• Dublin
• Negotiable
• Posted about 18 hours ago

Qualified Person Key Responsibilities: Serve as Qualified Person (QP) for the certification and batch release of clinical trial supplies in compliance with EU regulations. Act as Responsible Person (RP) on the Wholesale Distribution Authorisation (WDA) for Pre-Approval Access activities. Support ...

• Dublin
• Negotiable
• Posted about 19 hours ago

CQV Equipment Engineer Responsibilities: Develop and execute CQV testing documentation for utility systems within a sterile drug product manufacturing facility. Deliver on key project milestones, including safety, schedule adherence, and high-quality documentation/electronic records for assigned ...

• Dublin
• Negotiable
• Posted about 19 hours ago

The Site Utility Engineering Subject Matter Experts (SMEs) will act as Utility System Owners for Black and Clean Utilities. They will be responsible for providing engineering oversight, technical support, and continuous improvement for assigned utility infrastructure, systems, and equipment acros...

• Dublin
• Negotiable
• Posted about 19 hours ago

CQV Equipment Engineer Responsibilities: Develop and execute CQV testing documentation for utility systems within a sterile drug product manufacturing facility. Deliver on key project milestones, including safety, schedule adherence, and high-quality documentation/electronic records for assigned ...

• Dublin
• Negotiable
• Posted about 19 hours ago

CQV Equipment Engineer Responsibilities: Develop and execute CQV testing documentation for utility systems within a sterile drug product manufacturing facility. Deliver on key project milestones, including safety, schedule adherence, and high-quality documentation/electronic records for assigned ...

• Carlow
• Negotiable
• Posted 12 days ago

Are you looking to take the next step in your manufacturing or pharmaceutical career? We're currently recruiting on behalf of a leading global pharmaceutical company for a Production Operator to join their state-of-the-art facility in Carlow. This is a fantastic opportunity to work within a high-...

• Dublin
• Negotiable
• Posted 20 days ago

QC Material Management Analyst My client is seeking to recruit a QC Material Management Analyst to join the QC Site Operations team at its Multi-Product Cell Culture Drug Substance Facility. Reporting to the QC Material Management Supervisor, they will be responsible for supporting site activitie...

• Dublin
• Negotiable
• Posted 21 days ago

My Biopharma client is seeking to recruit a Snr Specialist, QA Compliance Materials Management. Reporting to the Senior Manager, QA Compliance Materials Management, the Specialist will support the material qualification and release activities for its biologic's commercial portfolio and clinical p...