Technical Writer
RESPONSIBILITIES:
Kforce has a client that is looking for a Technical Writer to join a fast-paced and innovative team that is developing a cloud-based enterprise platform that will be supporting 10K+ Users.
In this role, you will be responsible for:
- Customer support onboarding materials (i.e. user guide, etc.)
- Contributions supporting go-to-market requirements
- UX technical writing
- Deliver detailed user guides which will be used by the support team and that will also be embedded in our cloud-based enterprise platform
- Establish the user assistance practice and authoring tools / systems that can output to multiple targets such as: Text/PDF guides, HTML micro-sites from the same source material
- Work independently to gather information from UX Designers, Software Developers and Product Management about features / workflows, and create (helpful, interesting, well-organized, consistent, high-quality) user assistance content from scratch
- Write concise, persuasive, on-task content for the user interface that keeps users engaged and reduces their potential confusion by reducing user errors
- Think outside the box and imagine new learning flow / experiences or techniques that can be applied to enterprise web-application; Your techniques create a cohesive experience for initial learning and then scaffold a novice to become an efficient expert user
- Use the product, test each procedure and workflow, become an Expert User
About You:
You are a high-energy, start-up enthusiast crossed with a professional, polished communicator. You love learning about new technologies and industries, and love teaching what you have learned to others even more. You are naturally driven to become the expert in whatever product or space you are tasked to document. You care passionately about developing useful, accurate content, and have a knack for knowing the questions a user will ask before they do. You don”t wait for the information to come to you, you go out and get it.
REQUIREMENTS:
- Bachelor”s degree in Human Computer Interaction or Communications and 5+ years of content / documentation experience in the software industry
- 5+ years of technical writing experience in enterprise software
- Excellent written and verbal English language skills
- Excellent content planning and organization skills
- The ability to act as information designer, project manager, writer, editor, and publisher
- The ability to quickly learn complex concepts and technologies and clearly explain them to others
- Knowledge or experience with creating documentation in an Agile development environment
- Knowledge or experience with structured authoring, preferably using DITA and Oxygen XML Editor
- Knowledge of authoring documentation in Markdown
- Knowledge or experience with source control systems, preferably using GitHub
- Knowledge or experience with XML, HTML, and other web-development standards related to technical documentation
- Knowledge or experience with bug tracking systems, preferably using JIRA
Bonus:
- Previous experience documenting a web authoring / writing application
- Previous experience building on-boarding experience for new users
Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
Medical Writer
MedErgy, a scientifically-focused communicationsagency, is currently seeking Medical Writers and a Senior Medical Writers to join our energetic team of professionals in Yardley, PA. The core responsibility for these positions is developing content with the highest level of technical accuracy for various accounts. The senior writer also has incremental quality control responsibilities.
Candidates in postdoctoral positions or finishing graduate/medical school are encouraged to apply.
Specific responsibilities of Medical Writers/Senior Medical Writers include:
- Writing and revising draft outlines, abstracts, posters, reviews, primary papers, and slides
- Communicating with authors and clients regarding medical/scientific content
- Reviewing and editing manuscripts
- Attending internal and external team meetings
- Applying principles of good publication practice at all times
Qualifications include:
- Advanced life sciences degree; MD, PhD, or PharmD
- For Senior Medical Writer position, a minimum of 3 years’ experience is required; publication planning experience is a plus
- Working knowledge of good publication practice
- Excellent written and verbal communication skills
- Desire to work in a collaborative team setting
- Ability to thrive under challenging deadlines and in an energetic environment
We offer a competitive salary and benefits package including medical, dental, vision, ST/LT disability, life, 401(k), and tuition reimbursement.
If you would like to learn in a collaborative and challenging work environment, forward your resume with salary requirements to:
Human Resources: hr@medergygroup.comHelp
Senior Writer
- Deliver consistent and compelling messaging related to advancement and development efforts.
- Write, edit, and research as appropriate for a range of platforms, including print, digital, video, advertising, direct mail, email, sales letters, invitations, newsletters, features, interactive, social media, display and other touchpoints.
- Incorporate consumer insights and strategic messaging into writing.
- Work closely with design team to generate ideas, concepts, and content.
- Research and fact check as needed; edit and/or proofread on an occasional basis.
- Occasionally contribute to magazines and editorial products.
- Participate in strategy meetings; project management processes and adhere to deadlines and writing style guides and brand standards.
- Maintain awareness of trends and best practices in marketing, advertising, and communications.
- Strategic beliefs
- The University of Wisconsin-Madison has a transforming impact on students, alumni, and society;
- Authentic, lifelong relationships and engagement with alumni, donors and friends are fundamental to sustaining the reputation and continued success of the University;
- Philanthropy has an essential and growing importance on the future progress of UW-Madison;
- The highest level of stewardship and fiduciary responsibility in financial, investment, data and gift administration is vital to maintaining trust with our stakeholders;
- Diverse views, experiences and perspectives strengthen WFAA and the university community.
- Organizational values
- We are serious about delivering results;
- We work together and with our campus partners as a team;
- We are committed to alumni, donors, volunteers and others;
- We are open-minded;
- We create a positive work environment.
- Bachelor’s degree in advertising, marketing, journalism, English, or a related field;
- Five or more years of writing experience in an advertising or marketing environment;
- Outstanding written and overall communication skills;
- Portfolio of marketing or advertising work;
- Demonstrated creativity and idea generation that’s on strategy and produces clear, effective content;
- Open to feedback and being flexible with changes;
- Skills to manage multiple priorities and handle a high volume of work, while often producing copy at a fast pace;
- Talent for writing versions in different styles that appeal to various target audiences;
- Accuracy and attention to detail while meeting deadlines;
- Desire to seek and understand consumer insights to strengthen campaigns;
- Knowledge of Chicago Style, marketing concepts, standards and processes;
- Strong sense of accountability, knowledge of and passion for key issues;
- Ability to conduct research from primary and secondary sources;
- Knowledge of and passion for UW–Madison and higher education.
Advanced Technical Writer
EEO Employer – Minorities / Females / Disabled / Veterans / Sexual Orientation / Gender Identity.
Technical Writer (2 Roles)
- As a Technical Writer, you will work closely with team members to develop and maintain documentation and materials to ensure our security processes are accurate and streamlined.
- Write and maintain existing wiki documentation for organization, content, technical accuracy, and style.
- Simplify processes and procedures into understandable language, workflows, and instructions.
- Produce high-quality documentation that meets applicable standards and is appropriate for the intended audience.
- Work with internal teams to obtain an in-depth understanding of documentation requirements.
- Set-up reviews and walkthroughs with technical SME’s to complete documentation for ongoing use.
- Participate in all aspects of documentation development from product planning through product release.
- Work with clients and supervisors to identify and prioritize new and existing business initiatives.
- Provide key business partners with information and recommendations to assist in the development of training and communication supporting all areas of FCS operations.
Technical Writer
Tampa, Florida
Skills : Technical Writer, Content developer
Description : The Instructional Systems Designer (ISD) designs innovative learning products that are instructionally sound and accurate and that engagingly convey content. The ISD will be expected to coordinate the development and delivery of all client training courses.
• Employ the ADDIE Model and performance-based lean ISD processes to produce high-quality web-based and paper-based manuals on systems
• Create course design documents based on job task and user analysis
• Design instructional materials
• Develop end-user and facilitator training materials
• Develop content incorporating subject matter expert (SME) input into clearly written and structured materials
• Provide input for modifications to course content and activities
• Utilize multimedia, instructional technology, and authoring tools to create classroom training and eLearning content
• Suggest and assist with implementing new instructional technology for efficient and effective training delivery
• Communicate and work directly with the client in support of design and development efforts
• Work effectively as part of dynamic team that includes SMEs, graphic designers, course developers, and technical writers to provide deliverables
Technical Writer II
| Role: Technical Services Support Role Location: Andover, MA Duration: 6+ Months Contract Job Description: The technical services support position is a support role intended to provide technical, logistical, administrative, and documentation support for activities pertaining to biologics drug substance production at the Andover location. These activities may include, but are not limited to, production campaign readiness, validation studies, regulatory submission, technical studies, and project coordination. The key responsibilities for the technical services support role include the following: 1. Authoring of technical protocols, reports, memorandum, records, regulatory submissions, and related correspondence and facilitating review and approval process 2. Retrieve and compile data from electronic sources / databases and paper records 3. Data verification for reports, technical correspondence, and regulatory submission 4. Hosting and managing project collaboration tool 5. Provide administrative and logistical support for project management, validation studies, and technical studies
A strong candidate will have the following attributes: Hit the ground running:
|
Medical Writer
Eclaro is looking for a Medical Writer for an opportunity with our client in Princeton, NJ
Job Title: Medical Writer
Location: Scudders Mill Road Princeton. NJ 08543
Schedule: 40 hours/week
Qualifications:
- Doctor of Pharmacy or equivalent
- 3-5 years relevant industry work experience; recognized expert in medical communications
- Preferred: understanding of the payer landscape and of Health Economic and Outcomes Research (HEOR)
- Extensive, proven experience and skill in writing high-quality, evidence-based scientific medical communication materials
- Ability to write in a clear, concise, and persuasive manner
- Ability to conduct literature searches in databases such as EMBASE and Pubmed/Medline
- Strong project management skills
- Highly proficient in the use of Microsoft WORD and PowerPoint
Responsibilities: - Analyzes and interprets scientific data to update or develop comprehensive, balanced, credible and accurate documents that comply with applicable laws, regulations, guidance’s and BMS policies and procedures, and are used to appropriately respond to inquiries from payers and Health Care Providers.
- Developing and writing content for their specific projects as well as reviewing scientific content created by outside agencies. Responsibilities include, but is not limited to, developing, writing/editing and managing the production of AMCP Dossiers, and scientific PowerPoint slide presentations for payers as the primary audience; developing and/or editing responses to address specific unsolicited payer and Health Care Provider requests for health outcome information.
- Manages and prioritizes multiple projects, provides solutions to complex problems, and delivers complete and accurate information within deadlines
- Maintains awareness of current industry practices that pertain to Medical Information
- Complies with the reporting of adverse effects and product complaints to BMS Worldwide Safety and Surveillance.
Jane Bautista
201 285 – 8622
Jane@eclaro.comHelp
https://www.linkedin.com/in/froilyn-jane-bautista-88751612a
ECLARO is a company that delivers talent. We provide fully customizable, comprehensive talent acquisition and management of seasoned professionals through a number of business models, including: Consulting, Professional Hire, Global Integrated Delivery™ and Managed Services. ECLARO recruits and manages a staff of highly skilled individuals in an array of specialized disciplines. This approach enables our clients to leverage new opportunities, respond to increased and changing demands and increase their profitability. Please visit www.eclaroIT.com to see why the Right People are The Answer™.
Specialties: Customized solutions for Human Capital and Talent Acquisition, Permanent placement and retained search, Recruiting, Staff Augmentation, Contract Labor, Managed Services, RPO, MSP, VMS, IT solutions, management and support, offshore business process outsourcing.
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
Website: http://www.eclaro.com
Industry: Staffing and Recruiting
Type: Privately Held
Company Size: 501-1000 employees
Founded: 1999
Digital Content Writer
Digital Content Writer
Reach Marketing, an award winning, Inc 5000 fastest growing digital marketing agency, is seeking a talented and creative associate to be a Digital Content creator/editor/specialist on our marketing team.
The ideal candidate is a skilled professional with marketing or technical writing experience who can take a leading role in developing, implementing, tracking, and optimizing Reach’s digital marketing projects across multiple channels. We’re looking for a creative candidate who is inquisitive, reliable, thorough, detail oriented, self-motivated, prodigious, and comfortable working both independently and with our talented team in a fast-paced, deadline-driven environment.
Responsibilities:
- Create original content for different marketing channels including web, video, email, and print.
- Collaborate and brainstorm with department leaders in the ideation, planning, and execution of all original digital marketing content.
- Create, update, input, and implement an editorial calendar that promotes our firm’s products and services.
- Manage the distribution and promotion of digital content on Reach Marketing’s websites and blogs.
- Draft, schedule and manage daily posts on Reach’s social media in Facebook, Twitter, Instagram, Snapchat, YouTube, & LinkedIn.
- Collaborate with our internal marketing automation teams to create personalized email campaigns and landing pages to optimize acquisition and retention.
- Assist with the preparation and review of RFPs and speaking engagements.
Requirements:
- Experience as a digital writer/editor/creator.
- Excellent communication skills.
- Education: Four-year college or equivalent education and experience. Ability to work on multiple projects simultaneously.
- Background in one of the following: communications, marketing, journalism, screenwriting, PR, and/or advertising
- Minimum of one year of similar work experience
- Comfortable working in a deadline-driven environment with changing priorities.
- Self-sufficient, motivated to excel, well-organized.
Preferred:
- Experience working with Content Management Systems and related software
- Knowledge of HTML
About Reach Marketing:
Reach Marketing is the direct marketing company launched by the founders, former key marketing management and technology team of Edith Roman Associates. Based in Pearl River, NY (just 30 minutes from Manhattan), the Reach team is comprised of service-oriented professionals who are passionate about bringing innovative marketing solutions to their B2B and B2C clients.
Technical Writer
Chat with me now! – https://flashrecruit.com/jobs/298781
Manufacturing Support – Technical Writer
Job Summary
This role is an exciting opportunity to be a critical part of a high growth organization that is radically changing the biotech industry. Currently, the client is building a state-of-the-art, LEED certified, cGMP manufacturing facility in Norwood, MA. This 200k sq. foot campus is critical as we continue to move more of our therapies into the clinic and require in-house manufacturing. The client is seeking a cGMP Manufacturing Support team member focusing on technical writing for our new site in Norwood, MA.
The individual in this role will be part of a cohesive team responsible for producing high quality mRNA-based medicines for evaluation in human clinical trials. The Manufacturing Support Technical Writing team member uses knowledge of cGMP regulations and biopharmaceutical production processes to create and revise standard operating procedures, batch records, specifications, forms and other critical documentation. They will work directly with subject matter experts to ensure content accuracy, improve efficiency and documentation practices.
Job Responsibilities
Heavy documentation, revising and creating SOPs, writing and formatting standard operating procedures and batch records, good comms, word skills, some GMP background and process development – this is budgeted to September, but there is always a chance it can be extended. How documents fit into vision of overall scheme, might be quality control or assurance documents, communicate with groups on their needs, meeting deadlines is critical, ask the right questions when you don”t understand
• Practices and promotes safe work habits and adheres to safety procedures and guidelines
• Conducts document revisions and/or document management
• Utilizes manufacturing process knowledge and documentation skills to identify areas of improvement or gaps within documentation and resolve issues and drive continuous improvement
• Participates in cross functional teams to drive completion of document revisions or creation with a focus on prioritization and timelines for completion
• Participates in cross-functional continuous improvement teams with Engineering, Validation, Quality Assurance, Quality Control, Facilities, and Manufacturing Science and Technology
• Works independently with minimal supervision and direction
• Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion
• Creates and presents trending and metrics reports
Education & Qualifications
• Years of experience range from 2-6 years, but someone more senior than that we can work with.
• Bachelor”s degree in Engineering or Life Sciences is preferred
• High school diploma/GED or Biotech Certification with 2-4 years of experience, or Bachelor”s Degree with 1-2 years of experience in biopharmaceutical operations
• Understanding of biologics drug substance operations or a similar complex specialized environment
• An understanding of regulatory requirements and their applications in a cGMP environment
• Experience with electronic documentation systems for controlled documents in a cGMP environment
• Excellent written and oral English language skills
• Strong skills in the use of Microsoft Word including formatting Demonstrated ability to lead cross functional teams and deliver results with minimal supervision
• Ability to manage multiple competing priorities in a fast-paced environment
• Understanding of lean manufacturing methodologies and operational excellence
Benefits
• Medical, Dental, and Vision Insurance
• 401K Plan with Company Match
• Life and AD&D Insurance
Chat with me now! – https://flashrecruit.com/jobs/298781