Document Editor Team Lead (GMP)

Location: UK - Slough; fully site-based

Company

hirify.global is a global life sciences company that manufactures medicines across more than 30 sites on five continents.

What you will do

• Lead and manage the Technical Administrative Team through direction, coaching, mentoring, and performance management.
• Oversee the creation, editing, review, approval, and delivery of GMP documentation from MSAT through GMP manufacturing.
• Coordinate document activities with internal and external stakeholders, resolving issues and managing changes.
• Provide expertise on document content, formatting standards, document management systems, procedures, and GMP practices.
• Drive documentation process improvements, strategic initiatives, and efficiency enhancements.
• Lead root cause investigations and implement solutions for documentation and process issues.

Requirements

• BSc in a relevant scientific or engineering discipline, or equivalent experience in biopharmaceutical development or manufacturing.
• Strong people leadership skills, including coaching, team development, feedback, and performance management.
• Excellent communication and stakeholder relationship-building skills across functions.
• Sound judgement and initiative in identifying risks, escalating issues, and resolving challenges affecting quality, compliance, or delivery.
• Experience delivering accurate, high-quality results against demanding timelines while maintaining customer focus.
• Ability to work fully site-based in Slough, UK.

Culture & Benefits

• Agile career development and a dynamic working culture.
• Inclusive and ethical workplace focused on collaboration, accountability, excellence, passion, and integrity.
• Performance-recognition compensation programs.
• Benefits vary by role and location.
• In-person collaboration supporting technical precision and high standards for medicine manufacturing.