Posted on:June 29, 2016

Summary of the Sr. Technical Writer job at Integrated Resources INC

Integrated Resources INC is hiring a Sr. Technical Writer. Based in Bridgewater, NJ, US. Working arrangement: On-site.

About Integrated Resources INC

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Sr. Technical Writer job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Position: Sr. Technical Writer

Duration: 6+ contract

Location: Bridgewater, NJ

Direct Client: Immediate interview

SR tech writer. The person has to be very familiar with working in an R&D shop writing very detailed Functional Specifications working with developers and understanding the software development life cycle.

The candidate should be able to write very precise business and technical requirements in order to write Requirement Specification documents. I want a senior level persons who can self

Manage and motivate and some biology, life science, pharma, biotech or cro experience.

Sr Technical Writer/Lead to assist with writing requirements, FS, management of documents, coordination, knowledge of document management tools like Alfresco, SVN 9 version control, Robohelp, Adobe, Word, etc. Need excellent writing skills, technical background and experience of clinical trials domain/ CRO/Medical Device is must. . Experience in Pharma, CRO, Medical Device or Biotech industry is a must. Long Term Contract opportunity.

Additional Information

Regards,

Nagesh

732-429-1641

Apply now

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