Biopharma Quality Inspector – GMP & Root-Cause

Avantor Sciences; Hillegom; On-site; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Bonus

Job summary

Avantor's Hillegom site is seeking a dedicated Quality Inspector to ensure customer and regulatory requirements are met across manufacturing, filling, labeling, and documentation.

You will perform in-process and final inspections, review production documentation for GDP compliance, and support root-cause analysis and corrective actions while upholding GMP and GDP standards in a regulated biopharma environment.

Qualifications

• Must be able to balance multiple tasks and priorities efficiently.
• Knowledge of ISO 9001, ISO CFR 820, 21 CFR 11, EXCiPACT is preferred.
• Experience in root cause analysis related to non-conforming material investigations is desirable.

Responsibilities

• Inspect product and review documentation throughout manufacturing, filling, labeling, and assembly to ensure compliance.
• Perform pre-fill, in-process, and final inspections using established work instructions.
• Stop production when a non-conformance is observed and follow NCM procedures.
• Document non-conformances and trends; support investigation and corrective actions.
• Ensure audit readiness and maintain GDP and GMP compliance.

Skills

Multitasking

Root cause analysis

Communication skills

Education

High School diploma or GED

Bachelor's degree

Tools

Outlook

Word

Excel

Access

Job description

Avantor's Hillegom site is seeking a dedicated Quality Inspector to ensure customer and regulatory requirements are met across manufacturing, filling, labeling, and documentation.

You will perform in-process and final inspections, review production documentation for GDP compliance, and support root-cause analysis and corrective actions while upholding GMP and GDP standards in a regulated biopharma environment.