Integrated Resources Inc.
Sr. Technical Writer
Integrated Resources Inc., Bridgewater, Massachusetts, us, 02324
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.
Do you have the following skills, experience and drive to succeed in this role Find out below.Job Description
Position: Sr. Technical WriterDuration: 6+ contractDirect Client: Immediate interviewThe Sr. Technical Writer will be responsible for writing detailed Functional Specifications and collaborating with developers, demonstrating a strong understanding of the software development life cycle.The candidate should be able to write precise business and technical requirements to create Requirement Specification documents. We seek a senior-level individual who can self-manage and motivate, with experience in biology, life sciences, pharma, biotech, or CRO.Responsibilities include assisting with writing requirements, Functional Specifications, document management, coordination, and knowledge of document management tools such as Alfresco, SVN version control, RoboHelp, Adobe, and Word. Excellent writing skills, a technical background, and experience in the clinical trials domain/CRO/Medical Device are essential. Experience in the Pharma, CRO, Medical Device, or Biotech industry is a must. This is a long-term contract opportunity.
#J-18808-Ljbffr
Do you have the following skills, experience and drive to succeed in this role Find out below.Job Description
Position: Sr. Technical WriterDuration: 6+ contractDirect Client: Immediate interviewThe Sr. Technical Writer will be responsible for writing detailed Functional Specifications and collaborating with developers, demonstrating a strong understanding of the software development life cycle.The candidate should be able to write precise business and technical requirements to create Requirement Specification documents. We seek a senior-level individual who can self-manage and motivate, with experience in biology, life sciences, pharma, biotech, or CRO.Responsibilities include assisting with writing requirements, Functional Specifications, document management, coordination, and knowledge of document management tools such as Alfresco, SVN version control, RoboHelp, Adobe, and Word. Excellent writing skills, a technical background, and experience in the clinical trials domain/CRO/Medical Device are essential. Experience in the Pharma, CRO, Medical Device, or Biotech industry is a must. This is a long-term contract opportunity.
#J-18808-Ljbffr