Performs analyses, inspection, and tests of raw materials, packaging materials, quantitative assays on samples, and/or finished products from manufacturing, to ensure quality standards and compliance to customer and regulatory requirements, and tolerance specifications for the chemical or physical property. Performs a variety of qualitative tests or qualitative assays on samples, and to aid in maintenance and certification of test instruments and apparatus to ensure compliance. Performs required inspections, checks, analysis and documentation of studies. Prepares and monitors quality statistics and reports. Reviews production records for conformance to procedures. Conducts non-conformance tests of manufactured, packaged or tested product.

Major Responsibilities:

1. Supports the production process to prevent downtime (in-process audits and incoming inspection)

2. Operates in accordance with established policies and procedures to support production and quality commitments

3. Effectively communicates with managers, supervisors and technicians regarding quality matters

4. Maintains Novartis values and behaviors

5. Completes QC/Surveillance audits and/or incoming material release, according to standard operating procedures.

Key Performance Indicators:

Production indicators: In-process audits completed, IQA cycle time Quality Indicators: Final product release with no deviations. Regulatory Indicators: Maintain regulatory compliance with governing body requirements and maintain proper documentation.

Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to [email protected] and let us know the nature of your request and your contact information.

Company Name
Huntington, WV 25702



Minimum : High School diploma. Excellent knowledge of written and verbal English.


Minimum : 1 year directly related experience.
Preferred : Manufacturing / QA experience. Quality mindset. SAP knowledge. Proficient in Excel/Word. Knowledge of the Change control process.

How to Apply

Quality Control Technician - 2nd Shift (