Biovian Oy logo
Est. Monthly
Estimated €2,416 - €2,880
Posted August 26, 2026 · 2 days agoLast seen August 28, 2026Deadline September 14, 2026
Biovian Oy

Quality Assurance coordinator

How this salary compares
Salary Context: Quality Assurance coordinator

Hover or tap a row for full statistics (EUR / month on this chart).

Salary analysis

Compared with the selected benchmark ("All roles in Turku, Finland"), this listing's salary midpoint is about 94% lower. The offer sits below the benchmark range (€1,992–€4,889). The listed pay band (€201–€240) is tighter than the benchmark, which suggests lower salary variability. This benchmark is based on 648 comparable listings.

Monthly salary comparison for Quality Assurance coordinator
MarketLower bound (25th percentile)MedianUpper bound (75th percentile)
All roles in Turku, Finland€1,992/per month€2,648/per month€4,889/per month
About the role

Quality Assurance Coordinator role at Biovian Oy in Turku. The QA team focuses on quality assurance for biologics development and manufacturing. Responsibilities include maintaining the quality management system, device and facility qualifications, risk management, change and deviation handling, supplier evaluations, drafting and reviewing GMP documents, and assisting with materials management. The final job scope will depend on prior experience and interests. We expect several years of QA experience in a pharmaceutical manufacturing or GMP environment and a suitable university degree. Proficiency in Finnish and English is required, with strong written and oral communication skills. The role is full-time and temporary in Turku, Kupittaa, with a supportive QA team and a comprehensive introduction. We offer meaningful work in the drug development space, career development opportunities from a new factory project, and good employee benefits including extensive occupational health care, health insurance, and wellness and exercise benefits.

Job Details

Responsibilities

  • Maintaining the quality management system
  • Device and facility qualifications; assisting in qualification processes
  • Risk management, changes and deviations handling
  • Supplier evaluations
  • Drafting and reviewing GMP documents
  • Assisting with materials management

Requirements

  • Several years of experience in Quality Assurance in a pharmaceutical plant and/or GMP environment
  • A suitable university degree
  • Proficiency in Finnish and English, both written and spoken
  • Strong interpersonal and teamwork skills, responsibility, resilience, flexibility, and ability to manage larger tasks

Education Level

Bachelor
Seen 16 hours agoContent Complete
Financial overview
€30.6M
Revenue
€5.0M
Profit
16.0%
Profit margin
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Location

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