, and formatting, Coordinating meetings with various parties. Help with running management system, clean up, standardized class titles and working with vendors. Data entry with new records. Understanding relational databases. Already have format just filling out the data.

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 Title: CMC Technical Writer Location: Santa Monica, CA - 90404 Duration: 8 Months contract with possible extension Description: We are 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

Job Title: Technical Writer - III Location: Santa Monica, CA - Remote Duration: 8 months contract PR: $60/hr to $80/hr Description: CMC TW/Technical Role 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 ve

Job Position – CMC Technical Writer Location – Santa Monica, CA 90404 Duration – O8 Months Description: 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 an

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 quality writing Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing and analytical and process development Thorough knowledge of biologics analytical and process development is essential. Cell therapy process development experience is highly desired Knowledge of product lifecycle – Product and process development, clinical trials, validation and regulatory submissions, commercial GMP manufacturing Working knowledge of regulatory requirements for biologics, pharmaceuticals and medical devices

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