Technical Writer at Northborough

Job Description

Technical Writer in the Quality Control Raw Material (QCRM) Department.  This is an individual contributor role accountable for the creation, and review of QCRM related documents.

This position is for an independent, proactive, experienced technical writer with demonstrated experience managing competing projects and working across multiple functional groups.  The successful candidate will be project based. 

Description:

•  Ensure timely and efficient creation/review of QCRM documents (material specifications, standard operating procedures,  test methods, technical protocols and reports, etc) using an electronic document management system

•  Contribute scientific knowledge, analytical skills, and interpretation of the information to be captured on the document

•  Collaborate with QCRM subject matter experts to ensure the clarity of purpose, scope, and accuracy of document content

•  Work effectively with the Quality Documentation department, document management system and related tools, templates, and procedures in order to ensure an efficient publishing of the documents

•  Initiate document review and approval workflows according to the corresponding Quality Documentation procedures

•  Ensure a consistent style of presentation of QCRM documents to maintain quality and ease of review

•  Must have transportation and be willing to travel between our local facilities

•  Degree in a relevant scientific discipline coupled with

•  5 years of experience as technical writer in a cGMP regulated industry (drugs, biologics)

 

Preferred Qualifications:

•  Proven excellent spoken and written English Strong verbal, presentation and analytical thinking skills

•  Documented excellence in advance features of Microsoft Word and ability to work effectively with a document management system

•  Demonstrated ability to prioritize tasks and complete high-quality documents on aggressive timelines

•  Experience with laboratory control system and Quality Control programs

•  Able to guide others to improve their writing, editing and proofreading skills

•  Degree in a relevant scientific discipline coupled with 5 years of experience as technical writer in a cGMP regulated industry (drugs, biologics)

For Immediate consideration please email resume to [Click Here to Email Your Resum]

Job Requirements

Quality Control Raw Material, cGMP, Microsoft Word

Country: USA, State: Massachusetts, City: Northborough, Company: The Judge Group Inc.