Description 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.

Responsibilities:
• Create, revise, and organize standard operating procedures and related controlled documents for laboratory start-up and ongoing operations.
• Partner with scientists, quality personnel, and other stakeholders to gather technical details and translate them into accurate, user-friendly documentation.
• Ensure written procedures align with Good Laboratory Practice expectations and applicable regulatory s...