Senior Global Regulatory Affairs Lead (Hybrid)

West Pharmaceutical Services, Inc; Ireland; Hybrid; EUR 60,000 - 76,000; Full time

Benefits offered by this job

Hybrid work

Professional development

Job summary

West Pharmaceutical Services, Inc. in Ireland is seeking a Senior Regulatory Affairs Specialist to coordinate material compliance for parenteral packaging, devices and contract manufacturing portfolios in a hybrid work setting.

You will ensure timely regulatory deliverables, mentor team members, and guide cross‑functional groups on US and international regulations and environmental requirements.

Qualifications

• Bachelor's, Master's or PhD in science, math, engineering or equivalent.
• Minimum 5 years of experience in Regulatory Affairs or equivalent.
• Experience with US and international regulations and guidelines.

Responsibilities

• Coordinate material compliance for parenteral packaging and devices.
• Submit regulatory reports and manage timelines.
• Communicate with suppliers for documentation and inquiries.
• Develop compliance processes and tool requirements.
• Monitor regulations and provide cross-functional regulatory guidance.
• Mentor team members and provide training.

Skills

Regulatory affairs

Team leadership

Cross-functional collab

Project management

Education

Bachelor/Master/PhD in science or engineering

Tools

MasterControl

SharePoint

MS Excel

MS Word

Job description

West Pharmaceutical Services, Inc. in Ireland is seeking a Senior Regulatory Affairs Specialist to coordinate material compliance for parenteral packaging, devices and contract manufacturing portfolios in a hybrid work setting.

You will ensure timely regulatory deliverables, mentor team members, and guide cross‑functional groups on US and international regulations and environmental requirements.