Barry O'Mahony

Are you a proactive quality professional ready to take the lead in driving compliance and continuous improvement in a dynamic medical device environment? My client is looking for a Senior Quality Engineer to join their team and play a critical role in upholding the highest standards of quality an...

Are you a proactive quality professional ready to take the lead in driving compliance and continuous improvement in a dynamic medical device environment? My client is looking for a Senior Quality Engineer to join their team and play a critical role in upholding the highest standards of quality and regulatory compliance. Key Responsibil...

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 ...

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 regulatory authority inspections and aud...

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 ...

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 equipment and utilities. Ensure testing ...

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...

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 across the site. Key Responsibilities: Ensure...

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 ...

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 equipment and utilities. Ensure testing ...

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 ...

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 equipment and utilities. Ensure testing ...