Our Quality
Pharmaceutical
QASpecialist
Neural analysis suggests this role is
optimal for Mid candidates.
“QA Specialist at Our Quality. Skills: Quality Assurance, GMP, Process Improvement. Handle deviations. Investigate complaints”
What You'll Achieve.
Ensure products meet high quality standards; Comply with GMP and internal requirements; Maintain product quality; Maintain patient safety
Industry & Context.
Solution-oriented
What They're Looking For.
Must Have
Minimum 3–5 years of experience in a pharmaceutical or regulated environment, Understanding of GMP / quality processes, Good communication skills in English
Nice to Have
Dutch language skills
What You'll Do.
Investigate complaints
Investigate quality issues
Participate in inspections
Act as QA representative
Review quality documents
Approve quality documents
Support continuous improvement
How You'll Work.
Team & Collaboration
Work closely with different teams; Work with stakeholders across production; Work with stakeholders across QC; Work with stakeholders across operations
Communication Scope
Good communication skills in English; Communicates clearly
Process & Methodology
Act as QA representative in projects, Act as QA representative in changes
Full Job Description
## **JOB DESCRIPTION:** **QA Specialist B** Location: Weesp, The Netherlands The is a fully onsite position that requires you to be in the office 5/5 days weekly. **About the role** We are looking for a QA Specialist B to join our Quality Assurance team. In this role, you will help ensure that our products meet high quality standards and comply with GMP and internal requirements. You will work closely with different teams across the organization and play an important role in maintaining product quality and patient safety. **What you will do** * Handle and investigate deviations, complaints and quality issues * Support and participate in audits and inspections * Act as a QA representative in projects and changes * Review and approve quality documents (GxP / QMS) * Support continuous improvement activities * Work with stakeholders across production, QC and operations **Who you are** You are a structured and quality-focused person who enjoys working in a collaborative environment. You take ownership of your work and are comfortable handling tasks independently, while also working closely with others. You are curious and motivated to understand processes and improve them. You are not afraid to ask questions and speak up when something doesn’t look right. You would likely describe yourself as: * Detail-oriented, with a strong focus on quality and compliance * Good at organizing your work and managing priorities * A team player who communicates clearly and builds good relationships * Comfortable working with different stakeholders across the organization * Proactive and solution-oriented * Open to learning and developing your skills **Your background** * Bachelor’s degree in a relevant field (e.g. science, pharmacy, engineering) * **Minimum 3–5 years** of experience in a pharmaceutical or regulated environment * Understanding of GMP / quality processes * Good communication skills in English, preferably in Dutch. **What we offer** * A supportive and collaborative team envi
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