Job Description
We are seeking two (2) experienced Procedure Writers to support a critical laboratory documentation workstream. These consultants will partner closely with existing team members to accelerate, standardize, and expand laboratory procedures across multiple sites. This role is ideal for candidates with hands‑on lab operations or lab management experience who have written procedures end‑to‑end and can confidently work with stakeholders to bring existing documentation to a scalable, enterprise level.
Responsibilities:
Redline, revise, and write laboratory procedures, taking direction from existing team members
Accelerate and mature existing procedures developed by the current team, expanding them for broader, multi‑site use
Write procedures from start to finish, owning the process from initial draft through stakeholder alignment
Review current documentation, identify gaps, and standardize content so it can be applied consistently across all sites
Partner directly with lab stakeholders, subject matter experts, and operations teams to gather requirements and validate procedures
Translate lab processes into clear, compliant, and practical documentation usable by lab staff
Support a defined workstream, operating with a high degree of ownership and accountability
Contribute to a data management workstream, with exposure to lab technologies and/or LIMS considered a strong plus
Apply lab operations knowledge to ensure procedures reflect real‑world workflows and best practices
Focus on content quality and accuracy rather than routing or system administration (dedicated teams handle workflow routing)
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Required Skills & Experience
5+ years of experience writing procedures or SOPs in a cGMP manufacturing environment
Hands‑on background in lab operations or lab management
Proven experience writing procedures end‑to‑end, not just editing or formatting
Strong ability to read existing documentation and adapt it for broader, multi‑site use
Excellent written communication skills with strong attention to detail
Comfortable working independently within a defined workstream
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.