On-Site Quality Manufacturing Engineer – Groningen

randstad professional

Groningen

Sur place

EUR 65 000 - 85 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Monthly project allowance 4% of salary
25 holiday days
8% Holiday Pay
Travel allowance 0.21 per KM or NS BI
Pension scheme (flexsecurity)
Home workplace budget €750
Randstad Academy access

Résumé du poste

Randstad Professional seeks a Quality Manufacturing Engineer in Groningen to drive quality compliance on the production floor and lead investigations to secure GMP standards across lines.

The role is fully on-site with 36–40 hours per week, requiring 4+ years in pharma/manufacturing engineering, and fluency in Dutch and English. You will collaborate with manufacturing and operations to eliminate defects and embed continuous process improvements.

Qualifications

  • Hold a bachelor’s degree (hbo) or higher in engineering, life sciences, or a related field.
  • Have at least 4 years of experience in quality or manufacturing engineering.
  • Bring proven work experience within the pharmaceutical or medical device industry.
  • Speak and write fluently in both Dutch and English.

Responsabilités

  • Direct investigations into non-conformities and implement permanent CAPAs.
  • Guide and authorize planned process deviations following established quality guidelines.
  • Analyze production scrap and rejection metrics to eliminate process variation.
  • Detect performance trends and present actionable data to cross-functional teams.
  • Draft and revise standard operating procedures to secure continuous compliance.

Connaissances

Quality engineering
Manufacturing engineering
CAPA
Data analysis
Cross-functional collaboration
Dutch language
English language
Problem solving

Formation

Bachelor’s degree in engineering or life sciences

Outils

GMP compliance
SOP drafting

Description du poste

Randstad Professional seeks a Quality Manufacturing Engineer in Groningen to drive quality compliance on the production floor and lead investigations to secure GMP standards across lines.

The role is fully on-site with 36–40 hours per week, requiring 4+ years in pharma/manufacturing engineering, and fluency in Dutch and English. You will collaborate with manufacturing and operations to eliminate defects and embed continuous process improvements.

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