GMP & Regulatory QA Specialist — Quality & Compliance

Abbott Laboratories; Netherlands; Remote; EUR 60,000 - 90,000; Full time

Benefits offered by this job

13th month

Sport allowance

Personal development budget

Job summary

Abbott Laboratories in Olst, Netherlands, is seeking a QA Specialist A to join the Quality Assurance team. You will ensure products meet GMP and internal quality standards, and you will work with diverse teams to maintain product quality and patient safety.

You will assess regulatory dossiers, implement changes locally, and serve as QA/regulatory representative on projects. You’ll investigate deviations, support audits, and review GxP/QMS documents while driving continuous improvement across

Qualifications

• Bachelor’s degree in a relevant field; 5+ years in a pharmaceutical or highly regulated environment.
• Excellent understanding of GMP and regulatory processes.
• Good English communication; Dutch optional.

Responsibilities

• Ensure regulatory dossiers compliance and oversee regulatory product documentation.
• Act as regulatory compliance representative in projects and changes.
• Handle deviations, complaints and quality issues; investigate and resolve.
• Support audits and inspections and review quality documents (GxP/QMS).
• Collaborate with regulatory affairs, production, QC and operations.

Skills

English communication

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in a relevant field

Tools

MS Office

Job description

Abbott Laboratories in Olst, Netherlands, is seeking a QA Specialist A to join the Quality Assurance team. You will ensure products meet GMP and internal quality standards, and you will work with diverse teams to maintain product quality and patient safety.

You will assess regulatory dossiers, implement changes locally, and serve as QA/regulatory representative on projects. You’ll investigate deviations, support audits, and review GxP/QMS documents while driving continuous improvement across