22 jobs found
- We are looking for a sharp technical writer to bolster our growing documentation team. Our software, used by medical professionals across the country, is becoming increasingly complex, and we need someone who can translate intricate processes into simple, easy-to-understand user guides, API documentation, and troubleshooting manuals. As our technical writer in Minneapolis, you'll be instrumental in improving user experience and reducing support requests. **Responsibilities Include:** * Authoring, editing, and maintaining technical documentation, including user manuals, API guides, and release notes. * Collaborating with software engineers, product managers, and support teams to understand product functionality and translate it into clear, concise documentation. * Conducting thorough research on technical topics to ensure accuracy and completeness of documentation. * Creating diagrams, illustrations, and other visual aids to enhance understanding. * Ensuring documentation is consistent with company branding and style guidelines. * Managing documentation repositories and version control. * Identifying and addressing gaps in existing documentation. * Participating in documentation review cycles and incorporating feedback. * Staying up-to-date with industry trends in technical communication. * Optimizing documentation for search engine discoverability. **Skill Cultivation & Background:** * A minimum of 3 years of professional journey as a technical writer or similar role. * Superb writing, editing, and proofreading proficiencies. * Familiarity with software development lifecycles and agile methodologies. * Hands-on expertise with documentation tools, such as MadCap Flare, Confluence, or similar. * Practical knowledge of API documentation and related technologies (REST, JSON). * Working history with version control systems (Git). * Capacity to comprehend complex technical concepts and translate them into understandable language. * Intellectual foundation: Bachelor’s degree in technical communication, English, computer science, or a related field. * Bonus: Skill cultivation with video creation and editing. **What We Bring to the Table:** As a rapidly expanding software company deeply embedded in Minneapolis's growing tech sector, we believe in offering a robust and comprehensive compensation package. We provide competitive pay commensurate with experience and proficiency. Besides that, we believe in an inclusive culture fostering growth: * Health insurance: Comprehensive medical, dental, and vision plans available from day one. * Time Off: Generous paid time off policy, encompassing vacation, sick leave, and personal days. * Learning fund: budget for conferences and courses. * 401(k) plan: Contribute to our company supported 401k * Company events: Regular team-building activities and social events in Minneapolis. * Public transport benefits: For onsite workers, we offer a monthly metro pass. * Onsite Perks (if applicable): free coffee from a local Minneapolis roasterMinneapolis, MNOn-site, RemoteFull-time$70,000 - $90,000 per yearTechnical, Medical25 days ago
- Are you a detail-oriented wordsmith with a passion for both science and clear communication? Our Santa Ana-based medical device company seeks a contract medical writer to produce high-quality documentation and marketing materials. **Your Mission:** As a contractor, your main objective will be to create compelling and precise product descriptions for our catalog and online presence. You'll transform technical specs into accessible, benefit-driven copy that resonates with healthcare professionals and potential customers. Your writings will be part of a comprehensive suite of marketing collateral. **Responsibilities Will Include:** 1. Authoring original, technically accurate product descriptions and related marketing assets, incorporating essential terminology and clinical evidence where applicable. 2. Collaborating with engineers, product managers, and marketing professionals to ensure comprehensive product coverage and strategic messaging alignment. 3. Researching relevant literature, regulatory guidance, and competitive analyses to ensure accuracy and originality. 4. Maintaining quality control through rigorous self-editing and review of colleagues' work. 5. Adhering to internal style guidelines and best practices for medical communications. 6. Revising text in response to feedback from regulatory affairs, legal, and marketing teams. **The Artistic Profile We're Looking For:** * Previous involvement in writing and editing product descriptions for medical devices, healthcare software, or pharmaceuticals. * Comprehensive knowledge of medical terminology, anatomy, and physiological processes. * The capability of conducting in-depth background research of products. * An educational journey that has concluded with a degree in a relevant field, such as life sciences, journalism, or communications. * Experience and insight to effectively prioritize and manage multiple projects while adhering to challenging deadlines. * An aptitude for adapting writing styles and tone to reach different target audiences and align with the overall brand voice. * Expert-level mastery of grammar, punctuation, and spelling. **Benefits Package for the Independent Contractor:** We value your contributions and are committed to providing you with the necessary tools for project accomplishment. Because this position is a contract arrangement, you will have control over your work schedule. Furthermore, we are committed to compensating you for hours worked and all costs related to travel that must be completed as requested. **Our Santa Ana Based Company Vibe:** We're a passionate group dedicated to providing healthcare professional with best-in-class devices and products. Join our team of creators in Santa Ana to develop and build a better healthcare sector. Let's improve our presence with some amazing writing.Santa Ana, CAOn-siteContractor$45 - $60 per hourMedical Writing, Product Descriptions26 days ago
- Join our cutting-edge pharmaceutical company as a Medical Device Technical Writer in North Las Vegas, NV. This hybrid role blends the precision of technical writing with the dynamic requirements of the medical device industry. We're not just crafting documents; we're shaping user experiences and ensuring patient safety through clear, concise, and accessible technical information. **Your Daily Creations** * Author, revise, and maintain technical documentation for a range of medical devices, encompassing user manuals, installation guides, maintenance procedures, and troubleshooting guides. * Collaborate with engineers, product managers, and regulatory affairs specialists to capture the nuances of device functionality and regulatory prerequisites. * Organize and articulate complicated technical concepts into easy-to-understand language for both technical and non-technical audiences. * Ensure compliance with industry standards and regulatory guidelines (e.g., FDA, ISO) in all documentation. * Manage the documentation lifecycle, including planning, writing, editing, and version control. * Participate in usability testing to enhance the clarity and effectiveness of documentation. * Contribute to the development and refinement of our document control processes. * Proofread and edit documentation created by other team members. * Spearhead documentation updates in response to device modifications, software updates, or feedback from the field. * Craft visual aids such as diagrams, illustrations, and flowcharts to supplement written content. **Competencies That Matter** * Academic grounding in technical communication, engineering, or a closely allied discipline. * Established experience in technical writing within the medical device or pharmaceutical sectors. * Proficiency in documentation software and content management systems. * Profound understanding of regulatory necessities related to medical device documentation. * Demonstrated talent for grasping intricate technical subject matter. * Exceptional written and verbal communication prowess. * Detail-oriented work ethic with unwavering accuracy. * Team spirit combined with individual drive to satisfy deadlines. * An interest in novel medical technologies and the evolving regulatory milieu. **Rewards & Wellbeing** We deliver a competitive compensation package commensurate with expertise. Our total rewards program offers comprehensive medical, dental, and vision coverage, ample paid time off, a 401(k) plan with corporate contribution, and diverse wellness offerings. Additional benefits include professional development stipends and opportunities for career growth. **Company Culture & Perspective** We nurture a culture of cooperation, transparency, and incessant learning. Our team is united by a passion for impactful innovation and an unyielding commitment to patient-centric solutions. We celebrate originality and empower team members to push boundaries. Join us and contribute to enhancing the health and well-being of individuals globally.North Las Vegas, NVHybridFull-time$80,000 - $100,000 per yearMedical & Technical28 days ago
- Our biotech company in San Francisco is on the hunt for a meticulous and innovative Medical Writer to join our growing team. We need a highly skilled communicator who can transform complex scientific data into easily digestible content for a variety of audiences, ranging from regulatory bodies and healthcare professionals to patients and the general public. This role is essential for our company's mission to improve patient outcomes through cutting-edge therapies. This is a full-time, on-site position with opportunities for remote work. **Key Responsibilities:** * **Regulatory Writing Expertise:** Develop and maintain clinical study reports (CSRs), investigator brochures (IBs), and other regulatory documents. Ensure all materials are compliant with FDA and international guidelines. * **Publication Planning and Execution:** Participate in the planning and execution of scientific publications, including peer-reviewed articles, abstracts, and poster presentations. Collaborate with researchers and medical affairs professionals to generate high-quality publications. * **Medical Communications Content Creation:** Create a range of medical communication materials, such as slide decks, training modules, and educational resources for healthcare providers. Tailor content to meet the specific needs of different audiences. * **Literature Reviews and Data Synthesis:** Conduct thorough literature reviews and synthesize complex data from clinical trials and other sources. Translate data into clear, concise, and accurate written materials. * **Collaboration and Teamwork:** Work closely with cross-functional teams, including clinical development, medical affairs, and marketing. Contribute to the development of overall medical communication strategies. * **Maintain Current Knowledge:** Stay up-to-date with current medical literature, regulatory guidelines, and industry trends. Apply this knowledge to the development of innovative and effective medical writing solutions. * **Quality Control:** Ensure accuracy and consistency of all written materials through rigorous review and editing processes. **Essential Qualifications:** * A relevant scientific background, ideally in biology, pharmacology, or a related field. * Proven capability in crafting regulatory documents, such as clinical study reports, investigator brochures, and safety updates. * In-depth grasp of clinical trial designs, statistical analyses, and medical terminology. * Fluency in regulations concerning medical writing and publishing ethics (ICH guidelines, GPP, etc.). * Impeccable written and oral communication competencies. * A commitment to excellence, accuracy, and scrupulousness in all aspects of medical writing. **What We Offer:** * A competitive salary with performance-based bonuses. * Complete health, dental, and vision coverage. * Generous paid time off (PTO) and company holidays. * A 401(k) plan with employer matching. * Proficient growth potential within the company. * Engaging in projects and initiatives with real-world impact. * A positive, diverse, and inclusive work environment. We embrace new ideas and strive for continuous growth. If you possess a passion for medical communication and aspire to make a tangible difference in healthcare, we encourage you to apply. Your skill and dedication will play a crucial role in our mission to drive forward advancements in medicine.San Francisco, CAOn-site/RemoteFull-time/Contractor$90,000 - $130,000 per yearMedical Writingabout 1 month ago
- We're seeking a detail-oriented and highly skilled Medical Writer to join our growing team in Frisco, TX. In this hybrid role, you'll primarily be working remotely, with occasional in-office days for team collaboration and meetings. The Medical Writer will be responsible for creating accurate, informative, and engaging content related to medical devices, pharmaceuticals, and healthcare topics. Your contributions will support marketing initiatives, educational programs, and regulatory submissions. **Responsibilities of the Position** * Research and write comprehensive documents, including clinical study reports, regulatory documents, white papers, abstracts, posters, presentations, and journal articles. * Collaborate with subject matter experts, including physicians, scientists, and marketing professionals, to gather information and ensure accuracy of content. * Interpret scientific data and translate complex information into clear and concise language suitable for target audiences. * Maintain up-to-date knowledge of industry trends, regulatory guidelines, and medical advancements. * Manage multiple projects simultaneously, adhering to timelines and budget constraints. * Ensure all content is compliant with regulatory requirements and ethical guidelines. * Develop and maintain a thorough understanding of therapeutic areas and product lines. * Participate in the development of medical communication strategies. * Review and edit content for accuracy, clarity, and consistency. **What You Need to Succeed** * Advanced academic background in a scientific field such as biology, chemistry, or medicine. A Master’s degree is strongly preferred. * Proven professional journey of 3+ years of experience in medical writing, with a focus on regulatory documents. * Exceptional writing, editing, and proofreading abilities, with a keen eye for detail. * Deep understanding of medical terminology, clinical research, and statistical concepts. * Familiarity with FDA guidelines, ICH guidelines, and other relevant regulations. * Proficiency in Microsoft Office Suite and document management systems. * Excellent communication and collaboration skills, with the ability to work effectively in a team environment. * Ability to interpret complex data and present it in a clear and concise manner. * Solid organization skills and ability to manage multiple projects simultaneously. **Our Commitment to You** We provide a supportive and collaborative work environment that fosters growth and development. Benefits encompass: * Competitive base salary and performance-based incentives. * Comprehensive health, dental, and vision insurance plans. * Generous paid time off, including vacation, sick leave, and holidays. * 401(k) retirement plan with company matching contributions. * Professional development opportunities, including training programs and conference attendance. * Hybrid work arrangement offering flexibility and work-life balance. * Employee assistance program providing confidential counseling and support services. * Opportunity to work on challenging and impactful projects. * Collaborative and supportive team environment. * Company events and team-building activities.Frisco, TXRemote/HybridFull-time$70,000 - $95,000 per yearMedical Writingabout 1 month ago