The Procurement Manager for indirect spend at AGC Biologics will manage sourcing activities, ensure effective purchase order processes, lead procurement for services and products, achieve cost savings, and mentor the procurement team while collaborating with internal stakeholders.

The Lead Generation Associate II will identify new business opportunities for drug manufacturing by researching biopharma drug developers. Responsibilities include maintaining databases, collaborating with the BD team, analyzing lead generation metrics, providing insights to stakeholders, and networking at industry events.

The Global Marketing Specialist II supports the planning, execution, and operational management of global marketing events and tradeshows for AGC Biologics. Responsibilities include managing vendor agreements, coordinating logistics, and tracking budgets. This role enhances brand awareness through effective marketing strategies and requires strong communication and organizational skills.

The Senior Manager, Global Public Relations will lead AGC Biologics' PR strategy, manage media relations, secure media coverage, and support crisis communications. This role involves relationship-building with media outlets and providing strategic counsel to executives, ensuring alignment on messaging and company reputation management.

As a Payroll Manager, you will lead payroll operations ensuring compliance, optimize payroll strategies, resolve issues, and manage payroll systems. You'll also collaborate with HR and Finance while developing your team and driving process improvements in alignment with organizational goals.

The role involves cleaning designated clean rooms according to standard operating procedures, documenting cleaning processes, adhering to hygiene regulations, and managing inventory of cleaning supplies. Candidates should have experience in cleaning, preferably in biopharma environments, and must communicate in German.

As the Manager of Late Stage Process Development, you will lead a team of 12 scientists and technicians focusing on late-stage biopharmaceutical processes. Your role includes overseeing operations, fostering teamwork, ensuring compliance with quality standards, and supporting project execution while enhancing department effectiveness and staff engagement.

The IT Application Specialist will optimize the Salesforce environment, collaborate with business and tech teams to gather requirements, manage the design and implementation of solutions, and provide post-implementation support to enhance operational efficiency across the global sales organization.

The role involves cleaning and maintaining controlled environments in a biopharmaceutical setting, adhering to SOPs, documenting cleaning activities, ensuring personal hygiene standards, managing inventory, and performing tasks as directed by supervisors.

The Senior CMC Project Manager will lead projects from proposal to completion, managing communications with clients and the project team. Responsibilities include planning and organizing projects, assessing risks, and ensuring timely and budget-compliant project delivery while providing recommendations for future improvements and building high-performing teams.

The Principal Scientist will coordinate and conduct laboratory activities, ensuring data integrity while authoring protocols and reports. They will work on developing downstream processes for biopharmaceuticals produced from mammalian and microbial cell lines and collaborate with various stakeholders to advance products towards commercial manufacturing.

The SVP, Business Development – Global Accounts (EU) is responsible for driving sales to large biopharmaceutical clients, formulating strategies for business growth, and leading contract negotiations. The role involves establishing relationships, developing account plans, and achieving revenue targets while collaborating with internal teams.

The Lead Generation Specialist will identify new business opportunities for drug manufacturing in the biopharmaceutical sector. This role involves market research, maintaining databases, collaborating with business development teams, and presenting insights to stakeholders.

The Director of Mammalian Operations will lead a department of approximately 40 employees in the biopharmaceutical industry, ensuring regulatory compliance, managing talent, and driving continuous improvement in manufacturing operations. Responsibilities include overseeing production processes, strategic planning, and participating in regulatory inspections, all while fostering a strong team culture.

The Senior IT Application Architect will lead the design and implementation of functional solutions across ERP and CRM systems. The role focuses on integrating business processes with IT infrastructure, providing strategic advice on applications, and establishing standards that enhance operational excellence in alignment with AGC Biologics’ mission.

The Biologisch-Technischer Assistent (BTA) will support the production team by preparing and conducting fermentations, harvesting cells, and performing various filtration techniques, ensuring compliance with GMP standards, and assisting with equipment qualification and documentation processes.

The Cost Controller will oversee CSRD reporting, manage cost tracking and analysis, including profitability calculations, and support COGS and Reimbursed Revenue recognition. This role involves collaboration with various teams, financial audits, and improving reporting processes while ensuring accuracy and compliance with financial standards.

The Senior Scientist in the QA Mammalian team will ensure quality assurance for biopharmaceutical production, resolve quality issues, review and approve technical documents, support SOP development, collaborate with management on project issues, and assist in audits and quality agreements with clients.

The IT Application Specialist will manage configurations of PPM software, gather requirements, assist in testing and implementation, and create system documentation while collaborating with stakeholders. They will support integration with external applications and troubleshoot issues post-implementation, while also maintaining technical knowledge and best practices.

The Scientist in Quality Assurance - Systems will oversee supplier qualification, assist in audits and inspections, maintain and enhance the Quality Management System in compliance with GMP, manage documentation, ensure compliance during production, and handle deviations and regulatory processes.