Quality Specialist Benelux
Life Sciences
QA
- Locatie
- Eigen-Brakel, Waals-Brabant
- Type werk
- Consultancy
- Werkmodel
- Fulltime, Hybrid
Verantwoordelijkheden
Product Complaint Management
- Receive and manage product quality complaints from customers and internal stakeholders.
- Open and follow complaint cases in the electronic Quality Management System (eQMS).
- Coordinate investigations with relevant stakeholders.
- Organize return sample shipments and replacement products.
- Communicate complaint outcomes to customers.
Batch Release & GDP Activities
- Review inbound 3PL documentation and transport temperature data.
- Perform administrative GDP batch release decisions for saleable stock.
- Coordinate release-related communications with logistics partners.
- Ensure proper approval and archiving of documentation in Source CD.
Quality Systems & Compliance
- Support deviation management activities and investigation follow-up.
- Assist in CAPA and Change Control management processes.
- Maintain accurate document and record archiving
- Support audit readiness and inspection activities.
- Participate in recall and mock recall activities.
- Support narcotics management administrative tasks when required.
Vendor & Customer Management
- Act as quality contact for local 3PL partners.
- Manage distribution-related quality questions and temperature excursion decisions.
- Review and approve customer qualification documentation.
- Ensure compliance with local GDP/GMP requirements.
Profile & Qualifications
Education
- Bachelor’s degree required.
- Master’s degree preferred.
Experience
- Experience working with Quality Management Systems (QMS) within the pharmaceutical industry is considered a strong asset.
- Knowledge of GDP/GMP regulations is an advantage.
Skills & Competencies
- Strong attention to detail and accuracy.
- Excellent organizational and administrative skills.
- Ability to manage multiple priorities independently.
- Analytical mindset with problem-solving and risk assessment capabilities.
- Customer-oriented and collaborative approach.
- Ability to communicate effectively with internal and external stakeholders.
- Team player with a proactive attitude and openness to new ideas.
- Fluent in English and Dutch or French, both written and spoken.
Vereisten
Education
- Bachelor’s degree required.
- Master’s degree preferred.
Experience
- Experience working with Quality Management Systems (QMS) within the pharmaceutical industry is considered a strong asset.
- Knowledge of GDP/GMP regulations is an advantage.
Skills & Competencies
- Strong attention to detail and accuracy.
- Excellent organizational and administrative skills.
- Ability to manage multiple priorities independently.
- Analytical mindset with problem-solving and risk assessment capabilities.
- Customer-oriented and collaborative approach.
- Ability to communicate effectively with internal and external stakeholders.
- Team player with a proactive attitude and openness to new ideas.
- Fluent in English and Dutch or French, both written and spoken.
Aanbod
- Geniet van een competitief salarispakket met extra voordelen die je talent erkennen.
- Versnel je carrière met een helder groeipad, coaching en mentoring ter ondersteuning.
- Werk in een dynamische en ondersteunende omgeving waar je echt het verschil kunt maken.
- Werk waar en wanneer je het beste presteert voor een ideale werk-privébalans.
- Kies een flexibele mobiliteitsoplossing, van een bedrijfswagen tot een openbaar vervoer abonnement.
- Bouw je netwerk uit en beleef onvergetelijke momenten tijdens exclusieve events en afterworks.
- Breid je vaardigheden uit met externe opleidingen en onze in-house Pauwels Academy.
- Werk aan uitdagende projecten met toonaangevende klanten in Life Sciences, Engineering & Digital.
- Grijp kansen op elk niveau, van een sterke start tot doorgroeimogelijkheden en samenwerking met experts.
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