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.
Tech Writer
Tandym Group · Bedford, MA, USA ·
- Job type:
- Full Time