At Pharma-BioServ, we are recruiting a Technology Transfer Engineer to join our existing team of consultants working within the R&D department of our medical device client based in Cork. The purpose of this role is tolead from a Technology and Product Inspection perspective related to all Strategic Inspection/Compliance activities. Role Coordinate and deliver 2D Barcoding as per project timelines. Integrate with the Do It Right Program in supporting Process Characterisation activities and identifying ..... (continued)

At Pharma-BioServ, we are recruiting a Manufacturing Quality Engineer to join our existing team of consultants working within the R&D department of our medical device client based in Cork. The purpose of this role is to lead from a Technology perspective the implementation and development of vision and integrated Laser marking systems. Role Introduce new technologies in parallel for new product introductions and current processes to ensure compliance to all regulations/specifications. CNC Programming ..... (continued)

At Pharma-BioServ, we are recruiting a QA Validation Engineer to join our existing team of consultants working within the R&D department of our medical device client based in Cork. The purpose of this role is to support the development and implementation of new technologies in the CNC, Vision and Laser marking areas. Role Validation of Software/Hardware based systems involving CNC, integrated Vision and Laser marking systems. Document and maintain in good order all relevant Quality assurance sections ..... (continued)

At Pharma-BioServ, we are recruiting a Validation Engineer for a 12 month contract in Cork. The purpose of the role is to provide validation support to process, equipment, facility, utility and method validation activities. Role Have knowledge of and ability to provide Interpretation and Guidance on Regulations, Corporate, Divisional and Site Local procedures as they relate to validation activities. Develop and revise Validation Procedures and Templates to ensure that Current Regulatory Compliance ..... (continued)

At Pharma-BioServ, we are recruiting a Quality Engineer to join our existing team within the R&D department of our medical device client based in Cork . Role Produce and maintain appropriate and comprehensive quality process specifications as required during the development and implementation of new technologies/processes. Document and maintain in good order all relevant Quality assurance Design Controls as directed by Data Management. Generate URS for new technology / equipment as a part of the ..... (continued)

At Pharma-BioServ, we are recruiting a Project Engineer for an automation project in Limerick. This is an initial 8 month contract role. The Project Engineer will be responsible for developing a new State-of-the-Art Automated Manufacturing Process. Engineer will develop clear user requirements, identify solutions, develop solutions with the chosen Vendor, carry out FAT, Validation, Training and transfer to Production. Role Engagement and support the wider team in delivery of the Project. Development ..... (continued)

At Pharma-Bio Serv we are recruiting a Quality Engineer to support manufacturing for 10 month contract in Cork. Role Provide effective and responsive QA support to Operations to resolve in-house, customer and supplier issues. Ensure Regulatory compliance in area of responsibility to GMP of all medical devices regulatory agencies (i.e. FDA, IMB and BSI). Assist in development, review and approval of process and equipment validation (IQ, OQ and PQ). Lead Problem Solving meetings using the following: 4D ..... (continued)

At Pharma-Bio Serv we are hiring a Snr Planner for a 6 month contract for a biopharma plant in Cork. Role Maintains day-to-day interactions with production floor. Conduct excess and obsolete inventory reviews for Raw Materials and Components. Maintains Day to day interaction with Suppliers and confirm purchase orders as applicable. Interprets Material Requirements Planning (MRP) requirements and release/communicate requirements to Suppliers. Ensures inventory levels meet production needs as well as ..... (continued)

At Pharma-BioServ, we are recruiting a Supplier Quality Engineer for an initial 12 month contract in Cork. Role Liaising with the Manufacturing and Quality engineers in the Business Units, in assessing and addressing material quality issues. Perform supplier quality audits and management of the supplier corrective action process. Implement and develop mechanisms to monitor and identify supplier non-conformance trends Track supplier quality performance measurements for suppliers (KPI’s) and participate ..... (continued)

At Pharma-BioServ, we are hiring a CMM Programmer/Engineer to join our existing project in Cork. This is an initial 12 month project and you will be working as a Consultant with Pharma-Bio Serv. The purpose of the role is to provide support for the inspection strategy associated with all metrology equipment Role Standardize site wide CMM infrastructure by facilitating, encouraging and coordinating continuous improvement. Support day to day manufacturing requirements with respect to CMM’s CMM ..... (continued)

At Pharma-BioServ, we are recruiting a Manufacturing Validation Engineer to join our existing team of consultants working within the R&D department of our medical device client based in Cork. The purpose of this role is to support the validation of CIP processes to GAMP/FDA standards, and provide additional support to other projects as required. Role Continuous Improvement Focus Generate and review validation documents (URS, RA, FDS, VP, IQ’s, OQ’s & PQ’s) Execute validation protocols and generate ..... (continued)

At Pharma-BioServ, we are hiring a Snr Compliance Specialist for a project in Limerick. This is an initial 6 month project role working as our consultant on site. Role Maintains regulatory inspection readiness plans on site. Ensures that audit procedures align with MD&D expectations. In accordance with defined procedures and Master schedule perform required audits. Ensure proper reporting, response review and approvals, communication of issues, and use of tracking and trending tools. As appropriate ..... (continued)

At Pharma-Bio Serv we are hiring a Project Manager for a strategic role on a medical devices facility in Cork. This is an initial 12 month contract. The position will involve the management of Project Teams to deliver new business systems to the Operational and Engineering function. This role will have responsibility for the development of new standards for Technology Development and the implementation of those across the Engineering Function. Role Development and implementation of Advanced Business ..... (continued)

At Pharma-Bio Serv we hiring x 4 Project Engineers for 12 month projects on a regulated manufacturing facility in Limerick. Role Project Engineer working on high speed, highly automated, complex and integrated manufacturing equipment. Project manages discrete retrofit projects of various sizes to increase equipment output, while adhering to cost, schedule, safety and quality requirements. Lead the development and Improvement of new and existing equipment and/or process. Drive equipment OOE ..... (continued)

At Pharma-Bio Serv we are hiring a Project Engineer for a 12 month project on a medical devices facility in Cork. The primary purpose of this job is to support manufacturing through the continuous development of manufacturing processes and projects to achieve operational targets. Role Continuous Improvement Focus Deliver key projects to the Value Stream which will positively impact on the key metrics. Drive process improvements/capacity increases through New technology/equipment introductions ..... (continued)

At Pharma-BioServ, we are hiring a Supplier Quality Engineer to join our existing team and work as a consultant within the R&D department of our medical device client based in Cork . This is an initial 6 month contract role. Responsible for implementation of External Manufacturing Quality Systems to support outsourcing of products ensuring Quality, Operational, Process Improvement and Product Development/Transfer issues and projects are implemented in an efficient and effective manner that minimizes risk ..... (continued)

At Pharma-BioServ, we are hiring a Validation Engineer to join our existing team and work as a consultant in our medical device client based in Cork . This is an initial 12 month contract role. The Validation Engineer is a member of the Product Transfer team, playing a key role in the planning and execution of validation activities related to project. Provide support for the validation activities associated with equipment & processes ensuring that all compliance issues and requirements of Company ..... (continued)

At Pharma-Bio Serv we are recruiting a Production Supervisor for a medical devices company in Cork. Role People management - supervision of production teams to ensure targets for quality/service/costs are achieved. This will be achieved through the application of an empowering style of leadership which draws fully on resources and capabilities of the team coupled with a positive Employee Relations approach. Planning - including developing /maintaining a viable plan incorporating hiring, training, ..... (continued)

At Pharma-Bio Serv we are recruiting a Warehouse/Materials Supervisor for a medical devices company in Cork. Role People management - supervision of the warehouse team to ensure that all customer (both internal and external) metrics are serviced in line with expectations. This will be achieved through the application of an empowering style of leadership which draws fully on resources and capabilities of the team coupled with a positive Employee Relations approach. Through policy and procedure ..... (continued)

At Pharma-BioServ, we are recruiting a Laser Vision Engineer to join our existing team of consultants working within the R&D department of our medical device client based in Cork. The purpose of this role is to lead from a Technology perspective the implementation and development of vision and integrated Laser marking systems. Role Introduce new technologies in parallel for new product introductions and current processes to ensure compliance to all regulations/specifications. Programming and support ..... (continued)