PE Global is currently recruiting for a CQV Engineer on behalf of a leading biotech company based in Dublin South. This is an initial 12-month contract role. Overview Owns projects, equipment, responsible for document drafting and protocol execution Single Use / Formulation / Equipment Commissioning and Qualification (C&Q) engineer for a capital project. Ensure the C&Q activities associated with the capital project are completed safely, as per schedule and in compliance with GMP and Quality Requirements. Responsibilities Commissioning & Qualification of Single Use Systems / Formulation Equipment / Process equipment. Generation of all C&Q test documents (C&Q Plan/Set to Works/FAT/SAT/IV/FT/C&Q Summary Report Provide technical assistance during investigations and system design. Coordinates and Supervises all C&Q activities on their systems. Ensures the C&Q schedule is maintained. Manages Daily C&Q coordination meetings. Responsible for Tracking and Reporting of C&Q status and risks/issues. Ensures Startup of equipment/utilities is completed in a safe and coordinated manner. Assist in the development of User Requirement Specifications (URS’s) and Quality Risk Assessment for Equipment and Automated Systems (QRAES). Education / Experience 3+ years’ experience in Engineering or Commissioning and Qualification Management Technical qualification at third level or equivalent in Engineering. Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects preferred Knowledge of safety, GMP and environmental regulatory requirements. Demonstrated strong Communication and Leadership skills. Demonstrated ability to collaborate with senior stakeholders to achieve optimal outcomes. Strong understanding of a risk‑based approach to commissioning and qualification within the biotechnology industry Familiarity with paperless validation systems. Interested candidates should submit an updated CV. Please click the link below to apply, call Kellie on 0214297900 or alternatively send an up to date CV to kellie.hackett@peglobal.net ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** #J-18808-Ljbffr
PE Global Healthcare is delighted to assist its client, a Private Hospital that specialises in caring for patients with cardiac, vascular, eye, orthopaedic and spinal conditions, which also provides both Emergency and Urgent Cardiac Care services. They are now welcoming experienced Orthopaedic Clinical Nurses to apply for a permanent role at this leading health service provider based in Cork. Candidate Requirements Registration with NMBI Demonstrable commitment to patient Safety & Quality Minimum 3 years post‑registration clinical experience Excellent knowledge of contemporary nursing practice and skills Ability to make decisions with excellent organisational skills Benefits Market aligned paygrades Pension Maternity Benefit Continuous Professional Development Free Parking Please call Brenda at PE Global Healthcare on 083 4102611 or email brenda@peglobal.net Please note our clients cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland. #J-18808-Ljbffr
The role: PE Global is currently recruiting for a QA Operations Specialist – NPI on behalf of a leading pharmaceutical company based in Dublin. This is an initial 11-month contract role. Role Description Quality Assurance Operations NPI Specialist An exciting opportunity has arisen for a Quality Assurance Operations NPI Specialist at Biotech client site in Dublin. The role ensures that the New Product Introduction objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers, as well as meeting Health Agency regulations and all other applicable governing regulations. Role Functions (Functions include, but are not limited to, the following) With energy, knowledge & innovation, the QA NPI Specialist will: Review and approve change controls, corrective and preventive actions (CAPAs), deviations including investigation protocols, root cause analysis and final investigation reports. Review and approve batch records Review and approval of Equipment qualification including IOQ and PQ, process validation, development studies, hold time studies etc. Provide quality assurance support across functional and cross-functional forums. Oversee quality aspects of material and supplier management, including preparation of material qualification packages, supplier audit assessments, and maintenance of the supplier management system. Collaborate with stakeholders such as Quality Control (QC), Manufacturing Science & Technology (MS&T), Engineering, and Warehouse to develop, review, and maintain documentation and quality records throughout the product lifecycle (e.g., method validations, facility upgrades, qualification protocols, calibration records). Review and approve Good Manufacturing Practice (GMP) documentation and data to ensure accuracy, completeness, and compliance. Partner cross-functionally to support timely delivery of project milestones. Contribute to the identification, development, and execution of continuous improvement initiatives and action plans in collaboration with cross-functional teams. Ensure the highest Quality, Compliance and Safety standards. General A self-starter and results-focused, the successful candidate will have strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Strong collaboration and cross-functional leadership skills. Strong verbal and written communication skills, project management skills. Experience, Knowledge & Skills Technical Strong knowledge of qualification and implementation of Single Use technologies and raw materials and supplier qualifications for use in a GMP environment. Strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Proven track record in delivering excellence. Competency in the use of SAP, KNEAT, eVal and Veeva systems including change control is an advantage. Familiarity and participation in risk assessment processes Qualifications & Education Education Bachelor’s degree (or higher) in Chemistry, Biology, Microbiology, Engineering or Supply Chain in a relevant discipline. 5 to 8 years’ experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations, or Technical Operations. Interested candidates should submit an updated CV. Please click the link below to apply, call Audrey on 0214297900 or alternatively send an up-to-date CV to audrey.mccarthy@peglobal.net ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** #J-18808-Ljbffr
PE Global Healthcare is delighted to assist its client, a Private Hospital that specialises in caring for patients with cardiac, vascular, eye, orthopaedic and spinal conditions, which also provides both Emergency and Urgent Cardiac Care services. They are now welcoming experienced Orthopaedic Clinical Nurses to apply for a permanent role at this leading health service provider based in Cork. Candidate Requirements Registration with NMBI Demonstrable commitment to patient Safety & Quality Minimum 3 years post‑registration clinical experience Excellent knowledge of contemporary nursing practice and skills Ability to make decisions with excellent organisational skills Benefits Market aligned paygrades Pension Maternity Benefit Continuous Professional Development Free Parking Please call Brenda at PE Global Healthcare on 083 4102611 or email brenda@peglobal.net Please note our clients cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland. #J-18808-Ljbffr
A leading health service provider in Cork is looking for experienced Orthopaedic Clinical Nurses for a permanent role. Candidates must have NMBI registration and at least 3 years of post-registration clinical experience, with a strong commitment to patient safety and excellent nursing skills. The position offers market-aligned pay, pension, maternity benefits, and opportunities for continuous professional development. #J-18808-Ljbffr
PE Global Healthcare is delighted to assist its client, a Private Hospital that specialises in caring for patients with cardiac, vascular, eye, orthopaedic and spinal conditions, which also provides both Emergency and Urgent Cardiac Care services. They are now welcoming experienced Orthopaedic Clinical Nurses to apply for a permanent role at this leading health service provider based in Cork. Candidate Requirements Registration with NMBI Demonstrable commitment to patient Safety & Quality Minimum 3 years post‑registration clinical experience Excellent knowledge of contemporary nursing practice and skills Ability to make decisions with excellent organisational skills Benefits Market aligned paygrades Pension Maternity Benefit Continuous Professional Development Free Parking Please call Brenda at PE Global Healthcare on 083 4102611 or email brenda@peglobal.net Please note our clients cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland. #J-18808-Ljbffr
A leading pharmaceutical company in Dublin is seeking a QA Operations Specialist for an 11-month contract role. The successful candidate will ensure compliance and safety in New Product Introductions, collaborating across multiple functional teams. The ideal candidate will have strong knowledge of cGMPs and related regulations, with 5 to 8 years of relevant experience. Interested candidates should apply with an updated CV or contact via phone for more details. #J-18808-Ljbffr
A leading pharmaceutical company based in Dublin is seeking a QA Operations Specialist for an 11-month contract. The role involves ensuring compliance with quality standards, overseeing quality operations, and collaborating with cross-functional teams. Candidates should possess a Bachelor's degree in a relevant field, along with 5 to 8 years' experience in Quality Control or Assurance. Strong knowledge of cGMP regulations and proficiency in relevant systems are essential. #J-18808-Ljbffr
The role: PE Global is currently recruiting for a QA Operations Specialist – NPI on behalf of a leading pharmaceutical company based in Dublin. This is an initial 11-month contract role. Role Description Quality Assurance Operations NPI Specialist An exciting opportunity has arisen for a Quality Assurance Operations NPI Specialist at Biotech client site in Dublin. The role ensures that the New Product Introduction objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers, as well as meeting Health Agency regulations and all other applicable governing regulations. Role Functions (Functions include, but are not limited to, the following) With energy, knowledge & innovation, the QA NPI Specialist will: Review and approve change controls, corrective and preventive actions (CAPAs), deviations including investigation protocols, root cause analysis and final investigation reports. Review and approve batch records Review and approval of Equipment qualification including IOQ and PQ, process validation, development studies, hold time studies etc. Provide quality assurance support across functional and cross-functional forums. Oversee quality aspects of material and supplier management, including preparation of material qualification packages, supplier audit assessments, and maintenance of the supplier management system. Collaborate with stakeholders such as Quality Control (QC), Manufacturing Science & Technology (MS&T), Engineering, and Warehouse to develop, review, and maintain documentation and quality records throughout the product lifecycle (e.g., method validations, facility upgrades, qualification protocols, calibration records). Review and approve Good Manufacturing Practice (GMP) documentation and data to ensure accuracy, completeness, and compliance. Partner cross-functionally to support timely delivery of project milestones. Contribute to the identification, development, and execution of continuous improvement initiatives and action plans in collaboration with cross-functional teams. Ensure the highest Quality, Compliance and Safety standards. General A self-starter and results-focused, the successful candidate will have strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Strong collaboration and cross-functional leadership skills. Strong verbal and written communication skills, project management skills. Experience, Knowledge & Skills Technical Strong knowledge of qualification and implementation of Single Use technologies and raw materials and supplier qualifications for use in a GMP environment. Strong contemporary knowledge of relevant cGMPs, regulations and current industry trends. Proven track record in delivering excellence. Competency in the use of SAP, KNEAT, eVal and Veeva systems including change control is an advantage. Familiarity and participation in risk assessment processes Qualifications & Education Education Bachelor’s degree (or higher) in Chemistry, Biology, Microbiology, Engineering or Supply Chain in a relevant discipline. 5 to 8 years’ experience in Quality Control, Quality Assurance or Pharmaceutical, Vaccine or Biological Operations, or Technical Operations. Interested candidates should submit an updated CV. Please click the link below to apply, call Audrey on 0214297900 or alternatively send an up-to-date CV to audrey.mccarthy@peglobal.net ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** #J-18808-Ljbffr
PE Global Healthcare in partnership with our client, a leading service provider of specialist residential and respite services for adults and children who have an intellectual disability, autism or acquired brain injury are currently recruiting Community Nurses / Registered Intellectual Disability Nurses (RNID) to cover services in the area of Co. Cork Duties and Responsibilities : Under the direction of the Unit Manager/designated person, the staff nurse will be responsible for the following, ensuring privacy, dignity and respect of the resident at all times. (Full-Time & Part-Time Contracts) The successful candidate requires: RGN/RNMH/RNID qualifications or other suitable nursing qualifications, and to be a Community Nurse on the current register as maintained by An Bord Altranais. Have a strong interest and /or experience in working with children and young adults with an intellectual disability and their families. Excellent communication, teamwork, interpersonal, organisational, and initiative skills. Excellent understanding of Person-Centred Planning, Safeguarding, Risk Management, and Positive Behaviour Support for Children’s Rights. Have an in-depth knowledge and understanding of National Standards for Residential Services for Children and Adults with Disabilities and relevant legislation pertinent to the support of children. Full Driving Licence and Transport is required for this role. Benefits : Comprehensive induction process Extensive training programme On-going mentoring and support Continuous Professional Development support Career progression opportunities Competitive salary with increments based on scope of role, qualifications, and experience. 40 hour week (all breaks paid) 20 days Annual Leave Service based recognition awards €500 refer a friend initiative Employee Assistance Programme for staff and their families Bike-to-Work Scheme Free onsite Car Parking Please call Brenda at PE Global Healthcare on 083 4102611 or email brenda@peglobal.net ***Please note our clients cannot assist with any visa sponsorship, and candidates must have the correct visa to live and work in Ireland*** PE Global Healthcare specialises in providing contract and permanent Healthcare professionals to the private and public sectors. PE Global Healthcare finds jobs for Healthcare Staff in all specialities in Ireland. #J-18808-Ljbffr
