
Quality Specialist - Fixed Term - Blueprint Genetics Oy - Espoo, Finland
Quality Specialist
Tap this card for salary charts and full compensation details.
Expand to unlock full salary context
See benchmark placement, pay-band comparison graph, and localized salary narrative.
Job Description
Blueprint Genetics, a Quest Diagnostics company, is a clinical genetic testing company aspiring to bring genetic knowledge to mainstream healthcare. We want to improve the lives of individuals and families impacted by inherited, rare diseases. We are looking for a motivated and detail-oriented Quality Specialist to join our Quality team. This is an excellent opportunity for a quality professional who combines an interest in technology with solid understanding of quality management processes within the IVD medical device and clinical laboratory environment. In this role, you will support maintenance and development of our Quality Management System (QMS), with a particular focus on risk management, document management, and eQMS development activities. We are looking for someone who is not only able to coordinate activities, but also actively create and maintain QMS documentation, including risk assessment records. This position is fixed term until 30.9.2027. Key Responsibilities include participating in QMS process development and digitalization initiatives, managing maintenance of controlled documentation in QMS, driving risk management activities and improvements in line with ISO 14971:2019 and CAP requirements, assisting in preparation for audits, supporting follow-up actions including assessment of nonconformities and CAPAs, collaborating cross-functionally with internal stakeholders, and ensuring QMS documentation and processes comply with external and internal requirements. What We Are Looking For includes a Bachelor’s degree or equivalent in Life Sciences, Biotechnology, Biomedical Engineering, or related field, preferably 2-3 years of experience in Quality Assurance or IVD industry, experience with EU IVDR 2017/746, ISO 13485, and ISO 14971, digital skills including AI, hands-on risk management experience, ability to produce high-quality QMS documentation, partly on-site work, structured and proactive working style, and strong communication skills in English. What We Offer includes the opportunity to work for a company making a real difference, participate in quality management projects, a collaborative environment, a positive international work environment, and employee benefits such as bonus system, occupational healthcare, lunch benefit, sports & wellbeing, mental wellbeing support, gym membership, and team events. How to apply: submit your application and CV by July 5th, 2026. For more info, contact Minna Jänis at +358 50 516 9309 on June 17th and 18th between 10:00 - 11:00 EEST. About Blueprint Genetics: changing diagnostics with accessible genetic knowledge, founded in 2012, with 240 co-workers.
Company Information
| Location | Active listings |
|---|---|
| Espoo, Finland | 14 |
| Remote - Global | 1 |
| Role type | Active listings |
|---|---|
| Customer Service Representative | 2 |
| Software Engineer | 2 |
| Accessioning Specialist | 2 |
| Production Assistant | 1 |
| Human Resources Specialist | 1 |
| Scientist | 1 |
| Financial Analyst | 1 |
| Billing Specialist | 1 |
| Customer Service | 1 |
| Intern | 1 |
| Finance Analyst | 1 |
| Role level | Active listings |
|---|---|
| Senior | 1 |
| Mid-level | 1 |
Blueprint Genetics Oy appears in 15 indexed job postings in JobCrawls' Finland dataset since May 2025. In that historical index, the strongest location signals for this employer are Espoo, Finland and Remote - Global.
About
Includes details from the Finnish Trade Register.
Osakeyhtiö
Other health care services
Financial Overview (2024)
Blueprint Genetics Oy was profitable in 2024 with revenue of €29.2M and a profit margin of 0.1%.
Data shown is based on historical job postings from our database.
Job Details
Responsibilities
- Participate in QMS process development and digitalization initiatives
- Manage maintenance of controlled documentation in QMS
- Drive risk management activities and improvements in line with ISO 14971:2019 and CAP requirements
- Assist in preparation for audits, and support follow-up actions including assessment of nonconformities and CAPAs
- Collaborate cross-functionally with internal stakeholders
- Ensure QMS documentation and processes comply with external and internal requirements
Requirements
- Bachelor’s degree or equivalent in Life Sciences, Biotechnology, Biomedical Engineering, or related field
- Preferably 2-3 years of experience in Quality Assurance or IVD industry
- Experience with EU IVDR 2017/746, ISO 13485, and ISO 14971
- Digital skills including AI
- Hands-on risk management experience highly preferred
- Ability to produce high-quality QMS documentation independently
- Ability to work partly on-site
- Structured, proactive, and solution-oriented working style
- Strong communication skills in English
Skills & Technologies
Benefits & Perks
Recruitment Process
- 1Submit application and CV by July 5th, 2026
- 2Interviews during open application period
