Sr. Associate Facilities & Engineering Compliance (Day role)

amgen; Dún Laoghaire; On-site; EUR 60,000 - 81,000; Full time

Job summary

Amgen Dun Laoghaire is seeking an L4 Senior Sr Associate to manage Facilities & Eng Compliance. The role focuses on leading deviation investigations for fill/finish and packaging, ensuring GMP compliance, and producing audit-ready documentation.

You will drive root-cause analysis, develop CAPAs, and coordinate cross-functional teams to deliver investigations on schedule. The position requires strong technical writing and regulatory communication skills.

Qualifications

• Bachelor's Degree in Science or Engineering with 5+ years of directly related experience in biotech/pharma manufacturing or support roles.
• Associate's Degree in Science or Engineering with 8+ years of directly related experience in biotech/pharma manufacturing or support roles.
• 10+ years directly related experience in a biotech/pharma manufacturing or manufacturing environment.

Responsibilities

• Lead investigations for deviations across fill/finish, inspection and packaging.
• Develop CAPAs and product impact assessments; write compliant documentation of findings.
• Present complex investigations to regulators and internal auditors; communicate progress to leadership.
• Coordinate cross-functional teams; manage investigations end-to-end; drive improvements in processes.

Skills

Investigation leadership

Root cause analysis

Project management

Technical writing

Communication

Quality systems

Education

Bachelor's degree in Science or Engineering

Associate's degree in Science or Engineering

10+ years biotech/pharma experience

Job description

Career Category

Compliance

Job Description

L4 Senior Sr Associate Facilities & Eng Compliance

Overview: Reporting to Validation Management, this position will manage Facilities & Engineering Deviations and Compliance for Amgen Dun Laoghaire (ADL).

This L4 Senior Associate Validation (Facilities & Eng Compliance) will be primarily responsible for leading investigations for fill/finish/inspection and packaging deviations and ensuring compliance with GMP and regulatory expectations. Please note this is a day role.

This role will also be involved in applying process, quality, compliance, and analytical knowledge to complete the following:

Manage deviation investigations, including establishing investigation teams, leading root

cause analysis, development of CAPAs, completing product impact assessments and

writing compliant documentation of all findings.

• Clear and concise technical writing of complex investigations
• Drive improvements to the investigation process
• Present investigations to regulatory inspectors and internal auditors
• Clearly communicate investigation progress to impacted areas and leadership

Quality Systems & Compliance

• Ensure compliance with GMP regulations, company procedures, and quality standards.

• Support inspection readiness and regulatory commitments.
• Validation lifecycle compliance

• Ensuring validation documentation remains audit-ready and GMP compliant.

Coordinate and lead cross-functional teams through complex investigations, and complete

tasks on schedule.

• Project management of the investigations end to end

• Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues.
• Build effective relationships across functions.
• Navigate through ambiguity and provide a structured problem-solving approach.
• Able to apply inductive and deductive reasoning in the investigation process

Qualifications:

Bachelor's Degree in Science or Engineering and 5+ years of directly related experience in

a biotech/pharma manufacturing or manufacturing support role (i.e. process development,

engineering, quality)

OR

* Associate's Degree in Science or Engineering and 8+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (i.e. process development, engineering, quality)

* 10+ years directly related experience in a biotech/pharma manufacturing or manufacturing environment.

• Detailed technical understanding of fill/finish operations.

• GMP and regulatory knowledge (FDA, EU GMP, Annex 1)
• Experience with compliance, problem-solving, root cause analysis, critical thinking, project management, and quality systems.

• Experience leading complex investigations.
• Experience participating in and leading cross-functional teams.
• Experience in managing multiple, competing priorities in a fast-paced environment.
• Experience presenting to inspectors during regulatory inspections and internal audits.
• Excellent technical writing.

Excellent presentation and communication skills, ability to communicate and collaborate

with technical and management staff.

• Ability to be flexible and manage change.

Personal Attributes

• Detail-oriented with a strong focus on quality and compliance.
• Ability to work under pressure and manage multiple priorities effectively.
• Proactive and self-motivated with a continuous improvement mindset

Salary Range

60,090.75EUR-81,299.25EUR