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1+ months

Technical Writer 1

Kelly Services
Irvine, CA 92604
  • Jobs Rated
    43rd
Kelly FSP Science and Clinical is currently seeking a Technical Writer for a long-term engagement with one of our Global Pharmaceutical clients. This position is onsite 2-3 days per week in Irvine, CA.


This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vison, 401K, and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.


General Purpose


Reports to the TW 4 or higher. Support Engineers with preparing, technical documents and manuals, explain complex information in a clear and concise manner and working with scientific staff to ensure accuracy of product descriptions. Responsible for documenting and managing change requests and ECOs to ensure complete traceability in a compliance environment.


Duties And Responsibilities


+ Writes and/or edits technical materials such as reports of research findings, regulations in technical areas, technical manuals, specifications or scripts on technical subjects. Provides written and oral reports, abstracts, summaries, charts, graphs, or other products.

+ Develops information and analysis to select and present information on the specialized subject in a format and at a level suitable for the intended audience.

+ Analyzes and review the preparation and organization of complex research.

+ Prepares written documents, including reports, articles, formal proposals, memoranda, and formal correspondence.

+ Edits reports and assists in or directs the development and presentation of the information.

+ Analyzes changes to various projects and prepares reports of changes for review.

+ Organizes and coordinates assignments that involve complex, novel or obscure problems and/or special requirements for analyzing and organizing information.

+ Lead and/or participate in the development of new documents or update existing documentation used for new product development

+ Participate in the development and maintenance of document standards, naming/numbering conventions, and templates for procedures, work instructions, and other relevant document types

+ Support/manage document workflow and ensure compliance

+ Ensure that document reviews and approvals are managed in an efficient and effective manner

+ Assist in the identification and removal of old/obsolete procedures and work instructions, as required

+ Collaborate within department and cross-functionally to meet set objectives and execute against manufacturing schedule.

+ Performs other related duties as assigned


+ Responsible for communicating business related issues or opportunities to next management level

+ Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition

+ Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures

+ Performs other duties assigned as needed


Education/Training/Experience


+ Bachelor's degree

+ Technical writing knowledge in the medical device industry, preferably

+ Prior experience using word processing, spreadsheet, and presentation software

+ Excellent written and verbal communication skills, possess a strong sense of responsibility and urgency

+ Strong process improvement mindset; passion for quality

+ Demonstrated effective interpersonal and effective teamwork skills

+ Analytical & problem-solving skills/root-cause analysis

+ Strong organizational skills with high attention to detail

+ Practical knowledge of project management, preferably


**You should know:** Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.


**Why Kelly** **** **?**


Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.


**About Kelly** ****


At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm)

Categories

Jobs Rated Reports for Technical Writer

Posted: 2022-06-15 Expires: 2022-08-15

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Technical Writer 1

Kelly Services
Irvine, CA 92604

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Technical Writer
43rd2019 - Technical Writer
Overall Rating: 43/199
Median Salary: $71,815

Work Environment
Very Good
32/220
Stress
Medium
93/220
Growth
Fair
91/220
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