Specialist I, Quality Operations

Enable Injections

Enable Injections

Operations, Quality Assurance

Posted on Apr 27, 2026

Title: Specialist I, Quality Operations

Description:

Location: Onsite

Status Type: Full Time

QUALIFICATIONS

Required:

  • Bachelor’s Degree or equivalent combination of education, training, and experience.

Preferred:

  • Audit report writing skills
  • Strong communication skills
  • Strong problem-solving skills
  • Strong interpersonal skills
  • Understanding of product complaint requirements
  • Some understanding of device and/or pharmaceutical regulatory and compliance requirements

Skills & Competencies:

  • Strong computer skills including Microsoft Office and databases/excel spreadsheets
  • Knowledge of e-mail/scheduling software application
  • Ability to learn and utilize future software/applications as it is deployed
  • Ability to adapt to change and handle unexpected situations with close guidance.
  • Accepts direction on how to adapt approach to changing situations.
  • Ability to follow defined procedures
  • Ability to stay focused on tasks, organize, compare, interpret basic data, and assess problems with guidance.
  • Work to acquire and develop new skills
  • Ability to collaborate and maintain cooperative work relationships with others.
  • Engages colleagues with the Enable Values in mind
  • Ability to maintain a positive attitude, show empathy for others, and always do the right thing
  • Good time management skills

Physical Requirements:

  • Must be able to remain in a stationary position for extended periods of time
  • Ability to lift and lower boxes of documents or handle equipment weighing up to 25 lbs.
  • Ability to constantly operate a computer and other office equipment, such as printer, telephone, etc.
  • Position requires being physically present on the premises during regular company hours or as approved by management.

RESPONSIBILITIES:

  • Assist with Batch Disposition responsibilities for Materials, Components, and Sub-Assemblies
  • Assists with the assembly and execution of Management Reviews
  • Support Corrective and Preventive (CAPA) and Nonconformance programs
  • Assists Quality Management in providing guidance on compliance related issues
  • Ensures product safety, regulatory compliance, and compliance through proper management of quality documents and quality records
  • Updates quality procedures and work instructions, when required
  • Identifies areas of opportunity to reduce waste and improve efficiency
  • Assist with Management Review metrics and documentation
  • Provides assistance during Regulatory and customer audits


Nearest Major Market: Cincinnati