Technical Writer – Compounding
We are currently seeking a Technical Writer – Compounding, responsible for producing clear, accurate, and compliant technical documentation to support safe, efficient, and regulatory‑compliant compounding operations.
This role provides dedicated ownership of compounding‑related documentation, including investigation write‑ups, SOPs, and Work Instructions (WKIs), ensuring alignment with GMP, GDP, and site quality standards. The role acts as a critical interface between Compounding, Quality and Technical Support.
Key Responsibilities
- Investigation & Deviation Documentation – Author and structure deviation investigations, root cause analyses, and CAPA write‑ups related to compounding activities, working closely with Compounding, QA, and TSO. Ensure investigations are fact‑based, concise and compliant with Quality SOPs and regulatory expectations. Support timely closure of investigations by simplifying technical narratives and ensuring clear linkage between root cause, impact, and corrective actions. Review investigation documentation for GDP compliance, clarity and audit readiness.
- SOP & Work Instruction Development – Write, revise, and maintain Compounding SOPs and WKIs, ensuring consistency with approved templates and document control requirements. Translate operational practice into clear, operator‑friendly instructions suitable for use on the manufacturing floor. Partner with SMEs to ensure documentation accurately reflects current processes, equipment, and systems. Support change management by updating documentation in line with process changes, investigations, audit actions, or system updates.
- Documentation Governance & Compliance – Ensure all documentation meets GMP and GDP standards, including clarity, traceability, version control, and training impact assessment. Support audit and inspection readiness by maintaining well‑structured, valid documentation. Identify gaps, inconsistencies, or risks in existing documentation and proactively drive improvements. Align compounding documentation with site Quality and Document Management requirements. Act as a key documentation interface between Compounding, Quality and Technical Support. Support training effectiveness by ensuring SOPs and WKIs are fit for purpose, unambiguous, and aligned to how work is physically performed. Provide guidance to SME authors and reviewers on best practices for technical writing and compliant documentation.
Skills & Experience
- Essential – Proven experience as a Technical Writer or similar role in a GMP‑regulated manufacturing environment or suitable background in report writing (e.g., science degree). Strong experience writing SOPs, WKIs and investigation documentation, or proven ability to translate complex scientific content into clear, accessible documentation for non‑specialist audiences. Solid understanding of GMP/GDP principles and regulatory expectations. Ability to translate complex technical and operational information into clear, structured documentation. High attention to detail with a strong quality and compliance mindset. Strong stakeholder management and collaboration skills.
- Desirable – Experience within pharmaceutical, cosmetics, or regulated manufacturing compounding operations. Familiarity with deviation, CAPA, and investigation systems. Experience supporting regulatory inspections or audits. Knowledge of document management systems and controlled documentation lifecycle. Structured, methodical, and quality‑driven. Pragmatic and solutions‑focused. Confident working with both operators and senior stakeholders. Comfortable challenging unclear or undocumented practices to improve compliance.
Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.
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