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LO
Lonza
3d ago

Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)

Visp
Full-timeOn-siteSenior

Description

You will lead a specialized team and define the strategic direction for validation and commissioning, ensuring the synthesis facilities meet the highest quality and GMP standards.

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Requirements

  • •Leadership in CQV/CSV within biopharma
  • •Strong background in cGMPs
  • •Knowledge of engineering and manufacturing
  • •Leadership skills and team orientation
  • •Outstanding internal and external communication
  • •Structured and well-organized working attitude
  • •Agility, motivation, and success drive
  • •Proficiency in German and English

Work Experience

approx. 4 - 6 years

Tasks

  • •Lead and develop a specialized CQV and CSV team
  • •Hire and qualify team members
  • •Define the CQV and CSV strategy for synthesis facilities
  • •Provide technical expertise for equipment and clean rooms
  • •Bridge the gap between engineering and operations
  • •Make strategic decisions on validation standards
  • •Ensure compliance in commissioning and qualification phases
  • •Support GMP risk assessments
  • •Act as a subject matter expert during audits
  • •Contribute to the development of global CQV standards
  • •Manage resources and drive continuous process improvements
  • •Collaborate with manufacturing, QA, and engineering departments

Tools & Technologies

CQVCSVcGMPs

Languages

German – Business Fluent

English – Business Fluent

Benefits

Bonuses & Incentives

  • •High performance compensation programs

Family Support

  • •Lifestyle, family, and leisure benefits

Career Advancement

  • •Agile career

Informal Culture

  • •Dynamic working culture

Purpose-Driven Work

  • •Inclusive and ethical workplace

Other Benefits

  • •Relocation assistance
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