Specialist Quality Control

qiagen· QIAGEN Gdańsk Sp. z o.o.
Apply Now ↗
📍 GdańskFull time

About this role

Overview  

 
At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.  

We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. 

 

We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. 

At QIAGEN, every day is an opportunity to make a real-life impact. 

 

Join us, grow with us, and together, let's shape the future of biological discovery. 

‎

About the opportunity

Join QIAGEN's Quality Control team and contribute to ensuring the highest quality standards for products used in molecular testing and life sciences. In this role, you will perform analytical testing, support validation activities, and help implement and qualify new quality control methods. You will work in a dynamic environment where adaptability, proactive communication, and continuous improvement are highly valued.

 

Your tasks include

  • Perform analytical testing independently in accordance with approved analytical methods and quality standards.
  • Conduct analyses of samples collected during manufacturing processes to support in-process quality control activities.
  • Prepare buffers, reagents, laboratory materials, and other resources required for routine testing.
  • Create, update, and maintain quality control documentation, including SOPs, Control Cards, Validation Plans, and related records.
  • Support the implementation, qualification, and optimization of new quality control methods and laboratory processes.
  • Participate in validation activities and cross-functional projects involving internal and business stakeholders.
  • Identify opportunities for process improvement and proactively communicate laboratory, material, equipment, or process-related needs.

Your profile

  • Bachelor's or Master's degree in Biotechnology, Molecular Biology, Genetics, Biology, or a related life science discipline.
  • Minimum of 2 years of professional experience in a Quality Control, Laboratory or related scientific environment.
  • Experience supporting or participating in validation activities.
  • Ability to adapt to a dynamic environment and manage changing priorities effectively.
  • Strong communication skills, confidence in raising concerns, and a collaborative, solution-oriented approach.
  • Hands-on experience with molecular biology techniques such as PCR, qPCR, SDS-PAGE, or electrophoresis.
  • Experience with HPLC would be considered a strong asset.
  • Fluent Polish and English at minimum B2 level.

What we offer  

 

  • Private medical care

  • Multisport card

  • Training and development programs

  • Flexible benefits platform

  • Language classes

  • Friendly atmosphere

  • Casual dress code

  • Employee Assistance Program and internal QIAGEN communities 

 

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.   

 

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

 

Please make sure to send an English version of your CV! 

Frequently Asked Questions

Is the salary disclosed for the Specialist Quality Control position at qiagen?
The salary for this Specialist Quality Control role at qiagen is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Specialist Quality Control position at qiagen located?
This Specialist Quality Control role at qiagen is based in Gdańsk. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Specialist Quality Control role at qiagen full-time or part-time?
This is listed as a Full time position. It is posted as a Specialist Quality Control role in the QIAGEN Gdańsk Sp. z o.o. department at qiagen.
Which team or department does the Specialist Quality Control at qiagen belong to?
This Specialist Quality Control position is part of the QIAGEN Gdańsk Sp. z o.o. department at qiagen. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Specialist Quality Control position at qiagen?
Click the "Apply Now" button on this page. You will be redirected to qiagen's official application portal hosted on workday where you can submit your application directly.
When was the Specialist Quality Control job at qiagen posted?
This Specialist Quality Control position at qiagen was posted on Sep 30, 2026. Apply as soon as possible — early applications are often reviewed first.
Specialist Quality Control
qiagen
Apply for this role ↗

You'll be redirected to qiagen's official application page on Workday.