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Quality Engineer; Pharmaceutical

Job in Aurora, Kane County, Illinois, 60505, USA
Listing for: 6AM City, LLC
Full Time position
Listed on 2026-07-10
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Quality Engineer (Pharmaceutical)

Job Description

Job Title: Quality Assurance Engineer

Department: Quality

Reports To: Director of Regulatory Affairs & Quality

Summary: Leads quality assurance activities for medical device, over-the-counter, and prescription drug products.

Essential Duties and Responsibilities

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Interprets Code of Federal Regulations (21 CFR parts 211 and 820), ISO 13485, and other regulatory requirements and updates internal procedures to be compliant.
  • Manages the Corrective and Preventive Action (CAPA) program by investigating issues that have or may cause a product nonconformance and require actions to prevent reoccurrence. Determines the strategy for corrections, corrective actions, and preventive actions. Implements or oversees the implementation of these resolutions. Verifies implementation and effectiveness of actions taken. Documents all activities of the CAPA process in CAPA reports.
  • Conducts Out of Specification (OOS) investigations for nonconformances related to DTI’s manufacturing and filling operations. Where applicable, requests investigations and/or corrective actions from DTI’s suppliers. Supports and reviews laboratory OOS investigations to provide independent quality oversight of laboratory testing.
  • Reviews and supports investigation activities for the resolution of customer complaints.
  • Provides support on quality assignments relating to the development of internal procedures, training, and interpretation of existing and new international regulations.
  • Reviews product design, label or other changes for impact on quality.
  • Reviews product labeling and claims for compliance to applicable regulations.
  • Complies with cGMP, EHS guidelines, and all working procedures assigned to the position.
  • Performs other tasks, as assigned.
Supervisory Responsibilities

None.

Qualifications

Education and Experience: Bachelor’s degree (science‐related discipline preferred) with 2 years relevant experience. Master’s degree is preferred. Regulatory Affairs Professional certification preferred.

Language

Skills:

Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.

Mathematical

Skills:

Ability to calculate figures and amounts such as proportions and percentages.

Reasoning Ability: Ability to carry out instructions furnished in written, verbal, or diagram form.

Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.

Pay Range: The Quality Assurance Manager is an exempt position that is paid semimonthly. Pay rate will be dependent on a number of factors including but not limited to knowledge, skills, and experience.

EEO Statement: Dental Technologies Inc. is proud to be an equal opportunity employer.

Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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