Data Reviewer, Quality Control - HPLC Biologics (f/m/d)

Lonza; Oberwallis; On-site; Vertraulich; Full time

Benefits offered by this job

Relocation assistance

Competitive compensation

Global benefits

Job summary

Lonza in Visp, Switzerland, is seeking a Data Reviewer (m/f/d) to join its Quality Control team. The role focuses on reviewing analytical data generated during routine QC testing to ensure GMP compliance and timely batch release of monoclonal antibodies.

You will collaborate with QC scientists to ensure data integrity and documentation quality. The ideal candidate holds a BSc or MSc in chemistry, biochemistry, or a related field, with hands-on experience in HPLC and CE techniques (including

Qualifications

• A BSc or MSc in chemistry, biochemistry or a related field, or equivalent experience.
• Experience in a GMP-regulated Quality Control environment is highly preferred.
• Hands-on experience with HPLC and CE techniques, including icIEF, is highly preferred.

Responsibilities

• Review analytical data from HPLC and CE analyses.
• Evaluate quality parameters supporting stability studies and batch release.
• Investigate unexpected or ambiguous results in collaboration with the QC laboratory team.
• Ensure analytical data and documentation comply with GMP requirements, SOPs and internal procedures.
• Support timely batch release through accurate and thorough data review.

Skills

English fluency

Attention to detail

GMP knowledge

Education

BSc or MSc in chemistry/biochemistry or related field

Tools

HPLC

Capillary electrophoresis (CE)

icIEF

Job description

Switzerland, Visp

We are currently looking for a Data Reviewer (m/f/d) to join our Quality Control team in Visp, Switzerland. In this role, you will review analytical data generated during routine QC testing, ensuring compliance with GMP requirements and internal procedures to support the timely release of monoclonal antibody batches. Join our international team and contribute to the quality of innovative biologic medicines.

What You’ll Get

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• A variety of benefits dependent on role and location. The full list of our global benefits can also be found at lonza.com/careers/benefits .
• Relocation assistance for eligible candidates and their families, if needed

What You’ll Do

• Review analytical data from HPLC and capillary electrophoresis (CE) analyses
• Evaluate quality parameters supporting stability studies and batch release
• Investigate unexpected or ambiguous results in collaboration with the QC laboratory team
• Ensure analytical data and associated documentation comply with GMP requirements, SOPs and internal procedures
• Support timely batch release through accurate and thorough data review

What We’re Looking For

• A BSc or MSc in chemistry, biochemistry or a related field, or equivalent experience
• Experience in a GMP-regulated Quality Control environment is highly preferred
• Hands-on experience with HPLC and/or CE techniques, including icIEF, is highly preferred
• Strong attention to detail and a precise, structured approach to reviewing analytical data
• An inquisitive mindset and the ability to critically assess and investigate unexpected results
• Flexibility to adapt to changing priorities in a fast-paced environment
• Fluency in English; German language skills are advantageous

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Reference: R79955