Job Description
Description
Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where our company has codified its legacy for over a century. Our company's success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
The Maurice R. Hilleman Center for Vaccine Manufacturing is located in Durham, NC. The facility established in 2004, manufactures our lifesaving vaccines in bulk and finished forms. Due to the importance of this facility in our Vaccine Manufacturing network, the facility has seen rapid growth in production volumes and new employees over the last several years; currently Durham employs 1,000+ people.
Vaccines Science & Technology (S&T) in our Manufacturing Division is seeking a highly motivated individual for the role of Associate Director within the Vaccine Manufacturing Facility (VMF) Technology organization. The Technical Operations Associate Director will collaborate cross-functionally within the Integrated Process Team (IPT) to provide technical support to the manufacturing shop floor within the vaccine fill-finish facility. This role involves leading multiple individual contributors, driving change management, supporting complex investigations, and demonstrating deep subject matter expertise during proactive problem solving and troubleshooting. The Associate Director will be a key contributor to meeting our key strategic priorities associated with safety, compliance, delivery, cost and people.
Responsibilities (may include, but not limited to)
This role will serve as one of the Associate Directors within Technical Operations and will be responsible for the Thaw, Pool, and Filling operations within the VMF IPT.
Provide leadership and direction for a team of highly technical individual contributors and be responsible for all human resource activities including one-on-one meetings, team development, hiring, talent assessment and performance reviews.
Coordinate responses to process upsets, including short-term mitigation to return to service and assessment of product impact
Prioritize projects, timelines, and resource allocation to improve safety, compliance, stability, cost and capacity
Approve investigations, SOPs, change requests, protocols, CAPAs, Quality Risk Assessments
Support of regulatory audits with coaching Subject Matter Experts (SMEs) and presenting to auditors
Collaborates with internal/external partners, e.g. other sites, CMC-Regulatory, Procurement, Supply Chain / Planning, Quality Center of Excellence (CoE), etc.