Deadline Oct 19

Quality Assurance Specialist

Posted Oct 2 (14 days ago) · Last updated Oct 16 · Open 14 days. This role usually stays open about 21 days

Key facts

QA Specialist at a global biopharma contract development and manufacturing company in Turku.

How this salary compares

Estimated €2,635 - €3,223Benchmarked against mid-level roles

Too few postings state a salary to show this.

Monthly salary comparison for Quality Assurance Specialist
MarketLower bound (25th percentile)MedianUpper bound (75th percentile)
mid-level roles€3,500 per month€3,900 per month€4,300 per month
This offer€2,635 per month€2,929 per month€3,223 per month

Estimated from 1,255 comparable listings

Est. take-home €2,139 - €2,504

Where and how
TurkuOnsiteMid-Level
Languages required
Finnish, English
Education
Masters
Experience
3 years experience

Original job ad

Translated by JobCrawls from the Finnish ad.

Open the ad
We are seeking a Quality Assurance Specialist to join the QA team in development and manufacturing of biological medicines at our Turku site. The role involves diverse QA duties such as developing and maintaining quality systems, risk management, change and deviation handling, internal audits, supplier assessments, equipment and facility qualification, software validations, and acting as a QA expert in collaborative projects with Production and QC. The final scope will depend on your skills and interests. Requirements include a few years of experience in QA for drug development or manufacturing in a GMP environment, and an advanced university degree (for example pharmacist or chemist). Experience in biological drugs manufacturing or quality management, sterile product manufacturing, and clinical trial drug manufacturing is valued. You should be proficient in Finnish and English, both written and spoken, and demonstrate teamwork, proactive attitude, ability to work under pressure, and strong attention to detail. We offer a global company with opportunities to contribute to biologics development and contract manufacturing, a thorough onboarding, a supportive workplace, and good employee benefits including extensive occupational healthcare, health insurance, and wellbeing and fitness perks. The position is full-time and permanent, based in Turku, Kupittaa.

About the role

Summarised by JobCrawls from the job ad above.

Requirements

  • Several years of QA experience in pharma/ GMP environment

Responsibilities

  • Develop and maintain quality systems
  • Risk management and change/ deviation handling
  • Internal audits
  • Supplier assessments
  • Equipment and facility qualification
  • Software validations
  • QA support in collaboration projects with Production and QC

Skills & technologies

Quality Management Systems (QMS)GMPIVDR/IVIV (if Applicable)ValidationDocument ControlRisk Management

Benefits & perks

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About Biovian Oy

Financial overview
€30.6M
Revenue
€5.0M
Profit
16.0%
Profit margin
Biovian Oy logo
Biovian Oy · 2 open roles
Top locations (all time): Turku, Finland · 11
View company
Current open roles at Biovian Oy on JobCrawls
LocationActive listings
Turku, Finland11
Current role mix at Biovian Oy on JobCrawls
Role typeActive listings
Quality Assurance Specialist2
Production manager, DSP1
Analytical Technician1
Proposal manager1
Scientist, DSP1
Analytical scientist1
Warehouse and Equipment Maintenance Worker1
Open application1
Bioprocess engineer1
Quality Assurance coordinator1
Current role-level mix at Biovian Oy on JobCrawls
Role levelActive listings
Mid-Level9
Manager2

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