Job Title: Equipment Engineer Senior A1745 About the Company:Our client is a Multinational Biopharmaceutical company with more than 20,000 employees worldwide and approximately 500 workers in its D n Laoghaire (co. Dublin) facility, which is a 37,000-square-metre aseptic operations facility with freeze-dry product (lyophilization) and liquid vial-filling capabilities.Its Irish site specializes in secondary manufacturing activities formulation, fill, and packaging, and also includes a bioprocessing suite and laboratories. The local team is currently engaged in one of the largest and fastest technology transfer programs in the company s history. Make a difference in the lives of others, working at the forefront of biotechnology with the top minds in the field. Job Summary:The Project / Equipment Engineer reports to the Senior Manager for Strategic Engineering Projects and is responsible for scoping and executing technical projects supporting Drug Product manufacturing within Formulation, Component Preparation, Vial/Syringe Filling, Lyophilisation, Device Assembly, Inspection, Labelling and Packaging areas. This includes qualification of new equipment and implementation of associated reliability and maintenance programs. Job Duties: Project management and execution of assigned projects including project prioritization, resources management, status management and external communication. Working with various stakeholders, to scope projects and ensure requirements are satisfied. Project input will span from concept, through design, construction, commissioning and operation Coordinating the introduction of new processes, equipment and materials including problem solving and troubleshooting equipment issues prior to qualification & start-up Development and implementation of maintenance programs and spare parts inventory optimization with the introduction of new equipment. Ability to translate strategic/emerging technology solutions into pragmatic executable plans Development and management of change controls Participate as a member of multidisciplinary site and multisite teams Development of detailed specifications, engineering documents, protocols and standard operating procedures Work in a collaborative manner within the Process Teams structure and contributes to Root Cause Investigations and Cross Functional Investigations. Works in a collaborative manner with the System Owners, Maintenance Supervisors & Technicians, Capital Project Engineers and Vendors to perform equipment upgrade and/or retrofits. Perform all tasks with due care and attention ensuring compliance with Good Manufacturing Practices and company requirements, policies and procedures Support a safe working environment by complying with environmental health/safety practice, rules and regulations Travel may be required to support execution of projectsRequirementsExperience and Qualification: Bachelor s Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience Typically, 5+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection, Labelling and Ancillary processes. Filling or Packaging Experience preferred. Technology transfer experience preferred. Proven project management experience. Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous Demonstrated experience in a GDP Compliant environment. Experience in MS Office, MS Project, Change Control & Document Management Systems Proven ability working cross functionally, delivering technical solutions and implementing improvements. Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results Technical report writing and communication/presentation skills Data driven decision maker Ability to work to tight deadlines in a fast-moving environment*** No Visa Processing ***BenefitsBenefit from Independent Solutions ethical principles!We look after our team, we know the business, we have been working in the sector >20 years. We are not a recruitment agencyWhile placed on client sites you will be an integral part of our team, gaining support and access to the knowledge and experience of our cross functional LifeScience teamWe offer attractive rates - competitive margins compared to our competitorsPayment on time and in fullWe continue to partner and grow our client base and thereby ensure that we have a continuous supply of High-Value ProjectsWe work for you! Experience and Qualification: Bachelor s Degree in Engineering (Mechanical, Electrical or Chemical) or Relevant Experience Typically, 5+ years engineering experience, preferably in the biotechnology industry / aseptic pharmaceutical environment or Automated Inspection, Labelling and Ancillary processes. Filling or Packaging Experience preferred. Technology transfer experience preferred. Proven project management experience. Strong mechanical capability with hands on experience in a technical role within a high-volume manufacturing environment, is advantageous Demonstrated experience in a GDP Compliant environment. Experience in MS Office, MS Project, Change Control & Document Management Systems Proven ability working cross functionally, delivering technical solutions and implementing improvements. Solid leadership skillset and experience working in a team environment, embracing an interdependent working culture that delivers results Technical report writing and communication/presentation skills Data driven decision maker Ability to work to tight deadlines in a fast-moving environment *** No Visa Processing ***
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