Vacant job

Overview

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

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

We have played a central role in shaping modern science and healthcare, and we have only just begun. If you thrive on new challenges, value diversity, and want to make a tangible difference in people's lives, then QIAGEN is the right place for you.

At QIAGEN, every day is an opportunity to make a difference in real life.

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

About the opportunity

Join QIAGEN DNA Synthesis (QDS) in Västerås as a Development Engineer within our Technology Development & Process Excellence (TD/PE) team. This role offers the opportunity to contribute to cutting-edge advancements in analytical and preparative liquid chromatography, supporting the development of premium quality oligonucleotides for our customers.

Working within a collaborative and multidisciplinary team, you will play a key role in developing methods, techniques, and processes to ensure an optimized, best-in-class oligonucleotide production process. You will operate in a dynamic environment where continuous improvement, scientific curiosity, and ownership are highly valued.

Your tasks

• Developing and optimizing analytical and preparative liquid chromatography methods (e.g., HPLC, UPLC, LC-MS) for oligonucleotide production.
• Planning, executing, and evaluating development projects related to oligonucleotide manufacturing processes.
• Defining project scope, timelines, and deliverables, and communicating progress to internal and external stakeholders.
• Supporting deviation investigations and CAPA activities in collaboration with Quality Assurance.
• Contributing to continuous process improvement initiatives to enhance quality, efficiency, and robustness.
• Creating, reviewing, and maintaining SOPs and electronic lab documentation.
• Providing support to the onsite oligonucleotide production facility as required.

Your profile

Please submit your application in English

We are looking for someone whose drive and mindset match their skills – someone who sees challenges as opportunities. Work can be fast-paced, so we’re looking for someone who brings energy, ownership, and a growth mentality to both TD/PE and QDS.

• Bachelor’s or Master’s degree in subject areas related to Chemistry, Chemical Engineering, Biotechnology, Biochemistry, or equivalent.
• Hands-on experience with analytical and preparative liquid chromatography (e.g., UPLC, HPLC, LC-MS).
• Theoretical and practical knowledge of solid-phase oligonucleotide/peptide and/or organic synthesis.
• Ability to write, review, and follow SOPs related to oligonucleotide synthesis, as well as writing and reviewing electronic lab journals.
• Familiarity with working in regulated environments such as ISO9001, ISO13485, and/or cGMP standards would be advantageous.
• Experience of working with process development initiatives would be advantageous.
• An advanced ability to communicate in verbal and written formats in both English and Swedish is essential as the language onsite is Swedish.

What we offer

• Extra pension benefit
• Health allowance (2500 SEK/year)
• Volunteer day
• Opportunity to join internal QIAGEN communities
• Performance-related bonus
• Hybrid work (subject to your role)

Our people are the heart of everything we do. Passion drives us as we push boundaries to renew and develop. We inspire through leadership and influence through action. We foster a collaborative, supportive environment where every individual and team can thrive. We strive for 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, veteran status, or disability.