BD Medical | Staff Systems Engineer

Job Description Summary We are seeking a talented Product Security and Threat Analyst Engineer to join our Post-Market Vulnerability Team. You will be at the forefront of our product security cybersecurity defense. This role will focus on identifying, analyzing, and mitigating cyber threats and vulnerabilities affecting BD's medical products. The successful...

Overview The primary function of this role is to provide Quality Engineering support to Production, Quality Control, Purchasing, Facilities, IT, Regulatory, Analytical Lab, Research and Development and Engineering Sustaining teams This includes, but is not limited to, providing support to process validation, change requests, non-conforming product issues,...

Staff Systems Integration Engineer Role: Permanent Hybrid is aligned with the Limerick or Cork offices. The growth and demand for health monitoring has and will continue to grow exponentially. ADI is well positioned to leverage its core sensor and signal processing technology to take advantage of this growth. We are looking for an energetic,...

Overview The primary function of this role is to provide leadership and direction to the Post Market and Manufacturing Engineering teams, while taking overall responsibility for effective and efficient running of the department. The Director, Engineering is also responsible for working with Local and Global Functional Leaders, and Divisions to manage all...

Staff Systems Engineer My client, a leading medical device company, is seeking a Staff Systems Engineer to join their innovative team. In this role, you will contribute to cross-disciplinary product development, driving systems engineering activities throughout the product lifecycle and potentially leading key initiatives. Key Responsibilities: Manage and...

Overview The Manufacturing Engineer 2 (Test Method Validation) performs and documents validations of medical device manufacturing processes. Reporting to: Manager, Manufacturing Engineering Responsibilities Develop and execute Test Method Validations for Test Equipment per current QMS/Regulatory standards. Validate and implement medical device manufacturing...

Overview The Senior Manufacturing Engineer (Test Method Validation) Reporting to: Manager, Manufacturing Engineering Responsibilities Develop and execute Test Method Validations for Test Equipment per current QMS/Regulataory standards. Validate and implement medical device manufacturing processes as assigned. Identify equipment/fixture installation...

Overview The Manufacturing Engineer 2 (Test Method Validation) Reporting to: Manager, Manufacturing Engineering Responsibilities Develop and execute Test Method Validations for Test Equipment per current QMS/Regulatory standards. Validate and implement medical device manufacturing processes as assigned. Identify equipment/fixture installation qualification...

Overview The Global General Ledger (GL) team is responsible for the accuracy and consistency of the General Ledger. The main duty of the role is being responsible for GL processes with the goal of standardising, automating and manage exceptions. The Senior Accountant will have overall accounting responsibility for multiple entities including Cook France. The...

Overview The Regulatory Affairs Specialist 2 helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. The Regulatory Affairs Specialist 2 serves as a communication liaison between the Cook manufacturer and the Cook local affiliates,...

Overview Work as part of the Quality Engineering to provide an efficient service to our customers internally and externally in dealing with product complaints issues and other relevant quality assurance projects as they arise. Reporting to: Team Lead, Quality Engineering Department: Complaints Responsibilities Department:...

Overview The Manufacturing Engineer 2, New Product Introduction will be responsible for key activities within New Product Introduction. Key activities will include leading projects to either introduce new products or support and improve existing products. More specific details are listed below. Reporting to: Manager, Manufacturing Engineering...

Overview Come develop technology solutions that solve planetary-scale problems in the Analog Devices’ battery management business unit. The electric vehicle and green-energy revolution is here, and we are changing the world with our industry leading battery monitoring technology. From the high-performance and thrill that EVs deliver to the...

Overview ​​ The Manufacturing Engineering Specialist is responsible for the preventative maintenance schedule of equipment used in production and engineering. This also includes maintaining a database and all related documentation.​ Reporting to: Manager, Manufacturing Engineering Responsibilities ​​Maintain and implement the...

Overview The primary function of this position is to lead and/or participate in projects focused on design modifications of devices post release to market, for the purpose of maintaining device quality and compliance, as well as reducing costs and increasing yields. Reporting to: Team Lead, Post Market Engineering Responsibilities Lead or...

Overview The primary responsibility of this role is to provide Quality Assurance support as required within Cook Medical Europe Ltd. (CMEU) This includes completing internal audits and maintaining the internal audit system; providing support to software validation, change requests, non-conformance issues and the Company’s corrective and preventive...

Overview The primary purpose of this position is to provide technical support to Production, Manufacturing Engineering and Research & Development. In addition, drive process improvements to increase Manufacturing efficiency plus further develop manufacturing activities within the plant. Reporting to: Manager, Manufacturing Engineering ...

Overview The primary function of this position is to lead and/or participate in projects focused on developing strategy with respect to chemistry, manufacturing, and controls (CMC) of combination drug devices , specifically providing oversight in method development and validation, compendial method verification and transfer , specification/acceptance...

Overview The Tender Representative 1 is responsible for working with Cook Medical Divisions & other relevant departments within Cook, to ensure that Tenders to supply Cook Medical products to the European Market are submitted in a timely and accurate manner. This role is also responsible for ensuring Cook Medical product pricing is updated on the...

Overview The Regulatory Affairs Specialist 2 ensures regulatory compliance to the EU MDR at the office of the EU Authorised representative (AR). The EU AR Office is responsible for verifying compliance to the EU MDR on behalf of Cook Medical’s non-EU manufacturers. The Regulatory Affairs Specialist 2 serves as a communication liaison between the...