Senior Manager Automation

Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr Manager Automation to join our IT PMO and Business Operations team in Limerick in an onsite position. In this role, you will oversee the group responsible for the configuration and installation of new biopharmaceutical process and manufacturing laboratory equipment while collaborating with personnel in the Automation Department. This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide. When & where: • Location: Raheen, Limerick Discover your role: • Building and leading a team of OT engineers/specialists; providing mentoring, performance management, and career development • Responsible for ensuring training, development, and compliance of direct reports and subordinate staff • Coordinating activities related to configuration and support of laboratory and process equipment • Acting as a Subject Matter Expert during regulatory inspections and internal investigations • Managing projects related to process equipment and laboratory software automation • Leading the workflow within automation Support groups; setting priorities and vetting requests for automation services • Partnering with the Validation Department by providing technical personnel for configuration and qualification of equipment • Supporting the regulatory compliance and efforts through audit participation and quality systems development • Collaborating with Manufacturing, QC and Maintenance as a technical advisor • Ensuring integrity is maintained for data generated during manufacturing and testing of drug product • Owning the architecture and lifecycle management of OT equipment • Leading investigations and CAPAs related to OT system deviations, outages, or data integrity events • Managing OT-related capital and operational budgets, vendor relationships, and service contracts This role requires: • Requires BS/BA in Science, Engineering or Software Programming and 8+ years of experience (5+ years of supervisory experience) • Current knowledge of cGMP biotech/pharma operations, industry trends, regulatory and quality policies, procedures and documentation methods • Solid understanding of software Design Lifecycle and Quality Risk Management • Demonstrated project management expertise • Proven capability in resolving complex inter-departmental and organisational issues • Strength in influencing leaders in cross-functional roles regarding automation solutions #IRELIM #JOBSIEST #LI-Onsite Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.   Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employ