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The Senior Manager of Global Public Relations will oversee and execute AGC Biologics' PR strategy, build relationships with media and stakeholders, manage crisis communications, and support global marketing initiatives to enhance brand presence and reputation.

The Senior Vice President, Business Development – Global Accounts (EU) will oversee all sales activities for large biopharmaceutical companies, formulating and executing growth strategies. Responsibilities include developing client proposals, managing relationships, and achieving sales targets through effective negotiation and account management.

The Scientist in Quality Assurance Systems will support supplier qualification, audit supplier quality agreements, ensure GMP compliance, manage documentation, and handle deviation reports and batch record reviews in the biopharmaceutical industry.

Assist in the biopharmaceutical production process, including fermentation, cell harvesting, filtration, and conducting in-process controls while ensuring GMP compliance and documentation. Collaborate with a team in a fast-paced production environment with responsibilities including equipment qualification and calibration support.

The Lead Generation Specialist will research the biopharmaceutical market to identify new business opportunities, maintain updated databases, and collaborate with business development and marketing teams to nurture leads. The role involves data analysis and reporting on lead generation metrics, as well as providing customer service to stakeholders and networking at industry events.

The IT Application Specialist will optimize Salesforce solutions, collaborate with business and technology groups, and manage post-implementation support. This role involves gathering requirements, project planning, enhancing systems, and ensuring compliance while balancing multiple projects and teams.

The Principal Scientist in Late Stage Downstream Process Development will plan and coordinate laboratory activities, evaluate experimental results, and provide scientific and technical support. This role involves collaborating with stakeholders and requires strong experience in developing downstream processes as well as knowledge of regulatory aspects of biopharmaceutical production.