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Overview
Quality Manager / Senior Quality Engineer - Bioretec Oy - Tampere, Finland
Human Resources Specialist
Compensation
€3,000 - €3,500/month
Vacation: 5 weeks
Salary Context: Human Resources Specialist
Market Average: Human Resources Specialist
€13 - €19,532
In Tampere, Finland: Human Resources Specialist
€13 - €8,000
This Offer
€3,000 - €3,500
€13€19,532
per month
Location
Tampere
Remoteness
Onsite
Application Deadline
January 25, 2026
Posted: January 14, 2026
Management Tier
No People Management
Job Type
Full-time
Experience
Minimum experience: 3 years
Required:
EnglishFinnish
Specialisations:
Regulatory complianceQuality managementSupplier quality
Job Description
Seeking an experienced Quality Manager or Senior Quality Engineer for supplier quality management and QMS maintenance at Tampere site. Responsible for supplier audits, documentation, and continuous improvement in a regulated medical device environment.
Company Information
Manufacture of medical and dental instruments and supplies (excl. dentures)
Yrittäjänkulma 5 33710 TAMPERE
Business ID: 1474196-9
Headcount: 40
Financial Overview (2024)
Bioretec Oy was unprofitable in 2024 with revenue of €4.5M and a profit margin of -0.9%.
Data shown is based on historical job postings from our database.
Job Details
Requirements
- Bachelor’s or master’s degree in engineering or related field
- Experience in quality assurance or supplier quality in medical devices or regulated environments
- Knowledge of ISO 13485, FDA 21 CFR 820
- Experience with supplier audits and quality tools
- Good analytical and problem-solving skills
- Strong communication and collaboration skills in Finnish and English
- Good documentation skills in Finnish and English
- Ability to work independently and manage multiple priorities
- ISO 13485 or ISO 9001 internal auditor training or certification
Responsibilities
- Lead and develop supplier quality management processes
- Evaluate and monitor suppliers through audits and reviews
- Manage nonconformities, corrective actions, and risk assessments
- Collaborate with Operations and R&D
- Review and approve supplier documentation
- Support incoming inspection and qualification activities
- Drive continuous improvement in supply chain quality
- Maintain and update QMS documentation and records
- Conduct internal audits and contribute to external audits and inspections
Field:
Healthcare
Education Level
Bachelor
Specialisations:
- Regulatory compliance
- Quality management
- Supplier quality
Perks
- Health insurance
- Flexible hours
Competitive salaryHealth insuranceFlexible work hours
5 hours ago
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Overview
Quality Manager / Senior Quality Engineer - Bioretec Oy - Tampere, Finland
Human Resources Specialist
Compensation
€3,000 - €3,500/month
Vacation: 5 weeks
Salary Context: Human Resources Specialist
Market Average: Human Resources Specialist
€13 - €19,532
In Tampere, Finland: Human Resources Specialist
€13 - €8,000
This Offer
€3,000 - €3,500
€13€19,532
per month
Location
Tampere
Remoteness
Onsite
Application Deadline
January 25, 2026
Management Tier
No People Management
Job Type
Full-time
Experience
Minimum experience: 3 years
Posted: January 14, 2026Deadline: January 25, 2026
Required:
EnglishFinnish
Specialisations:
Regulatory complianceQuality managementSupplier quality
Job Description
Seeking an experienced Quality Manager or Senior Quality Engineer for supplier quality management and QMS maintenance at Tampere site. Responsible for supplier audits, documentation, and continuous improvement in a regulated medical device environment.
Company Information
Bioretec Oy
Manufacture of medical and dental instruments and supplies (excl. dentures)
Yrittäjänkulma 5 33710 TAMPERE
Business ID: 1474196-9
Headcount: 40
Company Age: 27 years
Financial Overview (2024)
Bioretec Oy was unprofitable in 2024 with revenue of €4.5M and a profit margin of -0.9%.
Data shown is based on historical job postings from our database.
Job Details
Requirements
- Bachelor’s or master’s degree in engineering or related field
- Experience in quality assurance or supplier quality in medical devices or regulated environments
- Knowledge of ISO 13485, FDA 21 CFR 820
- Experience with supplier audits and quality tools
- Good analytical and problem-solving skills
- Strong communication and collaboration skills in Finnish and English
- Good documentation skills in Finnish and English
- Ability to work independently and manage multiple priorities
- ISO 13485 or ISO 9001 internal auditor training or certification
Responsibilities
- Lead and develop supplier quality management processes
- Evaluate and monitor suppliers through audits and reviews
- Manage nonconformities, corrective actions, and risk assessments
- Collaborate with Operations and R&D
- Review and approve supplier documentation
- Support incoming inspection and qualification activities
- Drive continuous improvement in supply chain quality
- Maintain and update QMS documentation and records
- Conduct internal audits and contribute to external audits and inspections
Field:
Healthcare
Specialisations:
- Regulatory compliance
- Quality management
- Supplier quality
Education Level
Bachelor
Minimum Years of Experience
3 years
Perks
- Health insurance
- Flexible hours
Competitive salaryHealth insuranceFlexible work hours
5 hours ago