Medical & Clinical Writer Opportunities

Job Description Job Description Job Title: Clinical Documentation Specialist (RN/LPN) – Full Time Location: On-site – Staten Island, NY | Valley Stream, NY | Margate, FL Schedule: Monday to Friday, 9:00 AM – 5:00 PM Department: Clinical Reports To: VP of Clinical Operations Company: Revival Home Health Care Position Summary: Revival Home Health Care, a certified and respected home health agency, is seeking a dedicated Clinical Documentation Specialist (RN or LPN) to join our Clinical team. This…

Job Description Summary We are seeking an experienced Data Architect to design and develop a scalable, secure, and efficient data platform. The Data Architect will be responsible for designing and implementing the data architecture platform, will work on multiple Data & Information projects in GE HealthCare as a project leader or internal consultant. The successful candidate will have a strong background in cloud computing, software architecture and implementation with a passion for technology …

Description Role – Medical Scribe Trainee Main role of the scribe is to document doctor patient encounter in a real time . Documentation for some of the best US Hospitals across multiple specialties 1.Attend all the training Modules as per the set instructions and timelines. Successfully complete the entire course and clear the performance checkpoints to attain a Client Ready status. 2.Able to go live with the assigned provider and Scribe independently. 3.The Medical Scribe Trainee drives servi…

Summary This role is strictly involved in business analysis, requirements documentation, and healthcare reference data support activities and does not involve direct access to Protected Health Information (PHI), Personally Identifiable Information (PII), or any secured or confidential client data. The work is limited to analysis of healthcare claims, reference code sets, and system configurations using governed datasets and does not include handling or processing of sensitive health or personal…

<div class="content-intro"><p><strong>Who we are </strong></p> <p>At Twilio, we’re shaping the future of communications, all from the comfort of our homes. We deliver innovative solutions to<a class="c-link" href="https://customers.twilio.com/" target="_blank" data-stringify-link="https://customers.twilio.com/" data-sk="tooltip_parent"> hundreds of thousands of businesses </a>and empower millions of developers worldwide to craft personalized customer experiences.</p> <p>Our dedication to <a class="c-link" href="https://www.twilio.com/en-us/blog/open-work" target="_blank" data-stringify-link="https://www.twilio.com/en-us/blog/open-work" data-sk="tooltip_parent">remote-first work</a>, and strong culture of connection and global inclusion means that no matter your location, you’re part of a vibrant team with diverse experiences making a global impact each day. As we continue to revolutionize how the world interacts, we’re acquiring new skills and experiences that make work feel truly rewarding. Your career at Twilio is in your hands.<br><span style="color: rgb(255, 255, 255);">.</span></p> <p><strong>Hiring and how we work</strong></p> <p>We use Artificial Intelligence (AI) to help make our hiring process efficient. That said, every hiring decision is made by real Twilions! </p> <p>Also, while we are a remote-first company, you may be asked to report in person on an ad-hoc basis for team gatherings, functional off-sites or customer meetings. <br><span style="color: rgb(255, 255, 255);">.</span></p></div><p><strong>See yourself at Twilio</strong></p> <p>Join the team as Twilio’s next Senior Learning Experience Designer.</p> <p><strong>About the job</strong></p> <p>This position is needed within our Learning Experience Design team which is the engine that helps our GTM organization achieve their revenue goals. We are seeking an innovative Senior Learning Experience Designer to revolutionize how our global sales team learns, adapts, and executes. In this role, you will bridge instructional design, sales effectiveness, strategic priorities, and cutting-edge artificial intelligence. You won't just create training modules—you will design high-impact, AI-enhanced learning journeys, a range of modalities to match the sellers’ needs, interactive simulations, and performance support tools that shorten ramp times and drive revenue.<br>The ideal candidate is an agile instructional designer who actively tests, adopts, and masters modern AI design tools (generative text, AI video, code blocks, voice synthesis, automated assessments, and interactive simulation builders) to multiply design output quality and speed.</p> <p><strong>Responsibilities</strong></p> <p>In this role, you’ll:</p> <ul> <li> Leverage AI authoring tools, large language models (LLMs), and prompt engineering to rapidly draft, iterate, and refine learning materials, roleplay scenarios, pitch guides, and sessions.</li> <li>Build AI-driven roleplay simulations (e.g. objection-handling exercises, discovery calls, uncovering use case exercise, etc.)  where sales reps can practice realistic customer conversations with generative AI personas.</li> <li>Develop content into enablement that is driven by adult learning theory; enablement modalities are selected based on what best supports the seller. </li> <li>Collaborate with Sales Leadership, Product Marketing, and Revenue Operations to map learning pathways directly to seller competencies, product launches, and strategic sales methodologies </li> <li>Design just-in-time performance support assets (FAQs, Playbooks) integrated directly into seller workflows (CRM, Slack/Teams, Sales Engagement platforms).</li> <li>Transform complex product specifications and market insights/positioning frameworks into easily digestible, highly actionable learning experiences.</li> <li>Design dynamic, personalized learning paths based on rep tenure, role (AE, SE, SDR, DSR, etc)), performance data, and skill gaps.</li> <li>Implement AI-based automated feedback loops that evaluate sales reps' video pitches, call recordings, and written communications.</li> <li>Continually research, test, and integrate emerging AI tools and software into the enablement tech stack to accelerate enablement development cycles, increase outcome quality, and increase enablement impact.</li> <li>Establish guidelines, prompt libraries, and best practices for the team's ethical and effective use of AI design tools.</li> <li>Monitor learning metrics, tool adoption, sales ramp time, and quota attainment to continually optimize enablement programs.</li> </ul> <p><strong>Qualifications </strong></p> <p>Twilio values diverse experiences from all kinds of industries, and we encourage everyone who meets the required qualifications to apply. If your career is just starting or hasn't followed a traditional path, don't let that stop you from considering Twilio. We are always looking for people who will bring something new to the table!</p> <p><strong>*Required:</strong></p> <ul> <li>3–5+ years of experience in instructional design, learning experience design (LXD), or sales enablement—preferably within a fast-paced B2B SaaS or technology environment.</li> <li>Expert-level mastery of prompt engineering using LLMs (ChatGPT, Claude, Gemini) for curriculum design, scenario building, and content generation.</li> <li> Intermediate level familiarity/ building with modern AI-enhanced L&D platforms, adaptive learning engines, and/or AI roleplay platforms (e.g., Gong, Articulate 360, Quantified, AI, Allego).</li> <li>Hands-on experience with tools like ElevenLabs, Artlist.Io, RiversideFM, Synthesia, HeyGen, Midjourney, DALL-E, or Runway.</li> <li>Advanced proficiency with authoring tools (e.g. Articulate Storyline/Rise, Adobe CC, Google Suite,) integrated with modern AI plugins.</li> <li>A demonstrated ability to create engaging, application-based content (we’ll want to see examples of your work!).</li> <li>Understanding of the B2B sales cycle, buyer personas, and revenue metrics.</li> <li>Early adopter mentality with a passion for experimenting with emerging tech to automate tedious tasks and maximize creative output.</li> <li>Strong copywriting and visual communication skills tailored specifically to high-performing sales audiences.  </li> </ul> <p><strong>Location</strong></p> <p>This role will be remote,<em> </em>but is not eligible to be hired in CA, CT, NJ, NY, PA, WA.</p> <p><strong>Travel </strong></p> <p>We prioritize connection and opportunities to build relationships with our customers and each other. For this role, approximately 15% travel is anticipated to help you connect in-person in a meaningful way. </p> <p><strong>What We Offer</strong></p> <p>Working at Twilio offers many benefits, including competitive pay, generous time off, ample parental and wellness leave, healthcare, a retirement savings program, and much more. Offerings vary by location.</p> <p><strong>Compensation</strong></p> <p><em>*Please note this role is open to candidates outside of California, Colorado, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington D.C., and Washington State. The information below is provided for candidates hired in those locations only.</em></p> <p>The estimated pay ranges for this role are as follows:</p> <ul> <li>Based in Colorado, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, Vermont or Washington D.C. :  106,320.00 - 132,900.00.</li> <li>Based in New York, New Jersey, Washington State, or California (outside of the San Francisco Bay area): 112,560.00 - 140,700.00.</li> <li>Based in the San Francisco Bay area, California: $125,040.00  - 156,300.00.</li> <li>This role may be eligible to participate in Twilio’s equity plan and corporate bonus plan. All roles are generally eligible for the following benefits: health care insurance, 401(k) retirement account, paid sick time, paid personal time off, paid parental leave.</li> </ul> <p>The successful candidate’s starting salary will be determined based on permissible, non-discriminatory factors such as skills, experience, and geographic location.</p> <p><strong>Application deadline information </strong></p> <p>Applications for this role are intended to be accepted until <strong>October 25th</strong> but may change based on business needs. </p> <p> </p><div class="content-conclusion"><p><strong>Twilio thinks big. Do you?</strong></p> <p>We like to solve problems, take initiative, pitch in when needed, and are always up for trying new things. That's why we seek out colleagues who embody our values — something we call <a href="https://www.twilio.com/company/values">Twilio Magic</a>. Additionally, we empower employees to build <a href="https://twilio.org/support-and-resources/impact-fund">positive change in their communities</a> by supporting their volunteering and donation efforts.</p> <p>So, if you're ready to unleash your full potential, do your best work, and be the best version of yourself, apply now! If this role isn't what you're looking for, <a href="https://www.twilio.com/company/jobs#open-positions">please consider other open positions.</a></p> <p><strong><span style="color: rgb(255, 255, 255);">.</span></strong></p> <p><strong>Stay alert to recruitment fraud</strong></p> <p>We care about your safety. Scammers sometimes impersonate Twilio recruiters through fake job postings, emails, websites, or messages. Please ensure you are engaging with an official @<a href="http://twilio.com">twilio.com</a> email address. We will never ask for payment, gift cards, cryptocurrency, or banking information during the recruiting process. We do not make job offers without a formal interview process or conduct interviews exclusively through text-based messaging apps.<br><br><span style="color: rgb(255, 255, 255);">.</span><strong> </strong></p> <p><strong>Twilio is proud to be an equal opportunity employer.</strong> We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. Additionally, Twilio participates in the E-Verify program in certain locations, as required by law.</p></div>

At Magentus, our goal is to create a healthier society through technology. We do that by delivering smart workflows that connect people, systems, and data - making care more intelligent, efficient, and accessible. Whether it’s supporting clinicians, streamlining operations, or improving patient outcomes, we’re here to make a real difference in healthcare through digital innovation.About The RoleWe're looking for a talented and detail-oriented Technical Writer to join our Product team and support our Clinical Diagnostics portfolio across APAC.Reporting to the Head of Product, Pathology APAC, you'll play a key role in shaping how our customers understand and interact with our software products. Working closely with Product Managers, Software Engineers and Subject Matter Experts, you'll create and maintain clear, accurate and user-friendly documentation that enhances the customer experience and supports successful product adoption.This is an exciting opportunity for someone who enjoys simplifying complex information, collaborating across teams and driving continuous improvement in documentation practices.Key responsibilities:Develop, maintain and improve user manuals, product documentation and release-related content.Work closely with subject matter experts, developers, software engineers and product managers to gather and validate information.Translate complex technical concepts into clear, engaging and user-friendly content for a variety of audiences.Ensure documentation is accurate, accessible, consistent and aligned with product releases.Build strong stakeholder relationships and coordinate reviews to maintain documentation quality.Identify opportunities to improve documentation processes, templates and tools.Manage competing priorities and documentation deliverables to meet key milestones and release timelines.Contribute to continuous improvement initiatives that enhance usability, efficiency and customer experience.About YouYou are a collaborative and proactive communicator with a passion for creating high-quality documentation. You enjoy working in fast-paced environments and have a strong ability to make complex information easy to understand.You’ll bring:3+ years' experience in technical writing, software documentation or content development.Experience working within technology, healthcare, pathology or clinical diagnostics environments will be highly regarded.Exceptional written communication skills with strong attention to detail, grammar and accuracy.Proven ability to translate technical information into content suitable for both technical and non-technical audiences.Experience using documentation tools such as Confluence.Familiarity with Jira or similar software development lifecycle tools.Strong organisational skills with the ability to manage multiple priorities and deadlines.A curious mindset, commitment to continuous improvement and a focus on delivering high-quality outcomes.Join Today!At Magentus, we live our values every day:One Team – We collaborate and support each otherConstant Evolution – We embrace change and keep improvingWe Care – About our people, our customers, and our impactMake A Difference – We’re here to create real, positive changeTrust – We do what we say and act with integrityWhat’s in it for you:Flexible work options to support work-life balanceLearning and development programs to grow your careerA supportive, inclusive team cultureOpportunities to work across departments and expand your skillsA purpose-driven company where your work truly mattersReady to bring your energy and organisation to a team that cares? Apply now and help us make a difference at Magentus! Show more Show less Seniority level Mid-Senior level Employment type Full-time Industries Hospitals and Health Care

Direct message the job poster from HireTalent Samarth Shrivastava Samarth Shrivastava Lead Talent Acquisition Recruiter | Senior Talent Discovery Specialist | CBAP | Driving Recruitment Success & Business Alignment 🚀Senior Conversational Designer – Voice/IVR & Dialogflow CX | RemoteAre you passionate about creating intuitive voice and conversational experiences that actually make a difference? Client is looking for a Senior Conversational Designer to help modernize and innovate customer experiences through conversational AI.What You’ll Do:Lead conversational design and support migration from legacy IVR platforms to Google Dialogflow CX / Conversational Agents.Architect complex NLU-driven voice interactions, reusable components, and conversational design systems.Analyze customer interactions to identify pain points, gaps, and opportunities for experience improvements.Partner with product, engineering, data, and operations teams to develop innovative conversational AI solutions.Define and track KPIs/OKRs while supporting ongoing optimization of voice and chatbot experiences.What You’ll Bring:Bachelor’s degree or equivalent experience with 5+ years in conversational/product design.Strong hands-on experience designing IVR, voice, and NLU-driven experiences.Experience with Google Dialogflow CX, plus exposure to Genesys Cloud, AWS Lex/Connect, or similar platforms.Familiarity with LLMs, Gemini, Vertex AI, Python-based language analysis, and conversational analytics.Strong communication skills and experience building scalable design systems with cross-functional teams.Healthcare or Medicare experience is a plus.📩 Interested? Message me or apply below! Show more Show less Seniority level Mid-Senior level Employment type Contract Industries Hospitals and Health Care and Insurance

Direct message the job poster from HireTalent Samarth Shrivastava Samarth Shrivastava Lead Talent Acquisition Recruiter | Senior Talent Discovery Specialist | CBAP | Driving Recruitment Success & Business Alignment 🚀 Senior Conversational Designer – Dialogflow CX | RemoteAre you passionate about conversational AI, customer experience, and designing smarter digital interactions? Client is looking for a Senior Conversational Designer to help transform chatbot and voice experiences through Google Cloud and next-generation AI.What You’ll Do:Lead conversational experience design and support migration to Google Dialogflow CX / Conversational Agents.Design complex NLU-driven conversation flows, reusable components, and scalable design systems.Identify opportunities to improve chatbot, IVR, and conversational experiences across customer journeys.Analyze user interactions, conduct research, identify pain points, and drive continuous improvements.Partner with Product, Engineering, Data, Operations, and Design teams to define KPIs and conversational strategy.What You’ll Bring:5+ years of experience in design strategy, product design, or conversational UX.Hands-on experience with Dialogflow CX / Conversational Agents and chatbot/voicebot design.Experience with AWS Lex/Connect, Genesys Cloud, or similar conversational platforms.Knowledge of LLMs, Gemini, Vertex AI, Python-based language analysis, or conversational analytics is a plus.Healthcare or Medicare customer experience and accessibility experience is highly valued.📍 Location: RemoteReady to design the future of conversational AI? Message me or apply below! Show more Show less Seniority level Mid-Senior level Employment type Contract Industries Hospitals and Health Care and Insurance

Hybrid Role- Minimum 50% OnsiteLocation- Warren Preferably; Manager is open to hire at Princeton Pike or Summit West.M-F Business HoursJob Description:This individual will be responsible for delivering CMC documentation (dossier and supporting documents)to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application.This role requires effective collaboration across technical functions to deliver on timelines for submissions. The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences across CTDO. The successful candidate will work effectively in cross-functional project teams to accomplish company goals.Primary Responsibilities:Co-authors/authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical, commercial, and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports.Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.Provide input and scientific oversight for content generation for module 2.3 and 3.Review and adjudicate comments, facilitates comment resolution, revises draft sections.Ensures content clarity/ consistency in messaging across dossier.Represent Tech Writing and document management in cross-functional CMC teams.Manage the logistical process and detailed timeline for scientific and regulatory content creation for clinical, commercial, and life-cycle CMC regulatory submissions and responses to health authority questions.Assist with dossier creation and system compliance for regulatory submissions.Coordinate with CMC matrix team leaders to ensure timely submissions.Support and implement continuous process improvement ideas and initiatives.Mentor and train employees on the technical writing processes.Collaborate with cross-functional team for effective logistical process and detailed timeline for scientific/ regulatory content creation for clinical, commercial, and life-cycle CMC regulatory submissions and responses to health authority questions.Assist with dossier creation and system compliance for regulatory submissions.Must possess a thorough understanding of the source documentation requirements needed for regulatory submissions and the correlation to the authoring process.Manage the logistical process and detailed timeline for authoring, review and data verification of regulatory submissions.Collaborate with external suppliers as needed for CTD content and review.Manage data verification documentation.Review and adjudicate comments in collaboration with SMEs.Train others on procedures, systems access and best practices as appropriate.Must possess a thorough understanding of the source documentation requirements needed for regulatory submissions and the correlation to the authoring process.Work independently under supervision and collaborates with other teams.Competencies & Experiences:Bachelors degree or equivalent in relevant discipline with a minimum of 2 years experience (4-7 years for senior level).Cell therapy CMC experience required.Familiarity with eCTD structure for regulatory submissions is required; BLA experience is strongly preferred.Outstanding verbal and writing communication skills, strong attention to detail, planning, organizational and negotiating skills, demonstrated ability for timely delivery.Proficiency in commonly used Microsoft Office applications (Word, Excel, SharePoint, PPT)is required.Experience with regulatory documentum software (CARA, eSub, etc) is strongly preferred along with proficiency in compliance ready standards for final publication.Experience in bio tech/pharma e2e product development required. Must be capable of working in a fast-paced changing team environment, prioritizing multiple tasks to meet filing deadlines.Take ownership of the section formatting, language check, connections to other sections / tables etc.Works independently under supervision and collaborates with other team members from scientific functions, project management, document management in cell therapy and GPS organization. Show more Show less Seniority level Mid-Senior level Employment type Contract Industries Pharmaceutical Manufacturing

AMERICAN SYSTEMS is an employee-owned federal government contractor supporting national priority programs through our strategic solutions in the areas of Information Technology, Test & Evaluation, Program Mission Support, Engineering & Analysis, and Training.ResponsibilitiesLeads development, revision, quality control, and delivery of CDRLs, maintenance manuals, technical data, test plans/reports, implementation artifacts, onboarding documentation, and transition records.Maintains documentation supporting ICS/ICD/ISA updates, configuration control, RMF evidence, customer additions, operational procedures, and Government review packages.Writes, rewrites and/or edits material for reports, manuals, briefs, proposals, instruction books, catalogs, and related technical and administrative publications.Edits manuscripts by reviewing content for completeness, accuracy and correctness of language use and revises manuscripts to meet predetermined standards of style and accuracy.Looks for inconsistencies of thought, development or organization.Confers with authors to recommend treatment of material.Reorganizes, cuts or rewrites, as necessary.May edit copy as well.Allocates print space for story text, photos, and illustrations according to space parameters and copy significance, using knowledge of layout principles.Plans the contents of publications according to the publication's style, editorial policy, and publishing requirements.Verifies facts, dates, and statistics, using standard reference sources.Oversees publication production, including artwork, layout, computer typesetting, and printing, ensuring adherence to deadlines and budget requirements.QualificationsBachelor's degree8-10 years of related work experienceActive Top Secret ClearanceUS Citizenship Pay Transparency Statement AMERICAN SYSTEMS is committed to pay transparency for our applicants and employee-owners. The salary range for this position is USD $90,000.00/Yr. - USD $130,000/Yr. Actual compensation will be determined based on several factors permitted by law. AMERICAN SYSTEMS provides for the welfare of its employees and their dependents through a comprehensive benefits program by offering healthcare benefits, paid leave, retirement plans, insurance programs, and education and training assistance. EEO Statement EEO Race/Sex/Disability Status/Veteran Status Show more Show less Seniority level Mid-Senior level Employment type Full-time Industries IT Services and IT Consulting

Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.Position SummaryWe have an opportunity for a Technical Writer. This position is responsible for collecting, organizing, formatting and authoring documents. This role will make inputs into the site inventory management system for Manufacturing activities.Shift: Monday- Friday 8:00am-5:00pmLocation: Greenville, NC100% OnsiteThe RoleWork with Subject Matter Expert (SME) to gather the information needed to create new documents or updates of existing documents (i.e. Master Batch Records and protocols) and coordinate associated change control documents Review documents with SME and Operations personnel to ensure they are accurate, executable and the formatting is consistent and harmonized Ensure the documentation database is accurate, and inputs conform to company standards Ensure and assist in making inputs to the Manufacturing Resource Planning in preparation for manufacturing events Responsible to close out help desk tickets regarding document corrections and updates Provide requested information during client and FDA audits Participate and contribute to the activities of the cross functional project development teams Participate and contribute to the continued implementation of electronic document software system Coordinate document approval across the organizationProvide lean and agile response to changing priorities in service of multiple business units for both packaging and manufacturing activities Other duties as assignedThe CandidateMinimum RequirementsRequires Bachelor’s degree in a STEM-related field with at least 1 year of relevant experience; ORRequires Associate degree in a STEM-related field with at least 2 years of relevant experience; ORRequires High school diploma or equivalent with at least 3 years of relevant industry experienceAbility to administer quality system programs and resources Familiar with GMP documentation requirements Proficient with computer systems such as Microsoft Office Word, Excel and Adobe Professional and database management software Effective presentation/communication skills, project/resource management skills Position requires the ability to occasionally lift 40 lbs unassisted, and occasionally push and pull a maximum of 100 lbs Majority of workday is performed while sitting, standing, and walking Requires the use of hands for simple grasping and fine manipulations Ability to climb, bend, stoop, twist, and have full range of motion in upper and lower extremities Occasional exposure to dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments Preferred Skill And BackgroundStrongly prefer at least one year of technical writing experienceWhy You Should Join CatalentPositive and fast-paced working environment focusing on continual improvement and innovation.Competitive Paid Time Off plus 8 paid holidays.Medical, dental, and vision benefits effective day one of employment.Tuition Reimbursement to help you finish your degree or earn a new one.Engaging site-based activities such as Music Bingo, Puppy Supply Donation Program, and seasonal events.Employee Resource Groups promoting Diversity and Inclusion.Green initiatives and community engagement programs including highway clean-up.Defined career path with annual performance reviews and growth opportunities.WellHub program promoting physical and mental wellness, including onsite fitness center.Exclusive discounts through Perkspot from over 900 merchants.Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.personal initiative. dynamic pace. meaningful work.Visit Catalent Careers to explore career opportunities.Catalent is an Equal Opportunity Employer, including disability and veterans.If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Important Security Notice to U.S. Job Seekers:Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.California Job Seekers can find our California Job Applicant Notice HERE.Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment. Show more Show less Seniority level Entry level Employment type Full-time Industries Biotechnology Research and Pharmaceutical Manufacturing

Direct message the job poster from The Lead Realty Leody Lyn Panahon Leody Lyn Panahon Accounts Management / Real Estate Company Description The Lead Realty is a multi-awarded real estate consultancy firm in the Philippines, providing thorough, transparent, and fast end-to-end services in buying, selling, leasing, and property investment. The company serves local and international clients across mid to ultra high-end markets and offers support in marketing, property management, after-sales service, bank financing, and property loan assistance. The Lead Realty partners with leading developers such as Megaworld, Rockwell Land, AyalaLand Premier, Robinsons Land Corporation, and other major real estate companies. Founded in 2017 and based in Bonifacio Global City, Taguig, the firm has grown to more than 20 brokers, agents, partners, and associates. Its track record includes multiple industry awards recognizing excellence in brokerage performance and eCommerce for home and living and property marketplaces.Role Description The Documentation Specialist is a full-time, on-site role based in Taguig. This role is responsible for preparing, organizing, and maintaining accurate documentation related to property listings, client transactions, contracts, and internal processes. The Documentation Specialist will review documents for completeness and compliance, coordinate with brokers, agents, and financial institutions, and ensure that all records are updated and securely stored. Daily tasks include data entry, document formatting, version control, and creating clear guidelines for documentation workflows. The role also involves supporting process improvements, assisting with reporting requirements, and collaborating with team members to uphold high standards of accuracy and transparency.Qualifications Strong documentation skills, including experience with Documentation and Technical Documentation in a business or real estate context.Ability to apply Clinical Documentation and Technical Writing principles to produce clear, structured, and compliant documents.Demonstrated Analytical Skills for reviewing data, identifying inconsistencies, and ensuring accuracy in records and reports.Proficiency with office productivity tools (e.g., word processing, spreadsheets, document management systems) and basic database usage.Excellent written and verbal communication skills, with strong attention to detail and organizational abilities.Ability to work on-site in Taguig, manage multiple tasks, and meet deadlines in a fast-paced, client-focused environment.Prior experience in real estate, legal, finance, or administrative documentation is an advantage.Bachelor’s degree in Business Administration, Communications, Information Management, or a related field preferred. Show more Show less Seniority level Entry level Employment type Full-time Industries Real Estate

Job TitleQuality & Training Specialist with German💡 Why Join Us?✅ Make a direct impact on service quality and business performance✅ Develop and coach employees to reach their full potential✅ Work closely with Operations, Leadership, and Client teams✅ Gain exposure to both Quality and Learning & Development functions✅ Enjoy career growth opportunities within a global organization✅ Be part of a collaborative and people-focused culture✅ Access continuous learning and professional development programs🎯 Your Impact🔍 Quality ExcellenceAs a Quality Evaluator & Trainer, you will help ensure exceptional customer experiences by driving quality standards and continuous improvement.✔ Monitor and evaluate calls, chats, and email interactions to ensure quality compliance✔ Analyze performance trends, identify gaps, and recommend improvement actions✔ Share quality insights and evaluation results with internal and client stakeholders✔ Participate in calibration sessions to drive scoring consistency and best practices✔ Maintain a strong understanding of products, services, and program requirements✔ Support quality initiatives, documentation updates, and improvement projects✔ Partner with Operations to identify key performance drivers and optimization opportunities✔ Contribute to overall business performance, operational excellence, and customer satisfaction🎓 Training & DevelopmentYou'll play a key role in developing talent and supporting employee success through engaging learning experiences.✔ Deliver impactful training sessions using modern facilitation techniques✔ Coach and support employees throughout their learning journey✔ Monitor trainee progress and provide constructive developmental feedback✔ Prepare and facilitate classroom, virtual, and hands-on learning activities✔ Partner with Operations to ensure successful transition from training to production✔ Evaluate training effectiveness and recommend improvements to learning programs✔ Support the creation and enhancement of training materials and job aids✔ Foster a culture of continuous learning and professional growth👤 What We're Looking For✅ German(C1/C2) + English C1/C2✅ Experience as a Trainer or Quality Evaluator is mandatory.✅ Strong analytical skills and attention to detail✅ Excellent organizational and time-management abilities✅ Ability to work independently and manage multiple priorities✅ Excellent communication and facilitation skills✅ Proficiency in Microsoft Office applications✅ English and/or Polish language skills considered an asset✅ Availability to work from our Katowice office - OnSite role🎁 What We Offer💰 Stable full-time employment based on an employment contract🏥 Private healthcare package (Luxmed)🎯 MyBenefit Platform And Additional Employee Benefits🛡️ Life insurance coverage📚 Access to e-learning and professional development platforms🧠 Employee Assistance Program (psychological, legal, financial, and managerial support)🌍 Free language courses🎉 Employee events, competitions, engagement initiatives, and much more Show more Show less Seniority level Mid-Senior level Employment type Full-time Industries IT Services and IT Consulting

Direct message the job poster from CTC Resourcing Solutions Anil Dahiya Anil Dahiya Senior Recruitment Consultant at CTC Resourcing Solutions Medical Writer Documentation Specialist – 7103Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking for an experienced Medical Writer Documentation Specialist to act as a subject matter expert for the quality of clinical, nonclinical, and regulatory documentation.The role ensures that key deliverables are clear, accurate, consistent, compliant, and submission-ready, supporting development programs, health authority interactions, and global regulatory submissions.This is a 2 years’ contract based in Basel area with high possibility of extension(s) or turning into a permanent role.Main Responsibilities:Review clinical, regulatory, and nonclinical documents for clarity, conciseness, consistency, completeness, alignment with source data, and compliance with internal procedures, templates, ICH guidance, and relevant health authority requirements.Ensure documents are suitable for inclusion in critical regulatory submissions, including NDA, MAA, CSR, DSUR, and IND dossiers.Partner with authors, contributors, and cross-functional stakeholders to continuously improve the quality of clinical and regulatory documents.Contribute to the development and implementation of documentation templates, guidelines, standards, and best practices.Manage collaboration with external documentation quality specialists, including work allocation, quality oversight, and timely delivery of outputs.Coach and mentor external consultants and colleagues developing expertise in documentation quality control.Support due diligence activities when required.Qualifications and Experience:Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required;Master’s degree or equivalent qualification required; a science-related discipline is preferred.At least 7-10 years of relevant experience in clinical and/or nonclinical quality assurance, medical or regulatory writing, or the editing and quality review of clinical and nonclinical documents.Strong knowledge of regulatory documentation requirements, guidelines, submission standards, and document quality expectations.Good understanding of experimental methods, research design, and statistical analysis.Ability to analyze and interpret medical data generated in clinical trials.Excellent attention to detail, accuracy, judgement, and quality orientation.Ability to work independently, manage priorities, and deliver effectively within tight timelines.Excellent communication and interpersonal skills, with confidence working across functions and with external partners.Fluency in English, additional European Languages an advantage Show more Show less Seniority level Mid-Senior level Employment type Contract Industries Pharmaceutical Manufacturing

Nevvon is hiring an Instructional Designer – eLearning ScriptsWhere the future of work meets healthcare workers - that’s where you’ll find us! We’re here to make sure vulnerable populations are treated by highly trained and motivated healthcare professionals.Our mission is to empower caregivers and agencies to provide better care by addressing daily challenges and bridging performance gaps in the workplace. Through our innovative platform, we provide on-line training that aim to improve staff recruitment and retention, save time and money for agencies, and ultimately enhance the quality of care. Love writing, learning, or training? Excited about AI? This might be the role for you. Nevvon is hiring an Instructional Designer – eLearning Scripts to join our Content team and create training for people working in health and home care.We’re looking for someone with strong instructional design and writing skills who can identify what learners need to know, decide how best to teach it, and turn it into clear, accurate, and engaging eLearning scripts. You’ll use AI throughout the process to research, develop, and refine content and find more efficient ways of working.Here’s what you’ll be focused on:Research healthcare and home care topics using AI-assisted workflows Research and analyze a wide range of training topics using AI-assisted workflows and reliable sourcesApply instructional design principles to determine what learners need to know and how best to teach itStructure training into focused lessons with clear learning goals and an effective learning flowDevelop and update e-learning scripts that turn complex information into clear, practical**, and engaging** trainingUse AI efficiently across research, analysis, structuring, drafting, and QACritically evaluate AI-generated research and content, checking accuracy and identifying gaps or weaknessesReview and QA your own work, and review and proofread other writers' scriptsBalance audience needs, accuracy, scope, runtime, required content, and style when making content decisionsCollaborate with other team members to solve problems, share feedback, and improve contentExperiment with new AI tools, prompts, and workflows and help us find better ways of workingTake ownership of your work, use your own initiative, and raise questions or issues when neededSupport other Content team projects and priorities as neededIn order to be successful in this role, you’ll need to have:Strong, natural English writing skills and the ability to make complex or nuanced topics clear, accurate, and engagingExperience developing training, educational, or instructional contentStrong analytical and research skills, with good judgment about accuracy, relevance, and what matters to the learnerMeaningful hands-on experience using AI for research, analysis, structuring, and writing with the ability to use it efficiently and critically evaluate its outputA learner-first mindset and the ability to make thoughtful decisions about content, structure, and learning flowCurious about AI and motivated to keep exploring new tools, features, and ways of workingIndependent, proactive, and accountable for the quality of your workCollaborative and comfortable giving, receiving, and acting on feedbackFlexible and adaptable, and comfortable working with changing priorities and tight deadlinesPragmatic, with the judgment to distinguish meaningful improvements from personal preferenceStrong Advantage: Knowledge of healthcare, home care, caregiving, skilled nursing, or healthcare trainingExperience writing scripts for video-based or interactive trainingExperience with digital or e-learning contentSalary Range: 32-38 CAD/hour (part-time) OR 65-70k CAD (full-time)RemoteCanada-basedFull-time preferred, with flexibility to consider part-time for the right candidateHow to Apply:Please submit your resume along with a short sample of your writing. Ideally, this will be something you’ve created for teaching, education, or training. If you don’t have a relevant sample, send us something you feel is a strong example of your writing style and voice.Candidates who move forward in the application process will be asked to complete a short practical task.Sounds interesting? Here are the next steps:Submit your resume at jobs@nevvon.com We offer a generous compensation package including competitive salary, health benefits, and professional development opportunities. We work remotely, with the option to attend our Toronto based office. Show more Show less Seniority level Entry level Employment type Full-time Industries E-Learning Providers

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.A Day in the LifeAt Medtronic, we are committed to improving healthcare through innovative medical technologies that help people live healthier lives. As a global leader in healthcare technology, our products and solutions make a meaningful difference for patients and healthcare professionals around the world.As a Commercial Training Specialist, you will design and deliver impactful technical product and sales training for the ENT Sales organisation and supporting functions across Western Europe. You will work closely with commercial, clinical, regulatory and other cross-functional stakeholders to ensure colleagues have the knowledge, skills and confidence to effectively represent, demonstrate and teach the use of our products.Primary responsibilities: Design, coordinate and deliver technical product and selling skills training for the ENT Sales organisation, including onboarding for new hires.Assess training needs and identify knowledge and skills gaps, developing targeted learning solutions to address them.Develop engaging, learner-centred training content using adult learning principles, working with subject matter experts and cross-functional partners.Keep training curricula and materials up to date in line with new technologies, clinical practices, business priorities and regulatory requirements.Manage training programmes and learner data within the Totara Learning Management System, including progress tracking, reporting and content improvements.Plan and coordinate training events, including logistics, communications, attendance and feedback, using relevant event-management tools.Collaborate with Marketing, Commercial, Clinical, Regulatory and Legal stakeholders to ensure training programmes meet business needs and applicable policies and guidelines.Lead training-related projects, manage priorities and budgets, and identify opportunities to improve learning effectiveness and introduce innovative learning technologies.Required qualifications: 3+ years of relevant experience designing, developing and delivering technical, clinical or sales training programmes.Strong presentation and communication skills, with the ability to engage and educate clinical, technical and commercial audiences.Demonstrated ability to manage multiple projects and priorities independently with limited supervision.Strong collaboration and stakeholder management skills, with the ability to influence and work effectively across functions.Analytical mindset with the ability to assess training effectiveness, learner feedback and programme performance and use insights to drive improvements.Ability to develop clear, engaging and learner-focused training materials.High level of organisation and attention to detail, particularly when coordinating regional training programmes and events.High School Diploma, Associate's Degree or Bachelor's Degree.Preferred Qualifications:Familiarity with Totara LMS or similar learning management platforms.Background in medical devices, healthcare, clinical environments or field sales/support.Exposure to clinical laboratory settings or working directly with healthcare professionals.Knowledge of adult learning principles, instructional design or learning technologies.Familiarity with event-management platforms such as Cvent.Understanding of regulatory and compliance requirements relevant to medical device training.Experience supporting training across multiple countries or international/regional teams.Physical Job RequirementsThe above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. ‌‌Recruitment Fraud AlertWe are aware of phishing scams targeting job seekers. Please keep the following in mind:Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Netherlands: 52,800.00 EUR - 79,200.00 EUR | Spain: 37,600.00 EUR - 56,400.00 EUR |The final salary within this range will be determined based on objective, job-related criteria, including relevant experience, skills and qualifications, in accordance with our compensation framework.‌This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). Show more Show less Seniority level Associate Employment type Full-time Industries Medical Equipment Manufacturing, Hospitals and Health Care, and Pharmaceutical Manufacturing

Location: NetanyaModel: OnsiteScope: Fulltime - EmployedDescription: We are looking for a full‑time Medical Writer for a multinational organizationResponsibilitiesWrite and edit clinical and regulatory documents (protocols, CSRs, IBs, summaries).Translate complex scientific data into clear, compliant content.Lead document development and review cycles across global teams.Ensure accuracy, consistency, and alignment with international regulatory standards.Manage timelines and deliver high‑quality submissions.QualificationsDegree in life sciences4+ years of medical writing experience in clinical/regulatory environmentsSolid writing and editing skills of clinical regulatory documentsExcellent scientific writing, editing, and communication skillsFamiliarity with global regulatory guidelinesProficiency in MS WordEnglish MT level - exceptional written and spoken communication Show more Show less Seniority level Mid-Senior level Employment type Full-time Industries Hospitals and Health Care

Search by KeywordSearch by LocationShow More OptionsLoading...LocationAllCountry/RegionAllJob FunctionAllLanguageAllBusiness UnitAllClearSelect How Often (in Days) To Receive An AlertSelect how often (in days) to receive an alert:Apply now »Technical AuthorDate: 6 Oct 2026Location:Bristol, GB, BS35 4GGJob Function: TechnicalBusiness Unit: Plasma TechnologyWe are excited to announce an exciting job opportunity at our Severn Beach, Bristol location! We are looking for a talented Technical Author to join our dynamic and rapidly growing global team on a permanent basis. In this role, you will create and refine highly technical documentation, prioritising content validation and review. The ideal candidate will possess exceptional written and verbal communication abilities and will collaborate effectively across various departments with diverse stakeholders. At Oxford Instruments, our commitment to our customers is paramount; this position is pivotal in ensuring the quality, accuracy, and timeliness needed to exceed our customers’ expectations.What You'll DoPublish customer manuals: Use Framemaker and Flare to create bespoke customer manuals from existing content.Develop new documentation: Develop clear and concise documentation that meets users' needs.Validate technical details: Work with engineers and technicians to ensure the technical detail is correct through observation and hands-on testing in our lab.Review written content: Peer review content written by other members of the team.Edit CAD drawings: Edit drawings and other images used throughout the documentation. Answer product queries: Work with engineers and managers to answer technical queries. Follow internal procedures: Apply our document version control and branching procedures.Health and Safety: Uphold the company's health, safety, and environmental protection standards.Be part of Team: Be part of a collaborative and inclusive work environment that values and empowers you to contribute your unique skills and perspectives. Minimum three days per week on site.What We OfferComprehensive authoring experience: Be part of the lifecycle of documentation from analysis to publishing, using modern authoring tools.Wide range of projects: Work on a range of short and long term projects for different user groups.Collaborative environment: Join a team of supportive professionals focused on our customers' experience.Professional growth: Opportunities for continuous learning and development.What We're Looking ForTechnical Expertise: Proficiency in various software development tools and languages.Problem-Solving Skills: Ability to tackle challenges head-on and find effective solutions.Customer Focus: Strong written and verbal communication skills to understand and meet customer needs.Self management: Ability to deliver content that meets agreed objectives and timescales.Team Player: Collaborative mindset to work effectively with colleagues and clients.Commitment to Safety: Adherence to health, safety, and environmental protection standards.Education/ExperienceA recognised technical authoring qualification (ISTC, NVQ, Diploma, etc.) or equivalent experience.Minimum experience of two years in a technical author role. Proficiency in using authoring software such as MadCap Flare, Framemaker or Adobe Acrobat.Experience in writing procedures for the operation and maintenance of technical products.Ideally, experience in either the semiconductor, electro-mechanical or scientific sector.Experience in CAD software is helpful.Experience in using Simplified Technical English is helpful.Familiarity with document control procedures such as branching, versioning and document review cycles.Professional Skills/ AbilitiesExcellent technical writing and proofreading skills.Excellent communication and interpersonal skills.Good technical comprehension with the ability to summarise technical detail appropriately for the audience.Meticulous attention to detail.Good time management skills with the ability to deliver to deadlines.Ability to work independency and as part of a team.Personal QualitiesA professional manner in all interactions.A problem-solving approach, remaining calm under pressure.A good team player able to demonstrate emotional intelligence and an appreciation of other people’s skills, abilities and experience.Able and willing to travel on occasions.At Oxford Instruments Plasma Technology, we provide tools for the engineering of micro- and nano-structures, with customers using our process solutions to research and produce materials and semiconductors vital for everything from medical devices and diagnostics, to electric cars and quantum computers.BenefitsIn addition to a competitive starting salary, Oxford Instruments also offers structured career development opportunities, an excellent work-life balance, private healthcare, a share incentive plan, 25 days annual leave, half-days on Fridays, a defined contribution Group Personal Pension Plan, the convenience of our on-site canteen, where you can enjoy fresh, hot meals prepared daily with a varied menu and delicious options to choose from all at subsidised prices, and a flexible benefits package that you can tailor to your requirements.Follow us at www.twitter.com/oxinst or www.facebook.com/oxinstAll qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, or disability. We encourage applications from people of all backgrounds and would ask you to get in touch if you are concerned about any barriers you feel you may be facing in your application process with us.Note to recruitment agencies: Oxford Instruments operates a Preferred Supplier List, and we do not accept unsolicited agency CVs. Please do not forward candidate details in response to this advert, or to any Oxford Instruments employees or other company locations. Oxford Instruments is not responsible for any fees related to unsolicited CVs.Apply now » Show more Show less Seniority level Entry level Employment type Full-time Industries Nanotechnology Research

We are excited to announce an exciting job opportunity at our Severn Beach, Bristol location! We are looking for a talented Technical Author to join our dynamic and rapidly growing global team on a permanent basis. In this role, you will create and refine highly technical documentation, prioritising content validation and review. The ideal candidate will possess exceptional written and verbal communication abilities and will collaborate effectively across various departments with diverse stakeholders. At Oxford Instruments, our commitment to our customers is paramount; this position is pivotal in ensuring the quality, accuracy, and timeliness needed to exceed our customers’ expectations.What You'll Do:Publish customer manuals: Use Framemaker and Flare to create bespoke customer manuals from existing content.Develop new documentation: Develop clear and concise documentation that meets users' needs.Validate technical details: Work with engineers and technicians to ensure the technical detail is correct through observation and hands-on testing in our lab.Review written content: Peer review content written by other members of the team.Edit CAD drawings: Edit drawings and other images used throughout the documentation. Answer product queries: Work with engineers and managers to answer technical queries. Follow internal procedures: Apply our document version control and branching procedures.Health and Safety: Uphold the company's health, safety, and environmental protection standards.Be part of Team: Be part of a collaborative and inclusive work environment that values and empowers you to contribute your unique skills and perspectives. Minimum three days per week on site.What We Offer:Comprehensive authoring experience: Be part of the lifecycle of documentation from analysis to publishing, using modern authoring tools.Wide range of projects: Work on a range of short and long term projects for different user groups.Collaborative environment: Join a team of supportive professionals focused on our customers' experience.Professional growth: Opportunities for continuous learning and development.What We're Looking For:Technical Expertise: Proficiency in various software development tools and languages.Problem-Solving Skills: Ability to tackle challenges head-on and find effective solutions.Customer Focus: Strong written and verbal communication skills to understand and meet customer needs.Self management: Ability to deliver content that meets agreed objectives and timescales.Team Player: Collaborative mindset to work effectively with colleagues and clients.Commitment to Safety: Adherence to health, safety, and environmental protection standards.Education/Experience:A recognised technical authoring qualification (ISTC, NVQ, Diploma, etc.) or equivalent experience.Minimum experience of two years in a technical author role. Proficiency in using authoring software such as MadCap Flare, Framemaker or Adobe Acrobat.Experience in writing procedures for the operation and maintenance of technical products.Ideally, experience in either the semiconductor, electro-mechanical or scientific sector.Experience in CAD software is helpful.Experience in using Simplified Technical English is helpful.Familiarity with document control procedures such as branching, versioning and document review cycles.Professional Skills/ Abilities:Excellent technical writing and proofreading skills.Excellent communication and interpersonal skills.Good technical comprehension with the ability to summarise technical detail appropriately for the audience.Meticulous attention to detail.Good time management skills with the ability to deliver to deadlines.Ability to work independency and as part of a team.Personal Qualities:A professional manner in all interactions.A problem-solving approach, remaining calm under pressure.A good team player able to demonstrate emotional intelligence and an appreciation of other people’s skills, abilities and experience.Able and willing to travel on occasions.At Oxford Instruments Plasma Technology, we provide tools for the engineering of micro- and nano-structures, with customers using our process solutions to research and produce materials and semiconductors vital for everything from medical devices and diagnostics, to electric cars and quantum computers.Benefits:In addition to a competitive starting salary, Oxford Instruments also offers structured career development opportunities, an excellent work-life balance, private healthcare, a share incentive plan, 25 days annual leave, half-days on Fridays, a defined contribution Group Personal Pension Plan, the convenience of our on-site canteen, where you can enjoy fresh, hot meals prepared daily with a varied menu and delicious options to choose from all at subsidised prices, and a flexible benefits package that you can tailor to your requirements.Follow us at www.twitter.com/oxinst or www.facebook.com/oxinstAll qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, or disability. We encourage applications from people of all backgrounds and would ask you to get in touch if you are concerned about any barriers you feel you may be facing in your application process with us.Note to recruitment agencies: Oxford Instruments operates a Preferred Supplier List, and we do not accept unsolicited agency CVs. Please do not forward candidate details in response to this advert, or to any Oxford Instruments employees or other company locations. Oxford Instruments is not responsible for any fees related to unsolicited CVs. Show more Show less Seniority level Entry level Employment type Full-time Industries Nanotechnology Research

What are we looking for?We’re hiring a DevRel to own our public community and create unique, engaging content. Who are you? You are hands-on: you can debug, give architecture guidance, and jump on calls when needed You are creative: you can come up with unique, engaging content You are a great communicator and presenter: you can give demos, give talks, create videos. You are product minded: you can take repeated feedback, turn it into product ideas, and build the solution. What will you lead? Public forum: You help manage, support, and grow our public community Content creation: You create high quality, short-and-long form content (blog/video/whatever you are best at) Hands-on technical help: help users build apps, debug common issues, provide fixes/workarounds, and hop on calls to unbloc Community programs: ambassadors, rewards/recognition, office hours, AMAs, hackathons Feedback loop: triage/categorize/summarize themes and feed them into roadmap decisions; build lightweight fixes for recurring issues when needed What skills do we expect you to have? Strong TypeScript (you can actually debug and advise) Strong AI skills (prompting, agent workflows, debugging AI behavior) Excellent written and verbal communication High-energy, creative, community-first Experience running/scaling an online community What are Hercules’ operating principles?Hercules’ operating principles guide how we make decisions every day. We take them very seriously. Most of them are specifically choices that we as a company unique prioritize and so can be learned on the job. However, we do specifically filter for these principles our hiring process: We move with urgency. We ship fast, iterate, and correct mistakes quickly. Our bias for action speeds our learning and delights our customers. We strive for excellence. Doing things well is in our DNA. We have good taste. We get the details right. Our outputs are exceptionally simple and self-serve. We’re proud of our work. We are hungry. We are willing to work hard and break through walls to achieve the outcomes we want. We are willing to operate at any level to get things done. We are politely relentless. Is Hercules in-office or remote?Hercules founding team works in-office in San Francisco (Kearny and Bush). We have a very strong preference for in office. We are open to remote for exceptional candidates in US time zones who would be willing/able to travel to the office regularly.What are Hercules’ benefits? Healthcare, vision, and dental User whatever AI tools you’d like (you have an unlimited AI budget) Take what you need vacation policy Daily lunches, dinners and snacks in the office We guarantee you will do the best work of your career here What’s the compensation?$80k-$180k + equity (depends on seniority, equity, and location)Originally posted on Himalayas