On‑Site Batch Record Reviewer for Life‑Saving Medicines

Lonza Group AG; Oberwallis; On-site; CHF 90,000 - 130,000; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Job summary

Lonza Group AG in Visp is seeking a Batch Record Reviewer to ensure flawless compliance and data integrity across critical production projects. This fully site‑based role supports real‑time collaboration and precision required to manufacture medicines to the highest quality and safety standards.

You will review batch records, partner with Manufacturing and Quality teams, and drive continuous improvement while maintaining ALCOA+ data integrity.

Qualifications

• Degree in Life Sciences, Biotechnology, or related discipline (or equivalent).
• GMP‑regulated manufacturing or quality assurance experience.
• Hands‑on with electronic batch records (MES Syncade, DeltaV) and quality systems (TrackWise, SAP, LIMS).
• Strong GDP and ALCOA+ data integrity understanding.
• Good problem‑solving mindset; able to work independently and meet deadlines.
• Fluency in English (written and spoken) is required; reading proficiency is a plus.

Responsibilities

• Review batch records to ensure timely release and compliance.
• Collaborate with Manufacturing and Quality to investigate batch discrepancies.
• Analyze electronic and paper batch records in MES/DeltaV/SAP/LIMS environments.
• Evaluate process parameter failures and material consumption per ALCOA+ and GDP.
• Draft clear quality impact statements and post‑production documentation.
• Drive continuous improvement and data integrity across site production lines.

Skills

GMP experience

Data integrity

Problem solving

Independent work

Education

Life Sciences degree

Biotechnology degree

Tools

MES Syncade

DeltaV

TrackWise

SAP

LIMS

Job description

Lonza Group AG in Visp is seeking a Batch Record Reviewer to ensure flawless compliance and data integrity across critical production projects. This fully site‑based role supports real‑time collaboration and precision required to manufacture medicines to the highest quality and safety standards.

You will review batch records, partner with Manufacturing and Quality teams, and drive continuous improvement while maintaining ALCOA+ data integrity.