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Supervisor, Manufacturing Bioconjugates - Job Opportunity at Lonza

Visp, Switzerland
Full-time
Senior
Posted: April 20, 2025
On-site
CHF 120,000 - 150,000 per year based on Swiss market conditions and role seniority

Benefits

Relocation assistance for eligible candidates and families
Global career development opportunities
Impact-driven work environment
Ethical business practices focus
Comprehensive professional development

Key Responsibilities

Lead and manage Bioprocess Engineering team for ADC manufacturing
Oversee process procedures and MES recipe management ensuring GMP compliance
Serve as primary liaison for project teams, customers, and regulatory audits
Drive deviation and change management processes
Ensure manufacturing operations meet safety and quality standards

Requirements

Education

Master's Degree in Biotechnology, Biochemical Engineering, Biochemistry or related Life Science subject, or Bachelor's with relevant experience

Experience

Solid work experience in Downstream Processing or BioConjugates Manufacturing

Required Skills

In-depth knowledge of downstream processing techniques GMP understanding Excellent communication skills in English German language skills (advantage) Team collaboration Process management Documentation expertise Audit management
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Sauge AI Market Intelligence

Industry Trends

The bioconjugates and ADC market is experiencing rapid growth, with increasing demand for specialized manufacturing expertise particularly in oncology therapeutics Manufacturing supervision roles in bioconjugates are becoming increasingly critical as more ADC products enter clinical trials and commercial production The shift towards more complex biological therapeutics is driving demand for professionals with combined expertise in both upstream and downstream processing

Role Significance

Typically manages 5-8 Bioprocess Engineers in a GMP manufacturing environment
Senior technical leadership position with direct impact on product quality and regulatory compliance in critical therapeutic manufacturing

Key Projects

ADC manufacturing process optimization and scale-up Technology transfer and new product introduction Regulatory compliance and audit management Manufacturing process validation and documentation

Success Factors

Deep technical expertise in bioconjugation and downstream processing Strong leadership capabilities in a GMP environment Excellence in cross-functional communication and stakeholder management Ability to balance technical, regulatory, and operational demands

Market Demand

High demand with limited talent pool due to specialized nature of bioconjugates manufacturing expertise

Important Skills

Critical Skills

Bioconjugation expertise due to specialized nature of ADC manufacturing GMP compliance knowledge for ensuring regulatory standards Team leadership capabilities for managing technical staff Process optimization skills for maintaining manufacturing efficiency

Beneficial Skills

Project management capabilities for handling multiple production streams Quality systems knowledge for maintaining compliance Risk assessment and mitigation expertise Technical writing skills for documentation requirements

Unique Aspects

Role combines technical leadership with direct manufacturing oversight in advanced therapeutics
Position at one of Europe's leading biotech manufacturing hubs
Opportunity to work on cutting-edge ADC products
Strong focus on professional development and global career opportunities

Career Growth

2-4 years in role before advancement, depending on business growth and performance

Potential Next Roles

Manufacturing Department Head Technical Operations Director Site Head of Manufacturing Process Excellence Leader

Company Overview

Lonza

Lonza is a leading global contract development and manufacturing organization (CDMO) with significant presence in biological therapeutics

Top-tier CDMO with strong market position in bioconjugates and complex biologics manufacturing
Visp site represents one of Lonza's largest and most strategic manufacturing locations globally
Innovation-driven environment with strong focus on technical excellence and regulatory compliance
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