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LOLonza

R&D Project Lead(m/w/x)

Basel
Full-timeOn-siteExperienced

Leading pharmaceutical development projects for biotech products, ensuring QC delivery and documentation. MSc/PhD in relevant science with cGMP analytics experience required. Performance-based compensation programs.

Requirements

  • MSc or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
  • Experience in Analytics or Quality Control under cGMP regulations
  • Knowledge of analytical lifecycle for biotechnology products and CMC requirements
  • Strong communication and interpersonal skills with proactive attitude
  • Detail-oriented and ability to work in matrix organization
  • Business fluent English, written and spoken

Tasks

  • Lead pharmaceutical development projects
  • Ensure timely delivery of QC work-packages
  • Ensure timely delivery of documentation
  • Represent QC in internal meetings
  • Represent QC in customer meetings
  • Address risks proactively
  • Communicate effectively
  • Maintain compliance with cGMP
  • Maintain compliance with SOPs
  • Support audits
  • Act as SME for QC topics
  • Drive process improvements
  • Share best practices

Work Experience

  • approx. 1 - 4 years

Education

  • Master's degree

Languages

  • EnglishBusiness Fluent

Benefits

Bonuses & Incentives

  • Compensation programs that recognize high performance
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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