Senior Drug Product Engineer, Global Process Development

Amgen; Dublin; Hybrid; EUR 90,000 - 130,000; Full time

Job summary

Amgen Dun Laoghaire, Co. Dublin, Ireland, will remotely support manufacturing at European contract sites. The role spans aseptic drug product processing, tech transfer, and process validation, with international travel to partner sites.

You will lead cross-site teams, troubleshoot parenteral manufacturing, and drive improvements from NPI through commercial production. Qualifications include a science/engineering degree with 5+ years (or Master’s with 3+ years) and a driving license.

Qualifications

• Knowledge of cGMPs and regulatory requirements.
• Proven problem-solving ability demonstrated in prior roles.
• Excellent oral and written communications skills.
• Bachelor’s degree with 5+ years or Master’s with 3+ years related experience, or assoc. degree with 10+ years.
• Full clean driving license required to enable travel between sites.

Responsibilities

• Act as a drug product technical expert and provide leadership for troubleshooting parenteral product manufacturing.
• Lead cross-site teams, set agendas, and identify potential issues.
• Provide process development expertise for aseptic processing, transfer, validation, and characterization.
• Troubleshoot issues with drug product processing technologies and equipment.
• Identify and implement opportunities for improving sterile operations.
• Support commercial manufacturing and external supplier quality with NC/CAPA evaluations.
• Visit contract manufacturing sites to support key production milestones.

Skills

cGMP knowledge

Problem solving

Communication skills

Driving license

Education

Bachelor’s degree in Science or Engineering

Master’s degree in Science or Engineering

Associate’s degree with extensive related experience

Job description

Amgen Dun Laoghaire, Co. Dublin, Ireland, will remotely support manufacturing at European contract sites. The role spans aseptic drug product processing, tech transfer, and process validation, with international travel to partner sites.

You will lead cross-site teams, troubleshoot parenteral manufacturing, and drive improvements from NPI through commercial production. Qualifications include a science/engineering degree with 5+ years (or Master’s with 3+ years) and a driving license.