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LO
Lonza
last mo.

Senior QA Automation Specialist(m/w/x)

Visp
Full-timeOn-siteSenior

Description

In this role, you will collaborate with internal teams on quality assurance for electronic batch records, ensuring compliance and consistency. Daily activities will involve reviewing batch records, managing performance metrics, and supporting the QA department to maintain high-quality standards.

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Requirements

  • •Academic degree in Chemistry, Biotechnology, Life Sciences, or related field
  • •Solid experience in GMP-regulated pharmaceutical/API industry
  • •Experience in electronic batch records (execution and/or review)
  • •Ability to recognize non-compliance and gaps in quality standards
  • •Structured, detailed, and well-organized work attitude; open-minded to new ideas; agile, highly motivated, and dynamic
  • •Business fluent English; good German language skills advantageous

Education

Bachelor's degree

Work Experience

approx. 4 - 6 years

Tasks

  • •Partner with internal customers on quality topics related to eBR setup
  • •Check and approve master production records for consistency
  • •Review completed batch records within specified timeframes
  • •Review minor deviations, investigations, and CAPAs by due dates
  • •Ensure closure and archiving of batch records after completion
  • •Assist in managing and tracking performance metrics and quality data
  • •Support QA department in various meetings
  • •Take on additional tasks as assigned

Languages

English – Business Fluent

German – Basic

Benefits

Bonuses & Incentives

  • •Compensation programs that recognize high performance

Corporate Discounts

  • •Numerous lifestyle benefits
  • •Leisure benefits

Family Support

  • •Family benefits

Other Benefits

  • •Relocation assistance
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