Technical Writer - Medical Device Documentation
Philips Iberica SAU
Philips Iberica SAU is seeking a Technical Writer in Cambridge, MA, responsible for producing comprehensive documentation for patient monitoring products. This role involves developing user manuals, service guides, and adhering to strict quality templates. The ideal candidate will have at least 2 years of technical writing experience, a Bachelor's degree, and proficiency in Adobe FrameMaker. The position requires working in-person at least 3 days per week. #J-18808-Ljbffr Philips Iberica SAU
$101k - $160k
Job Title Job Description Technical Writer (Cambridge, MA) The Technical Writer plays a crucial role in producing precise and comprehensive documentation for a wide range of medical devices and solutions. This role will be responsible for creating customer-facing product...Medical deviceFull timeWork at officeWork visaRelocation package3 days per week$110k - $120k
...solutions, focused on delivering connected medical device platforms and mobile applications that... ...Requirements We need a sharp, detail-oriented Technical Writer to help engineering teams create and maintain high-quality documentation in Polarion. Write and maintain technical...Medical deviceTemporary workWork experience placementWork from homeFlexible hours- A consulting firm is seeking a Technical Writer for a long-term contract role based in Branchburg... ...and maintain high-quality labeling documents for medical products in a regulated environment.... ...in the pharmaceutical or medical device sector, along with strong skills in writing...Medical deviceLong term contractContract work
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- Contact Government Services, LLC is looking for a Senior Technical Writer based in Boston, MA. This role involves drafting and developing technical documentation for various IT projects and collaborating with project stakeholders to establish technical processes. The ideal...
$36.06 - $40.87 per hour
...Research, An Accenture Federal Services Company, in Boston, is seeking a Documentation Specialist responsible for developing various documentation products, including end-user manuals and technical documents. The role requires collaboration with team members to ensure...Hourly pay$72.8k - $127.1k
...Technology Solutions team, the Senior Technical Writer role for Medi‑Span is responsible for... ...understand customer‑facing technical documentation for a range of embedded drug data and... ...e.g., HIPAA, FDA guidelines, CE Mark/Medical Device Regulation). Follow industry best...Medical deviceWork at officeRemote work$110.39k - $151.81k
## Software Medical WriterApplylocations: US, MA, Wilmingtontime... ...R262555**About Analog Devices**Analog Devices, Inc.... ...Software Medical Writer - Medical Devices**We... ...of software lifecycle documentation for medical device... ..., engineering, or technical discipline (advanced degree...Medical devicePermanent employmentWork at officeDay shift- Technical Writer / Documentation Specialist BioPoint is currently hiring a contract Technical Writer / Documentation Specialist. Under general direction, the role involves gathering, analyzing, and interpreting technical information to compose IT and Security related processes...Contract workCurrently hiring
- ...We are seeking a Risk Assessment / Technical Documentation Specialist to support Quality Control Lab Systems in a GxP‑regulated pharmaceutical or biotech environment. This role will serve as a subject matter expert across IT systems and data integrity, ensuring solutions...Work at office3 days per week
- ...English language communication and writing skills. Bachelor's degree in engineering with 5 to 9 years of technical writing experience. Extensive knowledge of Document Development Life Cycle (DDLC), structured authoring, content reuse, and single-sourcing. Proficiency in...Local areaRemote work
- ...candidate will have a strong background in laboratory work, excellent technical documentation skills, and a commitment to safety and quality. This position will involve characterizing drug delivery devices, maintaining lab equipment, and supporting the development of...Medical device
- ...development team. In this hands-on role, you will drive advanced PCB systems design, implementing control systems and maintaining documentation through the hardware development lifecycle. Ideal candidates will have a Master's Degree in Electrical Engineering and 5-10+...Medical device
- ...Description Senior Quality Engineer - Medical Device Industry - Boston We are seeking... ..., and related procedures Provide technical guidance to Quality Control teams to improve... ...analytical, problem-solving, and documentation skills Excellent communication and...Medical deviceWork at office
$111k - $185k
...hands. Summary Of Role We are seeking a Document Control Senior Specialist who will be... ...Document Control in the pharmaceutical, medical device, or biological industries. Experience with... ...regulatory inspections. Proficient in technical writing skills. Expertise in MS office...Medical deviceLocal area3 days per week- ...sustaining engineering activities for drug delivery devices. This role involves maintaining design documentation while ensuring compliance with regulatory... ...functional teams to support the commercialization of medical devices with a focus on innovation and quality. #J...Medical device
$81.12k - $117.17k
Senior Technical Writer Employment Type: Full-Time, Experienced Department: Technology Support Skills and attributes for success: Drafting and development of technical documentation related to a variety of projects in the IT space. Work closely with project stakeholders...Full timeFlexible hours$31.83 - $63.65 per hour
...is looking for a motivated writer who is passionate about user... ...implementation and configuration documentation, and release text. You also... ...assistance developers and technical writers, engineering, and... ...which includes the following: Medical, dental, and vision...Hourly payTemporary workLocal areaFlexible hours- ...supports the pharmaceutical, biotech, and medical device industries with a proven, scientific... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and... ...bias Write and edit clinical development documents, including but not limited to, clinical...Medical deviceRemote jobWorldwide
- ...necessary.) Generate and execute life cycle documentation (FAT, SAT, IOQ, PQ) for cleaning,... ...commissioning, qualification or other technical documents, user requirement... ...within the biotech, pharmaceutical, or medical device industry. Knowledge and experience working...Medical deviceWork at officeRemote workFlexible hours
- ...Director of Regulatory Affairs in the medical device industry, you will play a pivotal role... ...(510(k)), pre-market approvals (PMA), Technical Files, and other submissions to global... ...development and maintenance of regulatory documentation, including design dossiers, technical...Medical device
$145.6k - $218.4k
...engineering activities for commercialized medical devices and drug delivery combination products. Maintain/update design history documentation, engineering records, and lifecycle... ...to implement lifecycle changes. Resolve technical issues from commercialization and post‑...Medical device$28 - $35 per hour
...Comprehensive Benefits Package: medical, dental, vision, 401K, PTO,... .... Work with, direct, and document the activities of subcontractors... ...accurate inventory of medical devices; maintain database accuracy;... ...Qualifications 2‑year degree in a technical/electronics field or...Medical deviceHourly payFor subcontractorRemote workWork from home$159k - $219k
...integral part of the Implantable Device Unit and Device Development... .... Serve as the primary technical authority with contract manufacturers... ...plans, and compliance documentation. Evaluate suppliers, manage... ...extensive experience in the medical device industry,...Medical deviceContract workTemporary workLocal area$24 - $28 per hour
...Description StemWave is a fast-growing medical device company based in Massachusetts,... ...ownership across assembly, troubleshooting, documentation, and lean initiatives, contributing to... ...High School Diploma, GED or equivalent technical degree with 1-2 years minimal...Medical deviceHourly payFull timeWork at officeFlexible hours$65k - $90k
...responsible for interfacing with medical advisory boards, economic... ...providing required order related documents (order confirmations;... ...delivery schedules Overcomes technical and business objections of prospective... ...knowledge of medical device industry. Exceptional verbal...Medical deviceRemote jobTemporary workFlexible hours$145.6k - $218.4k
...activity with drug delivery devices and combination products. You... ...processes and risk documentation associated with drug delivery... ...activities for commercialized medical devices and drug delivery combination... ...effectively. Evaluate technical issues arising during commercialization...Medical deviceSummer workFlexible hours- ...The Global Product Monitoring Vigilance Report Writer develops, establishes, and maintains quality assurance methodologies, systems, and medical device industry best practices which meet customer, regulatory, and client requirements; serves as a post‑market vigilance...Medical deviceWork at office
$18 - $20 per hour
...talented individuals interested in undertaking varied technical challenges, primarily in medical device and life science industries. Headquartered in Newark... ...making real medtech labs safer, smarter, and better documented. As a Lab Operations & Safety Intern, you'll help...Medical deviceHourly paySummer workInternshipSummer internshipWork at officeRelocation package3 days per week
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