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CH
CH12 Lonza AG
last mo.

QA Automation Specialist - Batch Record Review(m/w/x)

Visp
Full-timeOn-site

Description

In this role, you will work closely with various Quality and Operations teams to ensure compliance in manufacturing activities. Daily tasks will involve reviewing batch records, managing quality documentation, and collaborating with customers on automation topics.

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Requirements

  • •Basic GMP knowledge
  • •University degree in Biology, Biotechnology, Life Science, or similar educational background
  • •Basic understanding of GMP and bioprocess manufacturing
  • •Ability to identify non-compliance and gaps from Quality standards
  • •Professional fluency in English and basic German proficiency or willingness to learn
  • •Structured, precise, and well-organized working attitude; open-minded and pragmatic for new ideas and suggestions

Education

Bachelor's degree

Tasks

  • •Review executed electronic batch records in MES Syncade
  • •Participate in MES Syncade Recipe change management
  • •Collaborate with the Operations team to clarify ambiguities in batch records
  • •Manage Quality Records for Batch Record review observations
  • •Ensure completeness of documentation for batch release
  • •Engage with customers on batch record review and automation topics
  • •Collect and evaluate KPI data regularly

Languages

English – Business Fluent

German – Basic

Benefits

Other Benefits

  • •Lifestyle benefits
  • •Relocation assistance

Family Support

  • •Family benefits

Corporate Discounts

  • •Leisure benefits
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