Associate Director, Technical Operations Automation

Associate Director, Technical Operations Automation (Hybrid) Join to apply for the Associate Director, Technical Operations Automation (Hybrid) role at Merck Job Description The Associate Director, Automation within Global Clinical Supply (GCS) is responsible for developing and executing a systems and process automation strategy to support new and existing operations and supply technologies, capabilities, and performance monitoring. This role will partner regularly with Technical Operations and Capital Projects to ensure the compliant execution of automation-related aspects of our projects and will also lead the execution of projects within Technical Operations and upskill personnel on the basics of automation. Responsibilities Lead startup of systems-related aspects of new operational facilities and equipment. Lead system-related aspects of new technology deployment such as system development lifecycle (SDLC), assessments of data integrity, privacy, risk, and other aspects necessary for GxP use. Implement automation solutions, including both platform technologies and associated analytics, reporting, and visualization capabilities. Develop and complete appropriate system validation, Change Control and testing documentation, ensuring compliance with all requirements. Support systems upgrades/maintenance, and new software/systems install. Review automation documents, preventive maintenance, and Standard Operating Procedures to ensure compliance with Good Manufacturing Practice and safety. Partner with business areas to develop processes to enable use of technology & equipment. Develop and support corrective actions for investigations related to automation or IT systems. Conduct or support automation system-related investigations and implement necessary CAPAs. Qualifications Education Minimum Requirement: Bachelor's degree in Information Technology, Engineering, Scientific, or related field. Required Experience And Skills: At least 7 years of experience in an information technology and/or operations role within the pharmaceutical industry. Experience with pharmaceutical facility and equipment commissioning, qualification, and validation (CQV). Development and execution of equipment and facility automation-related CQV strategies. Strong compliance mindset and understanding of cGMP, including FDA and EMEA. Works effectively across boundaries to build strong collaborative relations with other groups. Direct support of validation activities and compliance-related requirements functions. Willing to constructively challenge the status quo and explore continuous improvement opportunities. Strong abilities in Stakeholder Management and building and strengthening cross-functional networks. Excellent communication skills. Preferred Experience And Skills: Experience with Operational Excellence methodology e.g. Six Sigma and Lean methods principles and tools. Leadership of cross-functional teams through project planning, execution, monitoring, and closeout phases to deliver successful completion to project target milestone dates. Experience with SAP or other production software. Networking, Virtual Machines, Database management and other general OT & IT administration. EEO Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. Hybrid Work Model Effective September 5, 2023, employees in office-based positions in the U.S. will be working a hybrid work consisting of three total days on-site per week, Monday - Thursday, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence. Salary and Benefits Salary range: $126,500.00 - $199,100.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits including medical, dental, vision, health care and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. How to Apply You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. Requisition ID: R . #J-18808-Ljbffr