Sr. Technical Writer

Integrated Resources Inc.; Bridgewater (MA); On-site; USD 80,000 - 120,000; Full time

Job summary

A leading company is seeking a Sr. Technical Writer for a 6+ month contract in Massachusetts. This role involves writing functional specifications and collaborating with developers in a fast-paced R&D environment. Candidates should possess strong technical writing skills along with experience in the biotech or pharma sectors.

Qualifications

• Senior-level professional with experience in biotech or pharma.
• Ability to self-manage and motivate.

Responsibilities

• Writing detailed Functional Specifications and Requirement Specification documents.
• Coordinating activities and managing documents in an R&D environment.

Skills

Excellent writing skills

Technical background

Document management tools

Education

Bachelor's degree in relevant field

Tools

Alfresco

SVN

RoboHelp

Adobe

Microsoft Word

Job 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+ months contract

Direct Client: Immediate interview

The Sr. Technical Writer will be responsible for working in an R&D environment, writing detailed Functional Specifications, collaborating with developers, and understanding the software development lifecycle.

The candidate should be able to write precise business and technical requirements to produce Requirement Specification documents. We are seeking a senior-level professional who can self-manage, motivate, and has experience in biology, life sciences, pharma, biotech, or CRO sectors.

The role includes assisting with writing requirements and functional specifications, managing documents, coordinating activities, and having knowledge of document management tools like Alfresco, SVN (version control), RoboHelp, Adobe, Word, etc. Excellent writing skills, a strong technical background, and experience in the clinical trials domain, CRO, or Medical Devices are essential. Experience in Pharma, CRO, Medical Devices, or Biotech industries is required. This is a long-term contract opportunity.