Merck
Associate Director, Engineering, Maintenance & Utilities
We're seeking an exceptional leader to join our team as an Associate Director, Engineering, Maintenance & Utilities. As a leader in our team, you'll have the opportunity to make a significant impact on our operations and drive business results. As a member of the Engineering, Maintenance, & Utility Department, the HEPA Certification Associate Director is accountable for the management of the HEPA certification personnel and program supporting our Manufacturing Division at the West Point, PA site. This group is responsible for improving asset reliability and manufacturing capacity by providing technical support in the field on engineering resolution of manufacturing mechanical or automation problems, processes incompliance with GMP, safety, and environmental regulations. Accountability Ensure that area objectives are achieved while reliably supplying quality product at a competitive cost consistent with our company, Regulatory Agency, and State and Local code requirements for quality, good manufacturing practices (GMP), equal employment opportunity, finances, labor, employee, environment, and safety; Tactical and strategic area management, including collaboration with indirect staff; Promote the behaviors and principles that drive continuous improvement. Duties Compliance - Responsible for creating and sustaining a culture that ensures that compliance (Safety, Environment, cGMP, etc.) are imperatives for the business. Responsible for establishing a Right First Time culture by reducing waste and constantly driving continuous improvement. Responsible to review and approve compliance documents, as per procedures or need. Supply - Lead area daily walkthrough. Exercise independent judgment and decision making to ensure quality product is reliably produced while managing cost. Responsible for area supply performance metrics (Schedule Adherence, Release on Time, Customer service performance, Product Lead Time, etc.). Continuous Improvement - Accountable for developing a company Production System (MPS) and continuous improvement culture while achieving MPS Targets and business results for the area. Develop strategic initiatives related to the manufacturing process, equipment, and human resources in support of long range operating plans. Report area monthly metrics and any action plans to address gaps to the IPT Leadership team. Identify, prioritize, and champion improvement projects to improve process efficiency, cycle time, and yield, reduce process variability, and eliminate waste. Financial Stewardship
Responsible for development and management of the area operating budget as defined with the profit plan. Accountable for meeting the operating budget and continuously reducing cost. Ensure members of the area have business acumen and understand how they may impact business finances. People Management
Responsible for creating and sustaining a highly engaged workforce through utilization of the companys Leadership Behaviors and Inclusion. Provide coaching on professional development and career paths. Provide timely feedback and performance evaluations for direct reports after obtaining the relevant input and evaluation. Provide feedback and input on performance evaluations for indirect staff. Support IPT Talent Management. Qualifications: Essential: Required: Bachelor's Degree in Business Administration, Science, Engineering or another technical field Minimum (6) years' experience in more than one functional area, such as Operations, Quality, Technical Operations, Technology, Engineering, Maintenance, and/or Supply Chain. Experience with HEPA certification Concurrently, minimum (2) years of line experience, with responsibility for direct reports. Preferred: Minimum of (2) years' experience in relevant manufacturing or processing (aseptic/sterile, bulk, solid oral dosage, packaging, etc.) Demonstrated knowledge of High Performing Organization tools and methodology, including MPS/lean processing Demonstrated ability to create an engaged workforce using Inclusion as the How Demonstrated experience of interacting with site, divisional or regulatory audits Demonstrated success with Talent Management Working Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis, knowledge in reliability engineering (including asset life cycle management). Computerized Management Maintenance Systems SAP), and CMRP certification desired.
We're seeking an exceptional leader to join our team as an Associate Director, Engineering, Maintenance & Utilities. As a leader in our team, you'll have the opportunity to make a significant impact on our operations and drive business results. As a member of the Engineering, Maintenance, & Utility Department, the HEPA Certification Associate Director is accountable for the management of the HEPA certification personnel and program supporting our Manufacturing Division at the West Point, PA site. This group is responsible for improving asset reliability and manufacturing capacity by providing technical support in the field on engineering resolution of manufacturing mechanical or automation problems, processes incompliance with GMP, safety, and environmental regulations. Accountability Ensure that area objectives are achieved while reliably supplying quality product at a competitive cost consistent with our company, Regulatory Agency, and State and Local code requirements for quality, good manufacturing practices (GMP), equal employment opportunity, finances, labor, employee, environment, and safety; Tactical and strategic area management, including collaboration with indirect staff; Promote the behaviors and principles that drive continuous improvement. Duties Compliance - Responsible for creating and sustaining a culture that ensures that compliance (Safety, Environment, cGMP, etc.) are imperatives for the business. Responsible for establishing a Right First Time culture by reducing waste and constantly driving continuous improvement. Responsible to review and approve compliance documents, as per procedures or need. Supply - Lead area daily walkthrough. Exercise independent judgment and decision making to ensure quality product is reliably produced while managing cost. Responsible for area supply performance metrics (Schedule Adherence, Release on Time, Customer service performance, Product Lead Time, etc.). Continuous Improvement - Accountable for developing a company Production System (MPS) and continuous improvement culture while achieving MPS Targets and business results for the area. Develop strategic initiatives related to the manufacturing process, equipment, and human resources in support of long range operating plans. Report area monthly metrics and any action plans to address gaps to the IPT Leadership team. Identify, prioritize, and champion improvement projects to improve process efficiency, cycle time, and yield, reduce process variability, and eliminate waste. Financial Stewardship
Responsible for development and management of the area operating budget as defined with the profit plan. Accountable for meeting the operating budget and continuously reducing cost. Ensure members of the area have business acumen and understand how they may impact business finances. People Management
Responsible for creating and sustaining a highly engaged workforce through utilization of the companys Leadership Behaviors and Inclusion. Provide coaching on professional development and career paths. Provide timely feedback and performance evaluations for direct reports after obtaining the relevant input and evaluation. Provide feedback and input on performance evaluations for indirect staff. Support IPT Talent Management. Qualifications: Essential: Required: Bachelor's Degree in Business Administration, Science, Engineering or another technical field Minimum (6) years' experience in more than one functional area, such as Operations, Quality, Technical Operations, Technology, Engineering, Maintenance, and/or Supply Chain. Experience with HEPA certification Concurrently, minimum (2) years of line experience, with responsibility for direct reports. Preferred: Minimum of (2) years' experience in relevant manufacturing or processing (aseptic/sterile, bulk, solid oral dosage, packaging, etc.) Demonstrated knowledge of High Performing Organization tools and methodology, including MPS/lean processing Demonstrated ability to create an engaged workforce using Inclusion as the How Demonstrated experience of interacting with site, divisional or regulatory audits Demonstrated success with Talent Management Working Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis, knowledge in reliability engineering (including asset life cycle management). Computerized Management Maintenance Systems SAP), and CMRP certification desired.