ISIJP00010374 Tehnical Writer 3 Not AVail for W2 Ref
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Job Posting ID: ISIJP00010374
Job Posting Title: TECHNICAL WRITER 3
Description: QMS
Technical Writer 3 (x2)
Duration: 1 year
Onsite/Hybrid/Remote: Hybrid (2 days a week) Only
Locals/Nonlocals can be submitted: Local time zone Mode of interview: Zoom No
of rounds of interview: 3 Top 3 skills: SOPs, Regulations, Document Control
Preferred Skills: Excel/Smartsheet/One note. Comfortable reaching out and
leading meetings with SMEs. Ability to thrive in a busy and fast-paced
environment
Primary Function of Position:
The Technical Writer ensures that development and
delivery of process documentation standard operating procedures (SOPs) is
consistent and compliant with company and regulated guidelines. The Technical
Writer writes, edits, and maintains usable, accurate, clearly presented, and
consistent internal process documentation. The Technical Writer requires
general guidance on new assignments and processes but is expected to complete
day-to-day work with little instruction. This is a self-directed role requiring
exceptional time management and communication skills.
Essential Job Duties
• Write,
edit, and maintain internal process documentation according to company template
and guidelines
• Provide
ongoing writing support to cross-functional teams as they transform their
processes to the new company templates and guidelines
• Develop
and maintain process documentation flow charts
• Collaborate
with department team members and with cross-functional team Subject Matter
Experts (SMEs) to learn their internal processes to write, edit, and maintain
process documentation
• Ensure
compliance with Quality, Document Control, and Good Documentation Practice
(GDP) guidelines
• Understand
the document control steps which are required to release documentation. Upload
files to the document control system.
• Resolve
complex issues in creative and effective ways, using skills as an experienced
technical communication professional with understanding of industry best
practices and company objectives
• Act
as the lead writer on projects and mentor other writers as needed
• Keep
abreast of the basic requirements for compliance in own area of work and
complies with those requirements. Participate as required in training on
regulatory issues affecting own area of work and share learned expertise with
others. Bring regulatory compliance questions/issues to the attention of
management
• Adhere
to policies, procedures, style guides, and quality documents. Collaborate with
project team members to share knowledge and best practices.
Required Skills, Experience, Education, & Training:
• 3-5+
years writing or editing experience in a regulated environment focusing on
internal process documentation SOPs
• Bachelor’s
degree in communications, professional writing, English,
biological/medical/engineering sciences, or equivalent
• Strong
writing and grammar skills in areas of content development and writing style.
Analytical ability to grasp and effectively communicate complex scientific and
engineering concepts
• Ability
to understand and create flow charts
• Strong
organizational skills and ability to manage deliverables for multiple projects
under tight deadlines, set priorities, and manage time effectively
• Expert
skill level using current versions of standard authoring tools, including
Microsoft Word and Microsoft Visio
• Working
knowledge of Adobe Illustrator, Adobe Photoshop, or equivalent
• Previous
experience with medical devices or a regulated environment
• Perform
assignments with minimal instruction and supervision
Preferred Skills, Experience, Education, & Training:
• Understanding
of Document Control processes preferred
• Understanding
of decision tracking software such as OneNote, Excel, and Smartsheet preferred
• Understanding
of localization process preferred
Job Posting Start Date: 02/17/2025
Job Posting End Date: 02/16/2026
Business Unit: Regulatory
Site: B108 - 1020
Kifer Road
Location: 1020
Kifer Rd, Bldg 108
Posting Information
Job Posting Owner: -
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