Specialist Operations

Confirmed live in the last 24 hours

QIAGEN

Gdańsk

On-site

Posted April 29, 2026

Job Description

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.

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About the opportunity

In this role, you contribute your scientific and technical expertise to the manufacturing of recombinant proteins within a regulated production environment. Working closely with cross-functional teams, you independently execute purification processes at production scale, support continuous improvement initiatives, and help introduce and validate new manufacturing solutions. The position combines hands-on laboratory work with problem-solving, documentation, and project involvement, offering the opportunity to make a tangible impact on high-quality production processes.

Your tasks include

Executing purification of recombinant proteins at production scale using chromatography (FPLC), filtration, and formulation techniques, in line with production schedules
Acting as shift lead when required, coordinating and supervising assigned laboratory staff during production activities
Operating and maintaining advanced laboratory equipment such as ÄKTA systems, filtration units, HPLC, and freeze dryers, including troubleshooting technical issues
Supporting the introduction, optimization, and validation of new or improved manufacturing processes and departmental projects
Identifying, analyzing, and resolving production-related issues while implementing sustainable solutions
Driving continuous improvement of processes, workplace organization, and technical documentation in collaboration with relevant stakeholders
Preparing and maintaining accurate production and quality documentation in compliance with ISO/GMP requirements

Your profile

University degree (Master’s or Engineer level) in Biotechnology, Biochemistry, or a related life science field
Several years of hands-on experience in purification of recombinant proteins from genetically modified microorganisms at production scale, within an ISO/GMP environment
Solid practical knowledge of chromatography-based purification and downstream processing techniques
Experience working independently in a regulated laboratory or manufacturing setting
Good communication skills in Polish and working proficiency in English
Experience with fermentation (yeast or bacterial), bioreactor operation, or coordination of laboratory staff is considered an advantage

What we offer 

Private medical care

Group Life Insurance

Multisport card

Flexible benefits platform

Language classes

Pension Scheme (PPE) after 12 months

Childcare subsidy

Training and development programs

Happy Monday (snacks provided)

Attractive location (Sky Tower)

Hybrid work (conditional to your role)

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!