SR MANAGER, VALIDATION

Job Summary The Sr.
Manager of Validation is responsible for supporting the facility with technical expertise, problem solving abilities, and facility qualification.
This includes overseeing all phases of validation projects from project proposal, concept design, commissioning, equipment validation, program maintenance and decommissioning.
They also provide technical support and maintain the site Validation Master Plan and revalidation requirements.
They are also responsible for formulating, reviewing, and approving qualification protocols related to; equipment, computer systems, facilities, and utilities.
The Sr.
Manager of Validation is part of the Senior Management Leadership team responsible for the plant's overall achievement and results.
They work collaboratively with the various teammates to implement operational improvements that support focus on improving quality, productivity, labor, and cost saving efficiencies.
This role is also key in ensuring a team culture that is driven by safety, discipline, transparency, and accountability.
Responsibilities

Responsible to establish the Validation strategy for new processes/equipment and translates those requirements to appropriate validation protocols and standard operating procedures
Develops, maintains, and updates the Validation Master Plan (VPM) for the overall project
Ensure that Validation Department conducts in accordance with current Good Manufacturing Practices, the company's quality goals and sustainable compliance initiatives, as well as the company's mission, vision, and values
Oversees activities of the project personnel to include assignment of tasks, scheduling, and coordination across the various plant functional areas
Responsibilities for qualification of new equipment/processes, computer-related system qualification and calibration program management
Reviews detailed plant layouts, procedures, and equipment specifications (URS) to ensure the project progress and regulatory compliance
Conducts and/or participates in deviation investigations to identify root causes and define corrective and/or preventative actions (CA/PA), maintaining compliance within the company
Communicates and reports the status of each project to the management and department that sponsors the project.
Communication includes project status, milestones, and any additions to the scope of the project as well as regular updates in the form of written reports and oral presentations to senior management
Works as part of a multi-disciplined team
Directs validation projects by coordinating contractors or site personnel, reviewing the generated reports, and implementing any changes or recommendations that result from the studies
Revise, review, and approve existing SOPs and develops new SOPs for systems/equipment
Manage creation of execution and adherence to the Departmental Budget
Mentors and develops staff regarding teamwork, validation techniques and procedures to ensure cGMP compliance
Communicates metrics, trends, and data summaries to senior management using a variety of media:
intranet, reports, and presentations
Interfaces with the FDA or other regulatory body relative to equipment and control system issues or critical processes as the primary Validation interface (SME)
Ensure department personnel are aware of Fresenius Kabi's Environmental and Energy Management
System including Environmental and Energy Policy.

Responsible for ensuring that Health, Safety and Environmental requirements are met under the requirements of ISO 14001 Environmental Management System and ISO 50001 Energy Management System.
Supports the needs of a 24 hour production facility
REQUIREMENTS

Bachelor's degree in science or engineering field or a combination of education, training, and experience.
10 years of related experience in a cGMP facility
5 years of leadership experience with direct reports
Experience in cGMP CA/PA, root-cause analysis, risk assessment, and investigation tools and techniques
SME oversite of all disciplines within Validation:
Commissioning and Qualification (IQ/OQ/PQ), Sterility Assurance, Cleaning Validation, Computer Systems Validation, Validation Maintenance/Risk Management, and Application of Statistical Technique
Current knowledge and understanding of cGMPs, industry guidance, and aseptic manufacturing, room classifications and airflow pattern testing tools and techniques, depyrogenation/sterilization requirements and techniques and associated statistical analysis tools and methods.
PC literate with standard Office application (Word, Excel, PowerPoint, Project, Access)
Previous experience and participating in with FDA, EU, ICH regulatory agency inspections
Must have excellent verbal skills.
The ability to communicate clearly and extemporaneously to a variety of audience types, included regulatory agencies.
Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company match, andwellness program.
Fresenius Kabi is an Equal Opportunity/Affirmative Action employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.