
Deadline Oct 2
Last seen Oct 2
Posted Sep 24 · 9 days ago
Open 9 days. This role usually stays open about 14 days
Quality Engineer
Quality Engineer at Pharmia Oy in Tuusula; permanent, full-time role.
We are seeking a Quality Engineer for Pharmia Oy in Tuusula, Finland. This is a permanent, full-time position. The role involves developing, maintaining and supervising the quality assurance system for dietary supplements and medical devices, ensuring that products, processes and documentation meet regulatory requirements and applicable standards. Key responsibilities include developing and maintaining quality management systems; analyzing and improving production and service processes for quality and efficiency; ensuring product and operation compliance with standards (ISO 13485, FSSC 22000, HACCP); conducting internal audits and preparing for regulatory inspections; creating and maintaining quality management documentation and reporting; training staff in quality-related practices; developing risk-based methods (FMEA, HACCP, risk assessment); supporting supplier quality assurance and product development from QA perspective.
The text above is the employer's original job description, extracted as written. Other details on this page, like salary, responsibilities, and requirements, are interpreted from that text by our system, not values the employer explicitly confirmed, so treat them as our best interpretation rather than verified facts.
Estimated from 266 comparable listings
| Market | Lower bound (25th percentile) | Median | Upper bound (75th percentile) |
|---|---|---|---|
| mid-level roles | €3,500 per month | €4,250 per month | €5,500 per month |
| This offer | €2,682 per month | €3,063 per month | €3,443 per month |
- Develop and maintain quality management systems for manufacturing
- Analyze and improve production and service processes for quality and efficiency
- Ensure regulatory compliance of products and operations (ISO 13485, FSSC 22000, HACCP)
- Conduct internal audits and prepare for regulatory inspections
- Create and maintain quality documentation and reporting
- Train staff in quality-related practices
- Develop risk-based methods (FMEA, HACCP, risk assessment)
- Support supplier quality assurance and product development from a QA perspective
- A relevant university degree (e.g., engineer, pharmacy, food science, biochemistry, biotechnology)
- Minimum about 5 years of experience in manufacturing
- Nice to have 1-2 years of experience in IVDR/MDR quality management and QMS process development
- Knowledge of key standards and regulations (ISO 13485, FSSC 22000, MDR, food legislation)
- Understanding of manufacturing technologies and processes
- Experience with ERP systems
- Fluent Finnish and English language skills
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|---|---|
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|---|---|
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| Role level | Active listings |
|---|---|
| Mid-Level | 439 |
| Manager | 27 |
| Senior | 14 |
| Junior | 8 |
| Intern | 2 |
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