medical technical writer

Mizuho OSI

<p></p><div><div><div><div><div><div><b>Date: </b>Mar 31, 2026
</div></div></div></div><div><div><div><div><b>Category: </b>Marketing
</div></div></div></div><div><div><div><div><b>Location:
</b>Union City, CA, US, 94587-1234
</div></div></div></div><div><div><div><div><div><b>About Company</b></div>
<div>
Mizuho OSI is the leader in the markets for specialty surgery and patient positioning. The company&rsquo;s portfolio includes specialty surgical tables for procedure-specific approaches that improve patient outcomes in spine and orthopedic surgeries along with disposable and reusable surgical patient care products.</div><br>
<div></div>
<div><b>
Job Summary</b></div>
<div>
The Technical Writer effectively writes technical manuals, product guides and other related required documentation. The Technical Writer also oversees writing, editing, updating and authenticating technical and promotional marketing materials for all Mizuho OSI products and services. The Technical Writer ensures documentation meets all standards and/or industry requirements. The position writes and reviews technical input and documentation for both new and sustaining product development. The Technical Writer provides expertise in understanding technical language and converting those specifications into product manuals or guides that will aid the user.</div><br>
<div>
</div><p><b>We are looking for you if you have the ability to:</b></p>
<ul><li>Provide creative solutions</li>
<li>Communicate well and do so in an organized and timely fashion</li>
<li>Inspire those around you with your vision and creativity</li>
<li>Work with a dynamic team to shape the future of our business</li>
<li>Partner with cross-functional departments to identify opportunities for improvement</li></ul><br>
<div></div>
<div><b>
Responsibilities:</b></div>
<ul>
<li>Write technical materials including but not limited to equipment manuals, product guides, operating and maintenance instructions, and other Marketing communication, as assigned.</li>
<li>Convert complex technical content into clear, concise, easily readable text or tables, charts, and graphics that focus on end-user needs.</li>
<li>Collaborate cross-functionally between marketing, engineering, regulatory teams, and others as appropriate, to create and update content in a timely manner to meet project needs.</li>
<li>Ensure that written content facilitates translation into multiple languages, checking for clarity, conciseness, consistency, and removing jargon or idioms.</li>
<li>Work with and manage vendors, including translation services, and graphics or creative services, as needed.</li>
<li>Ensure documents adhere to company&rsquo;s content and layout guidelines and meets company&rsquo;s graphic standards.</li>
<li>Maintain current technical product knowledge for new and existing products.</li>
<li>Analyze existing content to determine need for revisions in previously published materials.</li>
</ul><ul><li>Collaborate with the regulatory team to ensure compliance with all regulatory agency requirements and other applicable standards and regulations for labeling and publications.
</li></ul><ul><li>Ensure that the company website is up to date on all technical specifications for all products.</li>
<li>Train and instruct other members of the department and the company by passing along skills and information to assist them in their development and advancement, either with one-on-one or with platform training skills, as applicable.</li>
<li>Perform independently, as well as in a team environment, to analyze problems and formulate plans to overcome challenges and to get work done quickly with a high degree of quality.
</li><li>Make sound and logical decisions and choose the appropriate courses of action based on the available information.
</li><li>Continue to improve the Company and the Marketing department through personal action and by contributing ideas to support both the Department and Company&rsquo;s ongoing improvement efforts.</li>
<li>Understand Mizuho OSI&rsquo;s business objectives and the relationship between the Marketing Department and those objectives to support and follow the Corporate Vision, Mission &amp; Values Statements, to maintain the services and quality levels set by Mizuho OSI, and to continually enable Mizuho OSI to be a great place to work.</li>
<li>Understand, follow, and support Mizuho OSI&rsquo;s internal Quality System policies, procedures and work instructions including but not limited to applicable external regulations (21 Code of Federal Regulations Part 820 Quality System Regulations and applicable International Standards).</li></ul><br>
<div></div>
<div><b>
Qualifications &amp; Requirements:</b></div>
<ul>
<li><b>Requires 5-6 years of related experience; minimum of three years Medical Device experience.</b></li>
<li><b>BS/BA Degree or equivalent combination of education and experience.</b></li>
<li>Ability to decipher highly technical information and convert into content optimized for end user; skilled at organizing information into a clear, concise written form.</li>
<li>Excellent writing, editing, and proofreading skills.</li>
<li>Proficiency with DITA, Adobe Acrobat, FrameMaker, and InDesign, and Microsoft Office Suite.</li>
<li>Experience with Adobe Illustrator, Photoshop, Oxygen, and content management systems preferred.</li>
<li>Experience in a Quality Control environment; knowledge of ISO standards.</li>
<li>Ability to demonstrate strong analytical skills.</li>
<li>Ability to work independently to establish and accomplish goals and to be a positive and productive team member.</li>
<li>Detail oriented with the ability to learn new concepts and apply them quickly.</li>
<li>Excellent customer focus with a high sense of urgency.</li>
<li>Ability to provide excellent interpersonal and communication skills.</li>
<li>Ability to communicate effectively in English with employees and other business contacts in a courteous and professional manner (additional languages a plus).</li>
<li>Ability to function calmly in a fast-paced environment.</li>
<li>Ability to manage multiple projects and meet tight deadlines.</li>
<li>Flexibility in managing and reprioritizing projects based on shifting deadlines and proposing working solutions where conflicting priorities exist.</li>
<li>Respond sensitively to the needs and feelings of others regardless of position; accept interpersonal differences, maintain rapport, and interact effectively with all levels of employees within the organization.</li></ul><br>
<p></p>
<p>
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</p><br>
<p></p>
<p><i>
Pay Scale: $104,000- $125,000 DOE + potential annual bonus + comprehensive benefits</i></p><br>
<div></div>
</div></div></div></div><div><div><p><br>
<b>EOE STATEMENT</b><br>
<br>
Mizuho OSI is an Equal Opportunity Employer and makes business decisions based on job related criteria only. Company policy prohibits unlawful discrimination based on race, color, religious creed, gender, religion, marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition including genetic characteristics, sexual orientation, sexual identity, or any other consideration made unlawful by federal, state or local laws.</p>
<p>Mizuho OSI conducts criminal conviction background checks and drug screening through a third-party screening vendor which includes searches of address history, criminal convictions, court records, education verification, employment verification, and reference checks. In addition, depending on the nature of the position for which you are applying, a motor vehicle driving report, a credit report, and/or ID checks in other non-U.S. countries are also included.</p>
<p>Criminal conviction background checks will run after an applicant has received and accepted a conditional offer of employment. After a conditional offer is made and before any background check is performed, applicants will receive background check disclosure and consent forms under state and federal laws, such as the Fair Credit Reporting Act and the Investigative Consumer Reporting Agencies Act. Existence of a criminal record is not an automatic bar to employment. An assessment will be made about whether the conviction has a direct and adverse relationship to the job in question. No job offer will be withdrawn, and no adverse action will be taken against any employee, based on the results of a criminal conviction background check, without an individualized assessment of whether the applicant&rsquo;s conviction history has direct and adverse relationship with the specific duties of the job in question.</p>
</div></div></div><div><div><div><div><b>Top Reasons To Join The Mizuho OSI Team</b><br>
<br>
<ul><li>Privately held company with a tradition of market leadership and best-in-class innovation</li><li>Fast-paced entrepreneurial culture focused on dramatically improving patient outcomes through personal empowerment</li><li>Emphasis on continuous improvement and celebration of our values of R.E.S.P.E.C.T. and the Mizuho OSI Way.</li><li>Create innovative solutions designed and manufactured at our HQ in Northern California</li></ul>
<br>
<b>The Mizuho OSI Way</b><br>
<br>
In 1978, we set out to change the way patients undergo surgery. As a Mizuho OSI customer, you can expect our commitment to the following&hellip;<br>
<ul><li>We commit to your satisfaction. If you are dissatisfied, we will strive to make it right.</li><li>We do things the right way. We commit to hire people with competence, generosity and a caring attitude.</li><li>We motivate our employees to use their individual strengths to provide creative solutions, changes, and innovations.</li><li>We anticipate your needs through customer experiences, thus nurturing our relationships.</li></ul>
<br>
Collectively, this creates an environment that enables and inspires healthcare professionals to improve the lives of patients.<br>
<b><i>Dare to go further. Care to do more.</i></b></div>
<p><b>BENEFITS</b></p>
<p>At Mizuho OSI, we believe better solutions and decisions are born of diversity and are proudly an EEO/AA employer. We offer a comprehensive benefits package that includes: medical, dental, vision, life insurance, 401k with matching, educational assistance and more.</p>
<p><b>FOR OUR SERVICE MEMBERS AND VETERANS</b></p>
<p>Mizuho OSI values the service Veterans and their family members have given to our country and we support the hiring of returning Service Members and military spouses. If you are a Veteran or wounded warrior and would like assistance with the employment process at Mizuho OSI, please contact HR at (510) 429-1500.</p>
<p><b>FOR PERSONS WITH DISABILITIES</b></p>
<p>If you are a person with a disability or a disabled Veteran and are applying for a job with Mizuho OSI, we would like to ensure your application process goes as smoothly as possible. If you need additional assistance, information or answers to your questions, feel free to contact HR at (510) 429-1500.</p></div></div></div></div><p></p>

Technical Writer

Sanofi

<div><p><b>Work Schedule: </b>Mon-Fri; 9am-5pm ET (20-40 hours per week)</p><p><b>
Location: </b>100% Remote</p><div><b>
Contract Length:</b> 12-months<br>
<br>
Sanofi's contingent workforce program, FLEXT Direct, is seeking a Part Time Medical Writer II for a 12-month contract.<br>
<br>
Job Summary:<br>
We are seeking a detail-oriented and innovative professional to join our team in creating accurate, engaging, and compliant digital content for diverse promotional channels within the healthcare sector. This position focuses on developing high-quality marketing materials that resonate with target audiences while maintaining strict adherence to regulatory standards. The successful candidate will collaborate closely with marketing teams and leverage cutting-edge AI-driven tools to streamline content development processes. This role offers the opportunity to work at the intersection of healthcare communications, digital marketing, and emerging technologies, making a meaningful impact on how healthcare information reaches and engages audiences across multiple platforms.<br>
<br>
Responsibilities:<br>
<ul><li>Collaborate with marketing teams to develop and refine digital copy for websites, email campaigns, social media, and other promotional channels</li><li>Adapt content from existing commercial and medical assets, ensuring clarity and alignment with brand messaging</li><li>Utilize large language models and AI tools to generate initial drafts and enhance efficiency in content creation</li><li>Review and fine-tune AI-generated content to correct inaccuracies, improve tone, and ensure compliance with regulatory standards</li><li>Verify references and source materials to maintain accuracy, credibility, and adherence to healthcare regulations</li><li>Navigate the Medical, Legal, Regulatory compliance and review process effectively</li><li>Stay informed on industry trends, compliance requirements, and emerging AI technologies to optimize content strategies</li><li>Manage multiple projects simultaneously and meet deadlines in a fast-paced environment</li></ul><br>
Skills:<br>
<ul><li>Strong understanding of healthcare terminology, compliance standards, and promotional guidelines</li><li>Excellent writing, editing, and proofreading skills with exceptional attention to detail and accuracy</li><li>Familiarity with AI tools and content generation platforms</li><li>Knowledge of digital marketing strategies and SEO best practices</li><li>Understanding of FDA, EMA, or other regulatory guidelines for healthcare communications</li><li>Proficiency in content management systems and marketing automation tools</li><li>Strong collaborative and communication abilities</li></ul><br>
Experience:<br>
<ul><li>5+ years of experience in healthcare marketing, medical writing, or related roles</li></ul><br>
Qualifications:<br>
<ul><li>Bachelor's degree in Marketing, Communications, Journalism, or a related field</li></ul><br>
This is an exciting opportunity to work with a leading organization in the pharmaceutical industry while enjoying the flexibility of a fully remote position. You will be at the forefront of integrating innovative AI technologies into healthcare communications, helping to shape the future of digital marketing in this critical sector. The role offers the perfect balance of creative content development and technical innovation, allowing you to expand your expertise while contributing to meaningful healthcare initiatives that impact patients and healthcare professionals worldwide.</div></div>

Part - Time Medical Writer II (Clinical) (contract)

<div><b>Job ID</b> R-541637 <b>Date posted </b>03 April 2026
<div><h1 class="jobSectionHeader"><b>Job Description Summary</b></h1><p></p><h1 class="jobSectionHeader"><b>
Job Description</b></h1><p>
We are<b> the makers of possible</b></p><p></p><p>
BD is one of the largest global medical technology companies in the world. Advancing the world of health&trade; is our Purpose, and it&rsquo;s no small feat. It takes the imagination and passion of all of us&mdash;from design and engineering to the manufacturing and marketing of our billions of MedTech products per year&mdash;to look at the impossible and find transformative solutions that turn dreams into possibilities.</p><p></p><p>
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you&rsquo;ll be supported to learn, grow and become your best self. Become a <b>maker of possible</b> with us.</p><p></p><p>
The<b> Technical Writing Specialist </b>is responsible for developing clear, accurate, and user-friendly operator manuals and other customer-facing technical documentation for <b>Advanced Patient Monitoring devices</b>. Content is created and refined using product requirements, SME input, and device simulators to translate complex technical information into step-by-step instructions complemented by appropriate GUI images and visual workflows.</p><p></p><p><b>
This remote-based position must be within Pacific Standard Time (PST) time zone to ensure effective collaboration with cross-functional teams, including </b>periodic onsite visits to our Irvine, California office (approximately once per quarter).</p><p></p><p><b>
Key Responsibilities:</b></p><ul><li>
Develop and edit operator&rsquo;s manuals and other user facing technical documentation such as Service Manuals using technical specifications and input from project SMEs and/or Senior Technical Writers. Convert SME input into user instructions of text and images of appropriate graphical user interface (GUI) steps. SME input comes from System Engineers, Software Engineers, Regulatory Specialists, and Quality Engineers to refine content for regulatory submission and translation.</li><li>
Maintain documentation in a standard format, following established guidelines.</li><li>
Partner with team members to facilitate clarification or explanation of reference materials and technical documentation</li><li>
Review documents for style, clarity, grammar, and punctuation</li><li>
Identify and correct inconsistencies of thought, development, or organization and gain consensus with collaborators to make appropriate adjustment</li><li>
Other duties assigned by Leadership</li></ul><p></p><p><b>
Education and Experience required:</b></p><ul><li>
Bachelor&rsquo;s degree.</li><li>
2 years of relevant technical writing experience within the healthcare industry, including developing service manuals, interpreting requirements, and collaborating closely with cross functional teams to distill complex inputs into clear documentation. Skilled at filtering large volumes of technical information to identify what is essential for end users.</li><li>
Candidates must be prepared to submit writing samples demonstrating their technical writing capabilities.</li></ul><p></p><p><b>
Knowledge and Skills required:</b></p><ul><li>
Strong technical writing capability, with the ability to translate complex technical specifications into clear, precise, and user-friendly documentation under tight deadlines. Strong editing and proofreading skills ensure clarity, consistency, and accuracy across all materials.</li><li>
Highly collaborative communicator, skilled at building consensus across cross functional teams on content changes that promote consistency and content reuse. Adept at developing strong peer, departmental, and cross business relationships that support best practice sharing and team effectiveness.</li><li>
Strong stakeholder engagement, with the ability to work effectively within interdepartmental project teams and represent the organization in discussions with senior internal and external personnel on high impact, cross organizational matters.</li><li>
Advanced proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and demonstrated ability to quickly learn and adopt new software tools and technologies.</li><li>
Exceptional problem solving and critical thinking skills, with the ability to manage competing priorities and maintain high performance in fast paced environments.</li><li>
Independent and accountable work style, consistently producing high quality, accurate outputs while effectively integrating feedback and maintaining strict attention to detail.</li><li>
Excellent written and verbal communication skills, including negotiation, relationship management, and the ability to tailor complex information to diverse audiences.</li></ul><p></p><p><b>
Preferred qualifications:</b></p><ul><li>
Prior experience in the Medtech and/or medical device industry.</li><li>
Preferred prior experience interpreting and clearly deciphering clinical terminology, and translating complex scientific and clinical concepts into accessible, accurate language for clinicians, regulatory stakeholders, and FDA facing documentation.</li><li>
Degree in Stem, Science or closely related field preferred.</li><li>
Ability to produce and edit content in FrameMaker and Photoshop, with prior experience using DITA based Content Management Systems strongly preferred.</li></ul><p></p><p>
At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.</p><p></p><p>
For certain roles at BD, employment is contingent upon the Company&rsquo;s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD&rsquo;s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.</p><p></p><p><b>
Why Join Us?</b></p><p>
A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It&rsquo;s also a place where we help each other be great, we do what&rsquo;s right, we hold each other accountable, and learn and improve every day.
</p><p></p><p>To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you&rsquo;ll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place.
</p><p></p><p>To learn more about BD visit https://bd.com/careers</p><p></p><p>
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.</p><p></p><p>
Required Skills</p><p>
Optional Skills</p><p>
.</p><h1 class="jobSectionHeader"><b>
Primary Work Location</b></h1>
USA CA - Irvine Laguna Canyon<p></p><h1 class="jobSectionHeader"><b>
Additional Locations</b></h1><p></p><h1 class="jobSectionHeader"><b>
Work Shift</b></h1><p></p><p>
At BD, we are strongly committed to investing in our associates&mdash;their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You.</p><p></p><p>
Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates&rsquo; progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles.</p><p></p><p><b>
Salary Range Information</b></p></div></div><p></p>

Technical Writing Specialist

Prescient Edge

<div>Job Description:<p><br>
Prescient Edge is seeking a <b>Technical Writer/Editor</b> to support a federal government client.</p>
<p><b>Benefits:</b><br>
At <b>Prescient</b><b> Edge</b>, we believe that acting with integrity and serving our employees is the key to everyone's success. To that end, we provide employees with a best-in-class benefits package that includes:</p>
<ul><li>A competitive salary with performance bonus opportunities.</li>
<li>Comprehensive healthcare benefits, including medical, vision, dental, and orthodontia coverage.</li>
<li>A substantial retirement plan with no vesting schedule.</li>
<li>Career development opportunities, including on-the-job training, tuition reimbursement, and networking.</li>
<li>A positive work environment where employees are respected, supported, and engaged.</li>
</ul>
<p><b>Position Overview</b></p>
<p>We are seeking a meticulous and experienced Technical Writer/Editor to support a U.S. Navy program. The successful candidate will be responsible for developing, writing, editing, and managing a wide range of technical documentation for complex naval systems. You will work closely with engineers, subject matter experts (SMEs), and program personnel to ensure all documentation is clear, accurate, and compliant with all applicable Department of War (DoW) and Navy specifications.</p><br>
<p></p>
<p>The Technical Writer/Editor will work closely with Government security personnel, program leadership, and contractor team members to ensure compliance with security requirements while enabling mission execution. The Technical Writer/Editor must be capable of operating independently with minimal oversight and supporting a dynamic operational environment.</p>
<p><b>Key Responsibilities</b></p>
<p>The Technical Writer shall be capable of performing the following functions with minimal guidance:</p>
<div><ul><li>Document Creation &amp; Editing: Author, edit, and proofread technical documents including system manuals, operator guides, maintenance procedures, test plans, technical specifications, and training materials.</li></ul>
<ul><li>Compliance &amp; Standards: Ensure all documentation adheres to stringent military standards and program-specific style guides.</li></ul>
<ul><li>SME Collaboration: Proactively collaborate with engineering teams, technicians, and program management to gather and translate complex technical information into clear, concise, and accurate content for the intended audience.</li></ul>
<ul><li>Document Management: Manage the entire document lifecycle, including version control, review cycles, and archival, utilizing Microsoft Teams and CMPro.</li></ul>
<ul><li>Quality Assurance: Perform final quality assurance checks on all documents to ensure they are free of grammatical errors, technically accurate, and formatted correctly before delivery.</li></ul></div><br>
<br>
<br>
<b>Job Requirements:</b><p><b><br>
Qualifications &amp; Requirements</b></p>
<ul><li>Must be able to obtain and maintain a DoD Secret security clearance.
</li><li>Demonstrated experience as Technical Writer/Editor or similar role</li>
<li>Bachelor&rsquo;s degree in Technical Communication, English, Journalism, or a related technical field.</li>
<li>Minimum of [3-5] years of professional experience as a technical writer or editor.</li>
<li>Demonstrated experience working within a DoW, aerospace, hydrography, or defense contractor environment.</li>
<li>Ability to operate independently in an OCONUS environment</li>
<li>Strong organizational, communication, and problem-solving skills</li>
<li>Ability to manage multiple priorities in a fast-paced operational setting</li>
<li>Strong skills in the following:
<ul><li>Exceptional writing, editing, and proofreading skills with a strong command of English grammar and style.</li>
<li>Proven ability to understand and interpret complex technical concepts, engineering drawings, and schematics.</li>
<li>High proficiency with Microsoft Office Suite (Word, PowerPoint, Excel, Teams) and Adobe Acrobat.</li>
</ul></li></ul><p><b>Preferred Qualifications</b></p>
<ul><li>Prior experience supporting U.S. Navy or DoD programs</li>
<li>Experience in deployed or OCONUS environments</li>
</ul>
<p><b>Additional Requirements</b></p>
<ul><li>Limited travel (&lt;10%) as required by mission needs</li>
</ul>
<p><b>Location</b></p>
<ul><li>Panama City Beach, FL (remote position potential for qualified candidates)</li>
</ul>
<p><b>Security Clearance</b></p>
<ul><li>Secret (or ability to obtain)</li></ul></div><p></p>

Technical Writer/Editor

JHS PROFESSIONALS

<p><b>JHS Professionals Is Hiring &ndash; Healthcare Content Writer (Medical Billing)</b></p><p><b>Location: Gulberg Greens, Islamabad</b><br/><b>Job Type: Full-time (On-site)</b><br/><b>Shift Timing: Night Only</b><br/><b>Work Location: In person</b></p><p>We are seeking a highly skilled <b>Healthcare B2B Content Writer</b> with extensive expertise in <b>Medical Billing and Revenue Cycle Management (RCM)</b>.</p><p><b>Key Responsibilities</b></p><ul><li>Produce high-quality, human-centric articles, guides, and whitepapers on complex RCM topics</li><li>Translate dense financial and regulatory jargon into engaging, readable content</li><li>Conduct independent research on CMS updates, reimbursement trends, and billing compliance</li><li>Create E-E-A-T optimized and semantically rich content to establish industry thought leadership</li></ul><p><b>What We Are Looking For</b></p><p>✔ Minimum 1-2 years of experience in medical billing, or healthcare tech content writing<br/>✔ Strong ability to simplify complex billing workflows without losing accuracy<br/>✔ Human-first writing approach (no AI-generated filler content)<br/>✔ Deep SEO knowledge with focus on search intent and compliance accuracy</p><p><b>Perks &amp; Benefits</b></p><ul><li>Medical coverage</li><li>Probation &amp; annual increments</li><li>Performance &amp; punctuality bonuses</li><li>Food Allowance</li><li>U.S. federal holidays</li><li>Work-life balance initiatives</li><li>Accommodation provided</li><li>Porivdent Fund</li></ul><p><b>Why Join Us?</b></p><ul><li>Work with a team that understands the technical depth of your content</li><li>Build real industry authority not just content volume</li><li>Competitive compensation for specialized expertise</li></ul><p>Send your CV to:<br/>hr@jhsprofessionals.com</p><p>Start your Healthcare Content Writer Jounery with #TeamJHS -Apply now and grow with us!</p><p>Work Location: In person</p>

Healthcare Content Writer

Joint Relief Institute

<div><div><b>About Us</b></div>
<div>At the Joint Relief Institute, our mission is to improve the quality of life for people dealing with joint pain. Our medical clinic specializes in treating knee and joint pain, focusing on large joint pain relief with a minimally invasive approach called viscosupplementation. We strive to significantly impact our community and support each other in our collective pursuit of wellness. We believe that every role within our team contributes immensely to our success and the well-being of our patients.</div><br>
<div></div>
<div><b>Practice Philosophy:</b></div>
<div>Joint Relief Institute offers a very friendly and happy work environment and leads the healthcare market in the field. We are expanding and looking for a team player to grow with us. We understand the importance of a positive workplace environment and ensure this by promoting and encouraging our core values of honesty, teamwork, compassion, growth, and ownership.</div><br>
<div></div>
<div><b>About the Role</b></div>
<div>We are seeking an outgoing and compassionate receptionist to join our team. As a receptionist, you will play a crucial role as the face of the office! You will work in tandem with our administrative and clinical staff to deliver the best experience to our patients. We are looking for someone with a positive and energetic attitude who genuinely cares about our patients and team members. If you want to make a difference in the lives of patients with joint pain and arthritis, we encourage you to apply for this exciting opportunity at Joint Relief Institute.</div><br>
<div></div>
<div><b>Location: Joint Relief Insitute</b></div>
<div><b>Job Type: Full-time</b></div>
<div><b>Pay: $15.00 - $17.00 per hour (dependent on experience)</b></div><br>
<div></div>
<div><b>Responsibilities:</b></div><br>
<ul>
<li><br>
Scanning papers and documents and uploading them to practice EMR or wherever appropriate.</li>
<li>Checking in patients and greeting them in a warm and welcoming manner.</li>
<li><br>
Making patient appointments.</li>
<li><br>
Collecting copays.</li>
<li><br>
Tracking wait time in the waiting area.</li>
<li><br>
Maintaining a clean lobby that is stocked with essentials for our patients.</li>
<li><br>
Data entry of patient demographics and proper documentation in practice EMR.</li>
<li>Supporting the office with all other administrative duties.</li></ul><br>
<div>
</div><div><b>Qualifications:</b></div>
<ul><li>High school diploma or GED.</li>
<li><br>
Proven customer service experience.</li>
<li><br>
Effective communication and e<br>
levated attention to detail.</li>
<li>Comprehension of MS Office, with working knowledge of healthcare management systems, Microsoft Suite, and Google Suite products.</li>
<li>Bi-lingual (Spanish) is a plus!</li></ul><br>
<div>
</div><div><b>Benefits:</b></div>
<ul><li>Paid Time Off</li>
<li>Paid Sick Time</li>
<li>Paid Holidays</li>
<li>Paid Bereavement</li>
<li>Bonus Eligibility</li>
<li>Insurance Options:
<ul><li>Medical</li>
<li>Supplemental Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>Life</li>
</ul></li><li>NO WEEKENDS!</li></ul><br>
<div>
</div><div><b>Join Us</b></div>
<div>We believe that diverse, inclusive teams make our organization a more innovative and vibrant place. We encourage people from all walks of life to apply. If you have the skills and passion needed for this role, please apply!</div><br>
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<div>The Joint Relief Institute is an Equal Opportunity Employer. We do not discriminate based on race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.</div><br>
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<div><b>How to Apply</b></div>
<div>Interested applicants should submit their resume and a cover letter detailing their relevant experience and why they are interested in the role. The application period will close once the right candidate has been found. If you are enthusiastic about joining an organization that prioritizes teamwork, compassion, and excellence, submit your application today. We look forward to hearing from you!</div><br>
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<div><b><i>Compliance consent is required for all roles at Joint Relief Institute.</i></b></div></div>

Medical Technician and Scribe

Lincoln Electric

<div><div><div><div><div><p>Technical Writer
</p></div></div></div></div><div></div><div><div><div><div><div>Lincoln Electric is a high-performance industrial machinery and technology leader who helps customers manufacture and maintain vital equipment and infrastructure. Lincoln Electric&rsquo;s innovative solutions enable higher quality and productivity across a variety of processes including welding, cutting, brazing, machining, process automation, and field repair. The Company leverages proprietary technologies and expertise in materials science, power electronics, automation, and intelligent software to help customers build better and achieve resilience in their operations. Headquartered in Cleveland, Ohio, Lincoln Electric is the essential &lsquo;Linc&rsquo; that keeps the economy running. The Company operates 71 manufacturing and automation facilities across 20 countries and serves customers in over 160 countries. For more information about Lincoln Electric and its products and services, visit the Company&rsquo;s website at https://www.lincolnelectric.com.</div><br>
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Location: <b>Michigan City-North</b><br>
Req ID: <b>28785</b></div><div></div><div><br>
</div><div><div><div><div>About us</div>
</div><div><div>
Vanair&reg;, a Lincoln Electric company, has been an industry leader since 1972, working to bring our customers the very best in Mobile Power Solutions&reg;. Lincoln Electric is the world leader in the engineering, design, and manufacturing of advanced arc welding solutions, automated joining, assembly and cutting systems, plasma and oxyfuel cutting equipment, and has a leading global position in brazing and soldering alloys. We are recognized as the Welding Expert&trade;, which advances customers&rsquo; fabrication capabilities to help them build a better world.<br>
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If you like being challenged, want to be a part of something special, and desire being part of an exciting team that is always striving to be at the forefront of our industry, then we&rsquo;re looking for you &ndash; a driven and motivated new team member.</div></div></div><div><div><div>
Position Summary</div>
</div><div><div>
The Technical Writer is responsible for creating, revising, and maintaining high-quality technical documentation for Vanair&rsquo;s compressor and mobile power equipment product lines. This role works closely with engineering, manufacturing, quality, and service teams to translate complex technical information into clear, accurate, and user-friendly documentation for customers, service technicians, and internal stakeholders.</div></div></div><div><div><div>
Key Responsibilities</div>
</div><div><ul><li>Develop and maintain operator manuals, service manuals, installation guides, safety documentation, and technical bulletins.</li>
<li>Translate engineering designs, schematics, and technical specifications into clear written content.</li>
<li>Collaborate with engineering, product management, and field service teams to gather and verify technical information.</li>
<li>Edit and standardize documentation to ensure clarity, consistency, and quality.</li>
<li>Ensure documentation meets applicable safety, regulatory, and quality standards.</li>
<li>Maintain document control including revisions and change tracking.</li>
<li>Support new product launches by delivering documentation aligned with production timelines.</li>
<li>Create or coordinate diagrams, illustrations, and graphics as needed.</li>
<li>Review documentation for accuracy, grammar, and usability.</li>
</ul></div></div><div><div><div>Required Qualifications</div>
</div><div><ul><li>Bachelor&rsquo;s degree in Technical Writing, Engineering, English, Communications, or related field, or equivalent experience.</li>
<li>2+ years of experience in technical writing within a manufacturing or industrial environment.</li>
<li>Experience documenting mechanical or electromechanical systems, preferably compressors or mobile power equipment.</li>
<li>Ability to read and understand engineering drawings and specifications.</li>
<li>Strong written and verbal communication skills.</li>
<li>Proficiency with Microsoft Office and Adobe Acrobat tools.</li>
</ul></div></div><div><div><div>Preferred Qualifications</div>
</div><div><ul><li>Experience in compressor, heavy equipment, or industrial manufacturing industries.</li>
<li>Familiarity with document control systems or PLM platforms.</li>
<li>Understanding of safety and regulatory documentation standards.</li>
<li>Basic mechanical or electrical knowledge.</li></ul></div></div></div><br>
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<p></p>
<div><b>Lincoln Electric is an Equal Opportunity Employer.</b> We are committed to promoting equal employment opportunity for applicants, without regard to their race, color, national origin, religion, sex (including pregnancy, childbirth, or related medical conditions, including, but not limited to, lactation), sexual orientation, gender identity, age, veteran status, disability, genetic information, and any other category protected by federal, state, or local law.</div><br>
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<b>Nearest Major Market: </b>Michigan City
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<b>Job Segment: </b>Technical Writer, Document Control, Welding, Field Service, Machinist, Technology, Administrative, Manufacturing</p></div>

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