Tech Writer

A pharmaceutical manufacturing organization is seeking a Tech Writer to join their team in Massachusetts. In this role, the Tech Writer will support the creation, revision, formatting, and maintenance of GMP documentation for manufacturing operations. This role focuses on ensuring that controlled documentation remains accurate, compliant, and well-maintained throughout the document lifecycle. About the Opportunity: Schedule: Monday-Friday Hours: Standard business hours Setting: In-person Responsibilities: Author, edit, format, revise, and maintain SOPs, batch records, work instructions, forms, templates, and logbooks Ensure high standards of cGMP documentation practices are consistently followed Coordinate document reviews and approvals through the document management system Manage document lifecycle activities, including creation, revision, issuance, periodic review, and archival Collaborate with cross-functional teams to support documentation needs, project activities, and effective communication Qualifications: 2-3 years of experience with Document Management Systems Experience with CAPA Strong team-working and communication skills Highly motivated, detail-oriented, and able to solve problems independently Ability to read, write, and understand English Proficiency in Microsoft Excel, Word, and Outlook Desired Skills: Experience supporting GMP documentation in a manufacturing environment. Tandym Group