QC Analyst

Terumo Europe NV; Wülfrath; On-site; EUR 42,000 - 54,000; Full time

Benefits offered by this job

Competitive compensation

Professional development opportunities

Benefits package

Job summary

Terumo Europe NV is seeking a QC Analyst to perform routine and advanced analytical testing in biopharmaceutical QC. Based at our Wuppertal-Aprath site with some Leverkusen support, you will execute HPLC/UPLC, CE, and iCIEF assays, document results, and contribute to method transfers and validations.

The role requires a bachelor’s degree in a scientific field, 1–2 years of lab experience, strong attention to detail, and English proficiency.

Qualifications

• Bachelor’s degree or equivalent in a scientific field.
• 1–2 years of relevant laboratory experience preferred.
• Hands-on experience with chromatography, especially HPLC/UPLC.
• Exposure to GMP-regulated lab environments is an advantage.
• Willingness to learn new analytical techniques and quality systems.

Responsibilities

• Perform routine release, stability, and in-process testing according to procedures.
• Perform analytical testing using separation techniques (HPLC, UPLC, CE, iCIEF).
• Review, evaluate, and document analytical results per quality requirements.
• Support method transfers, verifications, qualifications, and validations.
• Draft, update, and review analytical procedures and SOPs.
• Prepare samples, solutions, reagents, and materials for testing.
• Maintain laboratory equipment and readiness for testing.
• Contribute to daily GMP lab activities and 5S improvements.
• Collaborate with QC and other teams to ensure efficient operations.
• Pursue continuous improvement and learn new methods and GMP requirements.

Skills

Chromatography

HPLC/UPLC

CE/iCIEF

English fluency

Attention to detail

Team collaboration

Adaptability

Education

Bachelor’s degree in Chemistry, Pharmacy, Biochemistry, Life Sciences, or related field

Tools

HPLC/UPLC

CE

iCIEF

Job description

At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations.

Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this might be the opportunity you're looking for.

As a QC Analyst, you will perform hands-on analytical testing of biopharmaceutical products, with a strong focus on chromatographic and electrophoretic separation techniques. You will support routine release, stability and in-process testing as well as analytical method transfers and the related documentation. Through your work in the laboratory, you will directly contribute to the quality and reliability of products that ultimately matter to patients.

This is an 18-month temporary position, primarily based at our Wuppertal-Aprath site, with occasional support at the Leverkusen site.

Your team

Terumo Pharmaceutical Services Germany (TPSG), with sites in Leverkusen and Wuppertal, is part of Terumo’s global Pharmaceutical Solutions division. We support pharmaceutical and biotechnology companies by providing high-quality contract development and manufacturing services.

Within our Quality Control department, we perform analytical testing to support the release and stability assessment of biopharmaceutical products. Our expertise spans physicochemical testing, chromatography, electrophoretic methods, bioassays, and microbiological testing. By bringing together expertise across these scientific disciplines, our teams help ensure that products consistently meet high standards for quality, safety, and regulatory compliance.

Your Responsibilities

• Perform routine testing of release, stability, and in-process samples according to approved procedures and specifications.
• Perform analytical testing using separation techniques such as HPLC, UPLC, CE, and/or iCIEF.
• Review, evaluate, document, and report analytical results accurately and according to applicable quality requirements.
• Support analytical method transfers, verifications, qualifications, and validation activities.
• Contribute to the drafting, updating, and review of analytical procedures, test methods, SOPs, and other relevant laboratory documentation.
• Prepare samples, solutions, reagents, and other materials required for analytical testing.
• Support laboratory equipment and instrument management, including maintenance and readiness for testing.
• Contribute to day-to-day GMP laboratory activities, including 5S and general laboratory organization.
• Collaborate with colleagues within QC and across other teams to ensure reliable and efficient laboratory operations.
• Contribute to continuous improvement and remain open to learning new methods, processes, and quality requirements.

Your profile

• Bachelor’s degree in Chemistry, Pharmacy, Biochemistry, Life Sciences, or a related scientific discipline, or relevant vocational training (Ausbildung) in a scientific or laboratory field.
• Ideally 1 to 2 years of relevant laboratory experience.
• Hands-on experience with chromatography, particularly HPLC and/or UPLC.
• Experience with other separation techniques, such as CE and/or iCIEF, is an advantage.
• Previous exposure to a GMP-regulated laboratory or Quality Control environment is an advantage.
• Strong interest in hands-on laboratory work, with good attention to detail, quality, and reliable documentation.
• Adaptability and willingness to learn new analytical techniques, quality systems, procedures, and company-specific GMP requirements.
• Collaborative and responsible mindset, with an interest in continuous learning and professional development.
• Fluency in written and spoken English.

What We Offer

At Terumo, our purpose is Advancing Healthcare with Heart. In this role, your analytical expertise contributes directly to the quality and safety of biopharmaceutical products within an international healthcare company with a strong sense of purpose. You’ll gain hands-on exposure to analytical techniques used in biopharmaceutical Quality Control while further developing your expertise in separations, GMP, method validation, and analytical method transfer. You’ll be part of a collaborative environment where teamwork, knowledge sharing, and continuous learning are valued, with opportunities to contribute your own ideas and help improve the way we work. Guided by our Japanese heritage, our culture is built on respect, ownership, and continuous improvement. We also offer opportunities for professional development, together with a competitive compensation and benefits package.