PRINCIPAL MAINTENANCE AND RELIABILITY ENGINEER
Canovanas
| Employer: | AstraZeneca |
| Job Type: | Full Time |
Description | |
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The Maintenance and Reliability Engineer is accountable for delivering maintenance excellence activities across assigned equipment, facilities and utility systems to deliver cost savings, energy reductions, improved uptime, and improved overall equipment and systems reliability. This role serves as the Technical Lead of the site Reliability and Total Productive Maintenance (TPM) processes. Executes/deliver the TPM strategy as per site goals targets. Serve as the System Owner for assigned systems, ensuring compliance with company policies, procedures, and all applicable regulations. Acts in a leadership role in providing engineering support and technical expertise for GMP and non-GMP related equipment and utilities systems. This role will foster a reliability focused mindset where equipment and related systems downtime impact becomes part of the day-to-day decision making. By working closely with cross-functional team disciplines, this role will ensure that the iPR manufacturing operation is working towards executing in an efficient and effective way. Plays a key role in supporting the strategy development, project/process improvements and representing the site on related regional or global forums. The incumbent is responsible for leading and maintaining, as applicable, process improvement of the PET (Process Execution Team) Formulation Department, including digital systems/platforms such as: AZ-SHE System, SAP (Finance, Maintenance, Calibration), Asset Life Cycle Management, Site Master Plan, Department Scorecard, with all sub-systems related to collect the data, Key Performance Indicators, dashboards, SABA and others. Lean Champion for the PET Formulation, promoting a continuous improvement culture. Works with the implementation and monitoring of projects/process improvements, including the development of Business Cases (benefit, return on investment, impact, etc). This role serves as the Maintenance Facilitator for the PET. Typical Accountabilities
Education, Qualifications, Skills and Experience Essential Education/Experience: Bachelor's degree in mechanical or electrical Engineering with a minimum of six (6) years related experience and/or training. Thorough knowledge of the pharmaceutical/medical device industry with emphasis in manufacturing, packaging, utilities, and related equipment (including automation). Project management experience and proficiency required. Knowledge and understanding of validation and qualification principles, project management, and change control principles. Ability to understand and utilize financial analyses to make good decisions in a manufacturing environment. Language: Fully Bilingual (English and Spanish) Ability to read, analyze, and interpret general business (Business acumen), professional industry trend, including SHE area /technical/GMP and government regulations. Ability to write business case project proposals, plans, budgets and relate project documents. Ability to write technical (both high and low level) specifications, procedures, plan, and reports. Ability to effectively present technical information and respond to questions from group of peers, managers, and customers/stakeholders. Digital Literacy: Working knowledge of MS Windows Operating Systems. Windows applications such as Word, Excel, Access, Power Point and Project, among others. Working knowledge on SAP, and GVLMS. Desirable
Why iPR Pharmaceuticals? At iPR Pharmaceuticals we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. A culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare. Next Steps - Apply today! To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them. iPR Pharmaceuticals embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. | |