We are looking for a Technical Policy Writer to support documentation efforts for a biopharma manufacturing environment in Somerset, New Jersey. This is a Contract position that will focus on developing and refining controlled procedures for a new laboratory operation while partnering closely with subject matter experts across the site. The ideal candidate brings strong technical writing experience, a solid understanding of regulated laboratory practices, and the ability to produce clear, compliant documentation in a fully on-site setting.<br><br>Responsibilities:<br>• Create, revise, and organize standard operating procedures and related controlled documents for laboratory start-up and ongoing operations.<br>• Partner with scientists, quality personnel, and other stakeholders to gather technical details and translate them into accurate, user-friendly documentation.<br>• Ensure written procedures align with Good Laboratory Practice expectations and applicable regulatory standards, including 21 CFR Part 58 requirements.<br>• Review existing content for clarity, consistency, and compliance, making updates where needed to support operational readiness.<br>• Manage document workflows and version control within established quality systems, including MasterControl when applicable.<br>• Facilitate discussions with cross-functional teams to confirm process details, resolve documentation gaps, and maintain approval timelines.<br>• Support on-site documentation needs five days per week while helping maintain a consistent format and writing standard across procedures.