Create, update, and standardize SOPs, work instructions, and process documentation
Support QE and CAPA documentation across full lifecycle (investigation to effectiveness check)
Ensure documentation is GMP-compliant, clear, and audit-ready
Collaborate with SMEs, lab teams, and QA to capture and structure content
Improve consistency and standards across documentation (“one way of writing”)
Support document lifecycle in eQMS (reviews, updates, versioning)
Identify gaps and drive continuous improvement of documentation quality
Experience in GMP-regulated environment (pharma, biotech, lab operations)
Strong technical writing skills (SOPs, CAPA, process documentation)
Understanding of quality systems (QE, CAPA, change control)
Ability to translate complex processes into clear documentation
Experience with eQMS systems (e.g., MasterControl, Labware LIMS)
High attention to detail and structured working style
Strong collaboration and communication skills
Proactive mindset with focus on standardization and improvement
Job details are sourced from the employer's original posting.
Open job postingAbout the company
Solvias is a leading provider of contract research, development, and manufacturing services for the pharmaceutical and biotechnology industries.