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• Build and lead the Viral Vector Operations unit
• Drive process development and GMP manufacturing for viral vector platforms (e.g. Lentivurus, MVA)
• Ensure reliable, scalable, and high-quality GMP execution
• Oversee tech transfer, scale-up, and manufacturing readiness

Ensure that the production plan is executed on time and in line with quality requirements, and set priorities according to the situation and business needs....

• Coordinate and lead group retrofit projects: prioritisation, intervention planning, management of urgent situations, and decision‑making.
• Implementation and development of steering tools, standards and dashboards to monitor the activity and its performance.

• Drive implementation and compliance of Product Assurance and quality requirements across space projects
• Lead all Product Assurance activities throughout the complete project lifecycle
• Act as the primary interface for quality-related topics with customers and suppliers

QSHE & COMPLIANCE Oversees the application of Kerry QSHE policies and standards across the engineering department and external service providers. Guides the development, implementation, and upkeep of engineering statutory and compliance requirements at local, national, and regional levels. Ensures...

Design, develop, and advance high‑performance optical thin‑film coatings for DUV, UV, VIS, and NIR applications used in next‑generation semiconductor inspection systems....

• Develop and execute the global product compliance strategy in alignment with business, technology, and sustainability goals
• Ensure globally harmonized compliance practices while adapting to regional regulatory requirements and customer expectations

Define and implement the R&D project management strategy, standards, and methodologies (e.g. stage-gatestage-gate, agile/hybridagile/hybrid) in alignment with business and R&D strategy, including a robust governance framework with clear decision bodies, review cycles, and escalation paths....

Team Leadership & Development: Lead, mentor, and develop a high-performing team of MSAT specialists. Drive the efficiency, structure, and continuous improvement of the group's operations....

• Management of the QC department, including responsibility for budget and personnel
• Ensuring the timely QC testing of relevant materials (e.g., raw materials, intermediates, drug substances, finished drug products)
• Responsibility for method qualification/validation

As a Development Engineer (f/m/div) you will drive and control innovative technology developments for complex products - including scheduling and as customer interface...

• Identify new application opportunities.
• Translate opportunities into technical concepts and application hypotheses.
• Monitor internal and external technology developments to identify further opportunities for innovation, differentiation, or platform expansion.

Defining, leading, and executing R&D programs focused on improving the technical value proposition of Tyvek® nonwovens in the market....

The position as QC Bioassay Manager is responsible for leading a team of seven employees within the Quality Control department of AGC Biologics Heidelberg. This role entails the management and oversight of analytical testing of Bioassay Methods for Proteins and Nucleic Acids, including PCR, ELISA,...

Govern Business Unit product quality performance across development and released products, ensuring alignment with tesa quality objectives...

Take overall P&L responsibility for the Water Line Integrity business in Europe, ensuring sustainable, profitable growth and efficient use of resources....