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Cencora

Distributes medicines and supports patient care

Quality Manager: Documentation and Training

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeColumbus, OH, USANo salary listed

About the Job

Requirements

  • Training in fields such as business administration, marketing, or computer sciences, generally obtained through a four-year Bachelor's Degree program, or an equivalent combination of experience and education.
  • A minimum of five years of experience in a regulated industry such as pharmaceutical, medical device, or biologics.
  • Knowledge of FDA regulations.
  • Experience with an electronic Quality Management System (eQMS).
  • Ability to lead and manage individuals.
  • Ability to develop and maintain cooperative working relationships.
  • Good verbal and written communication skills.
  • Proficiency in Microsoft Office applications.
  • Strong organizational skills for prioritizing workload and responsibilities.
  • Ability to handle multiple projects and a variety of tasks simultaneously.
  • Ability to work in a fast-paced environment and deliver projects and requests on time with respect to established timelines.

Responsibilities

  • Manage the Documentation and Training department, including design, planning, and implementation of onboarding methodologies, standards, programs, policies, and procedures.
  • Manage and administer the electronic Quality Management System (eQMS).
  • Consult with functional leaders to identify, prioritize, and facilitate specific training needs.
  • Lead, design, and implement effective training programs to close identified gaps.
  • Evaluate and monitor the effectiveness of training programs continually.
  • Create a training and development strategy to implement learning solutions across departments within the organization.
  • Lead the New Hire training team to ensure new team members are ready to begin on-the-job training.
  • Provide reports and updates to executive management regarding the status of training and documentation as required.
  • Ensure mandated compliance training programs related to cGMP/FDA, OSHA, DEA, and Cencora Compliance are current for all required team members.
  • Provide guidance to all departments on training programs and delivery methodologies, including instructor-led classroom, structured hands-on on-the-job training, independent study, and e-learning modules.
  • Design, execute, and evaluate continuous improvement to the Compliance Orientation Training Program.
  • Provide required input during audits and inspections regarding facility training and documentation practices.
  • Ensure all associates follow cGMP and safety procedures.
  • Perform related duties as assigned.

Desired Qualifications

  • Three or more years of leading teams and/or management experience is preferred.

About the Company

Cencora

Distributes medicines and supports patient care

Cencora buys and distributes medicines for pharmacies, hospitals and physician practices, while helping drug manufacturers bring treatments to patients. Its businesses combine wholesale supply networks with specialty distribution for complex therapies and services that support prescribing and patient access. Customers order medicines through its distribution systems, and its teams manage sourcing, storage and delivery alongside pharmacy operations and manufacturer support. It earns revenue from pharmaceutical sales and fees for logistics and healthcare services. The parent company was formed in 2001 through the merger that created AmerisourceBergen, adopted the Cencora name in 2023, and is headquartered in Conshohocken, Pennsylvania.

Company size
10,001+
Company stage
IPO
Headquarters
Conshohocken, PA
Founded
2001

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