Quality Assurance Specialist
1st RD. Cleveland, OH 44101 US
Job Description
Position Overview
Â
The Quality Assurance Specialist is responsible for supporting quality system processes and maintaining high standards of compliance, documentation accuracy, and process control. Â
Â
Duties & Responsibilities
Key responsibilities include, but are not limited to:
-
Generate, review, correct, and archive documents supporting Good Manufacturing Practice (GMP) production activities.
Â
-
Conduct internal and external audits as assigned.
Â
-
Review and release raw materials, intermediate products, and finished goods; assist with incoming material and container inspections.
Â
-
Review and approve OOS (Out of Specification), deviations, nonconformances, and investigations.
Â
-
Coordinate CAPA, OOS, deviation, nonconformance, and investigation activities.
Â
-
Ensure compliance with current SOPs and quality system requirements.
Â
-
Assist with investigations and support resolution of product quality issues to enhance operational efficiency.
Â
-
Create, revise, and approve standard operating procedures and work instructions.
Â
-
Review and approve SOPs, protocols, and reports as required.
Â
-
Coordinate and/or deliver GMP and SOP training.
Â
-
Generate, track, and publish quality system metrics to support continuous improvement initiatives.
Â
-
Scan and archive GMP records and documentation.
Â
-
Support Quality Control Laboratory functions such as calibration and product release activities.
Â
-
Provide assistance to Environmental, Health, and Safety programs as needed.
Â
-
Perform other duties as assigned by the Quality Assurance Manager.
Â
Â
General Requirements
-
Bachelor’s degree in a scientific discipline or equivalent experience.
Â
-
Minimum of 2 years' experience in a cGMP/FDA-regulated environment (preferred) and working with ISO 9001 within Quality Assurance or Compliance functions.
Â
-
Proficiency in Microsoft Office, especially Excel.
Â
Â
Skills, Qualifications & Experience
-
Strong knowledge of ISO 9001:2015, ISO 14001:2015, cGMP, CFR 210/211, FDA requirements
Â
-
Experience in a manufacturing environment (chemical manufacturing or processing preferred).
Â
-
Familiarity with Statistical Process Control (SPC) and relevant software tools.
Â
-
Ability to evaluate and quantify cost of quality using data-driven KPIs.
Â
-
Strong project management, time management, and conflict-resolution skills
Â


