Quality Assurance Manager

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere.

Apply today!

Sunday
- Thursday 10:30PM- 7:00AM (or complete)

Please note, flexibility in schedule will be required based on business needs, this can include working different hours or days.

This position is located onsite at our facility in Columbus, OH. There is no option for remote or hybrid work.

• Responsible for quality activities in each packaging room, coordinating with QA Packaging Technicians to direct activities in the packaging rooms, and maintain a regular visible presence on the floor.
• Has the overall responsibility for the performance of the QA Technicians, including quality, safety, and customer service on a given shift.
• Works closely with Operations Managers to ensure product produced meets all applicable standards.
• Maintains Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs) related to the quality of our packaging lines.
• Responsible for quality, operations, safety and security of the facility.
• Demonstrates an understanding and articulates to the team of quality concepts such as: cost of quality, analytical metrics and / or statistics, trending, quality planning, validation, CAPA and problem solving.
• Support production to meet customer delivery requirements on time, first time, every time.
• Responsible for ensuring that daily quality and manufacturing targets are met.
• Participant and leader of project teams.
• Responsible for overseeing CI activities on assigned shift to promote improved efficiency and effectiveness of quality process, including completion of gap assessments and actions plans. Also includes oversight of 5S and other lean activities on the shift.
• Responsible for various record keeping activities including but not limited to batch records and shift reports. Competent in editing batch records and compiling constructive narrative information pertaining to batch production. Reviews batch record for completion and proper documentation.
• Excellent management skills to supervise personnel and interact with other departments at all organizational levels. Facilitates team meetings and reviews.
• Demonstrates ability to perform investigations / root cause analysis and develop corrective actions.
• Creates an environment of inclusion and engagement.
• Inspects and releases quarantined packaging material or rejects. Inspects finished drug product and verifies reconciliation of labels and inserts.
• Over sees and performs on-the- job quality training.
• Assists in performance management review programs.
• Responsible for the hiring, training, development, and mentoring of QA Technicians. Coordinates shift staffing with Sr. QA Manager and other leadership personnel.
• Completes accident/incident reports and conducts investigation. Participates in follow-up meetings and CAPA.
• Assists in writing/revising and maintaining task, department, and general SOPs.
• Reviews and approves associates time and attendance for payroll. Approves/Denies time off request, ensuring that staffing is maintained appropriately to allow for Safe and Quality focused production to meet business demands.
• May provide backup coverage for other managers as needed.
• May be required to work various shifts, hours and weekends.
• Performs related duties as assigned.

• Requires a bachelor’s degree with at least five (5) years of experience in the Quality field or equivalent combination of experience and education.
• A minimum of one (1) year experience in leading and directing the work of others.
• Previous project management experience is preferred.

• Ability to lead and manage teams.
• Ability to communicate effectively both orally and in writing.
• Ability to develop and maintain cooperative working relationships with others across all levels of the organization.
• Strong organizational skills; attention to detail.
• Proven experience successfully managing projects
• Ability to resolve issues effectively and efficiently
• Strong problem solving skills
• Ability to use good judgment in order to carry out detailed instructions.
• Ability to work independently and lead others.
• Ability to handle a variety of tasks simultaneously.
• Ability to make decisions and implement changes as directed.
• Strong computer skills including intermediate to advanced skills in MS Office software.
• Experience with document control software is preferred.
• Intermediate understanding of KPIs for quality manufacturing operations.
• Strong knowledge of cGMP Regulations Part 210/211 and 820 as well as DEA regulations.
• Knowledge and understanding of pharmaceutical production and quality concepts and procedures is required.

We provide compensation,…