Associate Director, Quality Control - Athlone

Responsibilities

• Exercise full Quality Control authority and compliance oversight including approval or rejection of products and materials.
• Lead the establishment and continuous improvement of site Quality Control laboratories.
• Build, hire, and develop a high-performing QC organization.
• Support procurement, installation, and qualification of laboratory equipment.
• Participate in site Quality Management Review, providing oversight of QC performance.
• Establish, implement, and maintain compliant QC systems and procedures.
• Author, review, and approve complex GMP documentation.
• Support analytical method transfer, validation, and lifecycle management.
• Generate and assess current and future QC needs and manage associated department budget.
• Maintain effective oversight of outsourced activities.
• Partner cross-functionally to enable compliant product release and new technology introductions.

Requirements

• Required Skills:
• Bachelor's degree in science or directly related discipline.
• Strong experience within GMP compliant Quality Control or Analytical functions.
• Significant experience in pharmaceutical or biotech analytical environment.
• Strong experience of personnel and project management experience.
• Experience with analytical method transfer and validation.
• Preferred Skills:
• Start-up Experience.
• Complex Biologic Method Experience.
• Advanced degree in a related field.
• Eligibility for Qualified Person (QP) is a distinct advantage.
• Strong budget management and financial approval capabilities.
• Job Level: Management
• Why Biogen?

Additional Information

About This Role: As the Associate Director of Quality Control at our Athlone site, you will be a pivotal leader in ensuring the integrity and compliance of our Quality Control operations. This role is crucial for establishing and maintaining site-wide QC processes in alignment with EU GMP, FDA, and global regulatory standards. You will oversee incoming inspection, raw material, in-process, environmental monitoring (EM), utility testing, and finished product testing and release, including governance of the site EM program. The role focuses on enabling site start-up, ensuring sustained GMP compliance, and maintaining a continuous state of inspection readiness. Your leadership will extend to laboratories, personnel, equipment, analytical methods, and systems, guaranteeing they are aptly designed, validated, and maintained for use in line with regulatory expectations. By proactively shaping future QC capability and advancing technology and digital innovation, you will position the function to support evolving pipeline and manufacturing demands. Through strong cross-functional partnership, you will enable compliant QC operations, while leading the successful introduction of new programs and technologies that strengthen and future-proof the site in line with business needs. This role requires working on site for 5 days per week in Athlone.

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