analytical method validation consultant.

• Execute hands-on method validation/verification for raw materials in the laboratory.
• Author, review, and remediate all controlled validation documentation (plans, protocols, and reports) to be audit-ready.
• Troubleshoot analytical methods, instrumentation, and sample preparation issues.
• Collaborate closely with QC and QA teams to ensure compliance and data integrity across all testing.
• Provide knowledge transfer and training to QC analysts.

• Strong hands-on analytical method validation/verification experience in a GMP QC laboratory.
• Proven ability to write and defend regulated validation documentation (plans, protocols, reports).
• Expertise in common pharmaceutical analytical techniques, including HPLC/UPLC, FTIR, GC, Wet Chemistry, and UV-Vis.
• Exceptional data integrity and documentation discipline.

At Randstad, we are passionate about providing equal employment opportunities and embracing diversity to the benefit of all. We actively encourage applications from any background.