
Open since Jun 2026
Technical Writer
AI Summary
Authors technical protocols, reports, and correspondence for a biopharmaceutical manufacturing client, compiling data from electronic and paper sources and managing document review workflows.
About this role
A Few Words About Us
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.
Following is the position details. Please let me know if you are available/interested so we can further discuss this position. Also email me your resume and contact number where I can call you.
Location: Andover,MA
Duration: 10 months+
Job Description:
Our client is looking for a Technical Writer .
Responsibilities:
• Authoring of technical protocols, reports, memorandum, records, and related correspondence.
• Retrieve and compile data from electronic sources / databases and paper records.
• Reconcile comments from multiple reviewers on technical writing.
• Provide administrative support for the routing of documents for review and approval in conjunction with the use of an electronic documentum or record management systems.
• Provide administrative, logistical, and project management support for technology transfer and production campaign execution related effort.
Required skills:
• Prior experience in biopharmaceutical manufacturing is preferred.
• Proficiency in Microsoft Word and Excel, and experience in the use of web-based applications.
• Technical writing.
• Ability to carry out basic calculations in support of data compilation and technical writing activities (candidate with science or engineering background preferred).
• Experience in conducting meetings.
• Experience in conducting meetings, 2+ years experience in biopharmaceutical manufacturing preferred.
All your information will be kept confidential according to EEO guidelines.
Skills
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