Technical Writer/Documentation Specialist Quanterix
THIS JOB HAS EXPIRED Job Code: TW-100
Quanterix is an exciting early stage company whose mission is to develop a game-changing platform that combines proprietary single-molecule sensitivity, multiplexing, and full automation. We are seeking a talented and highly motivated Technical Writer/Documentation Specialist to join our Product Development Group. If you have experience in preparing technical documents in compliance with Quality system guidelines, this could be a very rewarding position for you.
Responsibilities will include:
Writing and editing technical documents to support the development and launch of the Immunoassay product line. Documents will include equipment and reagent manufacturing procedures, test methods, operating instructions, test protocols and reports, SOPs, specifications, package inserts and product labels.
Working closely with R&D and Manufacturing subject matter experts to understand the technical content and requirements of the documentation.
Ensuring documentation is accurate, complete, meets specifications and adheres to standards for quality and style.
Maintaining a high level of quality, clarity and consistency for all documents.
Identifying areas of improvement in processes, styles and formats.
Processing documents through the electronic documentation control system, maintaining revision control and managing reviewers on a tight schedule.
The position requires:
Bachelor?s degree in Science, Medical Technology, English, or Technical Communications.
2 years of professional experience in editing and/or writing for a technical audience.
Experience working in a regulated environment (ISO, GLP, GMP) preferred.
Excellent written and editorial skills.
Ability to critically review own work before sending out for review.
Demonstrated ability to work independently.
Fluent in word processing; good working knowledge of software programs; experience with electronic document management systems is a plus.
In addition: You need excellent organizational and communication skills, a strong work ethic, the ability to generate high quality documentation under tight deadlines, and a superior attention to detail. You will be working in a fast-paced environment, on multiple projects, with some of the brightest minds in the business. You will be a part of a rapidly growing company on a trajectory to have a major impact in the life science research and clinical diagnostics arenas.
Founded in 2007 and located in Lexington, MA, Quanterix is developing an ultra-sensitive diagnostic platform capable of measuring individual proteins at concentrations 1000 times lower than the best immunoassays available today. The Single Molecule Array (Simoa?) technology at the heart of the platform enables the detection and quantification of biomarkers previously difficult or impossible to measure, opening up new applications to address significant unmet needs in life science research, in-vitro diagnostics, companion diagnostics, blood screening, and more. Quanterix is a venture capital backed company and the exclusive licensee of a broad intellectual property portfolio initially developed at Tufts University by Dr. David Walt, scientific founder of Quanterix and Illumina.
Quanterix offers a dynamic, fast-paced, entrepreneurial environment. The company plans to launch its Simoa HD-1 Analyzer to the life science research market in mid-2013, and is growing rapidly to prepare for commercialization. Quanterix offers a competitive benefits package, including generous health and dental, 401k, and paid time off, and is an equal opportunity employer.
||One Kendall Square |
Cambridge, MA 02139
THIS JOB HAS EXPIRED