Contract Manufacturing Site Lead — Senior Manager

Amgen Inc. (IR); Dublin; On-site; EUR 102,000 - 137,000; Full time

Job summary

Amgen is seeking a Contract Manufacturing Senior Manager (Site Lead) to develop and lead robust business processes, manage budgets, contracts, and capacity planning across contract sites. You will drive operational excellence and work closely with external CMOs to ensure reliable performance.

This role requires 8+ years in protein/API/DS/DP or packaging, deep knowledge of cGMP and regulatory guidelines, plus 3+ years of cross-functional leadership.

Qualifications

• Bachelor’s degree required in Business Administration, Engineering, or a science-related field.
• 8+ years in protein, API, DS/DP, or packaging manufacturing environments.
• 8+ years knowledge of cGMP principles, FDA and regulatory guidelines, and validation principles.
• 5+ years working with external parties or leading cross-functional teams for clinical/commercial products.
• 3+ years project management leading multi-functional and multi-location teams.
• 3+ years experience across ACM or CMQ.
• Ability to travel +/- 20% (domestic and international).

Responsibilities

• Develop and lead robust business processes across contract sites.
• Manage budget development, monitoring, and reporting; contracts and information requests.
• Monitor contract site performance using lean tools and PDCA; lead operating reviews.
• Lead department-wide projects from conception to implementation and transfer activities to contract sites.

Skills

Cross-functional leadership

Budget management

Problem solving

Risk management

Education

Bachelor’s in Business Administration, Engineering, or Science-related field

Job description

Amgen is seeking a Contract Manufacturing Senior Manager (Site Lead) to develop and lead robust business processes, manage budgets, contracts, and capacity planning across contract sites. You will drive operational excellence and work closely with external CMOs to ensure reliable performance.

This role requires 8+ years in protein/API/DS/DP or packaging, deep knowledge of cGMP and regulatory guidelines, plus 3+ years of cross-functional leadership.