Job Description
Job Description
Adecco is seeking an experienced Technical Writer for our client to bring clarity and consistency to product development documentation through concise writing, accurate formatting, and collaborative communication. This global company is an American biotechnology and biomedical engineering firm and multinational manufacturer of medical devices used in interventional medical specialties. This role will support a cross-functional product development team and contribute to high-quality documentation in a regulated environment.
This role is hybrid (3 days onsite weekly) in Arden Hills, MN. Please only local candidates apply. The rate for this role is $37hr.
Key Responsibilities:
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Plan, write, revise, and organize content using technical writing principles, tools, and methods
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Translate complex technical information into clear, well-structured documentation
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Manage administrative authoring tasks, including document routing for approvals and accuracy checks
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Ensure document quality by organizing information for readability, consistency, and compliance
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Review and edit peer documentation to uphold content standards and consistency
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Collaborate cross-functionally with product development teams to gather source materials and deepen product understanding
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Identify and implement process improvements in technical writing workflows
Quality Responsibilities:
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Maintain compliance with quality systems by embedding quality and regulatory standards into all documentation work
Qualifications:
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2–5 years of experience in technical writing, preferably within a regulated industry (medical device industry strongly preferred)
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Bachelor’s degree in a related field
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Experience working with content management or labeling systems
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Proficiency in desktop publishing tools, especially Adobe InDesign and Adobe Creative Suite
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Experience writing for translated documentation
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Strong attention to detail, problem-solving abilities, and the ability to manage multiple projects simultaneously
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Comfortable navigating complex processes and fast-paced environments
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Excellent collaboration and communication skills
Preferred Qualifications:
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Experience in the medical device or life sciences sector
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Familiarity with regulatory documentation standards and processes
Pay Details: $35.00 to $37.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
- The California Fair Chance Act
- Los Angeles City Fair Chance Ordinance
- Los Angeles County Fair Chance Ordinance for Employers
- San Francisco Fair Chance Ordinance