Documentation Engineer Job Description Sample
Fpga Software Documentation Engineer
Microsemi Corporation is a leading provider of semiconductor solutions differentiated by power, security, reliability and performance. Microsemi's FPGAs are ideal for a wide variety of applications within the communications, industrial, and aerospace and defense markets. Our Libero™ SoC Design Suite enables high productivity with its comprehensive, easy to learn, easy to adopt development tools for designing with Microsemi's FPGAs. As a FPGA Software Documentation Engineer, you will:
Work in the Software Engineering team, learning cutting-edge Libero Software features, and how they are ideally used to implement customers' designs
Write clear, high quality, customer-facing documentation for new Libero features
Provide usability feedback on software tools and features
- Work in a fast-paced release environment with 8-12 software releases a year
* BSEE (or equivalent) with 5+ yrs. experience OR Advanced degree with 3+ yrs. experience OR PhD with 0+ yrs. experience using FPGA design software, other EDA software, or designing SoCs / ASICs
- Strong English writing ability (grammar and style) Preferred/Additional
* 2+ years experience sourcing documentation for software
Linux (running commands from command line) * Formatting and publishing documentation * XML or HTML * Adobe FrameMaker
Madcap Flare * MS Visio
Experience with SERDES/DDR or other high speed protocols a plus Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled
Custom/Contract Design And Documentation Engineer
SONNEMAN – A Way of Light is seeking an experienced engineer to provide design engineering support for our contract/custom department, and to generate product documentation for stocking and custom products. Position is for full-time employment in our Larchmont, NY office.
- Generating 2D and 3D CAD drawings for custom lighting products.
- Providing technical support for custom design requests.
- Generating product documentation including cut sheets, assembly instructions, etc. for new and custom products.
- Minimum 3 years of product design engineering experience, preferably in the decorative or architectural lighting fields.
- Highly skilled in SOLIDWORKS, 2D AutoCAD.
- Knowledge of Adobe InDesign and REVIT preferred.
- Excellent verbal and written communications skills.
- Bachelor’s degree in Industrial Design, Architecture, or related engineering field.
- US citizen or permanent resident (no VISA sponsorship available).
Energetic, fast-paced environment with a talented and capable team.
QA Engineer - Documentation Framework
Do you have a unique combination of collaborative, technical, and customer service skills? Our fast-paced team designs, builds, and maintains a modern and effective web experience that provides users of ArcGIS the answers they need, when they need them. Our mission is to deliver great online and offline content centered on our cutting-edge software products and their users. Responsibilities
Develop and manage tools and processes for efficient authoring, publishing, and translation of product content
Collaborate with developers and content owners to design, test, and validate enhancements to websites, content publishers, and supporting utilities
Create and execute robust test workflows across multiple browsers and platforms including Chrome, Firefox, IE, Windows, Linux, Android, and iOS
Establish and maintain baseline performance and quality bar for site deployments
Monitor health, performance, and usability of sites using web metrics and other tools
Support colleagues in their use of various technologies in our authoring/publishing stack, including GitHub, CSS frameworks, content management systems (CMS), XML editing tools, and QA tools
Troubleshoot and resolve content authoring and publishing issues
Manage and maintain GitHub repo workflows, including review and merge of changes, branch management, and builds
Ability to decompose complex problems and performing root cause analyses
Proven record of delivering quality customer service and solving problems
Experience working with and testing websites on multiple platforms and devices
Knowledge of Python or other comparable scripting language
Excellent written and verbal communication skills
Self-motivated and have an interest in continuous learning
- Bachelor's in GIS, computer science, or a relevant field, depending on position level Recommended
Experience with Git, Jenkins, Selenium, or comparable technologies
Familiarity with search technologies such as Google Search Appliance, Lucene, and Elasticsearch
Familiarity with web metric tools such as Google and Adobe Analytics Our passion for improving quality of life through geography is at the heart of everything we do. Esri’s geographic information system (GIS) technology inspires and enables governments, universities, and businesses worldwide to save money, lives, and our environment through a deeper understanding of the changing world around them. Carefully managed growth and zero debt give Esri stability that is uncommon in today's volatile business world. Privately held, we offer exceptional benefits, competitive salaries, 401(k) and profit-sharing programs, opportunities for personal and professional growth, and much more. Esri is an equal opportunity employer (EOE) and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Requisition #: 2017-6835 External Company Name: ESRI, Inc. External Company URL: www.esri.com
Cyber Engineer - RMF Package Documentation
Cyber Engineer - RMF Package Documentation Tracking Code 2260-987 Job Description Founded in 1980, COLSA Corporation’s team of cyber engineers, analysts and professionals across the US provide government customers with the latest and most sophisticated engineering, programmatic, and information technology services. Centered at the core of its values, COLSA knows its people are its most valuable resource. In addition to receiving a competitive compensation package, our employees enjoy offerings such as flexible work schedules, paid time off, benefits that begin on the date of hire, recognition programs, tuition and certification assistance, and immediate vesting in our matching 401(k) plan. Our WE CARE Wellness program provides support and initiatives to empower employees and their families to live healthy, balanced lives and our Association of COLSA Employees (ACE) provides a fun way for employees and their families to come together in times of both celebration and need. We invite you to connect your talents with opportunity, and be a part of our “Family of Professionals,” in supporting cutting-edge initiatives related to our country’s national defense! General Summary Under limited direction, supports the development of Risk Management Framework (RMF) packages and supporting activities. Principal Duties and Responsibilities (*Essential functions)
Develops RMF packages and works with customer to help them navigate the RMF process *
Conducts scans using ACAS and HBSS; runs SCAP compliance checker *
Works with and maintains entries in eMASS *
Develops RMF documentation including SOPs, Security Plans, and schedules *
Runs STIGs against all components of the system *
Evaluates and makes recommendations designed to promote economy, efficiency, and effectiveness in the security program *
May help patch systems and make configuration changes that increase security
Required Experience Required Qualifications
Bachelor’s degree in related field or equivalent
Minimum of 7 years work related experience
Experience developing RMF packages and writing supporting documentation
Demonstrated experience with STIGs, eMASS, ACAS, HBSS, and the SCAP compliance checker.
In depth understanding of cyber security policy, tools, threat mitigation, network topologies, and secured networks is required.
Ability to clearly present and communicate technical approaches and findings
A SECRET security clearance is required
Current Security+ CE certification is required Preferred Qualifications
Experience developing complete RMF packages from system categorization through the ATO Applicant selected will be subject to a government security investigation and must meet eligibility requirements for access to classified information. COLSA Corporation is an Equal Opportunity Employer, Minorities/Females/Veterans/Disabled. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin. Job Location Huntsville, Alabama, United States Position Type Full-Time/Regular
Quality Engineer Documentation
Job Title: Quality Assurance Engineer - Documentation Reports to:
Quality Process Manager JOB SUMMARY: The quality assurance engineer will be responsible for creating and updating technical documents to explain complex information in a clear and concise manner to a variety of groups with different levels of technical knowledge. Will collaborate with scrum masters, technical support, product IT and other identified stakeholder groups to create required technical documents (i.e. support notes, hardware and software system requirements, installation guides) across multiple products and platforms. Required Role-based Skills Determine the needs of end users of technical documentation Organize and write supporting
Documentation Specialist II Documentation Specialist II
Please stay to the low end of the rate card
1.Maintaining and coordinating the Record Retention process of cGMP documents for the Viral Platform. This responsibility Includes onsite and offsite record retention.
2.Updating documents within the Q eDoc system, whether administratively or through a Quality system such as Change Control or CAPA.
3.Creation and control of Production logbooks pre, post and during use.
4.Creation and control of cGMP forms.
5.Maintaining document control through Production Floor Support, including but not limited to exchanging inactive official copies of documents for Active official copies of documents in real time.
6.Supporting production needs and continuous improvement including change control, CAPA implementation, and operational optimization.
7.Coordinating document revisions between multiple groups to ensure Right the First Time environment, open communication, and to reduce the probability of rework and/or missed work.
8.Ensure cGMP regulations regarding documents, logbooks, and forms are adhered at all times for the Viral Vaccine Platform.
9.Tracking and reviewing change control documentation. Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
1.Attention to details
2.Working knowledge of cGMP
3.Good communication skills both written and verbal
4.Proficiency in WORD, and EXCEL, and have a working knowledge of other MICROSOFT OFFICE programs.
5.Excellent organizational skills
6.Sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
7.Work quickly with a high degree of accuracy.
Clinical Documentation Specialist – Clinical Documentation Improvement – Orlando
Under general supervision of the Director of Clinical Documentation Improvement and more closely the supervision of the Clinical Documentation Improvement Manager, and in collaboration with physicians, nursing and HIM coders, the Clinical Documentation Specialist (CDS), strategically facilitates and obtains appropriate and quality physician documentation for any clinical conditions or procedures to support the appropriate severity of illness, expected risk of mortality, and complexity of care of the patient, and to support ICD-10 implementation. The CDS educates members of the patient care team regarding documentation guidelines, including attending physicians, allied health practitioners, nursing, and care management. The CDS adheres to strict departmental and organizational goals, objectives, standards of performance and policies and procedures, continually ensuring quality documentation and regulatory compliance. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all. Knowledge, Skills, Education, & Experience Required:
Ability to learn/develop and fine-tune the skills necessary to perform Clinical Documentation Management
Organizational, analytical, writing and interpersonal skills
Dependable, self-motivated and pleasant
Critical-thinking, problem-solving and deductive-reasoning skills
Knowledge of Pathophysiology, disease process and treatments
Basic computer skills - familiarity with Windows-based software programs
Knowledge of regulatory environment
Strong interpersonal skills
Strong ability to organize/triage work and manage multiple priorities at once
Four - five years of acute care experience in med/surg, critical care, emergency room, or PACU
Knowledge of clinical documentation requirements that identify clinical conditions or procedures to support and enhance ICD-9 and ICD-10 coding. (Preferred)
BSN, MSN (Preferred)
Minimum of one year as a Clinical Documentation Specialist (Preferred) Licensure, Certification, or Registration Required:
Current active Florida State license as a Registered Nurse, Nurse Practitioner, or Physician’s Assistant
- Certified Clinical Documentation Specialist (issued by the Association for Clinical Documentation Improvement Specialists (ACDIS)) (preferred)
Demonstrates through behavior Florida Hospital’s Core Values of Integrity, Compassion, Balance, Excellence, Stewardship and Teamwork as outlined in the organization’s Performance Excellence Program
Reviews concurrent medical record for compliance including completeness and accuracy for severity of illness (SOI) and quality using the Compliant Documentation Management Program (CDMP) documentation strategies.
Develop an active, collaborative interface and structure with Florida Hospital Medical Staff
Completes accurate and timely record review to ensure the integrity of documentation compliance. Completes accurate and concise input of data into CDMP Trak resulting in accurate metrics provided by the CDMP program. Understands and supports CDMP documentation strategies (upon completion of training) and continues to educate self and team members using educational tools, videos and provided WebEx’s.
Recognizes opportunities for documentation improvement using strong critical-thinking skills. Uses critical thinking and sound judgment in decision making keeping reimbursement considerations in balance with regulatory compliance. Initiates/formulates CDMP severity worksheets and clinically credible clarifications for inpatients, sending/presenting opportunities for improved documentation compliance to physicians, nurse practitioners and other medical staff.
Transcribes documentation clarifications as appropriate for SOI, Core Measures, and Patient Safety to ensure documentation compliance is accomplished.
Strategically educates members of the patient-care team regarding documentation regulations and guidelines, including attending physicians, allied health practitioners, nursing, and care management. This includes quarterly compliance updates from Medicare.
Effectively and appropriately communicates with physicians and other healthcare providers as necessary to ensure appropriate, accurate and complete clinical documentation. Communicates with HIM staff and collaborates with them to resolves discrepancies with DRG assignments and other coding issues.
Completes well-timed follow-up case reviews on all concurrent cases with priority given for resolution of those with clinical documentation clarifications
Participates in Task Force meetings, including feedback on outstanding issues, presentations for educational opportunities and any other needs identified by the CDI group.
Assumes personal responsibility for professional growth, development and continuing education to maintain a high level of proficiency.
Performs other duties as assigned. If you want to be a part of a team that is dedicated to delivering the highest quality in patient care, we invite you to explore the Clinical Specialist opportunity with Florida Hospital and apply online today. *Bonus Details:
Applicable experience required.
Must live 50 or more miles from 601 East Rollins Dr., Orlando, FL to qualify.
Full Time employment contract required.
Rehires within 12 months are not eligible. Job Keywords: Clinical, Specialist, Documentation Improvement, East Orlando
Title:Clinical Documentation Specialist – Clinical Documentation Improvement – Orlando
Drafting / Quality Documentation Technician
Drafting / Quality Documentation Technician
The Drafting / Quality Documentation Technician plays a central role in the Quality Department by creating, tracking, and maintaining high-quality technical documentation for BestPack. This position will ensure records are organized and maintained in a centralized location to ensure ready access as needed to contribute to the overall consistent quality standards of our products. The technician will support the engineering team and reports to the Quality Assurance Configuration Manager. The individual will audit configurations, revise, and create quality documentation for industrial machines.
- Analyze schematics, assembly drawings, data sheets, and process documentation.
- Assist the Quality Assurance Manager with revisions and improvements to department documentation policies and structure.
- Physically audit components on assembled machines to update released documentation.
- Reverse engineer new components and draft custom modifications in AutoCAD.
- Produce AutoCAD footprint drawings.
- Quality assurance reconciliations documentation of parts and machinery.
- Develop engineering documents and CAD drawings from red-line documentation
- Maintain document version control.
- Study and edit drawings, specifications, and mockups for custom machinery builds.
- Create and publish machine manual documentation in Adobe InDesign.
- Entering parts and BOM’s into SAP MRP computer system.
- Audits documentation and records for accuracy and completeness
- Create and maintain easy-to-understand user documentation for a variety of material, including how-to guides, instruction manuals, procedures and reports.
- Prior experience with AutoCAD, Adobe InDesign and Adobe Illustrator.
- The ability to create AutoCAD standardized drawing environment.
- Experience with Windows Suites.
- Knowledge of MRP systems, preferably SAP.
- Ability to function successfully in a team with a good attitude.
- Ability to work independently and complete projects without constant supervision and correction.
- Ability to be knowledgeable of engineering measuring practices and the use engineering measuring tools (rulers, calipers etc.)
- Knowledge of materials, processes, and fasteners used in the mechanical engineering industry.
- Mechanical engineering and/or industrial machinery technical background preferred.
- Ability to use computer, mouse, and keyboard for extended periods of time.
- Carry/lift/move objects that may weigh up to 40 lbs.
- Bend, kneel, and reach on a regular basis.
- Sit or stand for extended periods.
- Strong work-ethic, self-direction, and an eagerness to complete and take on new tasks
- Detail-oriented with excellent organizational skills.
BestPack delivers answers to solving a wide range of needs from produce to eggs, and from packaging cosmetics to securing medical products, to name a few. With the support staff of field technicians throughout the United States, BestPack maintains the resources and parts to service and repair its over 100 carton sealer models and carton erectors, while providing the entire range of quality industrial machine and hand roll tape.
Mid-Level Specialized Support – Technical Documentation And Briefing Support Dodp9
E3 Federal Solutions (E3) is an award winning Veteran Owned Business specializing in providing acquisition management, financial management, and program management support to the federal government. E3's strong understanding of federal acquisition, contract, financial management and program management organization (PMO) lifecycles paves the way for mature organizational processes, experienced resources, responsive management and proven management methodologies to meet and exceed client goals. Excellence, Accountability, Community, Humility and Integrity are the core values of E3 as we continue to strive in becoming a recognized leader in the management consulting community that both federal agencies and industry partners value doing business with. We are an organization that offers both our employees and clients an exceptional experience; our culture will be contagious, while always maintaining a genuine reputation. E3 is currently seeking a Senior Engineer to support test and evaluation planning and oversight within the Office of the Secretary of Defense (OSD) Strategic Capabilities Office (SCO). Specific tasks will include:
Support the development of test objectives and procedures, analysis of performer progress, modeling objectives and techniques, and coordination of modeling and testing.
Support R&D program engineering and physical experimentation and testing efforts, including preparation of experimental R&D test plans, coordination with performers and facilities, and implementing and inspecting safety requirements.
Plan, coordinate, and support elements of prototype development, testing, and/or demonstrations, as required.
Conduct independent assessments of R&D results of lab and other test conducted by performers.
Provide data collection and documentation support.
Minimum of 10 years of recent and relevant programmatic and technical support experience.
Bachelor's degree in engineering, computer science, physics, or other S&T-related subjects is required.
Top Secret/SCI clearance required. E3 is an Equal Employment Opportunity / Affirmative Action employer, E3 Federal Solutions, LLC (E3) is dedicated to making all employment decisions without regard to race, color, sex (including gender and transgender status), age, religion, national origin, disability, marital status, veteran status, registered domestic partner or civil union status, gender identity, medical condition, genetic information, sexual orientation, or any other protected status in accordance with applicable federal, state, and local laws. E3 hires and promotes individuals solely on the basis of their qualifications for the job to be filled. Req #: 2017-3701 External Company URL: www.e3federalsolutions.com
Lead Engineering Documentation Administrator - 17-00647
Lead Engineering Documentation Administrator - 17-00647 # Irving, TX
Job Snapshot # Location: Irving, TX # Category: Miscellaneous # Employee Type: Direct Hire # Duration: 0 weeks
Pay Rate: $68,000.00 - $72,000.00 /Year
Apply Now Not ready to apply, but want to stay up-to-date in future job openings? Join our Talent Network for job alerts in your inbox. # Contact
1/6/2018 # Job ID: 79995 # Contact: Volt # Phone: 972/518-2500 # Fax:
Description Volt is seeking a dynamic, energetic and accomplished Lead Engineering Documentation Administrator with 5 years of engineering documentation (PLM) experience.
Scheduling and Supervision and Administration
Must schedule tasks based on workload, contents of the input queue, and any implied or explicit priorities, including product or project priority, requests, etc.
Supervise Engineering Documentation Administrator and Coordinator, setting their priorities, and conducting performance appraisals.
Chair the Engineering Change Control Board, facilitate discussions so that members have an adequate understanding in order to make approval decisions, promote attendance, and ensure that the proceedings are recorded and archived.
Ensure product definitions include information to describe any required conditions or process to insure integrity of what’s being purchased or manufactured.
Process Engineering Documentation Request forms and produce Release, ECO, Deviation, and Product Configuration documents that control the configuration of a product at the time of manufacture.
Maintain the orderly storage of all engineering change and release control documents as well as the associated drawings and specifications.
Help identify Engineering Documentation processes that could be improved, including computerization, automation, and changes to existing computer systems. # EDUCATION: BA/BS degree or equivalent experience requiredEqual Opportunity Employer
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