Technical Writer Medical Devices (100% REMOTE/NO C2C)

Our client, a US Fortune 250 company and a global Medical technology corporation serving customers in Clinical Labs, Health care research & Pharmaceutical industry, seeks an Technical Writer Medical Devices

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NOTE: THIS IS 100% REMOTE ROLE & ONLY W2 CANDIDATES (NO C2C/1099)

*** Candidate must be authorized to work in USA without requiring sponsorship ***

Position: Technical Writer Medical Devices (Job ID: 42122)

Location: San Diego CA 92121 (100% REMOTE)

Duration: 12 Months + Strong Possibility of Extension

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Job Description:

• Documents suites of products, including hardware and software user guides, installation guides, communication/service bulletins, tip sheets, product and device labels, and online documentation.
• Reviews product data, requirements, specifications, drawings, part lists, and prototypes to develop customer-facing and internal-facing documentation.
• Ensures accuracy, clarity, appropriateness, and consistency of documents; peer reviews documents developed by other writers when appropriate.
• Manages the labeling review process and prepares documents for production.
• Collaborates with quality, regulatory, clinical, marketing managers, engineers, and other subject matter experts to determine type of content and level of detail to be used in product labeling especially IFU and to suggest changes to enhance a document's readability, clarity, conciseness, and style.
• Communicates effectively with all levels of management, business units (corporate and international), and possesses a high degree of flexibility/selectivity in prioritizing business unit deliverables to meet company goals.
• Adheres to established templates and guidelines for developing product labeling (documentation).
• Manages the labeling review process and prepares documents for final production and release.
• Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements.
• Participates as required in training on regulatory issues affecting own area of work.

Qualifications

• Bachelor's degree in English, Journalism, Communications, or other liberal arts degree.
• Experience working in a regulated industry such as pharmaceuticals or medical devices.
• Extensive experience with regulatory compliance processes.
• Strong background in supporting regulatory requirements to ensure adherence to regulatory guidelines.
• Demonstrated ability to be highly collaborative with marketing, clinical, quality, and regulatory reviewers.
• Five or more years writing and editing hardware/software user guides (print and online) and other technical product documentation.
• Ability to effectively manage the delivery of prioritized tasks.
• Ability to demonstrate a high level of initiative to gather information for developing documentation.
• Ability to work independently with minimal supervision.
• Effective at thinking independently and solving problems with product core team members.
• Ability to work under compressed deadlines and must be able to deal with unresolved situations, frequent project changes, delays, or other events.
• Ability to handle multiple projects with excellent follow-up and project management skills.
• Familiarity with electro-mechanical concepts and software application usage.
• Experience in device labeling and/or packaging content development is a plus.
• Familiarity with large company engineering change control processes and Agile software development methodologies.
• Experience with Microsoft-based applications (Microsoft Office 365 )
• Minimum of two years' experience writing for online help
• Experience with SAP, Oracle, or similar enterprise resource planning (ERP) system.
• Experience in version control systems (VCS) such as, Perforce, Apache Subversion , Microsoft Team Foundation Server, or GitHub.
• Knowledge of screen capturing, photography, and image editing software such as Microsoft Paint or Adobe Photoshop .
• Skilled in both electronic and hard copy markup (Acrobat, tracked changes in Microsoft Word , standard editorial and proofreading symbols).
• Knowledge and experience with desktop publishing (DTP) software applications (MadCap Flare, Adobe FrameMaker , Adobe InDesign , Adobe Illustrator ) as applicable for technical documentation

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Bhupesh Khurana

Senior Technical Recruiter

Email:

Amerit Consulting is an extremely fast-growing staffing and consulting firm. Amerit Consulting was founded in 2002 to provide consulting, temporary staffing, direct hire, and payrolling services to Fortune 500 companies nationally; as well as small to mid-sized organizations on a local & regional level. Currently, Amerit has over 2,000 employees in 47 states. We develop and implement solutions that help our clients operate more efficiently, deliver greater customer satisfaction, and see a positive impact on their bottom line. We create value by bringing together the right people to achieve results. Our clients and employees say they choose to work with Amerit because of how we work with them - with service that exceeds their expectations and a personal commitment to their success. Our deep expertise in human capital management has fueled our expansion into direct hire placements, temporary staffing, contract placements, and additional staffing and consulting services that propel our clients businesses forward.

Amerit Consulting provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Applicants, with criminal histories, are considered in a manner that is consistent with local, state and federal laws.