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LO
Lonza
yesterday

QA Specialist, Batch Record Review(m/w/x)

Visp
Full-timeOn-siteJunior

Description

You will ensure manufacturing excellence by meticulously reviewing batch documentation and collaborating with cross-functional teams to maintain high quality standards and compliance.

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Requirements

  • •Degree in Biology, Chemistry, Biotechnology, or related field
  • •Advantageous experience in GMP pharmaceutical or API industry
  • •Ability to identify non-compliance and quality gaps
  • •Structured, precise, and well-organized working attitude
  • •Openness to new ideas and suggestions
  • •Agile, highly motivated, and dynamic drive
  • •Business fluent English
  • •Preferred good command of German

Education

Bachelor's degree

Tasks

  • •Review executed batch records and production documentation
  • •Examine test procedures, raw data, and logbooks
  • •Ensure documentation completeness to support batch releases
  • •Evaluate batch record comments with operations and QA managers
  • •Support deviations and investigations for review observations
  • •Collect and evaluate regular KPI data
  • •Write and revise SOPs within your area of expertise
  • •Collaborate with quality and operations functions

Tools & Technologies

GMPAPI

Languages

English – Business Fluent

German – Business Fluent

Benefits

Bonuses & Incentives

  • •High performance compensation programs

Career Advancement

  • •Agile career

Informal Culture

  • •Dynamic working culture

Purpose-Driven Work

  • •Inclusive and ethical workplace

Other Benefits

  • •Relocation assistance
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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