Technical Writer

posted:
Location
Colorado Springs, Colorado
Industry
Information Technology (Computer and Mathematical Occupations)
Job Type
Temporary
Salary
US$ 30.00 - US$ 35.00 per hour
Ref. Number
S_28744
Contact
Plunkett, Jeffrey, Spherion
Phone
719-2847220
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Job Description

Company:
Medical device manufacturer
North side of the Springs
Overtime available
massages/cafe onsite

Responsibilities:
Our fast-growing medical device company is hiring writers with experience writing technical documents in the field of science and engineering, and we are currently seeking a professional Technical Writer to join this expanding team. The successful applicant will be responsible for creating technical documents and manuals, explain complex information in a clear and concise manner and working with engineering teammates to ensure documentation accuracy. If you have previous experience as a Technical Writer, we encourage you to submit an application.
What You Will Learn: We attract and hire the best talent on the planet! You will be working with a great team of dedicated experts in the Medical Device Industry. You will learn from our Engineers, Clinicians and Manufacturing about our state of the art products.

What You Will Become: A highly influential teammate who can greatly impact the way we support and deliver our material handling and production process.

Working hours: 8:00 AM - 5:00 PM

Skills:
What Success Looks Like:

- Ideal candidate should be familiar with working in a GMP environment as it relates to medical device manufacturing and with writing, proofreading, submitting, and routing technical documents through the approval process.

- Create and revise various types of technical documents including validation protocols, work instructions, purchase specifications, CAD drawings, engineering reports, risk assessments, statistical analysis skills, and other project documents and specifications.

- The ideal candidate has experience establishing productive working relationships within a cross-functional team, including employees from various inter-facility departments (receiving inspection, manufacturing engineering, R&D, quality, purchasing, materials, etc.) and can work productively without supervision.

- Work with engineers as needed to prepare/complete documents, specifications and reports; may support completion of documents/tasks for pending projects

- Work with engineers to update dimensional and mechanical features as needed for protocols, reports, specifications, work instructions, etc.

- Communicate and negotiate document content and approval with internal employees and external suppliers as needed

- Track document review and approval routings; accurately track status of multiple documents

- Provide support to various engineering-based projects within an office environment; may be required to complete tasks in production areas. Apply technical writing skills in the form of protocols, test procedures, summary reports, flow charts, specifications and other documents as required.

- Create and distribute meeting minutes to document issues, resolutions and action items; follow-up on action items with responsible person(s).

- Ability to analyze documents to maintain continuity of style of content

Education:
Bachelors

Experience:
4-7 years

Qualifications:
What Success Looks Like:
? Ideal candidate should be familiar with working in a GMP environment as it relates to medical device manufacturing and with writing, proofreading, submitting, and routing technical documents through the approval process.

? Create and revise various types of technical documents including validation protocols, work instructions, purchase specifications, CAD drawings, engineering reports, risk assessments, statistical analysis skills, and other project documents and specifications.

? The ideal candidate has experience establishing productive working relationships within a cross-functional team, including employees from various inter-facility departments (receiving inspection, manufacturing engineering, R&D, quality, purchasing, materials, etc.) and can work productively without supervision.

? Work with engineers as needed to prepare/complete documents, specifications and reports; may support completion of documents/tasks for pending projects

? Work with engineers to update dimensional and mechanical features as needed for protocols, reports, specifications, work instructions, etc.

? Communicate and negotiate document content and approval with internal employees and external suppliers as needed

? Track document review and approval routings; accurately track status of multiple documents

? Provide support to various engineering-based projects within an office environment; may be required to complete tasks in production areas. Apply technical writing skills in the form of protocols, test procedures, summary reports, flow charts, specifications and other documents as required.

? Create and distribute meeting minutes to document issues, resolutions and action items; follow-up on action items with responsible person(s).

? Ability to analyze documents to maintain continuity of style of content

Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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