• Carlow
• Negotiable
• Posted about 4 hours ago

I am seeking a Compliance Engineer to support a leading pharmaceutical facility in Carlow. This role offers an opportunity to work in a dynamic, compliance-driven environment within the pharmaceutical industry. Role Overview The Compliance Engineer will be responsible for ensuring compliance, saf...

• Tipperary
• Negotiable
• Posted about 4 hours ago

I'm currently working with a leading global pharmaceutical company that is growing its QA function at a high-performing manufacturing site in Tipperary. This is an excellent opportunity for an experienced Quality Assurance Specialist to step into a senior-level position with a strong focus on GMP...

• Dublin
• Negotiable
• Posted 14 days ago

As a QC Microbiology Specialist, you will play a vital role in supporting Drug Substance and Drug Product activities through a range of microbiological testing and monitoring. Your contributions will directly impact manufacturing operations, product quality, and patient safety. Key Responsibiliti...

• Dublin
• Negotiable
• Posted 14 days ago

Are you ready to take the next step in your engineering career? Our client is seeking a Senior Engineer - Facilities & Soft Services to join their dynamic Engineering team. This critical role will ensure seamless site operations while meeting all regulatory and corporate requirements. What You'll...

• Wicklow
• Negotiable
• Posted 27 days ago

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...

• Dublin
• Negotiable
• Posted about 1 month 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 1 month 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 1 month 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 1 month 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 1 month 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 ...